Home >
24 September 2021
Make a donation

The resource to the Sickle Cell Disease Patient. We hope you find this website instructive.

If this website has been of help to you, feel free to make a donation to enable us investigate enquirers who wish to know whether they are carrying an ACHE gene or not, and thus help them make decisions that will prevent the burden of this hereditary ACHEACHE ailment of Sickle Cell Disease and other Haemoglobinopathy.

Your donation would be sent to Tadco@sicklecell.md



Publications
1965 to present day, click here
432Konotey-Ahulu FID. COVID-19: “WHAT WE EAT MATTERS ALL THE MORE NOW” SHOULD ANTICIPATE OTHER NON-VACCINE ADVICE. Re: Fiona Godlee. EDITORIAL. What we eat matters all the more now. BMJ 2020; bmj.m370 December 1 2020.
2020 | More
Donations
If this website has been of help to you, feel free to make a donation to enable us investigate enquirers who wish to know whether they are carrying an ACHE gene or not, and thus help them make decisions that will prevent the burden of this hereditary ACHEACHE ailment of Sickle Cell Disease and other Haemoglobinopathy.
book
FAQs (Click here for more)
1. Why is Sickle Cell Anaemia only found in Black people?
This is a very common mis-conception. Sickle cell anaemia (sca) is not "only found in Black people". White people in Greece, Sicily, Turkey, and their offspring around the world suffer from sickle cell anaemia (sca)... | More
2. Why do people with sickle cell anaemia not suffer from malaria?
A common mis-conception. A dangerous misconception. People with sickle cell anaemia do suffer from malaria, and very badly too. Doctors who have been wrongly taught have been known to advise... | More
3. Why then do Science teachers always talk about malaria protection in sickle cell anaemia?
Inadequate knowledge, or plain ignorance is the simple answer. I repeat: malaria affects sickle cell anaemia patients more seriously than it does others.... | More