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Camp Jumoke Archives

 

 

Parenting a Child with Sickle Cell?
2008 Poster-Child
2009 Poster-Child
2010 Poster-Child

2011 Poster-Child

How to do the turtlewalk

Look for more archived links in the near future, as we endeavour to give you valuable information about Camp Jumoke, Sickle Cell and how you can help.

 

The Best Way To Help

Blood Services

Many Sickle Cell patients are treated with blood transfusions to relieve their “crisis”. When a patient needs a blood transfusion, a compatible blood type is required.

In the case of Sickle Cell, the extent of the match may need to be more precise. The precise matching for special antigens is called phenotyping.

For further information, please contact Canadian Blood Services at
1-888-2-Donate or visit their website. Canadian Blood Services

What is Sickle Cell Disease (SCD)?

scd imagediagram

Resources and Form Downloads

Camp Jumoke is the only camp in Canada that serves the unique emotional and health-care needs of children living with Sickle Cell Disease (SCD).

Eligibility
Any child with SCD between the ages of 8 and 16 is eligible to attend Camp Jumoke. Our camp counsellors are trained to work with our children in cooperation with our staff of health care professionals.

Camper Selection is on a first come, first serve basis; subject to medical approval.

Please use the following links to access more detailed information.


Camp Jumoke is hosted at the site of Camp Wenonah near Bracebridge, Ontario which was specifically chosen for the picturesque surroundings, experienced staff and great programs.

Click the here for directions to Camp Jumoke's Head Office.
Join us at one of our Regular Board Meetings.

General Resources

Tools & Media Players

What is Sickle Cell Disease (SCD)?

Sickle Cell Disease (SCD) is an inherited blood disorder that causes the distortion, or “sickling,” of red blood cells. It occurs when a child inherits a sickle cell gene from each of their parents.

SCD affects millions of people throughout the world, in countries such as West and Central Africa, South America, Cuba, Central America, India, Middle East and Mediterranean countries.

One Family Dealing with SCAIt is particularly common among people of African ancestry. In Canada, approximately 1 in 600 have the disease and approximately 1 in 10 people are carriers of the sickle cell trait.

In SCD, the red blood cells contain an abnormal type of hemoglobin. Unlike normal red blood cells that are usually smooth and donut-shaped, these red blood cells become stiff and assume a sickle-shape (crescent shaped) and have difficulty passing through small blood vessels. When sickle-shaped cells block small blood vessels, less blood can reach that part of the body.