If you or yours have taken megadoses of solumedrol for an MS exacerbation, did you/they take it by IV at home or in the hospital? How did it go? (any improvements, what side effects, etc)
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debtahals wears a curiosity COAT
ANSWERS: 1
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Found a nice video on YouTube. Everyone is different, but I liked this one a lot. It's a woman with MS - talking about what it's like - what to expect - what the side effects are - and even some tips to make the journey easier - when you're on a 1 day, 3 day or 5 day treatment of solumedrol. (mega steroids by IV .. as a treatment for an MS flare-up) Asked this back in December. It's now April, and there are no answers here - but think it's worth adding this video for anyone who may need the information. I had solumedral about a year ago while hospitalized and may be looking at a respeat here soon. I realize this is no substitute for seeing and speaking with your primary doctor and your neurologist if you have MS. However, it's also nice to hear form others who have MS as well. So with that .. here's a video from someone who's "been there" ...
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