New here
I was diagnosed in 2003,RRMS and told by the looks of my MRI's I probably had MS for 10yrs previous to that. I have been on Copaxone since 2003, until this year I have only had a few big relapses and a few small ones. This year I h had 2 back to back. 1st one treated with solumedrol, the 2nd solumedrol didnt have any affect. Looking at IVIG right now.
I play the guitar and write music, sew, draw and swim.
Right now I am getting tired of pushing the same rock up the same mountain. Living in Houston TX, means a LOT OF HEAT....its July , I am in my air conditioned office, will go to my airconditioned car and the my airconditioned house. I am sure you all know the drill.
thanks for listening
I play the guitar and write music, sew, draw and swim.
Right now I am getting tired of pushing the same rock up the same mountain. Living in Houston TX, means a LOT OF HEAT....its July , I am in my air conditioned office, will go to my airconditioned car and the my airconditioned house. I am sure you all know the drill.
thanks for listening
welcome!!!! great to have you here! any questions, just ask, someone has advice. as for the heat, same routine here, all ac 24/7. i also live in nw pa. snow 6 months, then spring, summer, and fall, not always in that order! good luck.
It's tough having to stay indoors when there's so much to enjoy outside. I tell people that staying out of the heat is not a comfort issue for me. It's the difference between being able to move my arms and legs, and seeing clearly, or being darn near paralyzed. I'm sure it's difficult for people to understand that. I'm still amazed at how adversely affected my body is in the heat 
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