Vesna Aleksovska writes:
"As chair of the IGA, I am delighted to announce that Aviva Rosenberg the IGA representative for the National Gaucher Foundation has agreed to join the IGA Board as our new co-opted member. Aviva is a health care …
We have published our latest newsletter, you can read it here
We have always pledged to help any Gaucher patient that asks us for help wherever they live in the world, therefore advocating for charitable treatment has always been and will be our priority.
We are so pleased to be able to share with you (with …
We received a lovely letter from Hassan Suraw, a father of a Gaucher patient in Kenya:
“ I officially received sad news from Head of Hematology that my daughter is having Gaucher Disease last year 2018, while she was 15 months old, and it …
As part of its strategic imperatives, one of the goals of the IGA is to have a better understanding of the impact of being diagnosed with a comorbidity such as Parkinson’s Disease or Multiple Myeloma. The long-term objective is to put into …
Introducing our 2019 #RareStars - this year we celebrate those who have made a difference in the lives of our patients and/or their families with a montage for 1 October, followed by individual framed photos of each nomination throughout …