Lesson of the week – Dorothy S. Amanor-Boadu

How I, a sickle cell anaemia woman, hydrate myself intravenously at 36000 feet

Dorothy Amanor-Boadu SRN SCM
The Elite Nursing Agency & Health Promotion Centre P O Box AN 6519, Accra-North, Ghana. [Email: elitensg@yahoo.co.uk]

I was born with sickle cell anaemia [‘SS’]. My health, which had been pretty stable until a serious sickle crisis was precipitated by (I am embarrassed to say this) a dietary  indiscretion – overeating. This first severe crisis happened at the age of 21 when I was a nurse at the Nursing Training College, Korle Bu Hospital, Accra, and almost cost me my life. If it had not been for the expertise and dedication of my doctors Dr. F.I.D. Konotey-Ahulu and Dr. Alexander Bruce Tagoe who stayed on duty for 3 days with no rest, I would not be here to write this story.

They did not go home during my critical stage complicated by thrombo-embolism brought on after a ‘cut down’ on my right ankle, performed due to inability to find any veins during the crisis. I was in hypovolaemic shock. Overeating is a known precipitating cause of sickle cell crisis

[1]. I went on to qualify as a State Registered Nurse in 1976, and worked as a Staff Nurse in charge of the Dermatology Department and Institute of Clinical Genetics Sickle Cell Clinic at Korle Bu Hospital for a little over a year. I was specially chosen to work with the sickle cell patients because my doctors thought I could empathise with them, which I did. When they were in pain, I identified with them, and wiped their brow.

I then left for the UK, a cold country, where I underwent Midwifery training at the Jessop Hospital for Women in Sheffield. I chose to do midwifery in addition to my SRN, because my mother was a well-known midwife in Accra. After this, I proceeded to the USA to specialise in Oncology Nursing, and even wrote a book

[2]. In the USA, I began to have about two hospital admissions per year for sickle cell crises with hospitalisations lasting up to 10 days at a time. All other crises occurring approximately every three months or so, lasting up to four days, were treated at home. I am now over 50 years of age, but from 1992 or thereabouts, my health gradually, but noticeably declined progressively resulting in more frequent and more severe episodes of crises. This could be dated from when I (foolishly) indulged in overeating again and ended up with an extremely severe crisis in Georgia. During this crisis, I developed a bedsore on the heel of my left heel in less than 18 hours of admission; in fact, it occurred while still in the emergency room! This crisis, occurring after I had left the restaurant with my husband and daughter where we had all enjoyed a Chinese dinner, was the second most severe in my life. [I had been taught to look for a husband who was ‘AA’, and I found one, and we have a daughter with ‘AS’ Haemoglobin Type, just like my parents]. Within 4 hours after the Chinese dinner, I presented myself at the emergency room in severe pain all over the body. Being a nurse, I often directed the doctors what to do. Quite a few times I asked them to ring Dr Konotey-Ahulu in London who would always ask the doctors to listen to me [Oh the wonder of Mobile Phones! Felix was always contactable].

I had never encountered any problems with flying on the ‘long haul flights’ (e.g.6- 9 hours from Ghana to UK/ USA and vice versa) until I reached the age of 40 years; then ‘all hell broke loose’.

Crises became even more frequent. I found it difficult to avoid the precipitating causes like late nights and (dare I say it?) too much good food.

Blood vessels for intravenous fluid (not blood usually) in crisis became more and more difficult to find, so a central venous access device was implanted into my chest which connects to a major blood vessel (superior vena cava) which, when in use, permits blood to be drawn from, and administration of intravenous drugs and fluids (drip). The device is also known as a ‘portocath/infusaport’ (depending on brand inserted). I have had this device over the past fifteen (15) years or so (each device being surgically implanted and removed/changed should infection, leakage or blockage be noted). Mine has been changed five times so far at an interval of every 2- 5 years. My port was initially inserted following an extremely bad crisis where I went into shock and no peripheral veins could be found anywhere on my body including my feet; any line obtained infiltrated within less than 12 hours. Finally, an intravenous (IV) line was inserted into my neck (central line) as a temporary measure until the port was inserted. (This is generally done in the operating room with a mild general anaesthetic or in the radiology procedures lab/room under fluoroscopic guidance with ‘twilight sleep’ induced (awake, but not fully aware)).

It was not until I went to live in the USA that I decided I had had enough of going to hospital for every crisis not resolved by oral hydration and Paracetamol, or other stronger analgesics. In the USA I found patients could come on a daily basis for intravenous drugs to be administered using the same IV site for up to 3 days or more by attaching a ‘heparin well’ to the butterfly or angiocath.

This gave me the idea of having this venous device inserted for me so I could have my intravenous fluids (drip) administered in the comfort of my own home, rather than on the hard emergency room stretcher and be charged $250.00 per hour for those uncomfortable facilities!

Having convinced my physician (who in America were haematologists) to agree to this, I treated most of my crises at home, administering the IV fluids and drugs knowing I could go on admission with a call to my doctor, if I thought things were not progressing well or I could no longer cope. With the use of the ‘hep well’, I would go to the emergency room to have it inserted (and labs drawn as ordered) and return a few days later when better to have it removed. After the hepwell other venous access devices were developed over
the years, including the ‘Hickman Catheter’ (catheter surgically inserted into a major vessel protruding through the skin with catheter hanging out on the surface), and the ‘Port O Cath’ which is a central venous access device surgically implanted under the skin in the areas of the chest, arm, or groin. I acquired my first one in 1990. When not in use, it cannot always be seen, but since I do not have too much adipose tissue to hide it, mine protrudes, and looks like a little round lump under the skin – I call it my 3rd breast!

This device allowed me to avoid emergency room visits even more. I could now access (stick) myself with the ‘Huber needle’ and hook up my drip without assistance. All I had to do was call my doctor to let him know I was in trouble (i.e. in crisis) and he would call in my prescriptions to the hospital pharmacy. My husband would then pick them up and bring them to me at home, thus bypassing the Emergency Room altogether. Being a nurse, and working in the Haematology/Oncology areas, had really become useful to me in my personal life.

To think that if it had not been for Dr. FID Konotey-Ahulu and Dr. K.A Gbedemah my parents would not have allowed me to become a nurse as the latter thought the profession could prove physically taxing! I am glad I did nursing.

At this stage, I would like to acknowledge the following specialists: Dr. Jeffrey Giguere, in Greenville South Carolina, Dr. Laura de Castro, Durham North Carolina and Dr.Melanie Jacobs, Atlanta Georgia with gratitude for the trust and confidence they had in me to permit me to treat myself with minimal supervision, and without fear that I might become a drug addict and abuse the use of the port.

Well, back to our topic. After having flown on numerous occasions back and forth from the UK to USA and Ghana without incident (the planes by then were all using pressurised cabins and later prohibited smoking also which was helpful), I noticed after the age of 40 that on flights I was now tending to start ‘sickling’ approximately 3-4 hours into the flights. I was advised by Prof. F.I.D. Konotey-Ahulu to hydrate more before and after flights, to eat only a light meal prior to and during the flight, to move about more, and to start using Aerobic Oxygen 15-20 drops to a glass of water three times a day [3], which of course I drink on flights also. Following this advice and to make sure I got through without problems and inconvenience, I requested clearance from the medical department of the carrier I used most frequently (British Airways) for oxygen to be made available to me on the flights and permission for me to administer intravenous (IV) medications and fluids should it become necessary.

This procedure meant my physician and I had to complete a medical form which basically identified my condition and my requirements for the flight (oxygen for which an additional non-refundable charge of $150.00/£200.00 is required) and the physician’s opinion as to my fitness for the flight with confirmation that I did not need to be accompanied. With the assurance that I was a nurse and could take care of myself without assistance, the airline has to date always agreed to my requests.

After travelling yearly over a period of about 4 years, my physicians no longer have to fill forms for my medical clearance – a simple telephone call to the airlines medical division in London, U.K with confirmation of flight itinerary results in a printout attached to my ticket informing airline staff of my diagnosis and requirements always sufficed [Oh thank you British Airways! (and I hope I am not accused of advertising)]. I also request seating at the bulkhead/window (least inconveniencing to other passengers, should drip be required, also more legroom and space to manoeuvre in economy class).

During packing for my intended flight, included in my hand luggage is at least 1-2 litres of IV Fluids, Infusion sets, Syringes of different sizes 10/5/3ml with and without needles, Luer lock caps, adhesive tape, tegaderm dressing, normal saline and heparin flushes, alcohol swabs. Medications as prescribed including tablets and injection Phenergan, Pethidine, Paracetamol, Airtal or Percocet. One or two bottles of IV Ciprofloxacin and a small ‘sharps/biohazard’ container for disposal of needles and glass ampoules are also packed.

Finally, a letter from my physician giving reasons and the need for my possession of needles, lest some busybody security person suspect me of being a terrorist! Just a word here about my experience with pain killers on 3 continents. In Africa, neither Morphine nor Diamorphine are used for sickle crisis. In the USA Diamorphine is banned for clinical use. In the UK, both Morphine and Diamorphine are used for sickle cell crisis. In Ghana, we find Diclofenac, Airtal, and Ketorolac, with plenty of hydration, and occasionally Pethidine very briefly, more than adequate for the severest of crises.

Should I be flying with a carrier whose arrival and departure times are not always reliable a call to the airport to verify that flight is likely to depart on time is made. My goal here is to administer my intravenous fluids no more than an hour before checking in time to ensure adequate hydration for the flight. I have on occasion had to have my flight rebooked due to constant changes in flight departure time. Original departure of one airline that shall remain nameless was for 8pm, changed to 10pm, then 3am. Finally, the plane left without me at 5am. I took the flight 2 days later to get my hydration time right! The moral for other patients reading this article is this: ANTICIPATE PROBLEMS, AND PLAN HOW TO COPE WITH THEM! If necessary, cancel agreed plans (like a flight) in order to save your life.

My normal procedure now before any flight is to pack my bags about two weeks prior to the departure date (generally reduce stress – physical/emotional as much as possible several days/weeks before flight, and increase oral hydration three days before departure). On the date of departure I check in early where possible, return home to rest, take a bath prior to inserting my Huber needle into the centre of the port after cleaning it and an area of approximately 2” circumference with Betadine and alcohol swabs, using sterile technique secure/cover with appropriate dressing – Tegaderm/biocclusive (usually 3”x5”-this is a water repellent dressing applied to secure and protect port from invasion of pathogenic organisms etc) [Picture]. It is possible to shower/bathe without the insertion site becoming wet. Dressing change is required every third day and as necessary. Huber needle (90-degree angled needle) should be changed every 7 days, but should be removed as soon as no longer required for use to avoid risk of infection.

Once ‘hooked up’ I administer 500-1000ml of Dextrose/Saline or Normal Saline over 2-4 hours depending on total amount to be given and how I feel at the time. On completion, the Port is flushed with 10ml saline and 3ml U100 heparin flush, then capped and extension tubing tucked into my ‘bra’. IV infusion/tubing capped off and stored in a new clean self-sealing plastic bag, which is then added to my hand luggage.

Once on board the flight, with any signs of sickling (pain/discomfort) I first request for oxygen which, is either piped directly to my individual seat (from the cockpit) or via small portable tanks supplied by stewardesses. This is administered at 2-4 Litres/min depending on how acute the distress is. After 20 minutes or so, if no relief of symptoms are noted I inform the stewardess of my intent to administer IV Fluids and drugs, and request for a clothes hanger. (Usually at this point there is panic amongst the Air Crew because, despite the clearance printout from the medical department and the Ground Crew having all the details and specifics, the aircrew generally are left with only minimum information such as “they have a medical on board”).

At this point I usually get a visit from the Captain and Chief stewardess. Once everyone gets the fact that there was some miscommunication, I proceed to hang and prime the infusion tubing. The hanger is used to hang the infusion onto an appropriate fixture in front of or above me. Occasionally, depending on location of seat adhesive tape may be required to secure drip at a height to promote gravity drainage. Since the port is already accessed and ready for use all that is required is to flush the extension tubing with saline prior to administering IV medications and hooking up the infusion. Once the rate for infusion is regulated, a little nap with continuous oxygen usually averts any major crisis occurring even if not totally resolved. Most of the time, oxygen is not required for more than 2 hours and IV for 4 hours.

My IV line can be disconnected, flushed and capped off when I feel I no longer need it or at least thirty minutes before landing. To date there have been no complaints or concerns from other passengers. Everyone, crew and passengers alike have been considerate and helpful – willing to change seats where needed.

So now you know how Intravenous fluids can be safely and conveniently self- administered at 36000 feet!

Competing interests: None declared.

Acknowledgement: I thank Professor F I D Konotey-Ahulu for urging me to tell this story to encourage sickle cell disease patients never to give up.

1 Konotey-Ahulu FID. The sickle cell disease patient. Natural history from a
clinico-epidemiological study of the first 1550 patients of Korle Bu Hospital Sickle Cell Clinic. Watford, Tetteh-A’Domeno, 1996, page 122.

2 Amanor-Owusu D. Cancer Chemotherapy Manual. Legon, Accra. Ghana Universities Press, 2002

3 Konotey-Ahulu FID. Sickle-cell disease and the patient. Lancet 2005; 365: 382-83

Legend: Accessed Port covered with Tegaderm dressing. Note pallor of my nail: I have sickle cell anaemia with a cruising Haemoglobin level of 8 grams/dL.

Submitted by:Dorothy S. Amanor-Boadu

BMJ Rapid Response Hip pain in Sickle Cell Disease 8 January 2016

Re: Association of hip pain with radiographic evidence of hip osteoarthritis: diagnostic test study
Re: Association of hip pain with radiographic evidence of hip osteoarthritis: diagnostic test study Nancy E Lane, Thomas M Link, Steven Vlad, Irina Tolstykh, et al. 351:doi 10.1136/bmj.h5983

Rapid Response by Felix I D Konotey-Ahulu (8 January 2016) http://www.bmj.com/content/351/bmj.h5983/rr-2

Hip pain and radiographic signs of osteoarthritis: Sickle cell & other haemoglobinopathy differential diagnosis 

Dr M J Nieuwenhuijse and Professor Rob G Nelissen’s Editorial [1] linked to Kim and colleagues’ paper (doi:10.1136/bmj.h5983) is probably more suited for developing countries where MRI is often unavailable for investigating hip pain and “osteoarthritis” than for the UK, yet the authors appear to have only a Caucasian audience in mind for their message. We know that haemoglobinopathy is the commonest cause of hip pathology in Africa as I pointed out in The Lancet in “Hip disease in Africans” [2]


With every third West African at home and abroad possessing a beta-globin gene variant as Sickle Cell Trait (‘AS’) or Haemoglobin C Trait (‘AC’) we proved conclusively in Ghana that 3 out of every 100 births will have Sickle Cell Anaemia (‘SS’) or Sickle cell Haemoglobin C Disease (‘SC’) [3-9], thereby confirming veracity of the Hardy Weinberg gene frequency Equation p + q + r =1 producing phenotypes p2 + q2 + r2 +2pq + 2pr + 2qr =1 (the square of the gene frequencies) which was exactly what we observed on investigating 1,000 and 13,000 consecutive babies born at Korle Bu Hospital in Accra.[4 5]. Many of these babies grew to develop hip problems that often confused some radiologists [7], and which needed differentiating from Perthes’ disease [10]


Dr Nieuwenhuijse and Professor Nelissen are right to use phraseology like “clinical symptoms suggestive of degenerative hip joint disease” and “asymptomatic degenerative changes” [1] – terms that describe many patients with haemoglobinopathy [7 8]. The authors’ advice “Treat patients, not radiographs” also needs to be heeded because too often we clinicians refer patients for investigation without examining them, using the term “osteoarthritis” when osteo-arthropathy was better. Few Resident Doctors these days on both sides of The Atlantic practice the five cardinal “Introductory Course” drill before sending patients for investigations. These 5 are: 1. History 2. Inspection 3. Palpation 4. Percussion 5. Auscultation. Therefore, in answer to the authors’ question “How should we respond to patients presenting with hip pain?” [1] my first answer would be history: “Do you have hereditary rheumatism?”, using tribal names for sickle cell disease (chwechweechwe, ahututuo, nwiiwii, lakuragbee, etc) [6 7 8]. For many patients HISTORY alone gave me the diagnosis of hip pain. INSPECTION – Before he/she sat down I had observed the limp, and then I looked for jaundice and estimated straight leg raising, leg shortening, and elicited pain on hip rotation. PALPATION – I noted Corrigan’s pulse in my sickle cell anaemia patients and looked for abdominal signs, before pressure for groin tenderness. PERCUSSION: Liver enlarged? Spleen? AUSCULTATION – Precordial systolic bruit made me advise radiologists to comment on heart size, “cod fish vertebra”, and splenic calcification.


There is phenotype variation in incidence [11]: Sickle Cell Disease, ‘SC’ phenotype, has more frequent hip pain than Sickle Cell Anaemia (‘SS’) for the reasons explained elsewhere after personally surveying over 1,200 consecutive patients of all ages [6]. Seventeen of 600 consecutive Hb ‘SS’ ie 2.8% and 40 of 603 consecutive Hb ‘SC’ patients ie 6.6% with hip pain and limp had femoral head problem (p<00.1) [6 7 8 11 12]. Arthritic hip incidence in Sickle Cell Trait (‘AS’) is not different from that in the rest of the population with no ‘S’ gene, unless one’s definition of Sickle Cell Trait was the seriously flawed definition common in American publications where sickle cell disease ‘SC’ was often called Sickle Cell Trait merely because the mother of the patient with symptoms had Negative Sickling Test. Brilliant haematologists have been known not to proceed to haemoglobin electrophoresis when sickling test was negative, thereby missing Hb ‘C’ which, combined with Hb ‘S’ is sickle cell disease, ‘SC’ phenotype. In my 36 consecutive Haemoglobin ‘CC ’patients just the 35th presented with hip pain [7].


Results from cohort studies with varying degrees of expertise cannot be better than careful observation of consecutive patients over many years by the same clinician as in Ghana [7] and West Indies [13]. Both this Editorial [1] and Kim and colleagues’ paper it is linked to (doi:10.1136/bmj.h5983) mention cohort studies which fail to take into account the numerous non-Caucasians as well as white Mediterranean people with sickle cell disease whose hip pain has not alerted doctors to haemoglobinopathy. An exception was Professor Malcolm Milne who once asked me on a postgraduate ward round to examine a Greek patient.

INSPECTION: – Slight icterus. Nails pale. Right shoulder muscle wasting giving angular contour. Straight leg raising – only 450 from the bed on the left side, with pain on hip rotation. PALPATION: Murphy’s sign positive. Corrigan’s sign positive. AUSCULTATION: Precordial systolic bruit. I then announced: “This patient has Sickle Cell beta-Thalassaemia, with gall stones and articular bone necrosis of the right humeral head and left femoral head”. Professor Milne gave me full marks and showed us the detailed blood results from Professor J G Humble confirming the phenotype. But why did I not say Sickle Cell Anaemia (‘SS’), which was also very common in Greece? ANSWER: Because the patient’s nails and conjunctivae were not as pale as I had known them to be in Sickle Cell anaemia. I then announced to the impressed gathering that I knew much about sickle cell disease before I went to Medical School. My parents were among the 1 in 3 very healthy Ghanaians with Hb ‘S’ or ‘C’ Trait, and they produced 11 of us of whom 3 had sickle cell disease. Growing up in the Manya Krobo Tribe I was surrounded by close and distant relatives born with chwechweechwe-hemkom, and who walked with a limp [14]. No cohort studies were needed for my education.

Conflict of Interest: None declared.

felix@konotey-ahulu.com and Twitter @profkonoteyahul
Felix I D Konotey-Ahulu FGA MD(Lond) FRCP(Lond) FGCP, DTMH(L’pool)

1 Nieuwenhhuisje MJ, Nelissen RG. Hip pain and radiographic signs of osteoarthritis. BMJ 2015; 351:h6262 (03 December 2015)

2 Konotey-Ahulu FID. Hip disease in Africans. Lancet 1970; 1: 999

3 Ringelhann B, Konotey-Ahulu FID. Hemoglobinopathies and Thalassaemia in Mediterranean areas and in West Africa: historical and other perspectives 1910-1997 – A Century Review. Atti del’Accademia della Science di Ferrara 1998; 74: 267-307.

4 Gbedemah KA, Acquaye CTA, Konotey-Ahulu FID, Reindorf CA. Haemoglobin phenotype patterns in more than 1,000 consecutive new-born babies in Ghana. Ghana Med Journal 1976; 15: 253-256.

5 Bonney GE, Walker M, Gbedemah K, Konotey-Ahulu FID. Multiple births and visible birth defects in 13,000 consecutive deliveries in one Ghanaian hospital. In Proceedings of the Second International Congress on Twin Studies Part C. Ed Walter Nance. Progress in Clinical and Biological Research 1978; 24B: 105-108.

6 Konotey-Ahulu FID. The Sickle Cell Diseases: Clinical manifestations including the Sickle Crisis. Archives of Internal Medicine 1974; 133: 611-619.

7 Konotey-Ahulu FID. The Sickle Cell Disease Patient: Natural History from a Clinico-epidemiological study of the first 1550 patients of Korle Bu Hospital Sickle Cell Clinic. The Macmillan Press Ltd, London 1991 & 1992 and T-A’D Co Watford 1996.


9 Ringelhann B, Dodu SRA, Konotey-Ahulu FID, Lehmann H. A survey of haemoglobin variants, thalassaemia, and Glucoose-6 Phosphate Dehydrogenase Deficiency in Northern Ghana. Ghana Medical Journal 1968; 7: 120-124.

10 Konotey-Ahulu FID. Perthes’ Disease versus Sickle Cell Disease hip. October 24 2014 BMJ Rapid Response www.bmj.com/content/349/bmj.g5584/rr/778350 or http://bit.ly/1tGmuYm

11 Konotey-Ahulu FID. The spectrum of phenotypic expression of clinical haemoglobinopathy in West Africa. New Istanbul Contribution to Clinical Science 1978; 12: 246-247.

12 Konotey-Ahulu FID. Effect of environment on Sickle Cell Disease in West Africa: epidemiologic and clinical considerations – In SICKLE CELL DISEASE: Diagnosis, Management, Education and Research, Editors Harold Abramson, John F Bertles, Doris L Wethers. Saint Louis 1973 The C V MOSBY Company, pages 20-38.

13 Serjeant GR. Sickle Cell Disease. Oxford, Oxford University Press, 1992.

14. Konotey-Ahulu FID. Sickle Cell Disease in Successive Ghanaian Generations For Three Centuries (Manya Krobo Tribe) 1670 to 1970 – The Human Genome Diversity Project: Cogitations of an African Native. In Human Genome Diversity Project. POLITICS and The LIFE SCIENCES 1999; 18: 317-322.

Competing interests: No competing interests 08 January 2016
Felix I D Konotey-Ahulu Kwegyir Aggrey Distinguished Professor of Human Genetics University of Cape Coast, Ghana Consultant Physician Genetic Counsellor in Sickle Cell & Other Haemoglobinopathies Phoenix Hospital Group, 9 Harley Street, London W1G 9AL
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WORLD AIDS DAY – December 1, 2014

What is AIDS?

Allow me on World AIDS Day to do some self-advertisement which some Akoras may well be pleased I did.

My book “WHAT IS AIDS?” obtainable from Amazon has been commended by some prominent people not only because I was the first person ever to travel through the AIDS afflicted African countries when the Pandemic burst on the world, and interviewed over 120 International Prostitutes on duty, but also published my findings in peer re-viewed medical/scientific journals on both sides of the Atlantic. Just take a look at some of the comments:

  1. Professor (Justice) Thomas Mensah, Past Chairman of OAA-UK, in his most generous Book Review: “Experts generally find it easy to expatiate on their subjects to the comprehension of their fellow experts. But it takes a truly first-rate expert to make a highly technical subject understandable to laymen, without either trivialising the issues involved or sounding condescending in the process. When the technical subject in question happens to be emotive and encrusted with irrational fears and deeply ingrained prejudices, as is the case with AIDS, then it requires not just deep knowledge but also exemplary courage to undertake the task of discussing and explaining it to the uninitiated. And to be able to do this successfully calls for unique literary skills which one does not normally expect from practising scientists.
    “Fortunately for the reader, Dr Konotey-Ahulu brings to the task of writing about Acquired Immune Deficiency Syndrome (AIDS) an unusual combination of professional expertise, rare courage and integrity and supreme gift of language and style. …
    “Like the true scientist that he is, Dr Konotey-Ahulu would be the last to claim that his is the final word on the subject or that the prescriptions he suggests for prevention will be either successful or even feasible. What cannot be denied is that he has set the problem of AIDS in a totally different context by giving the individual man and woman, as well as African Governments and the world community in general, the information and perspectives on which to formulate a strategy for the future. For this he deserves the gratitude of all of us. Thomas Mensah”.
  2. Professor Maya Angelou (USA): “Compulsive reading. I could not put it down.”
  3. Mr J G Amamoo (London): “Scholarly. A remarkable book”.
  4. Dr Bill Turner (UK): “Excellent! A must for every medical student”.
  5. Dr Fred Wurapa (Congo): “The story of AIDS in Africa as it should be told”.
  6. Mr Louis Obosi (Nigeria): “Written for Africans, but should find its way to U.N.O.”
  7. Professor George Fraser (Oxford): “Excellent book … the most important topic in Medicine currently”.
  8. Group Captain John Weir (London): Remarkable book. Easily understood.”
  9. Mr K Gyang-Apenteng (London): “The most commendable aspect is its sheer readability.”
  10. Professor Geraint James and Professor Dame Sheila Sherlock (London): “Superb in every way.”
  11. Dr Nam Dunbar (Oxford): “Clearly dispelled many false notions about the causes and spread of AIDS”.
  12. Marion McTair (London): “ …a masterpiece of good descriptive writing”.
  13. Dr Ann Rudwick (London): “… a tour de force”. 

All the above is what others have said about my book. What do I myself say about it?


(a)  It is experiential in much of the discourse. What the sex ladies on duty told me is recounted in detail, forcing me to start the book with (Chapter One) TAFRACHER, that unique Ghanaian de-vulgarising prefix-word that I introduced into medical vocabulary in the British Medical Journal in 1975.

(b)  Photographs of me examining the sex ladies in their homes after their business demonstrating, with their permission, what AIDS looks like.

(c)  Disclosing names of self-confessed scientific liars or lying scientists  (Can you identify the 5 names?)

(d)  Akoras doing research will find a detailed list of references both of truth and the self con-fessed untruths to include in their work.

(e)  The book contains such unusual “stuff” that a lady from “USA TODAY” rang me in London at the Cromwell Hospital to ask “Who funded you to go to African countries to research AIDS?”. When I told her “I went to my bank in South Kensington, London, to borrow money for the 6-week tour to see what is happening at the grass roots on my Continent” she appeared less interested and hung up.

Perthes’ Disease versus Sickle Cell Disease Hip

Perthes’ disease versus sickle cell disease hip (18 Oct 2014)

www.bmj.com/content/349/bmj.g5584/rr/778350 or http://bit.ly/1tGmuYm

[Rapid Response to Perthes’ disease by Peter Kannu & Andrew Howard

(Published 23 Sept 2014) British Medical Journal – Practice Easily Missed?]

The instructive article [1] of Peter Kannu and Andrew Howard (Oct 4, p 32) has presenting clinical
features that can equally apply to children with sickle cell disease whose omission in differential
diagnosis does not help busy Residents and House Physicians in hospitals anywhere in the world.


While clinical presentation – the limp with the physical signs elicited – is identical in Perthes’
and sickle cell disease hip in children the radiological features help in differentiation [2 page
239]. The latter hip differentiation “from Calve-Legg- Perthes’ disease is not difficult” [3]
especially when “the significant differences in age of onset, degree and site of epiphyseal
involvement and changes in the femoral metaphyses are considered” [4 5]. Like in Perthes’ there was
no hip involvement in 157 consecutive children with sickle cell disease aged 4 and below [2 page
239], but between 5 to 9 years of age there was 1 case in 201 consecutive sickle cell disease
patients (0.5%) and between 10 to 14 years we had 7 (4%) of 177 consecutive patients [2]. Therefore
below the age of 15 years we in Ghana found 8 cases of avascular/aseptic femoral head necrosis in
200 consecutive sickle cell disease patients (2.5%) observed by one clinician (myself). The article
of Kannu and Howard [1] states: “The annual incidence of Perthes’ disease among children under 15
ranges from 0.2 to 19.1 per 100,000” which, while quoting the paper of Perry and colleagues on the
“racial and geographic factors on the incidence of Legg-Calve-Perthes disease” [6], failed to
comment that these so-called “racial factors” could be haemoglobinopathic.


Sickle cell disease is defined as possession of two beta-globin gene defects at least one of which
is the sickle cell gene [2], therefore the phenotypes constituting sickle cell disease are ‘SS’
known as sickle cell anaemia, ‘SC’ known as sickle cell haemoglobin C disease, ‘Sβ-Thal’ which is
sickle cell beta-Thalassaemia, ‘SF-HEREDITARY’ for sickle cell Hereditary Persistence of Foetal
Haemoglobin which 4 phenotypes comprised the commonest sickle cell diseases seen in Ghana. More
‘SC’ phenotype (6.6% of 603 consecutive patients of all

ages) than ‘SS’ (2’8 % of 600) suffered hip necrosis, but no disease phenotype is exempt [2]


Sickle cell disease occurs in significant measure in White people in Greece, Turkey, Sicily, and in
the Middle East, India, and in their descendants in the diaspora [2, pages 76-82]. Canada where
this article originates [1] has a good representation of these Mediterranean populations [7] as
well as Blacks and though the authors, as part of their investigations carried out for Perthes’
disease mention “a full blood count” there is need to remind Residents and House Physicians
anywhere in the world that haemoglobin electrophoresis must always be counted among the tests to be
carried out in any tentative clinical diagnosis of Perthes’ disease.


One Editor of a prestigious international medical publication once wrote asking me to limit my
references to articles published after the year 2000 AD. I wrote back to point out that clinical
signs were/are clinical signs and doctors needed reminding of their significance in any generation.
As part of their treatment regime Peter Kannu and Andrew Howard list “encouraging swimming” among
exercises to be recommended in Perthes’ disease. Well, fifty years ago bar 4 months I named in
Lancet swimming among the 17 commonest precipitating causes of sickle cell crisis [8]. Mistake
sickle cell disease for Perthes’ disease and this advice to encourage swimming would be misplaced.
Fortunately, Obisesan and Bohrer [5] knew how to diagnose Perthes’ disease in Black children in
West Africa 42 years ago. Should the present authors have mentioned this? Or were they dismissing
anything published before AD 2000 as being of little significance? Just two out of their 13
references are before the 21st Century. The increasing habit of starting articles with a clinical
dimension thus: “We did a MEDSEARCH going back 25 years” is neither academic nor helpful, because
quite significant clinical material may be missed. In 1972 I discovered and described in The Lancet
a new physical sign in sickle cell disease, to the extent of quantifying its incidence in the
different sickle cell disease phenotypes, the peripheral mental nerve neuropathy of sickle cell
crisis [9] – what came to be known on ward rounds as the “kanumblll sign”. Twenty-five years later
Sally Davies and L Oni published in the BMJ a comprehensive article on Sickle Cell Disease [10]
limiting their references to cover the previous 25 years, thereby (but not deliberately) omitting a
vital physical sign (numb lower lip) that could have drawn the attention of any doctor or nurse to
the fact that the person they were confronted with had sickle cell disease.

Competing interests: None declared

Felix I D Konotey-Ahulu MD(Lond) FRCP(Lond) DTMH(L’pool) Kwqegyir
Aggrey Distinguished Professor of Human Genetics University of Cape Coast, Ghana and Consultant
Physician Genetic Counsellor in Sickle Cell and Other Haemoglobinopathies, 9 Harley Street Ltd,
Phoenix Hospital Group, London W1G 9AL (E-mail felix@konotey-ahulu.com Web: www.sicklecell.md)
1 Kannu P, Howard A. Perthes’ disease. BMJ 2014; 349:g5584 (doi:1136/bmj.g5584)

2 Konotey-Ahulu FID. The Sickle Cell Disease Patient: Natural History from a
Clinico-epidemiological study of the first 1550 patients of Korle Bu Hospital Sickle Cell Clinic.
The Macmillan Press Ltd, London 1991 & 1992 and T-A’D Co Watford, 1996.

3 Golding JSR. The bone changes in sickle cell anaemia. Ann Roy Col Surg Eng 1956; 19: 296-315.

4 Barton CJ, Cockshott WP. Bone changes in Haemoglobin SC disease. Am J Roentgen Rad Ther Nuc Med
1962; 88: 523-532.

5 Obisesan AA, Bohrer SP. Perthes’ disease in Nigerians. Ghana Medical Journal 1972; 11: 298-302.

6 Perry DC, Machin DM, Pope D, Bruce CE, Dangerfield P, Platt MJ, et al. Racial and geographic
factors in incidence of Legg-Calve-Perthes’ disease: a systematic review. Am J Epidemiol 2012; 175:

7 Ringelhann B, Konotey-Ahulu FID. Hemoglobinopathies & Thalassemias in Mediterranean areas and in
West Africa: historical and other perspectives 1910- 1997 – A Century Review. Atti del’Accademia
della Science di Ferrara 1998; 74: 267-307.

8 Konotey-Ahulu FID. Sicklaemic Human Hygrometers. Lancet 1965; 1: 1003-

9 Konotey-Ahulu FID. Mental nerve neuropathy: a complication of sickle cell crisis. Lancet 1972; 2:
388 [The so-called kanumblll sign (Konotey-Ahulu Numb Lower Lip Lancet sign)]

10 Davies Sally C, Oni L. Management of patients with sickle cell disease. BMJ
1997; 315: 656-660.






Felix I D Konotey-Ahulu



Dr Kwegyir Aggrey Distinguished Professor of Human Genetics University of Cape Coast, Ghana and Consultant Physician Genetic Counsellor in Sickle Cell and Other Haemoglobinopathy, 9 Harley Street Ltd, Phoenix Hospital Group, London W1G 9AL

When The University of Cape Coast became the first in Africa to bestow a Personal Professorship and then chose me as the recipient, naming the Personal Chair after the legendary Educationalist Dr James E Kwegyir Aggrey, also known as Aggrey of Africa, UCC further honoured me by giving me the Honorary degree of Doctor of Science (Honoris Causa) on the same day that Dr Daniel Chapman Nyaho was given the Honorary Doctor of Literature Degree. As Rev Professor Samuel Adjepong, the then Vice Chancellor in the Year 2000 pronounced me “The Dr Kwegyir Aggrey Distinguished Professor of Human Genetics, University of Cape Coast, Ghana”, he commissioned me to use the honour to promote Education, Research and Service nationally and internationally in the field of “Sickle Cell Disease” in particular, and “Haemoglobinopathy” in general. The definition of these two terms follows the next paragraph, indicating how every Ghanaian family has reason to pay great attention to Haemoglobinopathy and Sickle Cell Disease.


I, here, record my profound gratitude for what the University of Cape Coast has done, because it did pave the way for other universities in Ghana to follow suit in creating Personal Chairs. A characteristic of my Distinguished Professorship has been that it has allowed me to latch on to one unique virtue of Dr J E Kwegyir Aggrey which was his Originality.  My own definition of Originality which was the hallmark of Dr Kwegyir Aggrey is this: To think what has not been thought before, to say what has not been said before, and to do what has not been done before. It is the essence of wisdom not only to emulate people like Dr Kwegyir Aggrey [Reference 1] who were known for their originality but also to identify young people, especially students, undergraduates and postgraduates, with originality. I promptly instituted an Annual Kwegyir Aggrey Prize Examination for the Faculty of Science to do just that. That annual examination, since 2001, has been the only one in the world that allowed Candidates to take anything (books, notes, and computers) into the examination room. Why? Because the questions I set were/are meant to test originality. Answers are not found in any text book or on the internet. The 3 month assignment given to Candidates before the 3-hour paper also probes Candidates for originality. For example, take this 3-month Assignment Question which I loved to give every other year: “Describe in great detail a problem whose solution has hitherto been unsatisfactory over many years, decades, or even centuries, and suggest, also in great detail, the way you think it can be satisfactorily dealt with. This assignment tests Originality and wisdom, and I have been able to indentify UCC geniuses who have gone on to do great things after graduation. Answers to this Assignment cannot be found in any textbook or on the internet and will, hopefully be published one day. The decision to give the prizes in Guineas rather than Ghana Cedis was to keep the memory of what Gold Coast’s special gold was worth. The gold weight that sold elsewhere for 20 Shillings fetched 21 Shillings if it came from Gold Coast’s GuineaCoast. The fact of Kwegyir Aggrey’s father being not only a Linguist but also an important goldsmith at Anomabu was recalled when successful Candidates were announced on the Day of Convocation/Congregation for First Prize 100 Guineas (£105 Pounds Sterling), 75 Guineas (£78.75 Sterling) and Third Prize 50 Guineas (£52.50 Sterling). When the overall standard was high a Consolation Prize of £10 was given to each Candidate who completed the Assignment successfully (raised to £15 in 2014). The decision not to tax the University with paying these sums was also original so that a Personal Professorship need not be a burden on university finances. But the most original aspect of my Kwegyir Aggrey Distinguished Professorship was how I approached the education of the public both nationally and internationally about the hereditary ailments that constitute Sickle Cell Disease or Haemoglobinopathy which may be defined as disease caused by abnormal haemoglobins. Haemoglobin is the protein of red blood cells needed for oxygen carriage in the body. “Haemoglobin Type” is inherited through genes.




Centuries before a certain Dr James Herrick MD in Chicago, USA, in 1910  found what he called “peculiar sickle shaped red cells” in the blood of a black man who was short of blood, in other words he had anaemia, plus periodic joint pains, Ghanaians knew of a medical condition which was characterized by cold season rheumatism, yellow eyes, hip problems, leg ulcers, occasional eye symptoms, difficulty in child birth, and some other complications. Although we knew that it ran in families parents may be perfectly healthy, yet their children, some of them, would have severe joint and bone pains under certain circumstances like the rainy season, fever, violent exercise, farming, sweating a lot from very hot weather, and when suffering from infections of various kinds. Every Ghanaian tribe had a name for this, and modern experts are amazed that even when we had no microscopes to see red blood cells kinked when they should be round in shape, we in Africa knew about the condition and called it Chwechweechwe (tswetsweetswe) in Gã, Ahotutuo in Twi, Dobakotiri (Dagbani), Niwiiwii (Fante), Nuidudui (Ewe), Hemkɔm (Krobo-Dãngme), Paa (Kasena-Nankani), Koba-tuem (Buili), etc [2]. The Yorubas call it Aromolegun or Lakuregbee. The disease is so well known that my own Konotey-Ahulu family has been able to trace it generations backwards to 1670 AD [See http://www.konotey-ahulu.com/images.generation.jpg with the names of sufferers “R” for Rheumatism (also http://www.sicklecell.md/images.generation.jpg) [3] My own parents had 11 children 3 of whom were born with Hemkɔm (Sickle cell disease).




How do I explain to illiterates that my father and mother did not have hemkɔm, yet 3 of us had the cold-season rheumatism? As body ache is the cardinal symptom of this illness, I use the word “ACHE” in my explanation of the inheritance of the condition. Now, every human characteristic derives its feature from contributions from both father and mother. Parents have a double code for every characteristic – skin colour, body build, type of blood protein called haemoglobin, type of Blood Group, body features, etc. Sometimes one parent’s characteristic predominates, nevertheless both characteristics are inherited. It is not always easy to say which of our characteristics is father’s, and which is mother’s but sometimes it is possible to isolate which characteristic is from father, and which from mother. The type of haemoglobin we inherit is like that. There is a code for the normal adult haemoglobin which is “A”, there is another code for a variation of normal haemoglobin known as Haemoglobin “S” which under certain circumstances like lack of oxygen stiffens up and causes the red blood cell to twist from round to sickle shape. I have given the label ‘NORM’ to normal Haemoglobin “A”, and ‘ACHE’ to any variant haemoglobin, like sickle cell haemoglobin “S”. There are many variants of normal haemoglobin, but the commonest in the world is haemoglobin “S” (for Sickle). Normal haemoglobin “A” does not cake up like “S” does with lack of oxygen. As with all other human characteristics each of us has a pair of codes (genes) for haemoglobin formation – one from father, the other from mother. The person inheriting normal haemoglobin “A” from one parent and a different haemoglobin, say “S” from the other parent is categorized “AS”, and is known as Sickle Cell Trait or “AS” phenotype [2].

Now, this is where an amazing thing happens which explains why some children of the same parents suffer from cold season rheumatism, while others do not. This is what happens: For a child to be conceived father’s sperm must unite with mother’s egg, and a father who possesses (as he must do) two hemoglobin codes and is characterized as “AS” divides his pair of codes into “A” and “S” for his millions of sperm discharged in coitus. In other words, there are sperm carrying just “A” code, and others with “S” code, never both. So you will never find a sperm with both haemoglobin codes “A” and “S” from a man who is “AS” phenotype. Is that not amazing? Similarly, a woman who is “AS” phenotype, releases her monthly egg which must carry just one of her two codes “A” or “S”, never both. Let us pause here: Dear reader, if you are not able to summarize what I have said so far about a man’s sperm, and a woman’s monthly egg, I am a poor teacher.

Now let us continue: When the man’s sperm meets the woman’s egg for fertilization 4 things can happen: (i) man’s sperm carrying “S” code meets woman’s egg carrying “A” code. The child conceived will have the phenotype “AS”, just like the parents, and will have no trouble at all with cold weather. (ii) Man’s sperm carrying “A” code meets woman’s egg with an “S” code, the child conceived will be “AS” and have no problems whatever. (iii) Man’s sperm carrying “S” code meets woman’s egg carrying “S” code conceives a child that will be “SS” who under certain circumstances will have the red cell changed into sickle shape in the blood, impeding easy flow around joints and in the bones, and causing severe pain. (iv) Man’s sperm coding haemoglobin “A” fertilizes woman’s egg coding haemoglobin “A” produces a child who will be “AA” who will not suffer cold season rheumatism. Now, the children who, like their parents, have one normal haenmoglobin “A” plus a variant haemoglobin called “S”, known as Sickle Cell Trait, cannot be distinguished except by blood test from those children who do not have any variant haemoglobin at all, “AA”. Those with haemglobin “S” from both father and mother have Sickle Cell Disease “SS”. Trait parents NORMACHE x NORMACHE produce children who may be NORMACHE (“AS” Trait – no problem), ACHENORM (“SA” Trait – no problem), ACHEACHE (“SS” sickle cell disease) and NORMNORM (no problem) [2 4] The term “Sickle Cell Disorder” is wrong because some Insurance companies  use it for both Trait (no problem) and Disease to defraud.

Figure 1 Probability of AcheAche hereditary disease from NormAche Traits 


CAUTION: (i) It must never be assumed that if the first child is ACHEACHE subsequent children will not be ACHEACHE. The so-called “1 in 4” Probability of a child being born ACHEACHE is quite deceptive.

(ii) The simple test that detects whether some healthy person is carrying “S” code or gene is called the Sickle Cell Test, and can also be very deceptive. If the result is negative, in other words if there is no sickle cell haemoglobin “S” it does not mean the person does not have another variant haemoglobin which is not “S”, but which can also cause body ache when inherited with another haemoglobin variant. Please read that sentence again, and again until you understand it. The commonest such haemoglobin in Ghana is haemoglobin “C”, which is also an ACHE haemoglobin. This Haemoglobin “C” will not be detected by the Sickle Cell test. Thus my father who was sickle  cell test negative was, on further investigation found to possess haemoglobin “C” that was passed on to 5 of his eleven children, 3 of whom also received the “S” code from our mother giving them two ACHE codes to form “Sickle Cell Haemoglobin C Disease”, ACHEACHE phenotype. Hence, apart from sickle cell disease “SS”, there is another haemoglobinopathy called Haemoglobin “CC” disease where the person complains of yellow eyes, tiredness, joint and abdominal pains. Sickle cell test is negative, but this is also ACHEACHE. [6 7]




Extremely common is the NORMACHE Ghanaian – 1 in every 3 healthy Ghanaian is NORMACHE “AS” or “AC”. To be precise, 20% of all southern Ghanaians are “AS” and 10% are “AC” while 20% of northern Ghanaians are “AC” and 10% are “AS”, so apart from other ACHE haemoglobins that are found in Ghana (like Haemoglobins D, F-heredirary [7 8 9], K-Woolwhich [10], Haemoglobin Korle Bu [11], Haemoglobin Osu-Christainsborg [12], beta-Thalassaemia [2], etc) 1 in 3 Ghaanaians will be found to be NORMACHE “AS” or “AC” which does them no harm whatever. This means that 1 in 9  male-female union for childbirth is that of Trait Carriers, namely NORMACHE x NORMACHE marriages, with the mother bearing ACHEACHE children. [13]

Let’s get real: : One in 3 readers of this article, 1 in 3 of the Professors at UCC, 1 in 3 members of Parliament, 1 in 3 Paramount Chiefs, 1 in 3 of the Black Star footballers, 1 in 3 market women, 1 in 3 of the Konotey-Ahulu family, 1 in 3 of all fishermen, 1 in 3 thieves, 1 in 3 prostitutes, 1 in 3 pastors, including bishops and archbishops in Ghana, 1 in 3 of the “prophets” and “faith healers”, 1 in 3 of our herbalists, is carrying an ACHE code and they probably do not know it, 1 in 3 nurses, doctors, medical students, undergraduates and post graduates are “AS” or “AC”. So are 1 in 3 rogues, and 1 in 3 liars. One in 3 of past Ghanaian Heads of State were NORMACHE. At least one of those Heads of State married an ACHEACHE lady who once consulted me. Also First Lady Mrs N M Atta Mills who was widowed not long ago told the international gathering of a thousand delegates at the International World Sickle Cell Conference, Accra in June 2010, to my astonishment, that when she was at Aburi Girls’ School I went there from Korle Bu Teaching Hospital to lecture the School on Sickle Cell Disease, then took her blood for analysis, and I later informed her in writing that she, like my own mother, had Sickle Cell Trait (“AS”)! Reader, this thing is very common paa!




A lot of unhelpful advice is given all around the world in connection with the possession of the ACHE gene. In Britain black pregnant women are advised to have what is called pre-natal diagnosis to see what the phenotype of the unborn baby would turn out to be. If the test reveals that the child will be ACHEACHE advice for abortion is given. I totally repudiate such advice if only because many ACHEACHE persons I know from my experience as previous Director of the largest Sickle Cell Clinic in the world have inherited from the same parents some extraordinarily brilliant genes along side the ACHE genes. Some of these ACHEACHE people are university Professors, International Judges, Senior Doctors, Diplomats, and Businesses men and women. These geniuses would have been recommended for abortion by today’s genetic counselling in Great Britain where I trained to be a doctor. A human being is far more than ACHE genes. Because of the pains they suffer when they have what is called sickle cell crises, some of these brilliant ACHEACHE persons make sure they themselves do not have ACHEACHE children. I have invented the kanad which allows them and others who are determined not to burden the next generation with ACHEACHE children to predict with 100% certainty which man-woman pairings will avoid this. This new invention [14] illustrates the kind of Originality Aggrey of Africa would have approved of. .




Ghanaians belong to 1 of three genetic blocks when it comes to counseling with respect to what to expect when one marries whom: NORMACHE, NORMNORM, ACHEACHE. (a) A NORMNORM Ghanaian possesses no ACHE at all (b) A NORMACHE Ghanaian possesses one ACHE and one NORM code (c.) A Ghanaian possessing two ACHE haemoglobins is ACHEACHE. All 3 categories are found in my own family. There are no other categories apart from these three. My parents had abnormal haemoglobin trait so were NORMACHE. They had 11 children of whom 3 were ACHEACHE, 4 were NORMACHE, and 4 were NORMNORM. It is vitally important to know if one possesses an ACHE, and what type it is. I developed this in a pictorial form as shown below – Two groups of 3 male phenotypes, and 3 female phenotypes seeking whom to marry.



Figure 2. The kanad Male and Female Groups 

I developed two groups of the three phenotypes as cubes with NORM as green, and ACHE as dark red. So NORMACHE has three sides as green, and three as dark red. ACHEACHE has all six sides of the cube as dark red, and NORMNORM has all sides of the cube green. One group of three cubes is female, and the other group of 3 is male. The six cubes are packed together into one bag to form the unit which every Ghanaian family should possess. Every Ghanaian should know which cube represents her/him. My father, for instance would be a NORMACHE green/red cube, and so would be my mother.




There are six possible results of Ghanaian mating when a known kanad phenotype (male) is hurled on the table together with another known kanad (female). If the parents are determined not to have an ACHEACHE child the kanad gives unequivocal results.

With relevance to sickle cell disease (scd) and other haemoglobinopathies there are 6 demonstrably different phenotype pairings of Ghanaians in procreation. Of the six pairings, as shown below, 4 produce predictable outcomes and 2 can be referred to as genetic gambling. Of the predictable outcomes one is 100 per cent disease outcome (ACHEACHE) and 3 predict 100% non-disease outcome

NB: If you carry an ACHE gene as Trait or double ACHE as hereditary disease ACHEACHE, and you do NOT want to increase the sickle cell disease burden, then go for the union that predictably leads to no births of ACHEACHE child   – Respectively Number 5 and Number 3 as shown below:  Marrying a NORMNORM is the only option. If, as a NORMACHE Trait, you marry an ACHEACHE person you may yet avoid having an ACHEACHE offspring, but this is gambling! If you, a trait ie NORMACHE have children with another trait NORMACHE you may produce no ACHEACHE offspring, but this is also genetic gambling which has paid off though! I have known couples then limit procreation rather than gamble further.  Males need to heed this advice seriously because they have a higher MPSI (Male Procreative Superiority Index) [2 15 16 17] than females. However, if ACHEACHE children arrive, do not despair. Many are known to carry brilliant genes which their non-aching siblings do not possess. They can achieve great things in life when managed properly. (See www.sicklecell.md or www.konotey-ahulu.com) [2 18]    


Predictability & Unpredictability of Producing Sickle Cell Disease (ACHEACHE) Children Using the kanad [Konotey-Ahulu Norm Ache Dice]

1. ACHEACHE x ACHEACHE     [Predictable Outcome – All will be ACHEACHE]

2. ACHEACHE x NORMACHE                 

[Unpredictable Outcome – Some ACHEACHE, Some NORMACHE]

3. ACHEACHE x NORMNORM               

[Predictable Outcome – None will be ACHEACHE, All will be NORMACHE]

4. NORMACHE x NORMACHE               

[Unpredictable Outcome – Some NORMNORM, Some ACHEACHE, Some NORMACHE]

5. NORMACHE x NORMNORM               

[Predictable – None will be ACHEACHE – Some will be NORMNORM, Some NORMACHE] These are healthy indistinguishable phenotypes so, please, identify Ache carriers by blood test and do genetic counselling before marriage.  

6. NORMNORM x NORMNORM             

[PredictableNone will be ACHEACHE – All will be NORMNORM]




1. A Fante man, Methodist Lay Preacher, married a seamstress. They both knew they had Nwiiwii, but little did they know that however many children they had they would all be ACHEACHE. Mrs ‘D’ became pregnant 12 times, and had 13 children including twins.

This ACHEACHE x ACHEACHE couple produced an all time world record in Medical Genetics which we published in the British Medical Journal (Konotey-Ahulu and Ringelhann 1969; Bentsi-Enchill and Konotey-Ahulu 1969). The ACHEACHE of Mr ‘D’ consisted of sickle cell gene “S” and Haemoglobin “C” gene, while Mrs “D” was Sickle Cell gene “S” and “beta- Thalassaemia” for Sickle cell beta-Thalassaemia disease [19 20]


Figure 3: ACHEACHE x ACHEACHE produce 13 ACHEACHE offspring [19 20]


2. A Ghanaian Physician Specialist married a doctor, and they had 4 children with no health problems whatsoever. They thought they had “finished”, but 5 years after the last child what they called “an unplanned pregnancy” occurred and they had a lovely little girl. By the age of 12 months the child began to have signs and symptoms of what they both knew implied sickle cell disease (hand-foot syndrome). They realized they must both have been carrying sickle cell trait NORMACHE (“AS”) and never tested themselves before. Although the girl was lovely, and was indeed the most brilliant of all their children they said they found the need for Genetic Counselling and Voluntary Family Size Limitation even when couples did not suspect they carried Sickle Cell Trait.

3. This “T-S” Kwahu family knew they were both sickle cell trait NORMACHE “AS” and said they were told that 1 in 4 of any children they had would be “SS” ACHEACHE. They thought that was fair enough Genetic Gambling, and as they were tremendously in love they went ahead to produce a family. When first child, a boy, was “SS” they thought, they could have more children because the 1 in 4 had already come, and they were looking forward to the following 3 children without the ACHEACHE combination. Read the story in my book “The Sickle Cell Disease Patient”, pages 500 & 501: Second child, boy, “SS”, third “SS”, fourth “SS”, fifth “SS” and sixth “SS” [2]. But why did they continue having so many children? Answer: Because the only girl among the 6 children had died young, and Mrs T-S desperately wanted a girl. Moral of this true story is that it is wrong to tell people that Genetic Gambling will produce the different phenotypes in a certain order. As the first 4 children of the NORMACHE doctors mentioned above turned out without being ACHEACHE phenotypes so it does happen that other NORMACHE parents have been known to produce children all of whom are ACHEACHE – the term gambling will not have any relevance otherwise. The “1 in 4” prediction advice is deceptive and must be pointed out in any competent genetic counseling exercise. 

4. Male Procreation needs to be curbed as part of Genetic Counselling and Voluntary Family Size Limitation (GCVFSL). On Saturday June 19 1971, Mr Kofi Sampani pulbished in The MIRROR (Accra) a front page story from Sunyani of Okomfo Klutse with a picture of his 23 wives who produced 94 children [21]. Okomfo Klutse could be NORMACHE, or NORMNORM or ACHEACHE “SC”, and no less than 8 of his wives would be carrying an ACHE gene. If he was ACHEACHE then all 94 children would have one of his ACHE genes, and any of the wives who gave an ACHE gene would have a child or children suffering from Ahotutuo.  If this man was NORMACHE, like my own father was, then 47 of his children would receive an ACHE gene, and some of the children would be ACHEACHE that resulted from some of the 8 wives passing on their ACHE genes. A year earlier in 1970 I had said in the Journal of Tropical Medicine and Hygiene in England that polygamy could increase the burden of sickle cell disease [22], so males with the Trait (NORMACHE) should limit family size because of their high MPSI (Male Procreative Superiority Index) a genetic index that I invented [2 15-17] to prove that geneticists must not say that Malaria/Sickle Cell Trait Balanced Polymorphism was the main reason for the high incidence of the sickle cell trait in African populations. [23 24]. Professor George Bonney and I showed mathematically the role of polygamy in Population Genetics [25]. Incidentally, there is a high incidence of sickle cell trait among white populations in Greece, Turkey, and India [13 26].


Populations all over the world are looking for governments to solve their health problems for them. We must be careful not to extend this “Government will do it all for me” attitude to Genetic Disease. Governments can make it easier for each of us to find out whether we are NORMACHE or NORMNORM or ACHEACHE to determine what exactly does our ACHE represents: “S”?, or “C”?, or “F-hereditary”?, or “beta-Thalassaemia”? or “Haemoglobin Korle Bu”? or Haemoglobin Osu-Christiansborg?”, or “K”?, or “D”?. True, our governments can help us [27], but we need ourselves to do something about our health, and our children’s health. My Distinguished Professorship advises you thus: “DO IT YOURSELF!”


Figure 4: Service, Education, and Research Dimensions of Genetic Counselling

This SCHEMA is the way forward. Let us know that if we are NORMNORM our grand children could be ACHEACHE. How is this possible? ANSWER: Because our husband, or wife may be a trait carrier – quite harmless – your son or daughter with the Trait may marry another Trait, like my parents did, and your grand child may then become ACHEACHE. This reasoning is quite simple, so please take this Genetics on board. As I have implied earlier it is no business of Genetic Counselling to ask a NORMACHE never to marry another NORMACHE, or to tell people how many children to have, or to tell them that the chances of hereditary disease in the offspring are such and such. No, my business as a Counsellor is to tell people the facts about the illness, and in this I seek the help of those who have ACHEACHE and who have become great Achievers in various fields of endeavour despite their medical history, and to ask them to join me in advising people to find out what phenotype they belong to, and then put to them their options: (1) Go in for Genetic Gambling, that is the “Probability” route, (2) Go in for the “I have made up my mind to avoid ACHEACHE” route which can be done by using the kanad – the Konotey-Ahulu Norm Ache Dice – to predict with 100 per cent certainty which pairings will always, without fail, avoid the ACHEACHE burden. This involves some painful decisions but has to be done, especially in the UK where many ACHEACHE patients have died from being given Morphine and Diamorphine (Heroin) for sickle cell pain [28 29 30]. Ghanaians have protested about this [31-37], but the Opiods (Opiates) for pain in sickle cell crisis have been officially sanctioned for the UK [38].If you are going to bring up children in the UK, and there is the possibility that if you have more children they will take their parents’ ACHE genes then take note that when they develop pains they will be put on Heroin and Morphine. Think seriously of limiting your family size even when you are most anxious to have another child.

A warning here for Ghanaian Doctors: Please do not adopt British or American methods of managing sickle cell disease when Ghana has produced the largest number of ACHEACHE Achievers in the world [39] without using Morphine or Diamorphine or Hydroxyurea or monthlty blood transfusions as they do abroad.



I heartily congratulate The University of Cape Coast at their 50th Anniversary for evidences of their Originality – thinking what has not been thought before, saying what has not been said before, and doing what has not been done before. Ayenyekoo!  – The plural for “Well Done!” Please extend your Originality to advising every student, teacher, administrative staff, and their families to find out (at their own cost) what their haemoglobin phenotype is. Let this University be the First in the world to have this policy. “At their own expense” is always better because it separates the really serious from the rest. “Save some money to enable you test yourself and your present family, and potential family” must be a Motto. One of the reasons for my KÁGÈ SICKLECELL FOUNDATION (KÁGÈ is Konotey-Ahulu Genetic Epidemiology) [38] is that governments every where have a great reluctance in dealing with genetic disease (except to decree that pregnancies should be terminated), and I want a Foundation that lays emphasis on teaching and on ethical matters in prevention processes. I have been spreading the message in lectures and international medical journals, and I have a website that is consulted around the clock from around the world [14] Since the Year 2000 when the University of Cape Coast made me The Kwegyir Aggrey Distinguished Professor of Human Genetics I have by August 2014 published 172 articles [40] most of which can be Googled and read on line, and all of which include the University of Cape Coast address, emphasizing ethical practice in Human Genetics and Clinical Medicine. May this University go from strength to strength, and may we thank GOD and take courage.




University of Cape Coast: I thank Vice Chancellor Rev Professor Samuel Adjepong and University Council, and subsequent Vice Chancellors Rev Professor Emmanuel Adow Obeng, Professor Jane Naana Opoku-Agyemang, Professor D D Kuupole, Pro-Vice Chancellors Professor Haruna Yakubu and Colleagues, and Registrars Mr Kofi Ohene and Colleagues of the Vice Chancellor’s Office and the remarkably cooperative Deans of the Faculty of Science since Year 2001 Professor Kobina Yankson, Professor Victor Gadzekpo, Professor Samuel Yeboah-Mensah, Professor B K Gordor, Professor Basuah, and their extremely hardworking Faculty Officers Rev Evelyn Nickel, Mr P K Mensah, Dr Alexis Akanson, Mr Barsi-Serbeng, Mr Ebenezer Aggrey, Ms Mary Obimpeh and their Administrative Staff Ms Emma Bedzo, Mrs Marian Aidoo, Ms Ernsetina Pokua all of whom supervised the Annual Dr Kwegyir Aggrey Prize Exams most admirably. Encouragers were Professors Jeurry Blankson, Eric Anum, Lawrence Owusu-Ansah, John Micah, and Mr Daniel Essel, Mr John K Edumadze, and Mr Sitsofe Tettey.

Indebted I am to a multitude – I am most grateful to the following who were generous in their help, financial and otherwise: Adomako, Albert & Fitnat; Acquaah-Harrison, Asabea; Chapman Nyaho, Mawunu; Akufo-Addo, Edward & Mrs Irene; Owusu, Maxwell; Botchway, Dr Kwesi; Vanderpuije Nii Oti Ahmed and Mrs Risikatu; Firth Drs Peter and Jean; Chew Dr George and May; Tettey Rev Ben and Mrs Margaret; Draisey Dr Mike; Norris Dr Geoff; Djabanor Dr Frank and Mrs Amelia; Matekole Professor Mike Ossom; Archampong Professor E Q; Addy Professor Jonathan H; Asirifi Professor Yaw; Laryea Mr Reginald; Amanor-Boadu, Dorothy; Thompson, Mrs Rosemary; Bruce-Tagoe, Professor Alexander; Codjoe, Lawyer Raymond; Mould-Iddrisu, Mrs Betty; Ekem, Dr Ivy; Tsikata, Capt Retired Kojo; Allotey, Professor Francis; Djangmah, Professor Jerome; Wosornu, Professor Lade; Hamidu, General (Retired) Joshua; Senanu, Professor Kojo; Perbi, Reindorf B; Konotey-Ahulu, Dawid & Rachel; Konotey-Ahulu, Mrs Rosemary; Madubunyi, Boniface; Awoonor, Professor Kofi; Baffour Ankomah; Nene Sakite II, Konor of Manya Krobo; Odoteye Samuel; Gbedemah, Mensah and Sophie; Omaboe, Nortey; Omaboe, Mrs Letitia; Ampim, Kofi & Deborah; Djamson, Dr Eric and Mrs Gladys; Shoetan, Samuel & Cecilia; Bonney, Professor George and Mrs Efua; Dodoo, Professor Benjamin; Awwad, Mr Awwad FRCS; Tetteh, Richard; Savage, Hugh; Badger-Laryea, Ms Christiana; Gorbett, Miss Ann; Bukar, Alhaji Ibrahim; Falae, Mr Samuel; Madueke, Mr Chike; Frimpong-Boateng, Professor Kwabena; Quartey, Dr Samuel (Philadelphia); Angelou, Professor Maya; Kofi, Tetteh J; Mlapa, Joel; Whest, Mrs Adelaide; Kofi-Tsekpo, Professor Mawule; Thairu, Professors Kihumbu and Wanja; Mensah Dr Justice Thomas and Mrs Akosua; Alexandra Road Congregational Church Hemel Hempstead, Herts, England; Ghana College of Physicians and Surgeons (Rebecca Amoh, Professors Paul Nyame, David Ofori-Adjei, J T Anim, Alex Bruce-Tagoe); Ghana Academy of Arts & Sciences (Presidents F T Sai, Letitia Obeng, R F Amonoo; F K Allotey); Academy for the Developing World (TWAS – Triest, Italy, Professor Mohamed Hassan); African Academy of Sciences (Nairobi – Professor Eng. Shem Arungu-Olende).


1   Konotey-Ahulu, FID. Aggrey of Africa: “Only the best is good enough for Africa”. New African, October 2004, pages 50-51

2   Konotey-Ahulu, FID. The Sickle Cell Disease Patient. Macmillan Education Ltd London 1991/1992. Foreword by Roland B Scott, MD (HowardUniversity) – 36 chapters with 4,500 references, 643 pages. ISBN: 0-333-39239-6 [Also Tetteh-A’Domeno Company (T-A’D Co 1996) UK – P O Box 165 Watford WD17 3ZH]

3   Konotey-Ahulu FID. The Human Genome Diversity Project: Cogitations of An African Native. Politics and the Life Sciences (PLS) 1999, Vol 18: No 2, pp 317-322. [Invited Commentary on Professor David Resnik’s article: The Human Genome Diversity Project: Ethical Problems and Solutions.] PMID: 12561789

4    Konotey-Ahulu, FID. Sickle Cell Disease. The Case for Family Planning. Accra, Astab Books Ltd, 1973; 32 pages.

5   Konotey-Ahulu, FID. Survey of Sickle Cell Disease in England and Wales. British Medical Journal 1982; 284(6309): 112 doi: 10. 1136/bmj.284/6309/112a Jan 9 1982


6   Konotey-Ahulu FID. The spectrum of phenotypic expression of clinical haemoglobinopathy in West Africa. New Istanbul Contribution to Clinical Science 1978 Dec; 12(3-4): 246-257. PMID: 756535 [PubMed – indexed for MEDLINE]

7   Ringelhann B, Konotey-Ahulu FID, Lehmann H and Lorkin PA. A Ghanaian adult, Homozygous Persistence of Foetal Haemoglobin and Heterozygous for Elliptocytosis. Acta Haematologica (Basel) 1970; 43(2): 100-110. PMID: 4986189 [PubMed – indexed for MEDLINE]  http://lib.bioinfo.pl/pmid:4986189

8   Ringelhann B, Acquaye CTA, Oldham JH, Konotey-Ahulu FID, Yawson G, Sukumaran PK, SchroederWA and Huisman THJ. Homozygotes for the hereditary persistence of fetal haemoglobin: The ratio of G to A chains and biosynthetic studies. Biochem Genet 1977 Dec; 15(11-12): 1083-1096. PMID: 603615 [PubMed – indexed for MEDLINE

9   Acquaye CTA, Oldham JH and Konotey-Ahulu FID. Blood-donor homozygous for hereditary persistence of fetal haemoglobin. Lancet 1977 April 9; 1(8015): 796-797. PMID: 66588 [PubMed – indexed for MEDLINE]

10   Ringelhann B, Konotey-Ahulu RID, TalapatraNC, Nkrumah FK, Price B and Lehmann H. Haemoglobin K Woolwich ( 2 2 132lys –> Gln) and its combination with Hb.S and C in two Ghanaian tribes. Acta Hematologica 1971; 45(4): 250-258. PMID: 4999133 [PubMed – indexed for MEDLINE] http://lib.bioinfo.pl/pmid:4999133

11   Konotey-Ahulu FID, Gallo E, Lehmann H and Ringelhann B. Haemoglobin Korle Bu (alpha2 beta2 73 Aspartic Acid –> Asparagine), showing one of the two amino acid substitutions of Haemoglobin C Harlem. J Med Genet 1968 June; 5(2): 107-111. (This is an example of intra-genic cross-over) http://lib.bioinfo.pl/pmid:5722880 | http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1468514

12   Konotey-Ahulu FID, Kinderlerer, JL Lehmann H and Ringelhann B. Haemoglobin Osu-Christiansborg. A new chain variant of Haemoglobin A (beta 52 D3 Aspartic Acid –> Asparagine) in combination with Haemoglobin S. Journal of Med Genet 1971 Sep; 8(3): 302-305. [PubMed – indexed for MEDLINE] PMCD: PMC 1469179 & PMID: 5097135 http://pubmedcentral.nih.gov/picrender.fcgi?artid=146917&blobtype=pdf


13   Ringelhann B, Konotey-Ahulu FID. Hemoglobinopathies and thalassemias in Mediterranean areas and West Africa: Historical and other perspectives 1910 to 1997 – A Century Review. Atti dell’Accademia dell Science di Ferrara ( Milan) 1998;74: 267-307

14    Konotey-Ahulu FID. Sickle Cell Resource website from Year 2000 -2012. http://www.sicklecell.md or http://www.konotey-ahulu.com

15   Konotey-Ahulu FID. Male procreative superiority in African populations: The fact established and quantified and Papp Z (Eds). Medical Genetics, Exerpta Medica 1977; 600-607.

16   Konotey-Ahulu FID. Male procreative superiority index (MPSI): The missing co-efficient in African anthropogenetics. BMJ Dec 20-27 1980; 281(6256): 1700-1702 doi:10.1136/bmj.281.6256.1700 http://www.bmj.com/cgi/reprint/281/6256/1700.pdf


17   Konotey-Ahulu FID. The Male Procreative Superiority Index (MPSI): its relevance to genetical counseling. In FIFTY YEARS OF HUMAN GENETICS A Festschrift and liber amicorum to celebrate the life and work of GEORGE ROBERT FRASER Edited by Oliver Mayo and Carolyn Leach. Wakefield Press 2007 (www.wakefieldpress.com.au)

1 The Parade West, Kent Town, South Australia 5067

18   Konotey-Ahulu FID. The Third International Conference On The Achievements Of Sickle Cell Disease (ACHEACHE) Patients -19th July 2010, International Conference Centre, Accra. Taking part were adult Sickle Cell Disease Patients in various Professions. Chairman was Professor Kofi Awoonor, Chairman of the Council of State, Ghana. The first ever such Conference was in London at the Royal Society of Medicine, 1 Wimpole Street in 1993. The Second was in Accra in 1995.

19   Konotey-Ahulu FID and Ringelhann B. Sickle-cell anaemia, sickle-cell thalassaemia, sickle-cell haemoglobin C disease and asymptomatic haemoglobin C thalassaemia in one Ghanaian family. BMJ 1969 Mar 8; 1(5644): 607-612. doi:10.1136/bmj-1.5644/607

PMID: 5766126 [PubMed – indexed for MEDLINE] March 8 1969

http://www.bmj.com/cgi/reprint/1/5644/607.pdf | http://lib.bioinfo.pl/pmid:5766126

20   Bentsi-Enchill KK, Konotey-Ahulu FID. Thirteen children from twelve pregnancies in sickle-cell thalassaemia. http://www.bmj.com/cgi/reprint/3/5673/762.pdf BMJ Sept 27 1969; 3(5673): 762 doi:10.1136/bmj.3.5673.762 [In Medical Memoranda Sept 27 1969]

21   Sapanin Kofi. Man with 23 wives and 94 children. Okomfo Klutse. The Mirror, Accra, Saturday 19 June, 1971, No. 932, Front Page.

22   Konotey-Ahulu FID. Maintenance of high sickling rate in Africa: Role of polygamy. J Trop Med Hyg 1970 Jan; 73(1): 19-21 (38 references). PMID: 4906442

23   Allison AC. Protection afforded by sickle cell trait against subtertian malarial infection. British Medical Journal 1: 290-294.

24   Konotey-Ahulu FID. Balanced Polymorphism and Hereditary Qualitative and Quantitative Erythrocyte defects. Ghana Med J 1972; 11: 274-285. [Chapter 8 in Ref. 2]

25   Bonney GE and Konotey-Ahulu FID. Polygamy and genetic equilibrium. Nature 1977; 265: 46-47 (January 6 1977). doi:10.1038/265046a0 …n5589/pdf/265046a0.pdf PMID: 834239 http://www.nature.com/nature/journal/v265/n5589/abs/265046a0.html

26   Choremis C et al. Blood group of a Greek Community with high sickling frequency. Lancet 1957; 2: 1333-34

27   Boyo AE, Cabannes R, Conley CL, Lehmann H, Luzzatto L, Milner PF, Ringelhann B, Weatherall DJ, Barrai I, Konotey-Ahulu FID and Motulsky AG. Geneva WHO Scientific Group on Treatment of Haemoglobinopathies and Allied Disorders. (Technical Report) 1972; 509:83 pages.

28   Mason S. Enquiry shows poor care for patients with sickle cell disease. British Medical Journal 2008; 336: 1152

29   NCEPOD (National Confidential Enquiry into Patient Outcome and Death). Sickle: A Sickle Crisis? (2008) [Sebastian Lucas (Clinical Coordinator), David Mason (Clinical Coordinator), M Mason (Chief Executive), D Weyman (Researcher), Tom Treasurer (Chairman) info@incepod.org

30   Konotey-Ahulu FID. Poor care for sickle cell disease patients: This wake up call is overdue BMJ Rapid Response May 28 2008 BMJ 2008; 336: 1152 to Susan Mayor “Enquiry shows poor care for patients with sickle cell disease” on National Confidential Enquiry into Patient Outcome and Death (NCEPOD) REPORT “SICKLE: A Sickle Crisis? (2008)

http://www.bmj.com/cgi/eletters/336/7654/1152a#196224 | http://www.info@ncepod.org

31   Konotey-Ahulu FID. Current “hit and miss” care provision for sickle cell disease patients in the UK. BMJ Rapid Response 22 July 2008


32   Chapman Nyaho Mawunu. Poor care for sickle cell disease patient: “Pain won’t kill him, but Morphine could”. British Medical Journal Rapid Response June 17 2008. http://www.bmj.com//cgi/eletters/336/7654/1152-a#197301

33   Shoetan Cecilia. I lost my Sickle Cell Disease adult daughter minutes after being given Diamorphine intravenously when she could not breathe. British Medical Journal Rapid Response June 3 2008 http://www.bmj.com//cgi/eletters/336/7654/1152-a#196520

34   Blankson Emmanuel Jeurry. Sickle Cell Disease is managed, NOT treated. British Medical Journal http://www.bmj.com//cgi/eletters/336/7654/1152-a#197350 18 June 2008

35   Frimpong-Boateng Kwabena. Poor care for sickle cell disease patients: This wake up call is overdue http://www.bmj.com//cgi/eletters/336/7654/1152-a#196359 BMJ Rapid Response May 30 2008 BMJ 2008

36   Ekem Ivy. Care for sickle cell patients. British Medical Journal Rapid Response 9 June 2008 http://www.bmj.com//cgi/eletters/336/7654/1152-a#196848

37   Dankwa Akosua M. Sickle Cell patients deserve to live. Brit Medical Journal Rapid Response http://www.bmj.com//cgi/eletters/336/7654/1152-a#197350 11 July 2008

38   Konotey-Ahulu FID. Management of acute painful sickle cell episode in hospital: NICE guidance is frightening! British Medical Journal Rapid Response 7 June 2012 http://www.bmj.com//cgi/eletters/344/bmj.e4063?ti

39   Konotey-Ahulu FID. KAGE SICKLE CELL FOUNDATION [Konotey-Ahulu Genetic Epidemiology Sickle Cell Foundation] Launched 2 September 2011 Ghana College of Surgeons, Accra.[Professor Kofi Awoonor as Chairman, and Nene Sakite II, Konor of Manya Krobo as Guest of Honour]

40 Konotey-Ahulu FID. Publications year by year from 1965 to 2014 great proportion on Sickle Cell Disease http://www.konotey-ahulu.com/publications_articles.asp

Conflict of Interest: None declared except that 3 siblings had sickle cell disease and a family genealogical history to 1670 AD www.sicklecell.md/images/generation.jpg or www.konotey-ahulu.com/images/generation.jpg  [Reference 3]





 Kwegyir Aggrey Distinguished Professor of Human Genetics University of Cape Coast, Ghana and Consultant Physician Genetic Counsellor, 9 Harley Street Ltd, Phoenix Hospital Group, London W1G 9AL, England


Felix I D Konotey-Ahulu
Felix I D Konotey-Ahulu



Kwegyir Aggrey Distinguished Professor of Human Genetics University of Cape Coast, Ghana and Consultant Physician Genetic Counsellor, 9 Harley Street Ltd, Phoenix Hospital Group, London W1G 9AL, England






Sickle Cell and Allied Haemoglobinopathy:

The Genetics that touches You and Me

Felix I D Konotey-Ahulu

Kwegyir Aggrey Distinguished Professor of Human Genetics, University of Cape Coast Ghana and Consultant Physician Genetic Counsellor 9 Harley Street Ltd, Phoenix Hospital Group, London W1G 9AL, England

 Originality, without doubt, is a hallmark of the University of Cape Coast. I define Originality as thinking what has not been thought before, saying what has not been said before, and doing what has not been done before. Right from the beginning when Head of State Dr Kwame Nkrumah decided to create a Third University in Ghana national and international eyebrows were raised.  But this 50 year’s Anniversary of what skeptics called “an experiment” has proved many wrong because UCC has many things to show that reflect sheer originality. Not least of which was the creation of the First Personal Chair on the African Continent to be linked to the name of an Educational Legend Dr James E Kwegyir Aggrey who thought things that had not been thought before, said things that had not been said before, and did things that had not been done before.

When Vice- Chancellor Rev Professor Samuel Adjepong, with the University Council made me The Dr Kwegyir Aggrey Distinguished Professor of Human Genetics in the University of Cape Coast and at the same time gave me an Honorary Doctorate in Science (when Dr Daniel Chapman Nyaho was also honoured with a Doctorate) I was greatly humbled and extremely grateful. I knew that work displaying originality was expected of me. This chapter contribution to the Golden Jubilee gives a little glimpse of what I have used the University of Cape Coast title to achieve. Quite apart from identifying UCC Science Graduates with genius through the Annual Dr Kwegyir Aggrey Prize Examinations, I have been ceaselessly engaged in skirmishes at the frontiers of Medicine especially where Ethics is made to take a back seat and commercial concerns promoted to the fore at the expense of patients’ health. A 32 year old son of a UCC Professor (Haemoglobin ‘SC’ phenotype) walked into a British Teaching Hospital on a Friday, and by the following Tuesday he was dead on a Heroin drip. A 32 year old Ghanaian lady (also Hb “SC” phenotype) walked into a London hospital, and within 18 hours she too was dead, with her mother, a nurse, looking on while Heroin was injected. I give the British Medical Journals ‘Full Marks’ for publishing not only my informed protests from the UCC platform, but also those of other Ghanaians including the Professor whose son died. You need to pay attention to what I have said here because Haemoglobinopathy affects all of us. Look up all the 40 references.

This article has also been published here on the Cape Coast website http://bit.ly/1DzHceM

History Versus Limits of Science: Is Solomonic Genius a Y Chromosome Phenomenon?

At least two groups of scientific thinkers or thinking scientists will frown on this article. First, those who base their atheism on reason, and secondly anti-Semitics. My plea is that both these groups – brilliant atheists and brilliant Jew haters read carefully what I have presented here and comment. There are some historic events whose explanation
defies scientific scrutiny [1]. Yet some aspects of these events can, within limits, have scientific explanations. Nobel laureate Sir Peter Medawar is one of the few original thinkers who recognize that there are limits to Science [2]. One such is origins (Ultimate questions) that are “beyond the explanatory competence of science” [2]. Medawar explains what he means by ultimate questions: “That there is indeed a limit upon science is made very likely by the existence of questions that science cannot answer and that no conceivable advance of science would empower it to answer.” [2, page 66]. Scientists can only hypothesize about origins but their theories do not change the fact that origins are historical events. The paradigm which says historical events that cannot be explained scientifically must be deemed not to have happened is contrary to Professor Medawar’s cogitations. And who am I to disagree with him?

Is Solomonic Genius a Y Chromosome Phenomenon?
History Versus Limits of Science: Is Solomonic Genius a Y Chromosome Phenomenon?

To read more click to open the PDF document above.

Management of sickle cell disease patient in the community

Re: Management of sickle cell disease patient n the community

FELIX ID KONOTEY-AHULU, Kwegyir Aggrey Distinguished Professor of Human Genetics, University of Cape Coast, Ghana

Consultant Physiician Genetic Counsellor in Sickle Cell and Other Haemoglobinopathies, 9 Harley Street Ltd., Phoenix Hospital Group, London W1G 9AL

British Medical Journal  Rapid Response www.bmj.com/content/348/bmj.g1765/rr/694233

13 April 2014

Re: Management of sickle cell disease in the community. Valentine Brousse, Julie Makani, David C Rees. 348:doi:10.1136/bmj.g1765

Valentine Brousse and colleagues’ Clinical Review [1], gives doctors little guidance for patient management. “Serjeant’s and my combined experience of 80 years covering thousands of patients in sickle cell crisis” can help. [2].


Graham Serjeant’s Jamaican experience [3] and my Ghanaian [4] differ from NICE’s Guidance [5] in UK where patients died from Morphine/Diamorphine overdose. [6 7] We managed sickle cell disease (scd) patients to university without Morphine/Diamorphine, Hydroxyuurea, or regular transfusions. Our experience (References 1965 to 2014} could save UK patients.

PROOF OF EXPERTISE http://bit.ly/1gDdMlN [8]

(1) Two brothers and one sister suffered from scd “Hereditary Rheumatism” traced back to 1670 AD www.konotey-ahulu.com/images/generation.jpg [9-11]. Siblings’ commonest cause of sickle cell crises characterized by convulsions and priapism [9 10] was Malaria. One brother had ‘gnathopathy’, my invented word for maxillary marrow hyperactivity [10 12 13 14].
(2) Directing largest Sickle Cell Clinic I catalogued 133 Illustrative Case Histories [10] including alcohol-induced myocardial infarction [10, p 503] and mental nerve neuropathy [15], kanumblll sign. Investigate any numb lower lip for scd. [15]
(3) Haematologist Helen Ranney published “There is no single clinical experience in the United States comparable to that of Dr Konotey-Ahulu” [16].
(4) Receiving with Linus Pauling and others “Martin Luther King Jr Foundation Award for Outstanding Research in Sickle Cell Anaemia” my Keynote Address “Difference between Sickle Cell Disease and Sickle Cell Trait” that exposed fraud of Insurance Companies led to being given 4 bodyguards in Philadelphia. [17] By saying Sickle Cell Trait was “largely asymptomatic” [1] Brousse et al repeated Insurance Companies’ misinformation/disinformation [18-21] used to levy Traits 150% Premium.
(5) On WHO Expert Genetics Advisory Panel with Haemoglobinopathy Greats who valued Ethics in Human Genetics. [22]


“In Jamaican experience morphia or its derivatives are rarely used or necessary” [23] and “the most painful crises may be treated in a day centre, the patient returning home in the evening” [24]. See more of Serjeant’s publications from 1968 [23-38].


(1) KEEP A DIARY! Circumstances [10 39], some patient-specific, precipitate crises eg Ghanaian scd man had sickle crisis on eating oranges [10]. Would Grousse et al start Hydroxyurea [1] after twice eating oranges?
(2) ALWAYS CARRY UMBRELLA. One rain-soaked scd boy got sickle crisis and stroke [44]. Trans-cranial Doppler [1] better prophylactic than raincoat? Hot weather too causes sickle crisis [39].
(3) NOSE PICKING causes Epistaxis [39 45].
(4) VALSALVA MANOEUVRE: In 18 causes of ocular bleeds [10] “six were related to sneezing, blowing nose, shouting, bending down, lifting heavy objects, and vigorous exercise” [46]. Avoid Valsalva in labour; Caesarian Section advised.
(5) DOCTORS BEWARE! Ectopic pregnancy, gall stones [47], appendicitis, splenic infarct [10] misdiagnosed as “Abdominal crisis”. Squatting (Tourniquet effect) can start crisis [10]. Opiates cause “Chest syndrome” [48]. Pulmonary embolism missed [49]. Note Intra-family scd phenotype differences [50 51]
(6) EXAMINE COMMUNITY RUMOUR. Medicated bed nets [1] no better than usual nets and may harm babies [52]. Malaria kills scd patients quicker [10 53-55]. Patients shun Hydroxyurea [56 57] and prenatal diagnosis [58 59] Drinking up to 4 L of water a day has stopped crises for past 25 years, as has “Aerobic Oxygen” 20 drops tds in water [60] Coconut juice clearing jaundice? [60.]
(7) STATIONERY BICYCLE aborts early morning priapism [10, 43]
(10) SICKLE CELL DISEASE PATIENT ACHIEVERS teach doctors 1993-2010 [70]
(11) G6PD Deficiency: 1 in 4 male and 1 in 16 female scd patients have this. [71 72]


NCEPOD discovered “9 out of 19 patients with sickle cell disease who had pain on admission and who then died had been given excessive doses of opiods” [6 7]. Yet NICE still recommends “a strong opiod intravenously” [5]. But Why? [2 4 10 48 75-87]. Patients complain to BMJ [88-90].

1 Brousse V, Makali J, Rees DC. Management of sickle cell disease in the community. BMJ 2014; 348:g1765 doi:10.1136/bmj.g1765

2 Konotey-Ahulu FID Opiates for sickle cell crisis? Lancet 1998: 351: 1438 “The question that puzzles me is why do west African and West Indian patients with sickle cell disease who did without morphine in our countries have to be given morphine pumps during sickle cell crisis when they come to the UK?”

3 Serjeant G. The case for dedicated sickle cell centres. BMJ 2007; 334: 477

4 Konotey-Ahulu FID. Dedicated sickle cell centres. BMJ Rapid responses March 20 2007 http://www.bmj.com/cgi/eletters/335/7618/462#167455

5 NICE GUIDELINES. Management of acute painful sickle cell episode in hospital; summary of NICE Guidance. BMJ 2012; 344: doi:http://dx.doiorg/10 1136/bmj’e’4063

6 NCEPOD – National Confidential Enquiry into Patient Outcome and Death. SICKLE: A Sickle Crisis? 2008 [Sebastian Lucas (Clinical Coordinator), David Mason (Clinical Coordinator), M Mason (Chief Executive), D Weyman (Researcher)/ Tom Treasurer (Chairman) info@incepod.org

7 Mason S. Enquiry shows poor care for patients with sickle cell disease. BMJ 2008; 336: 1152 “In 2 years 9 out of the 19 patients with sickle cell disease who had pain on admission and who then died had been given excessive doses of opiods”

8 Konotey-Ahulu FID. http://bit.ly/1gDdMlN International request to manage patients, for example, sicklecell.md/blog/index.php/2007/06/request-from-geneva-for-patient-in-hospital-in-colorado-usa June 2007

9 Konotey-Ahulu FID. Pattern of Sickle Cell Disease in Ghana (A Study Of 1,550 Consecutive Patients) – A Thesis Presented For The Degree of Doctor of Medicine (M.D.) In The University Of London 1971 Awarded Feb 1972.

10 Konotey-Ahulu FID. The Sickle Cell Disease Patient. Clinico-epidemiological study of 1550 consecutive patients at Korle Bu Hospital, Accra. T-A’D Co, Watford 1996 http://www.sicklecell.mde/aboutscd.asp
(Reprint of Konotey-Ahulu FID. The Sickle Cell Disease Patient. Natural History from a clinico-epidemiological study of the first 1550 patients of Korle Bu Hospital Sickle Cell Clinic. London & Basingstoke, Macmillan Press Ltd 1991/1992. Foreword by Roland B Scott MD, Howard Univ, Washington DC)

11 Konotey-Ahulu FID. Sickle Cell Disease In Successive Ghanaian Generations For Three Centuries (Manya Krobo Tribe) In The Human Genome Diversity Project: Cogitations of An African Native. Politics and The Life Sciences (PLS) 1999; Vol 18: No 2, pp 317-322.

12 Konotey-Ahulu FID. Effect of environment on sickle cell disease in West Africa; epidemiologic and clinical considerations. Chapter 3 in SICKLE CELL DISEASE – diagnosis, management, education and research. Eds Ahramson, Bertles JF, Wethers Doris L; St Louis – CV Mosby Co 1973, pp 20-38.

13 Konotey-Ahulu FID. The Sickle Cell Diseases: Clinical manifestations including the Sickle Crisis. Archives Intern Med 1974; 133: 611-619. http://archinte.ama.assn.org/cgi/reprint/133/4/611.pdf

14 Konotey-Ahulu FID. The liver in sickle cell disease. Clinical aspects. Ghana Med J 1969; 8: 104-118. (First ever use of word “Gnathopathy”)

15 Konotey-Ahulu FID. Mental nerve neuropathy: a complication of sickle cell crisis. Lancet 1972; 2: 388 [Constitutes discovery of a new physical sign in Clinical Medicine – The kanumblll sign spells out who discovered it, what it is, and where published: “konotey-ahulu numb lower lip Lancet” sign 1972]

16 Ranney Helen. Summary of Symposium 1972 on Sickle Cell Disease – Diagnosis, Management, Education and Research – In SICKLE CELL DISEASE, Eds H Abramson, John F Bertles, Doris Wethers (C Mosby Co), 1973, page 320: “There is no single clinical experience in the United States comparable to that of Dr Konotey-Ahulu”

17 Konotey-Ahulu FID. Four bodyguards and the perils of unmasking scientific truths www.bmj.com/cgi/reprint/335/7612/210.pdf BMJ 2007; 335: 210-11 BMJ July28 2007.

18 Konotey-Ahulu FID. Beware of symptomatic sickle cell traits. Lancet 1992; 339: 555. Doi:10.1016/0140-6736(92)90377-F (Pointing out that the Sickle Cell Trait ‘AS’ may not be true Sickle Trait, and that the Haemoglobin C Trait ‘AC’, may be something else, as the “A” has been shown could stand for Hb Quebec-Chori, by Witkowska et al – New Eng J Med 1991; 325: 1150-54 http://www.thelancet.com/journals/lancet/article/PII0140-6736(92)90377-F/fulltext

19 Konotey-Ahulu FID. Blaming sudden death on Sickle Cell Trait? Flaws in article of Charis Kepron, Gino Sobers, Michael Pollanen Exposed Sept 14 2011 www.sicklecell.md/blog/?p=105 or www.konotey-ahulu.com/blog/?p=105

20 Konotey-Ahulu FID. Sickle cell Trait Misinformation and Disinformation Nov 30 2011 www.sicklecell.md/blog/?=108 [Comprehensive Review]

21 Konotey-Ahulu FID. Further Communication on “Sickle Cell Trait Misinformation and Disinformation” and Sickle Cell Terminology: Disease or Disorder? www.sicklecell.md/blog/?p=127 April 16 2012

22 Boyo Alex E, Cabannes R, Conley CR, Lehmann H, Luzzatto L, Milner PF, Ringelhann B, Weatherall DJ, Barrai I, Konotey-Ahulu FID, Motulsky AG. WHO (Geneva) Scientific Group on Treatment of Haemoglobinopathies and Allied Disorders. (Technical Report) 1972; 509: 83 pages.

23 Serjeant GR. Sickle Cell Disease. Oxford, Oxford University Press, 1985.

24 Serjeant GR. Sickle cell disease. Lancet 1997; 35: 725-730.

25 Serjeant GR, Richards R., Barbor PRH, Milner PF. Relatively benign sickle cell anaemia in 60 patients aged over 30 in the West Indies. BMJ 1968; 3: 86

26 Serjeant GR, Serjeant BE, Milner PF. The irreversibly sickle cell: a determinant for haemolysis in sickle cell anaemia. Br J Haematol 1969; 17: 527-533.

27 Serjeant GR, Galloway RE, Gueri MC. Oral zinc sulphate in sickle cell ulcers. Lancet 1970; 2: 891

28 Serjeant GR. The clinical picture of sickle cell anaemia in Jamaica. MD Thesis, University of Cambridge, 1971.

29 Serjeant GR, Ashcroft. Shortening of the digits in sickle cell anaemia. A sequel of the hand-foot syndrome. Trop Gegraph Med 1971; 23: 341-346.

30 Serjeant GR, et al 1972. The conjunctival sign in sickle cell anaemia. JAMA 1972; 219: 1428-31

31 Serjeant GR, et al. The clinical features of sickle cell beta-thalassaemia in Jamaica. Brit J Haematolol 1973; 24: 19-30

32 Serjeant GR, et al. The clinical features of haemoglobin SC disease in Jamaica. Brit J Haematolol 1973; 24: 491-500.

33 Serjeant GR et al. Screening of cord blood for the detection of sickle cell disease in Jamaica. Clim Chem 1974; 20: 666-69.

34 Serjeant GR et al. The internal auditory canal and sensori-neural hearing loss in homozygous sickle cell disease. J Laryngol Otol 1975: 89: 453-455

35 Serjeant GR. Sickle Cell Disease, 2nd Ed. Oxford, Oxf Univ Press, 1992.

36 Serjeant GR, De Ceulaer C, Lethbridge R, et al. The painful crisis of homozygous sickle cell disease. Br J Haematol 1994; 87: 586-591.

37 Serjeant GR, Serjeant B. Sickle Cell Disease, 3rd Ed, Oxford, OUP, 2001.

38 Serjeant GR. Blood transfusion in sickle cell disease. A cautionary tale. Lancet 2003; 361: 1659-60 [Graham Serjeant’s adult not-transfused patient in Jamaica went on holiday in USA, was transfused and died!].

39 Konotey-Ahulu FID Konotey-Ahulu FID. Sicklaemic human hygrometers. Lancet 1965; 1:1003 1004 [Listing precipitating causes of crises eg hot weather etc] [http://www.pubmedcentral.nih.gov/picender.fcgi?artid=1846286&blobtype=pdf

40 Konotey-Ahulu FID. Torrential epistaxis associated with symmetrical facial skin ulceration in sickle cell anaemia. BMJ 1965; 2:859-860 doi:10.1136/bmj2.5466.859

41 Konotey-Ahulu FID, Kuma Eunice. Skeletal crumbling in sickle cell anaemia complicated by Salmonella typhi infection. Brit J Clin Practice 1965; 19: 575-578.

42 Konotey-Ahulu FID. Acute osteomyelitis in African children unmasks un-masks sickle cell disease with salmonellosis BMJ Rapid Response February 1 2014 http://www.bmj.com/content/348/bmj.g66?tab=response

43 Konotey-Ahulu FID. Erectile dysfunction: Test, please, for Sickle Cell Disease www.bmj.com/content/348.g129

44 Konotey-Ahulu FID. Sickle cell disease and the patient Lancet 2005; 382-383 Jan 29-Feb 4 [Importance of Circumstances in initiating crises]

45 Konotey-Ahulu FID. Epistaxis from sickle cell disease must not be forgotten www.bmj.com/content/344/bmj.e1097/rr/576087 28 March 2012

46 Konotey-Ahulu FID. Valsalva vitreous haemorrhage and retinopathy in sickle cell haemoglobin C disease. Lancet 1997; 349: 1774

47 Archampong EQ, Konotey-Ahulu FID. Biliary tract disease and sickle cell anaemia in Korle Bu Hospital, Accra. Ghana Med J 1975; 14: 176-180

48 Ringelhann Bela, Konotey-Ahulu FID. Haemoglobinopathies and Thalassaemias in Mediterranean areas and in West Africa: Historical and other perspectives 1910 to 1997. Accademia del Scienze Ferrara Atti, volume 74, Anno Accademico 174 1996-97, pages 297-307 [A Century Review]

49 Shoetan Cecilia. I lost my Sickle Cell Disease adult daughter minutes after being given Diamorphine intravenously when she could not breathe. http://www.bmj.com/cgi/eletters/336/7654/1152-a#196520 June 3 2008 BMJ

50 Konotey-Ahulu FID, Ringelhann B. Sickle cell anaemia, sickle cell thalassaemia, sickle cell haemoglobin C disease, and asymptomatic haemoglobin C thalassaemia in one Ghanaian family. BMJ 1969; 1: 607-612. http://www.bmj.com/cgi/reprint/2/5648/48.pdf [4 Hbnopathy phenotypes]

51 Konotey-Ahulu FID. Patterns of clinical haemoglobinopathy. East African Med J 1969; 46: 149-156 (With tables that distinguish phenotypes clinically)

52 The Globe and Mail, Toronto. Tough flights for mosquito nets. “If they are safe for babies and mothers in Africa, why are they not safe enough in Canada for a week?” 18 August 2006.

53 Konotey-Ahulu FID. Malaria and sickle cell disease. BMJ 1971; 2: 710-11.

54 Djabanor FFT, Reindorf CA, Konotey-Ahulu FID. The effect of sickle cell disease on Ghanaian children. In First International Publication No (HSM) 1974; 73-9141: 70-87

55 Konotey-Ahulu FID. Malaria and sickle cell: “Protection?” Or “No Protection?” – Confusion reigns. BMJ Rapid Response October 13 2008. http://www.bmj.com/cgi/eletters/337/oct01_3/a1875#203067

56 Olujohungbe A, Cinkotal I, Yardumian A. Hydroxyurea therapy for sickle cell disease in Britain. BMJ Editorial 1998; 316: 1689. “Many patients are unwilling to take the drug.”

57 Olujoungbe Ade. Bi-directional trust is needed in pain management in sickle cell disease. BMJ Rapid Response 2 July 1999 to Maxwell K, Streetly A, Bevan D BMJ 1999; 318: 1585-1590.

58 Konotey-Ahulu FID. Ethical issues in pre-natal diagnosis. BMJ 1984; 289: 185 http://www.bmj.com/cgi/reprint/289/6438/185-a.pdf

59 Konotey-Ahulu FID. Refusing to provide a pre-natal test for refusing later termination of pregnancy; can it ever be ethical? BMJ Rapid Response. November 20 2006 http://www.bmj.com/cgi/eletters/333/7577/1066#149662

60 Konotey-Ahulu FID. The Sickle Achievers (1). Ghanaian Times, July 23 2005 “I cannot think of a single Ghanaian family that did not have or know of someone with sickle cell disease – known by Tribal names”

61 Konotey-Ahulu FID. The Sickle Achievers (2) Ghanaian Times. August 13 2005 “Some time ago I coined the term for cold season Rheumatism which Europeans call Sickle Cell Disease … The ACHEACHE Syndrome (1 ACHE from each parent”. Makes it easy for Genetic Counselling.

62 Konotey-Ahulu FID. Genetic Counselling in sickle cell disease. BMJ 1969; 3: 235 http://www.bmj.com/cgi/reprint/3/5664/235.pdf (Put ‘ACHE’ for ‘BAD’) PERSONAL VIEW doi:10.1136/bmj.2.5648.48

63 Konotey-Ahulu FID. Sickle cell disease. The Case for Family Planning ASTAB Books Ltd, Accra, 1973

64 Konotey-Ahulu FID. Need for ethnic experts to tackle genetic public health. Lancet 2007; 370: 1836 [doi:10.1016/50140-6736(07)61771-1]

65 Ringelhann B, Konotey-Ahulu FID, Yawson G, Bruce-Tagoe AA, Miller A, Huisman THJ. Alpha Thalassaemia in West Africa. Symposium in Medical Genetics, Debrecen-Hajduszoboslo, Hungary (April 26-29 1976), pp 614-616 in Szabo G and Papp Z, Eds Medical Genetics, Excerpta Medica 1977

66 Konotey-Ahulu FID. Maintenance of high sickling rate in Africa: Role of polygamy. J Trop Med Hyg 1970 Jan; 73(1): 19-21 (38 References)

67 Bonney GE, Konotey-Ahulu FID. Polygamy and genetic equilibrium. Nature 1977; 265: 46-47 doi:10.1038/265046a0..n5589/pdf/265046a0.pdf

68 Konotey-Ahulu FID. Male procreative superiority index (MPSI): The missing co-efficient in African anthropogenetics. BMJ 1980; 291: 1700-02.

69 Konotey-Ahulu FID. The Male Procreative Superiority Index (MPSI): It’s relevance to genetical counselling. In FIFTY YEARS OF HUMAN GENETICS – A Festschrift and liber amicorium to celebrate the life and work of GEORGE ROBERT FRASER. Ed: Oliver Mayo & Carolyn Leach. Wakefield Press 2007, 1 The Parade West, Kent Town, Sth Australia www.wakefieldpress.com.au

70 Omaboe Letitia, Konotey-Ahulu FID. The Second International Conference on The Achievements of Sickle Cell Disease Patients. Accra 19th July 1995 Conference Brochure

71 Acquaye CTA, Gbedemah KA, Konotey-Ahulu FID. Glucose-6-phosphate Dehydrogenase Deficiency Incidence in Sickle Cell Disease patients in Accra. Ghana Med J 1977; 16: 4-9

72 Konotey-Ahulu FID. G6PD Deficiency in Ghanaians. How to recognise it.
Click ‘BLOG’ on www.sicklecell.md and click on January 2008 for 20 answers.

73 Konotey-Ahulu FID. WORLD SICKLE CELL DAY 19th June 2012 www.sicklecell.md/blog/?p=132 Featuring (i) The Inheritance of Sickle Cell Disease (ii) The Person with Sickle Cell Disease (iii) The Teenager with Sickle Cell Disease (iv) The Adult with Sickle Cell Disease.

74 WORLD SICKLE CELL DAY 19th June 1013. Broadcast Interview by Tunu Louise Roberts emphasising Public Health Approach to management, and Genetic Counselling with NORMACHE as Trait and ACHEACHE as Disease www.sicklecell.md or www.konotey-ahulu.com (Home Page) Also accessed as http://youtu.be/wEyebVIhr7Q [Suitable for patients and parents

75 Konotey-Ahulu FID. Morphine for painful crises in sickle cell disease. BMJ 1991; 302: 1604 (Commenting on Professor Chamberlain’s recommendation of morphine in pregnancy in sickle cell disease – BMJ 1991; 302: 1327-30). “In obstetrics what happens too foetal respiration when morphine is used?” http://www.bmj.com/cgi/reprint/302/6792/1604-c.pdf

76 Konotey-Ahulu FID. Management of patients with sickle cell disease. African Journal of Health Sciences 1998; 5: 47 [On Sally Davies and Lola Oni in BMJ 315: 656-60 “The Central Middlesex management protocol uses morphine infusions”] Response: “I fear Davies and Oni’s statement will make morphine the accepted drug for sickle crisis management. The consequences for such an approach are dire, especially when some UK hospitals are already making diamorphine their first choice”. And what did NCEPOD find in 2008?

77 Konotey-Ahulu FID. Opiates for sickle cell crisis. Lancet 1998; 352: 651-2

78 Konotey-Ahulu FID. Opiates for pain in dying patients and in those with sickle cell disease www.bmj.com/cgi/eletters/335/7622/685#177986 BMJ Response 11 Oct 2007

79 Konotey-Ahulu FID. Current “hit and miss” care provision for sickle cell disease patients in the UK. BMJ Rapid Response 16 July 2008. http://www.bmj.com/cgi/eletters/337/jul11_2/a/771#199135

80 Konotey-Ahulu FID. Management of sickle cell disease versus management of the sickle cell disease patient. BMJ Rapid Response 17 Sept 2008 http://www.bmj.com/cgi/eletters/337/sep08_1/a1397#202088

81 Konotey-Ahulu FID. Clinicians facing conflicting recommendations. Use common-sense? http://ww.bmj.com/cgi/eletters/337/nov28_2/a2530#205377 December 2008.

82 Konotey-Ahulu FID. Poor care for sickle cell disease patients: This wake-up call is overdue. BMJ Rapid Response (May 28) BMJ 2008; 336: 1152 http://www.bmj.com/cgi/eletters/336/7654/1152-a#196244 to Susan Mayor’s “Enquiry shows poor care for patients with sickle cell disease” on National Confidential Enquiry into Patient Outcome and Death (NCEPOD) REPORT “SICKLE: A Sickle Crisis? (2008)” http://www.info@ncepod.com

83 Konotey-Ahulu FID. Inquest into diamorphine deaths: Does NCEPOD sickle cell patients report warrant a similar inquest? BMJ Rapid Response March 7 2009 http://www.bmj.com/cgi/eletters/338/mar03_3/b903#210208

84 Konotey-Ahulu FID. UK Drug related deaths are still rising: So where is NICE? http://www.bmj.com/cgi/eletters/sep01_1/b3536#219836 BMJ Rapid Response to S Mayor: “UK drug related deaths are still rising.” Sept 6 2009. .

85 Konotey-Ahulu FID. The politics and economics of pain relief in the West and Third World. http://www.bmj.com/cgi/eletters/341/aug11_2/c3800#240684 Response Aug 24 to T Anderson doi:10.1136/bmj.c3800 Aug 11 2010

86 Konotey-Ahulu FID. Management of an acute painful sickle cell episode in hospital. NICE Guidance is frightening! BMJ Rapid Response Sept 7 2012 www.bmj.com/content/344/bmj.e4063/rr/599158 (42 References)

87 Konotey-Ahulu FID. Opiods for chronic non-cancer pain – Chemotherapy – Clinical Guidelines: Where does ultimate responsibility lie? BMJ Rapid Response www.bmj.com/content/346/bmj.f2937/rr/651421 June 25 2013

88 Dankwa Akosua M. Sickle Cell patients deserve to live. BMJ Rapid Response to NCEPOD Report 11 July 2008 [Adult “SS” wrote to the BMJ:
http://www.bmj.com/cgi/eletters/336/7654/1152-a “I know 60 and 70 year olds (yes, sickle cell patients) who have got to that age without ever receiving this as treatment”.

89 Chapman Nyaho Mawunu. Poor care for the sickle cell disease patient: “Pain won’t kill him, but Morphine could”. BMJ Rapid Response to NCEPOD by adult Sickle cell haemoglobin C disease grand-mother 17 June 2008 http://www.bmj.com/cgi/eletters/336/7654/1152a

90 Amanor-Boadu Dorothy, Bruce-Tagoe Alexander, Konotey-Ahulu Felix. The Third International Conference On The Achievements Of Sickle Cell Disease (ACHEACHE) Patients, Accra – 19th July 2010. Adeko Ltd, Accra ISBN: 978-9988-1-3927-8 “One known ‘SS’ man with a PhD, who had never in his 63 years been transfused though Hb level was never above 8.8 g/dL and who had never been prescribed Hydroxyurea, astonished delegates when he announced ‘I do not remember when I last took a pain killer for my sickle cell anaemia. Drink plenty of water, avoid malaria, and have a positive attitude to life’” [page 15] Quoted in full in link of Reference 85 above. [Dorothy Amanor-Boadu herself is a 59-year old “SS” Nurse Oncologist in Accra].

Competing interests: Coming from a family with 3 Sickle Cell Disease (scd) siblings I find it very difficult to remain detached when the received wisdom in the management of scd patients that was proven by NCEPOD to be harmful is still endorsed by NICE.

FELIX ID KONOTEY-AHULU, Kwegyir Aggrey Distinguished Professor of Human Genetics, University of Cape Coast, Ghana

Consultant Physiician Genetic Counsellor in Sickle Cell and Other Haemoglobinopathies, 9 Harley Street Ltd., Phoenix Hospital Group, London W1G 9AL

JFK Assassination, sermon by Dr Martyn Lloyd-Jones 24 Nov 1963 now online!

President J F Kennedy Assassinated Friday November 22 1963

Westminster Chapel with Dr Martyn Lloyd-Jones Sunday pm Nov 24 1963

Diary Entry of Dr Felix I D Konotey-Ahulu in London

LORD’s Day 24th Nov 1963: The Doctor preached as usual on John 1 v 16 in morning, and Gal. 6 v 14 in evening and he made it most relevant to President Kennedy’s assassination – The Cross as the only thing that makes peace, and brings people together. “I would wish President Kennedy’s murder to bring peace, but I know it won’t. I tell you of a MURDER that reconciles sinful man to GOD!” It was tremendous. Spent day at Mum’s with my beloved & Dawid. Evening prayer together. We heard after chapel the suspect of Kennedy’s killer shot dead.


On the 50th Anniversary, our Baby Dawid who was then 3 months old when JFK was killed, has now reproduced the entire Sunday evening Service at Westminster Chapel in which the words of the preacher, Dr Martyn Lloyd-Jones, quoted in bold letters above were said. See www.soundcloud.com/dawid1 and click on JFK, and join those of us who were there half a century ago in a Remembrance Worship:-

Prayer (Short)

Hymn: Before Jehovah’s awful Throne

Scripture Reading: Ephesians 2 verses 1 to 22

Hymn: My GOD I thank Thee

Prayer (Comprehensive)

Hymn: In the Cross of Christ I glory

Sermon: Galatians 6 v 14 “God forbid that I should glory save in the Cross of Christ”

Hymn: Abide with me

Prayer and Benediction