Bernadette Scarduzio – a CMT patient and advocate! I reside in Drexel Hill, PA with my 2 dogs.
Author Archive
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Summit Panelist Spotlight: John Maddox
John is Founder and Managing Director of Infusion Pharma Consulting LLC, a leading business strategy consultancy focused on the Orphan Drug and Hospital Therapeutics
Summit Panelist Spotlight: Dr. Xinliang Albert Liu
Dr. Liu shares the consensus that CMT is a lesser known disease and more research is needed to shed light on the experiences of patients with CMT.
Summit Panelist Spotlight: Joy Aldrich
After her genetic diagnosis, Joy connected with HNF for advice on AFOs and a letter writing campaign to tell family and friends about her diagnosis.
Summit Speaker Spotlight: Allison Moore
Allison Moore founded HNF in 2001 in an effort to improve the quality of life for people with Charcot-Marie-Tooth.
Summit Speaker Spotlight: Dr. Timothy R. Coté
HNF has invited Dr. Coté to lead the discussion on Public Policy. We will cover issues such as better AFO (leg-bracing) options, fast-tracking drug discoveries and clinical trials, applying for disability benefits, Medicare/Medicaid and services.
Summit Panelist Spotlight: Dr. David Walk
We’ve invited Dr. David Walk to join the panel discussion on “Genotype and Phenotype: Managing Symptoms, The Role of Researchers/Clinicians.”
Register for the Patient-Centered CMT Summit
Don’t wait, reserve your spot at the first Patient-Centered CMT Summit!
Summit Speaker Spotlight HNF’s CSO Sean Ekins
Leaders in Charcot-Marie-Tooth research need to be progressive visionaries, willing and able to push the boundaries to explore every opportunity available to advance therapeutics and clinical trials for CMT.
Summit Panelist Spotlight Matt Downing
Matt Downing, a CMT1A patient, will join HNF’s Founder and CEO Allison Moore in a panel discussion on the good, the bad, and the benefits of participating in a clinical trial.
Summit Speaker Spotlight: Kim Goodsell, The Patient Of The Future
Advocating for her own health, Kim was able to harness the power of genetic information to devise a treatment plan that not only reduced, but reversed much of her disability with CMT.
Summit Speaker Spotlight: Lori Sames of Hannah’s Hope Fund
HNF has the honor of knowing one such GAN patient, Hannah Sames. She was diagnosed with GAN at four years old, and now at age eleven, Hannah can no longer walk on her own.
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