Profil
Wendy Erler has held positions as a Director at Rare-X and as a Member-Board of Trustees at Huntington's Disease Society of America.
Postes actifs de Wendy Erler
| Sociétés | Poste | Début |
|---|---|---|
Huntington's Disease Society of America
Huntington's Disease Society of America Miscellaneous Commercial ServicesCommercial Services The Huntington's Disease Society of America is a nonprofit organization dedicated to supporting individuals and families affected by Huntington’s disease, a fatal genetic disorder causing progressive nerve cell breakdown in the brain. The non-profit company is based in New York, NY. The organization provides resources including education on symptoms, stages, genetics, and care management; support groups; social workers; telehealth services; and a network of centers offering clinical care. It funds research to advance scientific understanding and develop treatments, supports researchers through grants and fellowships, facilitates patient participation in clinical trials, and offers continuing education for healthcare professionals. The society emphasizes community engagement through donations, volunteering, advocacy, and events, including youth-focused programs. It also provides caregiver resources, professional training, and promotes physical therapy guidelines. | Directeur/Membre du Conseil | - |
Rare-X
Rare-X Packaged SoftwareTechnology Services Operates as a patient data processing platform | Directeur/Membre du Conseil | - |
Expériences
Fonctions occupées
Actives
Inactives
Sociétés cotées
Entreprise privées
Relations
Relations au 1er degré
Entreprises liées au 1er degré
Homme
Femme
Administrateurs
Exécutifs
Sociétés liées
| Entreprise privées | 2 |
|---|---|
Huntington's Disease Society of America
Huntington's Disease Society of America Miscellaneous Commercial ServicesCommercial Services The Huntington's Disease Society of America is a nonprofit organization dedicated to supporting individuals and families affected by Huntington’s disease, a fatal genetic disorder causing progressive nerve cell breakdown in the brain. The non-profit company is based in New York, NY. The organization provides resources including education on symptoms, stages, genetics, and care management; support groups; social workers; telehealth services; and a network of centers offering clinical care. It funds research to advance scientific understanding and develop treatments, supports researchers through grants and fellowships, facilitates patient participation in clinical trials, and offers continuing education for healthcare professionals. The society emphasizes community engagement through donations, volunteering, advocacy, and events, including youth-focused programs. It also provides caregiver resources, professional training, and promotes physical therapy guidelines. | Commercial Services |
Rare-X
Rare-X Packaged SoftwareTechnology Services Operates as a patient data processing platform | Technology Services |
















