NF2 Resources
- NF Clinic/Hospital List
- Top Hospitals
- Medical News Sources
- Medical Coverage
- Research Sources
- Assistive Options
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NF2 News
NF2 Support
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Resources In This Category -
NF2 Crew, NYC NF2 Support Group, The Children's Tumor Foundation, NF2 Network, NF2 Germany, UK Neuro, Living with Facial Paralysis, nfCanada, Australia, Texas, Brazilian NF Association, Catalana de les NF, NF Society of Ontario,
 NF2 Crew The NF2 Crew is an online-based support community for patients and family members (or loved ones) with Neurofibromatosis Type 2. We are one of the largest NF2 based support groups in existence with hundreds of members spanning the globe. Our "meet-ups" are held through a variety of Internet-based communication mediums. |
 NYC NF2 Support Group |
 The Children's Tumor Foundation Read about the Children's Tumor Foundation's comprehensive approach to improving the lives of individuals and families affected by neurofibromatosis (NF). |
 NF2 Network NF Network is a national non-profit network serving families and individuals affected by Neurofibromatosis. |
 NF2 Germany |
 UK Neuro The Neuro Foundation, Neurofibromatosis Association, is the authoritative voice of Neurofibromatosis in the UK. tHEY achieve this by providing first class information, support and advice; facilitating and promoting innovative research, and being an advocate for those with Neurofibromatosis. |
 Living with Facial Paralysis This group is looking for people affected by facial paralysis who live in the Peterborough area of the UK, people affected by Bell's Palsy, Moebius Syndrome and all other causes of facial palsy. We want to contact the local media to raise awareness, please contact us if you can get involved, three people are already on board. |
 nfCanada |
 Australia |
 Texas |
 Brazilian NF Association |
 Catalana de les NF |
 NF Society of Ontario |