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Annie Sedoric's Fundraiser
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Support Children's Brain Tumor Foundation and my Chicago Marathon run!
Because of your donation, brain tumor families will know they are not alone!
In April, 2022 I underwent brain surgery at BWH in Boston. Only a month prior I was diagnosed with a rare, incurable, disease called acromegaly. I was 24 years old, and just had moved to NYC to start “adulting”, but really I felt like a kid. I could not have gone through the experience of brain surgery or receiving a lifelong diagnosis without the support of my family, and they could not have gone through it without the support of others.
I felt like my life was over, but it really had only begun at the age of 24. I want the young kids that go through these incredibly hard experiences to know that their lives are just beginning and traumatic medical experiences are not defining. In November, 2024 I ran the NYC marathon for the National Organization of Rare diseases and this coming October I could not be more proud than to raise money for CBTF while showing myself, and others, that I am strong and capable even when living with Acromegaly.