Will's Power

CHAMPIONING LYMPHATIC DISEASE TREATMENT & RESEARCH FOR KIDS IN CANADA

Funds raised will support treatment and research of complex lymphatic anomalies within the Vascular Anomalies Clinic at SickKids. The Vascular Anomalies Clinic treats a variety of lesions, including hemangiomas, venous malformation, arteriovenous malformations and lymphatic malformations. Although the age limit for patients is from birth to 18 years of age, this clinic also assesses fetal vascular anomalies. To learn more click here!

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Meet Will

Hi I'm Will, I have a Complex Lymphatic Anomaly.  It is a very rare condition and there are not many others like me.  When I get sick my lungs fill with lymphatic fluid and I cannot breathe well.  I need to have chest tubes and oxygen to help me.  The chest tube hurts me a lot and I have to take special medicine to help with the pain. It is very hard to walk and move and I stay in bed a lot which I do not like. 

The last time this happened to me I was in the hospital for 50 days and 50 nights.  No one was able to visit me because of COVID, only my Mom or Dad could stay with me.  I really missed my brothers, sister, and friends.  I just wanted to go home and play with them and have fun.  Once I missed my brother's birthday and Father's day.  I just want to get better so I don't have to miss anything else.  

I have done so many things to try and help me to get better.  In the past 2 years, I have seen over 70 doctors, physiotherapists, respiratory therapists and registered dietitians at different hospitals and institutions.  They were all so nice to me and tried to help.  I have had x-rays, CT scans, MRIs, sclerotherapy, ultrasounds, echocardiograms, MR lymphangiograms, electrocardiograms, chest tubes, bone density scans, biopsies, lots of blood work, chemotherapy, TPN (Total Parenteral Nutrition), medium chain triglyceride (MCT) and high protein diet.  I even had to go on a low fat diet!  That was so hard, I missed my favourite foods.  Me and my Mom tried new recipes, but I was SO happy when my doctor told me I could eat normal food again!  We made a blog if you are on a low fat diet too, you can see my favourite recipes here: Zero For My Hero

We do not know what type of anomaly I have so I don't know what medicine to take to help me.  The way to find out is through genetic testing.  Canada does not have a lymphatic center. We also do not know of any research happening in Canada now that can help me and kids like me.  I may be travelling to the United States to get the help I need.  I would like to stay in Canada with my family.  I hope we can create a place in Canada to help all the kids like me.  Somewhere that research and genetic testing can happen and to one day find a cure!  I really hope that you can help me and others like me to make this happen.  Thank-you for supporting us!

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