AFMS Foundation

The AFMS Foundation helps families diagnosed with Multiple Sclerosis to live a better life through financial support and medical advocacy.

The AFMS Foundation is an IRS approved 501(c)(3) not-for-profit and all contributions will be tax deductible.

04/29/2026

We still have tickets remaining for this awesome night to raise money for AFMS Foundation! We hope you can join us!

03/12/2026

We are excited for this wonderful fundraising event for AFMS Foundation and hope to see you there!

08/29/2025

Help Us Make This Home Safe & Accessible 💙

We are raising funds for a local Glastonbury mom living with MS who urgently needs a hoyer lift, handicap bathroom remodel, accessible van, cleaning support, and evening care.

These essentials will make her home safe and accessible, giving her and her family the care and independence they deserve.

A heartfelt thank you to and for joining us in supporting this special family.

Every donation 🩵big or small 💙 makes a direct impact. Please navigate to our website to donate!

08/24/2025

Insurance doesn’t always cover what MS patients really need.

Not the wheelchair upgrade. Not the ramp. Not the shower bar.

Out-of-pocket costs can reach $10,000+ for basic safety and mobility equipment.

💙 That’s why AFMS Foundation exists … to step in where coverage falls short.

We fund the essentials, like vehicle modifications, walkers, bathroom safety tools, and more.
Because mobility should never be a luxury.

Open the door to independence.
• Click the link in bio to donate or learn how to help a family near you.

08/21/2025

MS is hard to diagnose - and harder to live with while waiting for answers.

There’s no single test. Symptoms can look like stress, migraines, or anxiety.

Many patients spend years searching for clarity while living in fear.

At AFMS, we step in once the diagnosis is clear but the path forward is still foggy.

We fund essential tools, therapy, and advocacy, so MS families aren’t left alone after hearing the words “You have MS.”

If you’ve been through the long road to diagnosis or are still on it - we see you.

Donate, share, and advocate with us. Because the wait is hard enough.

08/17/2025

MS damages the nerves … but not the spirit.

As the immune system attacks the protective layer of nerves, messages between the brain and body get disrupted.

This leads to unpredictable symptoms: numbness, weakness, imbalance, and pain.

Coping means adapting and AFMS helps make that possible.

We provide wheelchairs, car ramps, grab bars, walkers, and financial support for families adjusting to new normals.

You can help someone regain stability, dignity, and peace of mind.

Support our mission - one step, one ramp, one family at a time.

08/13/2025

This is impact.

When someone with MS tells us their life is safer, more manageable, or filled with a little more peace - that’s the power of your donation.

We don’t just provide financial help. We provide relief, dignity, and the tools to move forward.

Your gift today could be the next story we get to share. 💙

Click the link in our bio to help us keep going.

08/10/2025

You can’t always see MS - but people living with it feel it every single day.

Pain. Fatigue. Brain fog. Numbness. Anxiety.
It’s no wonder MS is known as an “invisible illness.”

💙 That’s why AFMS shows up in visible ways, funding what insurance doesn’t: home modifications, walkers, therapy, ramps, and peer support.

You can help bridge the gap between unseen symptoms and real support.

Let’s stop assuming and start supporting.
Tag someone who understands and someone who needs to.

08/06/2025

It’s the small things that make the biggest difference.

A grab bar. A safe ramp. A therapy session paid for when it mattered most.

This patient’s story is a beautiful reminder that compassion paired with action can change lives.

We’re proud to stand beside families living with MS—and we’re grateful for every donor who makes it possible.

💙 To continue this work, we need your help.
Donate via the link in our bio.

08/03/2025

Blurred vision. Double vision. Sudden blindness.

For many, this is how MS first reveals itself - and it’s terrifying.

Vision problems caused by optic neuritis are a common first symptom, and they disrupt far more than sight: they challenge confidence, mobility, and daily life.

At AFMS, we provide grab bars, adaptive home tools, and therapy funding to help MS patients regain control.

Because vision problems shouldn’t lead to fear or falls - they should lead to support.

Your donation helps restore safety, independence, and dignity.

💙 Let’s create a more visible impact for an invisible disease.

Address

Glastonbury, CT
06033

Telephone

+18609225678

Website

http://www.afmsfoundation.org/

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