Hello, I have been diagnosed for a year with MS, and have been on Rebif since diagnosis. I recently had to stop while we moved and a bunch of life changes, including losing my 4th job since my diagnosis due to frequent relapses. I am in the process of getting some assistance to get back on Rebif ASAP, and have been off of it for well over a month. The past couple weeks I've noticed my symptoms acting up a little, more spasms in my legs and arms, some worsening of depression, and worse fatigue, but this makes sense where I'm off of my meds and under a lot of stress (my husband is end stage kidney failure too). So the past week I've had a constant pressure in my head, its gets worse then a little better, then worse, then a little better and so on. It's almost constant, worse with bright light.
Yesterday I woke up with my R eye feeling like it was swollen and it's pretty sore. It hurts to blink and to move my eye. I've had stye's before but I don't feel a bump. I have taken my migraine medication and it doesn't help my headache, I take Vicodin to get by a few hours. I've never had an issue with my eyes in past relapses (I've had 4 relapses in the last year). I was curious as to what symptoms people had with optic neuritis and if this sounds like it could be. I am a nurse and normally I would recommend someone to go see their neuro, but I have no health insurance and if it's not the MS then I'd rather not go and have another bill on my plate. I'm looking more to see if I should see my neuro, my PCP, or an eye doc.. Any suggestions?? Thanks.
**Post broken into paragraphs by Moderator for easier reading. Many people with MS have visual difficulties that prevent them from reading large blocks of print.**
Yesterday I woke up with my R eye feeling like it was swollen and it's pretty sore. It hurts to blink and to move my eye. I've had stye's before but I don't feel a bump. I have taken my migraine medication and it doesn't help my headache, I take Vicodin to get by a few hours. I've never had an issue with my eyes in past relapses (I've had 4 relapses in the last year). I was curious as to what symptoms people had with optic neuritis and if this sounds like it could be. I am a nurse and normally I would recommend someone to go see their neuro, but I have no health insurance and if it's not the MS then I'd rather not go and have another bill on my plate. I'm looking more to see if I should see my neuro, my PCP, or an eye doc.. Any suggestions?? Thanks.
**Post broken into paragraphs by Moderator for easier reading. Many people with MS have visual difficulties that prevent them from reading large blocks of print.**
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