Four young girls fighting their rare disorder NF2 (Neurofibromatosis type 2) скачать в хорошем качестве

Four young girls fighting their rare disorder NF2 (Neurofibromatosis type 2)

Together, Jessica, Laurel, Victoria and Karen bond and support one another in their journey with living with this rare disease. Donate at https://nf2biosolutions.org/donate (more options below) In January 2020,these 4 young girls met for the first time. They had been socializing online for a year but were keen to meet in person, so they became the official cheerleading squad for the NF2 BioSolutions team in the Walt Disney World Marathon, and literally from all different parts of the world they were united together at the marathon starting line. During this visit, the girls had the incredible opportunity to meet in person the very talented and dedicated scientists/researchers that are fighting so hard behind the scenes in their own marathon to develop a gene therapy cure. If these researchers ever needed reminding of the importance of their work, then these four girls did just that. Tragically, these four friends collectively have over 50 tumours, and that’s just the ones reported on MRIs. There are most likely many more tumours growing on their nervous system undetected – until they start to cause clinical problems – by which time it is often too late to prevent permanent nerve damage. Please help us accelerate a cure together. To donate please go to: Facebook fundraiser:   / 695034994732797   OR USA residents can donate to NF2 BioSolutions US: https://nf2biosolutions.org/donate/ OR Canadian residents can donate at KBF Foundation (on behalf of NF2 BioSolutions): https://www.kbfcanada.ca/en/projects/... UK residents can donate to NF2 BioSolutions UK: https://nf2biosolutions.org/nf2-bioso... All of the above will issue you charitable tax receipts. Special thanks to Jamie Urman (camera), Cray Novick (camera/edit) and Karl Rausch (edit) that volunteered to film and edit this video.