Dear Friends
Every day welcomes more birth of children with Sickle Cell Disease. As the children grow and had to endure the pains and complications associated with this disease, many parents wish they could save their children from the pain and agony of the disease. We now know that many children were/will continue to be born with Sickle Cell Disease due to the ignorance of parents about their Carrier status at the time of procreation.

Hence I submit to you that in the absence of a viable cure, the only way to truly reduce/eliminate sickle cell disease in our community is by encouraging Haemoglobin Electrophoresis testing and by educating our children generation after generation about the importance of this testing.

Creating a family History around Sickle Cell Disease has been a favorite a mine and I encourage each and every one of you to start documenting the Genotype Status of each member of your family. Test & Educate the children and the grandchildren. No age is too young to be educated. Thank you for visiting Seed of Life and we hope you will support this great cause both financially and with your time. Volunteers are always needed.

You may donate online by going to our donate page OR call/e-mail us to set up a monthly pre-authorized payment for you. No amount is too small. We will love to hear from you.
Send us a line at sol@seedoflifepo.org OR call 416-745-4267

Sincerely,
LanreTunjiAjayi
Lanre Timothy Tunji-Ajayi
President,
Seed of Life Philanthropic Organization
president@seedoflifepo.org
Ph: 416-745-4267 OR 905-830-1388

SOLPO Scholarship
Sunday Afolabi was born with Sickle Cell Anemia to a middle class family in Nigeria West Africa. He grew up knowing that he was very special and brilliant as well. He would sometimes made comments such as “God must know why I have to bear this cross; but I look for a day when nobody will ever have to suffer from Sickle Cell Anemia again”.... More
SOLPO Acitivites
Oct 31   SOLPO Community Forum
Events
Ontario Government has listened
Many thanks to the Ontario ministry of health for listening to patient groups and funding Exjade for patients living with Sickle Cell Disease and Thalassemia. Thanks to you all for supporting the initiatives that made it possible.
Sickle Cell Patients that need Exjade are now able to receive it without worrying about being able to afford it.
You made it possible...... More