My name is Josh and I've had MS since October 2009. From what other people are dealing with it sounds like I don't have it too bad. But I'm definitely tired of dealing with it. I just finished my dose of Lemtrada that my neurologist prescribed. So far so good now I'm just dealing with the post medication aftermath. Having to flush my system about a gallon of water a day so I don't have cytokine release syndrome. I started my Ms by being on avonex back in 09 for about 6 years, then tried tecfidera that did not work well at all as far as side effects. Next was plegridy which seem to do okay but I got tired of all the shots and being a pincushion. After that was Aubagio which I thought was going to be good but ended up not working at all for me which is why I had this last major flare-up which led to Lemtrada.
Hopefully this will be the last night I ever take and my body will go back to somewhat normal. The One symptom I'm still currently dealing with but I'm hoping we'll go away or correct itself is overactive bladder issues with frequency and urgency. I can't spend the rest of my life being 20 minutes away from the bathroom if I drink something while trying to live daily life. Anyways that's me in a nutshell.
Hopefully this will be the last night I ever take and my body will go back to somewhat normal. The One symptom I'm still currently dealing with but I'm hoping we'll go away or correct itself is overactive bladder issues with frequency and urgency. I can't spend the rest of my life being 20 minutes away from the bathroom if I drink something while trying to live daily life. Anyways that's me in a nutshell.
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