Ask Kate! Genetics testing when there is neurofibromatosis in your family

Рет қаралды 785

5 жыл бұрын

In this "Ask Kate!" video, Kate responds to an email from Tim, who has NF in his family, and has some great questions about the genetics of NF.
If you have a question or comment for an upcoming "Ask Kate" video, please include it in the comments below, or email Kate at kkelts@ctf.org
Kate Kelts, RN, is the Patient Support Coordinator at the Children's Tumor Foundation.
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What is the Children's Tumor Foundation?
Children’s Tumor Foundation (CTF) began as the first grassroots organization solely dedicated to finding treatments for NF. Today, CTF is a highly recognized global nonprofit foundation, the leading force in the fight to end NF, and a model for other innovative research endeavors.
Visit our website at www.ctf.org/
Donate today at www.ctf.org/ways-to-give/
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Пікірлер: 1

@manriqueboys 2 жыл бұрын

My son just got diagnosed with NF one he is now four months old I have some of the maxi he has but when they test me I do not have an but my mom had a lot of this spot she was never tested but she passed away when I was younger with young babies that knows early what can I do to make a better life for my son I do not understand a lot about this NF one but I am learning