Saw the rheumatologist about a hour ago. It didn’t go as bad as I had thought .
Firstly they had moved the clinic AGAIN and hasn’t bothered to tell me in a letter 🙄
I saw the nice one again, I had my list and was honest .
I am going to try methotrexate again , 5 for one day then 1-2 folic acid depending on how I feel with side effects. I have asked her for a referral to physio to help strength and keep the movements I have.
I told her how I weren’t having blood test and that and she has given me the forms and I’m waiting for a letter in the post for appointment with the nurse in about 2 months time to see how I am getting on with the tablets .
She had explained to me that my lupus is current inactive , I was very confused as I didn’t understand what that meant ! It’s a good thing so the only problem I am having at the moment is the arthritis pains .