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Camp Jumoke – Info Sheet
http://www.jumoke.org/

ABOUT CAMP JUMOKE
 
Camp Jumoke (pronounced joo-MOH-keh) is a non-profit, charitable organization whose mandate is to enrich the life experiences of children affected with sickle cell disease by sending them to summer camp for two weeks each year. Camp Jumoke, the first and only summer camp for children with sickle cell disease, was co-founded in Canada in 1994 by members of The Association for the Advancement of Blacks in Health Sciences (AABHS). 
 
 “Jumoke” is a word from the Yoruba language of Nigeria that means, “Everyone loves the child”. Since our second year of operation, the turtle has been our symbol. The turtle lives longer than any other animal except man. In ancient cultures, the turtle was revered as a symbol of perseverance; some cultures believed that turtles possessed mystical healing powers. In nature, only the strong survive, and the turtle does this best. For these reasons, Camp Jumoke has chosen the turtle as a symbol of the struggle and strength of all of our children, especially those with Sickle Cell Disease.
 
What is the Camp Jumoke Program?
 
Since 1994, Camp Jumoke has been a special place for children affected with Sickle Cell Disease and has sent more than 400 Ontario children to summer camp. Our responsibilities include finding an accredited campsite and staff, medically screening the children to ensure they are healthy enough to attend camp, and providing an organized, medically supervised camping experience.
 
Approximately 500 children with sickle cell disease are treated medically at the Hospital for Sick Children in Toronto. The overwhelming majority of these children are visible minorities. Some families are recent immigrants to Canada and the cost of camp represents an expense beyond their means. Camp Jumoke covers the cost to send each child to camp, which is currently greater than $1,750.
 
This year, our plan is to send 35 children to camp between the ages of 7 and 16. Currently our camp is hosted by Camp Wenonah in Bracebridge, Ontario. They have welcomed us with open arms for the past 6 years. Ultimately, our goal is to be able to send every child to camp that expresses an interest and one day to have a camp that we can call our own.
 
FUNDRAISING INITIATIVES
 
In addition to our Annual Bowl-a-thon, Camp Jumoke engages in a number of other fundraising efforts to support the children, including:
 
Annual Walk-a-thon
Please join us for our Annual Camp Jumoke Walk-a-thon at Nathan Phillips Square in Toronto. The Annual Walk-a-thon, also known as the Turtle Walk, is Camp Jumoke’s main fundraiser. Through your generous support of this event, we raise a large portion of the funds needed to send our kids to camp. Last year, thanks to your contributions, we were able to send 36 children to camp. Our plan is to send 35-40 children to Camp Wenonah, near Bracebridge, Ontario. As usual, the Walk-a-thon  will offer a fun-filled day for the whole  family featuring exercise (6Km walk), live entertainment and lots of prizes.
Pledge forms will soon be available; please contact our office to receive yours. Hope to see you all there!
 
Scholarship Award
Camp Jumoke will be hosting their  Annual Scholarship Award. This is the event where we present a scholarship of $1,500 to a child who will represent Camp Jumoke for the year as our Poster Child. All children of Camp Jumoke or any child with Sickle Cell Disease is eligible and encouraged to apply for the scholarship after the camping session. Please join us either as guest, sponsor, or contributor to our endowment fund.
 

 

Seed of Life Philanthropic Organization Inc
 
 
Seed of life has been approved to:
Educate the public on the subject of Sickle Cell Anemia by providing lecturers in Schools, providing Seminars and by collecting and disseminating information on that topic.
Provide support for patients living with Sickle Cell Anemia by organizing support groups.
Advance education by providing scholarship to students with Sickle
Cell Anemia.
Relieve poverty by providing seminars, workshops and mentorship to persons of low income.
SOLPO’s Beliefs:
We believe that education is the cure to ignorance.
We believe that even though there is no cure for Sickle Cell Anemia at this point, educating the populace with the goal of reducing the number of children born with this disease is a must.
We believe in protecting our children and our future against the pain and agony of Sickle Cell Anemia through outreach campaigns and programs.
We believe that less children and eventually less adults will have to live with this deadly disease if we keep on educating those who are in the procreating stage of their lives about Genes and Genotype testing.
We believe that poverty could be reduced within our community if we educate people on how to set their minds on great things and use the right tools to achieve them.
We believe that many are poor in the African-Canadian Community not because they chose to but because of lack of needed tools and information on how to succeed
 


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