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A World With Out Myasthenia Gravis

Organized by Alexandra Castro
Po5410072 front
A World With Out Myasthenia Gravis Fundraiser - unisex shirt design - front
A World With Out Myasthenia Gravis Fundraiser - unisex shirt design - back
A World With Out Myasthenia Gravis shirt design - zoomed
A World With Out Myasthenia Gravis Fundraiser - unisex shirt design - front
A World With Out Myasthenia Gravis shirt design - zoomed
A World With Out Myasthenia Gravis Fundraiser - unisex shirt design - front
A World With Out Myasthenia Gravis Fundraiser - unisex shirt design - back
A World With Out Myasthenia Gravis shirt design - zoomed
Gildan Ultra Cotton T-shirt

Help us find a cure for Myasthenia Gravis

Custom Ink
All funds raised will be paid directly to Myasthenia Gravis Foundation of America for Research, Treatment, and a cure!.
$450 raised
64 items sold of
50 goal
Thanks to our supporters!
$16
Gildan Ultra Cotton T-shirt, Unisex - Sports Grey
Gildan Ultra Cotton T-shirt
Unisex - Sports Grey
  • A World With Out Myasthenia Gravis Fundraiser - unisex shirt design - small
  • A World With Out Myasthenia Gravis Fundraiser - unisex shirt design - small
  • A World With Out Myasthenia Gravis Fundraiser - unisex shirt design - small
Organized by Alexandra Castro

About this campaign

Tens of thousands of Americans are affected yet so few have ever heard of it.Myasthenia Gravis is a chronic autoimmune disease in which antibodies mistakenly attack and destroy neuromuscular connections, causing weakness in muscles that control basic movements that include walking, swallowing, blinking, breathing, and smiling. Many patients are unable to enjoy their daily lives, attend school, or work.

My name is Alexandra Castro and I have Myasthenia Gravis. Myasthenia Gravis is a chronic autoimmune disease in which antibodies mistakenly attack and destroy neuromuscular connections, causing weakness in muscles that control basic movements that include walking, swallowing, blinking, breathing, and smiling. Many patients are unable to enjoy their daily lives, attend school, or work. MG can affect every one in different ways. I was diagnosed at the age of 24 (9yrs ago). Since then my life has changed. I struggle everyday to live a normal life and do thenormal things that people take for granted. Such as taking in a full breath, eating a steak, chugging a coke, having a normal conversation with out losing my voice in mid conversation, and myfavorite of all;singing a song at the top of my lungs in the shower. These are just a few of the things I wish I could do againbut there is somuch more to this disease thannot being able to drink a cup of water with out choking.I have spent many years just trying to blend intrying, not tobe known as the girl with theweird disease, but today I am putting myself out there and hoping that by doing sopeople will take notice and join me inthiscause.

Supporters

Brenda High 1 item
Anonymous 6 items

alexandra castro

Debby 1 item

Rare diseases are overlooked and underfunded for research.

Ellis & Berdene Miller 2 items

My husband has had it for over nine years. His has been controlled with medication. However this year for the first time it is not covered by our insurance which is very unfortunate! He is living proof it works!

DUSHYANT CHAUDHARY 1 item
Anonymous 1 item + $50
Orqui 2 items

For a friend I dearly love! Alexandra

Brian Zintel 2 items
Joe and Laura Spearot 3 items + $10

To support our song single mother who raised us despite also battling MG!

laura 1 item

I have MG!

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