Neurofibromatosis Tumor Foundation
The Neurofibromatosis Tumor Foundation was established in 1979 as a support organization to provide information about neurofibromatosis (NF) to individuals and families affected by this tumor disorder of the nervous system. Appropriate referrals to health professionals and other resources are provided upon request without charge. We also provide peer counselling to NF families at no charge. The culturally diverse Board of Directors ensures the commitment to providing dignity to all individuals affected by NF. The organization stimulates and provides funds for research into neurofibromatosis and related disorders. The Professional Advisory Board is comprised of recognized NF experts, and after almost 40 years of local and national influence has gone global.
Founded
1979
0
Web
nfmidatlantic.org
Address
Towson
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1. How can NGOs effectively raise awareness about the impact of neurofibromatosis on individuals and families, and what strategies can be employed to support those affected by this condition?
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Brooklyn Simmons
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2. In what ways can we leverage technology and online platforms to promote conservation efforts for endangered species, and what role can NGOs play in facilitating these initiatives?
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Brooklyn Simmons
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Together, we can make a real impact in communities around the world. Help us bring hope and support.
What an amazing initiative! It’s so heartwarming to see organizations like the Neurofibromatosis Tumor Foundation providing support and resources to those in need. Together, we can make a difference! 🌟
Brooklyn Simmons
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Kudos to the NF community for working tirelessly to raise awareness and support research! Every effort counts and can help change lives. Let’s keep the momentum going! 💪💚
Brooklyn Simmons
Product Manager
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