If you know anyone with Cushing’s Syndrome, or if you are a physician interested in collaboration, please get in touch with the ORDI team. Write to us: contactus@ordindia.in Rare Disease helpline -+91 8892...
If you know anyone with Friedreich’s Ataxia, or if you are a physician interested in collaboration, please get in touch with the ORDI team. Write to us: contactus@ordindia.in Rare Disease helpline -+91 8892...
If you know anyone with Spinocerebellar Ataxias (SCA’s)(Type 1 to19), or if you are a physician interested in collaboration, please get in touch with the ORDI team. Write to us: contactus@ordindia.in Rare Disease...
If you know anyone with Post-Infectious Ataxia, or if you are a physician interested in collaboration, please get in touch with the ORDI team. Write to us: contactus@ordindia.in Rare Disease helpline -+91 8892...
If you know anyone with Paraneoplastic Cerebellar Degeneration (PCD), or if you are a physician interested in collaboration, please get in touch with the ORDI team. Write to us: contactus@ordindia.in Rare Disease helpline...
If you know anyone with Olivopontocerebellar Atrophy (OPCA), or if you are a physician interested in collaboration, please get in touch with the ORDI team. Write to us: contactus@ordindia.in Rare Disease helpline -+91...
If you know anyone with Marie’s Ataxia, or if you are a physician interested in collaboration, please get in touch with the ORDI team. Write to us: contactus@ordindia.in Rare Disease helpline -+91 8892...
If you know anyone with Hereditary Spastic Paraplegia (HSP), or if you are a physician interested in collaboration, please get in touch with the ORDI team. Write to us: contactus@ordindia.in Rare Disease helpline...
If you know anyone with Gluten Ataxia, or if you are a physician interested in collaboration, please get in touch with the ORDI team. Write to us: contactus@ordindia.in Rare Disease helpline -+91 8892...
If you know anyone with Episodic Ataxia, or if you are a physician interested in collaboration, please get in touch with the ORDI team. Write to us: contactus@ordindia.in Rare Disease helpline -+91 8892...
Our Executive Director Mr. Prasanna Shirol was a part of First Ever summit dedicated to advancing equitable care for rare diseases in older adults. The meeting was attended from 25 countries across Canada, Latin America, Europe, and Asia, representing patient and caregiver communities, patient advocates, healthcare professionals, and healthcare policy experts. This is a short video highlighting the impact of the initiative to date, in the words of the COLLABORATE Community.
