Infussions

Stuart and I had a really good meeting with the head of transplant on friday afternoon. He was pretty positive about my chances after the reccurance of the disease. He personally went to pathology to look at the biopsy. The damage has just started, so we have caught it very early. So far there is no measurable effect on kidney function. In short the doctors think I have a good chance of going into remission for several reasons; I have achieved remission in the past with my native kidneys, I respond to the treatments they have available and the progression of the illness in me in the past has been slow.

Choices are limited but there are a few treatment options. There is a new discovery OS, a sugars treatment which we might try as a trial. He is investigating further to see if I could be a candidate. If desperate we could try Cyclophosfomide again, but I have had two courses of that in the past and another one increases the risk of cancer alarmingly.

The option we are going to try is infussions of Albumun with high dose of steroids. For this I had to have a new permacath put in yesterday. I also had the first session of plasma exchange.

( you may recall they used this treatment before the transplant to reduce the FSGS in my blood). I can already feel the difference in my adema (swelling due to fluid retention). Apart from the localized pain of the recent surgery I feel good.

I will have three infussions per week for 2-4 weeks, possibly followed by Retuximab infussion/s.

I am back for my second session today it starts at 9.30am and we expect I'll be out by 2pm.