5 Ways to Help Fund SMA and Muscular Dystrophy Charities

Wendy Henderson avatar

by Wendy Henderson |

Share this article:

Share article via email


Non-profit organizations for spinal muscular atrophy (SMA) and muscular dystrophy are reliant on help from people to raise both funds and awareness of the diseases. The money used goes towards research for better treatments, drugs, and understanding of the disease and to assist patients who have unique needs and may require special equipment and support.

Participate in an Event
Organizations such as the Muscular Dystrophy Association and Cure SMA regularly hold fundraising events. These events are fun and participants can either pay to enter or have their friends and family sponsor them to take part.

Events include gala dinners, fun walks, golf days, full and half marathons, and other sporting events. If you don’t like the look of the official events, you could always host your own event with the proceeds going to your favorite MD or SMA charity.

MORE: Five ways Cure SMA offers help to newly diagnosed families.

Non-profit organizations are always looking for volunteers to offer their free time. Whether it’s to help out at a specific event or to lend an area of expertise to the running of the organization, all are welcome.

MORE: Find out about educational resources offered by the Muscular Dystrophy Association.

Become a Partner
Partnering businesses with a local charity or chapter of a non-profit helps to encourage a sense of pride and team building in employees.

MORE: Find out about 12 SMA resources available for young adults.

Donate Money
If you don’t have the time to participate or organize an event to raise money for MD or SMA, you could simply donate money to your favorite non-profit organization. This can either be a one-off donation or a monthly payment plan.

Many people choose to leave an amount of money in their will to their favorite non-profit.

MORE: Find out about seven support care areas that can help with SMA.

Become an Advocate
Advocates help non-profit organizations to address congress about important issues on disability law, treatment and research for SMA and MD.

MORE: SMA comes to making key U.S. newborn screening list.

SMA News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or another qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.