Multiple Sclerosis In Almaguin

Multiple Sclerosis In Almaguin We are a small group of people in the Almaguin Highlands area that have been touched by Multiple Sclerosis, (MS). Raising awareness & Funds.

Funds will go to 1st; assist family's registered with us, 2nd appropriate chosen research & education.

08/10/2026
This is Great News for those with Multiple Sclerosis In Canada! 🇨🇦     NO MORE DROP FOOT
08/10/2026

This is Great News for those with Multiple Sclerosis In Canada! 🇨🇦
NO MORE DROP FOOT

Below is an incredible testimony from an MS patient that wishes to remain anonymous. This is his story of recovery and his experience with Muscular Acoustic Modulation (MAM).

TESTIMONY:

My footdrop has been eliminated through Muscular Acoustic Modulation (MAM) treatment.

What is Muscular Acoustic Modulation? This video should explain it. https://www.omeostatic.it/mam-clinic/

Diagnosed with relapsing remitting MS in the early 1990s, I transitioned to Secondary Progressive disease in 2003. I’ve had mild symptoms of foot drop since the early 2000s. As the footdrop progressed, I was fitted for an in-shoe leg brace in 2007 by a physiatrist at the MS Rehabilitation center. It was a piece of uncomfortable hard plastic that fit inside the shoe, causing much discomfort. I decided against wearing it.

In the early 2020s, a friend with MS recommended an AFO (ankle foot orthosis) that attached to the outside of the shoe and helped mitigate footdrop. Using these I only occasionally required extra assistance.

In April of 2025 I travelled to Italy for a consultation with a Vascular Surgeon/professor at the University of Rome, creator of MAM technology. A clinical trial on MS patients showed evidence of improved quality of life in more advanced MS patients (EDSS score of 6 or more). https://pubmed.ncbi.nlm.nih.gov/39493439/ After 9 treatments the numbness in my lower limbs greatly diminished over the course of the next several months. I still required my AFO leg braces for the foot drop.

Before treatment my right foot was completely immobile; not even my neurologist could rotate my right ankle which had stiffened because of the MS. The first round of treatment restored a lot of feeling, but I still required AFO ankle braces.

After about eight months some of the numbness came back, so I returned to Rome.

In July of 2026 I had another 10 MAM treatments. The first six treatments brought me back to the place where I was at the end of the treatment in 2025. Treatment 7 was the transition point for me. Something happened in my right foot as the numbness had almost completely subsided and my ability to lift my foot on its own had returned.

On July 17, 2026, I was able to slowly walk a few hundred feet without canes, crutches or the leg braces I had worn for years. I returned to Canada and I no longer require assistance for walking.
Restoring my ability to walk independently has been my dream since 2003. It will still require discipline.

Dr. Mandolesi was very clear that exercise and good diet are keys to success. He recommended the Best Bet Diet, daily exercise and maintaining a healthy weight. Should I require more MAM treatments in the future I will seek out where it is offered. It is painless and non-invasive.

Shoutout !!To Home Comfort Care Services in Huntsville for being another Big Supporter of Multiples Sclerosis In Almagui...
07/31/2026

Shoutout !!
To Home Comfort Care Services in Huntsville for being another Big Supporter of Multiples Sclerosis In Almaguin. They make it a Monthly Ritual to wear there T-shirts at the end of every month.

Thank you for being a proud supporter. 🧡
They have offices in Gravenhurst, Bracebridge Huntsville and Parry Sound.

You can find them here on Facebook ⬇️
https://www.facebook.com/profile.php?id=61585095238048

07/30/2026

This is so true! This is MS!
We all have our own symptoms that flare up when stress hits us.


07/23/2026

Message from MS Hope! What is Epstein virus?  It’s known more by; “ Mono”.

Symptoms that may people with MS don’t talk about and can’t be seen. 🧡
07/23/2026

Symptoms that may people with MS don’t talk about and can’t be seen. 🧡

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Sundridge, ON

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