The Hereditary Neuropathy Foundation (HNF) has a new initiative aimed at identifying expert Health Care Providers (HCP) for the CharcotMarie-Tooth (CMT) community.
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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.
Pizza with a Purpose Various Locations -September 2015
Visit one of these locations on the designated day and present the flyer to your server and HNF will receive 20% off the sales that will fund CMT research.
My last month in numbers
It has been entirely too long since I’ve updated my blog and so much has happened since late April. I thought I would share some info on what I’ve been up to since my last post on April 29th
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.
Greensboro Survey Study for Genetic Counseling and Genetic Testing
The goal of this study was to explore the perceptions and utilization of genetic counseling and testing by people with Charcot-Marie-Tooth (CMT)
Introducing Our Newest Scientific Advisory Board Member
Dr. Stromatt has conducted over 55 Phase 1 to Phase 4 clinical trials in a wide variety of clinical indications, including oncology, rheumatology, pulmonology, gastroenterology, and neurology.
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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