HNF is proud to report that over $36,000 was raised for research for CMT2A at this annual event!
Blog Category
CMT Update
Total posts in Category: 74
Update on Michael Watkins – Team CMT Member
Michael Watkins completed the Leadville Trail 100 MTB race on August 15, 2015 in Leadville, CO. The trail race is widely considered one of the toughest mountain biking races in the country.
September is Charcot-Marie-Tooth (CMT) Awareness Month
In September, HNF has many ways to participate in our ongoing efforts to find a cure for CMT. Here are a few exciting and fun ways for you to join us in our efforts to raise awareness and funds
HNF Sponsors 2015 Peripheral Nerve Society Conference in Canada
Allison Moore, HNF CEO, and Joy Aldrich, HNF Advocacy Director, represented HNF as sponsors at this important conference, which was held in Chateau Mont Sainte Anne, Canada, from June 27 – July 2
Introducting HNF’s Health Care Providers Directory
The Hereditary Neuropathy Foundation (HNF) has a new initiative aimed at identifying expert Health Care Providers (HCP) for the CharcotMarie-Tooth (CMT) community.
HNF Physician Spotlight: Dr. Wayne Berberian
Dr. Wayne Berberian is a specialized orthopedic surgeon who repairs complications of the foot and ankle.
A Bi-Directional, Translational Model of Resistance-Type Exercise Training in the Management of Charcot-Marie-Tooth (CMT) Disease
This model examines the effects of a validated, evidence-based mechanical loading “resistance-type” exercise protocol in the management CMT.
Accepting Myself for Who I Am
Growing up, I always knew I was different than my friends. I couldn’t run fast, tripped often (the scars on my knees are a reminder), was lousy at any sports-related activity, and was generally weak and uncoordinated.
Our CMT Inspire Community, Soon to be 2,000 Strong!
HNF has partnered with Inspire to provide a safe online health and wellness community in which patients, families, friends, and caregivers connect with one another for support and information.
The Long Road to Diagnosis Renews Dedication to Advocacy
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.
A New Mouse Model for Charcot-Marie-Tooth (CMT2)
We were recently informed that The Jackson Laboratory (JAX, a nonprofit biomedical research institution headquartered in Bar Harbor, Maine) had taken delivery and will be distributing a newly generated CMT-related mouse model. The new model expresses mutant mitofusin 2, a mitochondrial membrane protein involved in mitochondrial fusion and regulation of vascular smooth muscle cell proliferation.
New Strategic Alliance with Rare Disease Report (RDR)
We are excited to announce our new collaboration with Rare Disease Report (RDR) to increase awareness of Charcot-Marie-Tooth (CMT) among the medical community. RDR’s website, e-newsletter, and print publication offers an independent voice for the Rare Disease Community.
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Awareness (34)
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CMT (1)
CMT en Español (1)
CMT Summit (53)
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CMT-Connect Webinars (10)
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Burke Insitute (3)
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Types of CMT (1)
CMT Type – CMT1A (22)
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