Join us as we turn "I CAN'T" into a "I CAN" MOVEment to cure VCP disease.

Most people don't understand the burden of VCP disease. The I CAN MOVEment is a great chance to highlight your challenges and show the world what you CAN DO! Our goal is to raise awareness and donations to support research and patient programs at Cure VCP Disease.

Invite your family and friends to join our team as we celebrate what we CAN DO!

What: A Virtual Move-A-Thon

When: May 4-10

Where: ANYWHERE

Why: To raise critical funds for Cure VCP Disease

Who: Everyone

HOW IT WORKS:

Pick a movement challenge- Walk, run, bike, or swim, finger-raises or wheelchair miles. It is up to you- get creative!
Sign-up!- Click the button to create your personal page and story. Join a team or create your own.
Share- Once you’ve created your page, share with your network. Send emails, texts and post on your socials. Let people know how and why to support you. Educating them about VCP disease, their donation impact, and your efforts is a great way to encourage donations.
Fundraise- People want to support you, but you need to let them know how and why. Check out our fundraising toolkit for some tips!
Challenge Week- Plan out your final fundraising push. Record yourself, take photos and don’t be afraid to ask people directly to support your efforts. Most importantly, HAVE FUN!
Post Event- Celebrate your achievement! You turned your “I Can’t” into an “I CAN!” and you raised some incredible funds for Cure VCP Disease. Thank your donors and let them know about your achievement.

IMPORTANT NEWS:

A donor is matching all donations up to $10,000! Let your supporters know that for every $1 they donate, Cure VCP Disease will get $2.

Need Ideas For How To Participate?
For those with a disability:
-"I can't run a 5K, but I can walk 500 steps this week."
-"I can't walk a mile, but I can walk three laps in the pool."
-"I can't lift a 4 lb weight, but I can get 10 spoonfuls of cereal to my mouth."
-"I can't run, but I can bike a mile."

For those without a disability:
-"I can't imagine not being able to walk, but I can raise awareness by walking for a cure."
-"I can't imagine what it is like living with VCP disease, but I can bike 20 miles for a cure."

Donate or sign-up to participate today.

About Our Organization:
Cure VCP Disease is a patient advocacy organization dedicated to driving the development of a cure for valosin-containing protein associated multisystem proteinopathy. It also known as IBMPFD (Inclusion Body Myopathy, Early Onset Paget’s Disease of Bone and Frontotemporal Dementia), but we call it VCP disease. It is hereditary and adult-onset, meaning that symptoms of the genetic mutation are not seen until a person is in adulthood. VCP disease can affect any combination of a patients’ muscles, bones and brain and can cause degenerative diseases including ALS, frontotemporal dementia, Parkinson’s, and Charcot-Marie Tooth. This devastating disease runs in families, and it is our mission to stop it.

2025 I CAN MOVEment

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