- A Tribute to RARE DISEASE DAY
- February 26th 2017
- Venue: IRIB International Conference Center (IICC)
The 8th international congress on the occasion of rare disease day
Dr. Ali Davoudian said:
Our aim is protecting all the rare disease patients regardless of geographical borders.
RDD 2017
25 January 2017, Paris – Patients around the world will mark the tenth annual Rare Disease Day on Tuesday 28 February. In the build up to Rare Disease Day 2017, the official video launches today.
Rare Disease Patients without Borders
35 days remain to Rare Disease Day in IRAN, “Rare Diseases Patients without Borders”
The story of a boy who just opens his eyes by his mother’s voice
He lived normally and he didn’t have any problems till the age of 5. One day when he was playing in the yard in his grandmother’s house he fainted suddenly. His mother cuddled him and kept calling his name “ Mohammad” and that was the beginning of their new life.
Helping doesn’t depend on the number of help wanted
Solidarity with Iranian patients
EURORDIS-Rare Diseases Europe has recently signed an agreement with the Rare Disease Foundation of Iran, a non-profit and non-governmental institution that provides services for rare disease patients and their community in Iran.
Research Class is held for Students in Dana Primary School
Research lesson added to the lessons for students who are studying at Dana school, affiliated to Rare Diseases Foundation of Iran.
Cooperation wtih the pharmaceutical company “Vegal” Spain
General manager of Rare Diseases Foundation of Iran has traveled to Spain to remove obstacles on the way of delivering orphan drugs to Iran. “Vegal Farmaceutica” is a pharmaceutical laboratory that began operations in 1994. They are nowadays present in most foreign markets.
President of Malaysian Rare Disorders Society will travel to Iran by next month
Rare Diseases Asia conference 2016, is held for 3 days from 27th of Aban (17th November) in Malaysia.
All rare diseases organizations from Asia and beyond participate in this event and Mr. Mehdi Mahkam attends as Rare Diseases Foundation of Iran representative.