Help CMT Kids

Take our quick survey to improve clinical trials for CMT kids.

CALLING ALL PEDIATRIC NEUROLOGISTS!

TAKE OUR QUICK SURVEY TO IMPROVE CLINICAL TRIALS FOR CMT KIDS!

New clinical trials are underway to treat Charcot-Marie-Tooth disease. Your input is needed to gain a better understanding of clinical endpoints and outcome measures for children living with CMT.

The Hereditary Neuropathy Foundation (HNF) is committed to improving endpoints and functional outcomes in the pediatric patient population with Charcot-Marie-Tooth (CMT). Until recently, there was little hope for a treatment to help the thousands of children living today with CMT…nor for the thousands more being born each year. That is changing, however, as possible therapeutics are moving rapidly from the laboratory to the clinic!

HNF has launched an on-line pediatric neurology survey to gain a better understanding of pediatric neurologists’ evaluation techniques in assessing young patients with CMT and pediatric neurologists’ perspective of the impact of CMT on their patients’ quality of life.

Just a few minutes of time can strengthen our mission to improve the lives of the many children and families affected by CMT!

If you are a pediatric neurologist, please share your valuable time with us and take our survey.

Your input is invaluable to us—and to the lives of CMT kids. Thank you!

Click here to complete the survey in a separate window…or simply fill it in using the form below.

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