10 September 2016

After visiting the rheumatology at the hospital and rheumatology said they were happy resigned to the idea of me increasing my Fumaderm as long as the Dermatologist was agreeable although they both have said there is no evidence of it having any effect on psoriatic arthritis,
My dermatologist has written to them saying he had no objection .
So as I had enough tablets to get me through to the next appointment I decided to start before getting the official nod from my dermatologist, I want it to have a chance to work before I go back to rheumatology as I asked them to bear with me for 6 months and if it didn't work I would have to change to something else

Ten days ago I increased my dose to 5 tablets a day for I week then 3 days ago I increased again to 6 tablets a day 3 with my breakfast and 3 with my evening meal

I have noted a bit more flushing of the face and body but no additional cramps

My bloods were good when I started to increase with lymphocytes 1.35 so will be interesting to see my next blood results that were taken on the first of September

I don't want to tempt fate but I'm sure the pain in my fingers is markedly less my feet don't hurt when I get up in the mornings, and my shoulders don't ache ache as much.
It might be my imagination or wishful thinking but at the moment I'm thinking it might be working    

21 October  2016

Went to see my GP 3 weeks ago  to have my last hormone injection so I'm hoping normal service will resume soon, that's two and a half years since I finished my Radiotherapy for my prostate cancer
I was pleased that my blood test for prostate specific antigen ( PSA ) was undetectable
So for my prostate cancer I now go to just 3 monthly blood tests to make sure it doesn't creep back
But no more damn hormone injections  

I was told my lymphocyte count was good from the beginning of of September at 125 so it was well within the normal range, took more blood at beginning of October

Having increased my dose of Fumaderm to six tablets a day 3 with breakfast and three with my evening meal I was a bit concerned that the lymphocyte count would fall again but my doctor took my bloods while I was with him.
I told him that I had increased my dose of fumaderm to 6 tablets a day and need to keep an eye on my lymphocytes,

Later that evening I got a call from my doctor telling me he had the results of bloods and unfortunately they had dropped to .95 not dangerous at that level but non the less the rapid drop from 1.25 to .95 in under a month has caused me to reconsider the increase and have dropped down to 5 tablets a day and am due another blood test in a few days ....it will be interesting to see the results before I have to see my dermatologist in December

I have noticed since dropping to the lower dose that my finger joints are getting more painful ...but I'm still reluctant to give up on Fumaderm  unles I'm offered something to deal with both problems like stelara or Cosentyx     

3 November 2016

Went to have a blood test Monday  this week as my last results the lymphocyte count had dropped  to .95.....not too worrying as it was only just out of the normal range.......So I was delighted this morning when my GP phoned and said guess what your lymphocytes have recovered and are back up to 1.23 a great result

I will continue on 5 tablets a day as my psoriasis is well under control and I only have a tiny patch on my left elbow
The arthritis is not too bad the finger joints are a bit tender and my feet are less painful when I get up in the morning so I will try to stick to this medication as it has been so good to me for the last four and a half years