My father was recently diagnosed with MDS and I was hoping someone could share with me any information on a relative (or personally) on how they are being treated for this? He is about to begin a series of treatments using Vidaza and I'm not sure what to expect?
I saw one post from 2008 from Geno that stated his wife had the disease at that time for 3 years but was still receiving blood transfusions? It's been a little over 2 month's now for my Dad and he has just recieved his 3rd transfusion. His tranfusions have been mainly red blood cell packed so the issues with white blood cells and platelets have not been as bad.
Any insight anyone?
I saw one post from 2008 from Geno that stated his wife had the disease at that time for 3 years but was still receiving blood transfusions? It's been a little over 2 month's now for my Dad and he has just recieved his 3rd transfusion. His tranfusions have been mainly red blood cell packed so the issues with white blood cells and platelets have not been as bad.
Any insight anyone?