The following article is one that I have written for Rare Disease Day 2024 and it appears on the Genetic Alliance UK website.
It tells the story of my 18 years of ITP, the ups and downs of an often tricky voyage.
Also included in the piece is my take on why we should all get involved in the Rare Disease Day campaign.
Here is the link - geneticalliance.org.uk/news...
#RareDiseaseDay #RareDiseases #ITPAware #ITPAwareness #RareDiseaseUK #GeneticAllianceUK
Coronavirus and ITP ???
ITP/autoimmune disease
My 14 year old brother was diagnosed last month with ITP.
