solu medrol used treat

Debs, It sounds like you mights as well take the Medrol - try it his way and then if it doesn't work out, you can go back and as for the solu-medrol. I'm guessing it is very close- just the "solu" means it is a liquid form (soluble) - again that's just my guess. Sorry you have to tough it out and take the meds - we all are taking stuff we would rather not ingest but do so because we're adults and understand the alternative. :-) Let us know how it goes...

I will have my first solu-medrol treatment at the end of this week. I have read the opinion of one person who has had this treatment before and they said that you should not drive or work. It was not clear if they were referring to just hours after the treatment or the entire five day course. I really need to work, and in order to work, I really need to be able to drive. Please tell me your experience with solu-medrol, especially if you continued to work during the treatment course.

Famliy Dr started a Decadron taper saying that it looks like MS but symptoms worsened. Neuro started IV Solu-Medrol 500mg x5 days and today was the last dose. Still numb arm. Just curious if any of you have experienced anything like this or how long it may take to get some relief from Solu-Medrol. Any information is very much so appreciated. Kinda freaking out here!!! Thanks!

My question is whether this feeling is a side effect of Solu-medrol or an MS symptom that his not being relieved by the Solu-medrol? I would be grateful for any insight!

For those of you who have had to get the solu-medrol treatment IV for 5 days, how did this affect you and your body? It has been a couple weeks since I stopped the out-patient treatment for the IV. I am still awake a lot of the time when I should be sleeping. I got about 2 hours of sleep last night, and today, I lay down to rest and I can't still.

I was diagnosed with Lupus Nephritus IV , my doctor had me do a 3 day IV treatment of 1g solu Medrol , each, that was a week ago. I was already on prednisone 60 mg a day and right before the treatment Cellcept was added. I am feeling like I got hit by bus ! I read elsewhere that most of my current issues are withdrawal from the Solu Medrol . I was wondering if anyone else has had this treatment and how long it took to feel" normal" ?

i had on hand a solu-medrol had my boyfriend give me inj 1.5cc Im glute but he gave it too me about 1 inch to the left and now i have swelling at the site about the size of a quarter i am a nursing student and try to walk him through it and made sure he aspirated will i be ok???

Anyone have any ideas how to cope with the solu-medrol headaches? I slept about 3 1/2 hours, nurse is coming back in 2 1/2 for round 2 of the infusion, so have a couple of more days with the headaches.

I have a quick question for you all... My neurologist says he doesn't want to give me Solu-Medrol for this "flare" because he said it would affect the MRI results as well as the LP if we do it fairly soon. Is what he told me true or is he just making me suffer for no reason? I don't know any better and thought who best to ask than you guys. Thanks so much.

Has anyone had an injection of solu-medrol, not an infusion, but an injection to treat their symptoms? If so what was your result...good, bad, no difference? If you improved how long did the effect last? I am asking this because on Monday I received and injection of solu-medrol. It was ordered by my GP. He said if you show improvement it is just one more indication it is MS. Monday - Wednesday, my gait was improved, the pain and burning in my hips and kness was gone.

I HAD CONSULTED ON OF THE MOST EXPRIENCED CHILD SPECIALIST IN MY CITY LAHORE ,FROM LEADING HOSPITALS

I had my first experience with Solu-Medrol infusion in early August. My relapse had just started and was worsening daily-right before I was due to start training for my new job! The immediate side-effects were quite obvious and well documented. I'm having less success finding out about long-term side-effects-in particular, rapid weight gain. I noticed the bloating quite early in my treatment, especially in my face and abdomen.

I see a lot of people going on solu-medrol lately, some multiple courses within a short period of time. This really concerns me, especially in regards to the potential serious side effects - some which I have experienced personally. My neurologist is very conservative about prescribing solu-medrol He's explained to me that he doesn't give steroids for sensory symptoms like tingling or feeling numb unless it is a new symptom. He orders an MRI to see if there is any change.

I started my exacerbation in April of this year and immediately got on Solu-Medrol. I took the Solu-Medrol for 6 days at maximum dosage and tapered off with Prednisone. While my Optic Neuritis went away after only a couple of weeks or so, I soon had a Trigeminal Neuralgia attack. This only happened once, thank God, but a few days later, I began to experience difficulty walking. I still have difficulty walking, some days good, some days really bad, but the other symptoms have vanished.

Hi, I am 33 Years old, 7 months back I was masturbating and it seems I pressed too hard on my penis, the day after I felt severe pain on flaccid, I visited a urologist who diagnosed me initially with peyronies disases, and injected me with steroid injection (Solu Medrol 1g), which did nothing with pain. I have done 4 Ultrasounds during the last 7 months and all shows normal. Today I visited the urologist again, and he said there is no fibrosis, it is maybe the dorsal nerve.

Mine seem to last anywhere from six to twelve weeks. They used to resolve completely, but now they seem to leave lingering symptoms- makes it harder for me to tell if they are really over or not.

Yeah I was on IV solu medrol right before Christmas and now I am on oral solu medrol so that is why I think that is what it is but now you all got me worried, I never even thought of heart attack lol. Not sure if I should wait and see or go to the ER lol.

Hi Jan - Just a few words on my personal experience with solu-medrol. I was on a 5-day infusion for loss of vision. Took a month afterward before I started to see results, but who knows if it was b/c the steroids or natural wane?... Next time I had the 5-day infusion was in March for heat band and down my leg. Felt better after 2 weeks.

I have since had my first exacerbation in the form of ON and just finished a 6 day course of oral Solu-Medrol at home. The course of Solu-Medrol was initially supposed to be for 3 days, but there was no improvement of my condition, so the Doc decided to prescribe 3 more days worth. When I asked the Doctor about beginning D.M.D.s again, she said that I would need to discuss it with my Neurologist. I did so, and my Neurologist booked me an appointment for the end of this month.

I then have to sit for approximately 20 minutes and I can than walk normally again. Last week I went for an infusion of Solu-Medrol. I had one infusion for 3 days at 3 hrs. each. I feel pretty good afterwards and am not limping much at all anymore. My question is regarding side effects of Solu-Medrol. I realize that everyone is different but is there an average time frame for side effects? Today is the 3rd day AFTER the infusions were completed.

A week later I had double vision which prompted my first round of Solu-Medrol. The drug did seem to help, and I saw a steady improvement until the beginning of April, where I estimate I was about 95% of normal. Only if I looked to the far left I saw double. Well, I began a new relapse mid April (other sensory symptoms) which I was given another round of Solu-Medrol in the beginning of May.

Solu medrol used treat

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