Hello, I want to raise awareness for the National MPS Society to help them raise funds for MPS I and other related diseases. MPS has made me who I am today. I was diagnosed at the age of 11 but started showing signs at the age of five.
It has been a long hard road to diagnosis and the road was not easy. I have had 5 surgeries since diagnosis and will have many more in my near future.
This disease is so complicated and yet so simple to understand. I am missing an enzyme that helps remove waste from my body. Enzyme Replacement Therapy helps provide an artificial enzyme back into cells to remove this waste. Still, this is not a cure.
We are in need of funding to help create different treatments and hopefully a cure one day. Please make a donation and help us out.
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