HNF Launches the Ultimate CMT Amazon Wish List

by Estela Lugo | May 10, 2021 | 1 comment

HNF Launches the Ultimate CMT Amazon Wish List

HNF’s focus is to support people living with CMT and their families with critical information to improve quality of life and we are dedicated to finding treatments for CMT. We provide a strong, organizational voice to those living with CMT all over the world.

The HNF team and supporters came up with an ULTIMATE wishlist of CMT-friendly products on Amazon to make life with CMT easier!

We hope you find this list helpful and choose HNF as your AmazonSmile Charity before you shop!

View HNF’s Ultimate CMT Amazon Wish List here.

Simply start your shopping at smile.amazon.com/ch/13-4137654 to confirm “Hereditary Neuropathy Foundation Inc” as your charity of choice, and AmazonSmile will donate a portion of your eligible purchase price to our organization.

Have a product that helps daily life with CMT?

Send [email protected] an email with “AmazonSmile” in the subject line. Please provide a product name, link, and how it helps you!

Learn more on this topic

One More Rep: Ed Moore Is Working Out For Charcot-Marie-Tooth Awareness

by Courtney | Oct 18, 2015 | Living with CMT | 0 Comments

Ed Moore, a Team CMT leader who is committed to spreading awareness of CMT with a pretty creative and bold fundraising strategy.

Charcot-Marie-Tooth Won’t Stop The ‘Karaoke King

by Allison Moore | Sep 23, 2015 | Living with CMT | 0 Comments

Patrick was an accomplished athlete in high school, participating in many sports and even boasting a 85mph fastball. But his deformed feet prevented him from running, eliminating any chance to pursue sports past high school.

Every Voice Makes A Difference: Social Media Awareness For Charcot-Marie-Tooth Disease

by Allison Moore | Sep 18, 2015 | Living with CMT | 1 Comment

it’s so important for you to join The Hereditary Neuropathy Foundation on all of our social media channels.

What It’s Like To Live With Charcot-Marie-Tooth Disease: The Stories Of Those Who Know It Best

by Courtney | Sep 7, 2015 | Awareness, Living with CMT | 10 Comments

The study is a collection of over 80 intimate and candid interviews, painting a vivid picture of those living with CMT. These interviews brought to light a range of different experiences: from devastating and heart-wrenching, to courageous and inspiring.

The Long Road to Diagnosis Renews Dedication to Advocacy

by Courtney | Jun 1, 2015 | CMT Type - CMT2C, CMT Update, Living with CMT | 7 Comments

Growing up we called it “Steffi disorder.” My friends and family were as baffled as my expert neurologists. I had been diagnosed with typical Spiral Muscular Atrophy (SMA) as a toddler but never followed its progression; I never seemed to get weaker. My myriad of symptoms was distinctly different than anyone else’s I had ever met in a lifetime living in the neuromuscular community. I thought I might never find my true diagnosis, let alone others who share it with me.

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1 Comment

Kaye Pauley on March 18, 2023 at 9:25 am
Want to talk with someone around the age of 65 through 80 that has CMT
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HNF Launches the Ultimate CMT Amazon Wish List