Support people affected by neurofibromatosis NF1-Nf2-Schwannomatosis alberta Canada
Support people affected by neurofibromatosis NF1-Nf2-Schwannomatosis alberta Canada
Our resources aim to educate the global community on neurofibromatosis, and provide resources to those living with NF. As this condition is relatively rare, but not absolutely uncommon (1/3500 people live with NF), it is often those living with NF that must inform and educate the medical and community on our condition.
This video shows a day in the life of a couple who both have Neurofibromatosis. Many times, people with Neurofibromatosis do not go out in public as often, many hide their appearance. Tim and Gail get out there and lets their tumours show. They embrace life and encourage others to do the same.
This is the latest video that Tim and Gail were invited to participate in. It is an updated version that provides new perspectives of how we cope with NF. We hope to encourage others to get out and enjoy life. If you have neurofibromatosis, don’t let it keep you from getting out and enjoying your life.
Please reach us at ABTF2019@gmail.com if you cannot find an answer to your question.
The tumor foundation provides research on NF for practitioners in the medical community that need to learn more about the condition to help their patients living with NF.
The tumor foundation provides a parenting guidebook for parents wanting to learn more about their children's diagnosis and condition.
Tumor Foundation stories: https://www.tumourfoundation.ca/nf-stories/
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