Hi Molly, I really think you should push for an MRI if you can they can tell a lot from that. I put all the things that had occurred and I could remember on a time line and gave it to the doctor. You need to start keeping a diary so that you dont forget things. The treatment is controversial but there were trials carried out which showed the DMD's reduced the number of attacks by a third, the only controversy I can see is that there are side effects which ou get with the drugs but these are not as bad as the after effects you get with attacks. What do i do to cheer myself up?......you are not going to be impressed but i have a glass of red wine and a cigarette, i figure if i'm going to go i will go happy. I love your name too, not so keen on mine ha ha. Ruby X
Hi Molly, how are you today? I'm fine its Saturday and can put my feet up for a little while anyway. Spoke to MS nurse yesterday about Copaxone, blood suagrs and bumps. She wants me to try another drug. I'm still thinking about it. Havent made my mind up yet. cant cope with the bumps, sore 7 itchy all the time. The weather here is lovely, sunshiene real sign of spring.Ruby X
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