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Ask Kate! Am I doing all I need to be doing for my child with NF1?

In this video, Kate responds to a mom with a child who has neurofibromatosis type 1, who wanted to know if she is covering all the bases regarding autism, precocious puberty, MRIs, and more. Do you have a question about neurofibromatosis? Ask Kate! Kate Kelts, RN BSN, is the Patient Support Coordinator at the Children's Tumor Foundation. Submit your question in the comments below, or email Kate at [email protected]. To enable Closed Captioning click the CC button. 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 https://www.ctf.org/ Donate today at https://www.ctf.org/ways-to-give/ Follow us on our social media platforms: Facebook -   / childrenstumor   Instagram -   / childrenstumor   Twitter -   / childrenstumor   LinkedIn -   / children's-tumor-foundation   #endnf #nf1 #nf2 #nf2swn #swn #childrenstumor #neurofibromatosis #schwannomatosis #nervetumor #tumor