solumedrol life

I know steroids can make you susceptible to infections, but has anyone developed a UTI on solumedrol? I had the unmistakable first inklings of one a bit ago. I rushed out for cranberry juice and a blueberry smoothie (blueberries are supposed to have the same effect as cranberries, and it's a good excuse for a fruit smoothie!!) and I'm hoping I can keep it at bay this way, but I guess I'll know in a few hours. These things tend to come on fast for me.

I am scheduled Monday to do an IV for three days of Solumedrol. Has anyone else done that and if so, what is your opinion. I am alittle nervous about it.

Sister had ITP, platelet count 2 when found. Hospitalized & given IV solumedrol in massive doses which saved her life. On prednisone after for a while. She can handle the diabetes connection. Unfortunately, continues to have psychotic effects almost 2 years later: voices & people when none there, bouts of extreme anxiety and multiple other symptoms. Acts as if suddenly struck with alzheimers. Can this be from the solumedrol IV & then prednisonne?

I am currently being treated with 1 gm Solumedrol once/month. I had a three day course last spring and felt AWFUL afterwards. I did eventually feel a bit better overall, so maybe it was worth it. Even the one day dose makes me feel pretty lousy. My sx actually seem to get worse for a few days afterward! I'm not dx, but symptomatically fit the diagnostic criteria (we'll see what the 3T MRI has to say...

Searching, I found you and am excited that there is a group that may actually be able to answer some of my questions. The first thing he wants to do is put me on solumedrol for 5 days, I am not currently in a flair. Any reason I should put myself through that if I am not currently having symptoms?

just last week I started having ridiculous trouble with my right legs/hips/knees and am walking with am limp and wanting to drag that leg..am STARTING DAY 3 of solumedrol and feeling slightly improved but the pain/difficulty walking has moved from hip to knee to ankle on the right side. my question is..will this go away or will it remain? does it sound like spacticity? Do I need to see an orthopedist? PT? meds? talk with the neuro?? any advice??

These are the same problems I have with Solumedrol. Diabetics have a hard time with Solumedrol and it seems that insulin or diabetic pills, cannot work hard enough to get high blood sugar levels down. Here where we live in Virginia, they will not do a treatment, if your blood sugar level is about 200. This is a good drug, but very hard on someone that is prone to high blood pressure and high blood sugar.

So today is 2nd day of solumedrol, plus about 3 other IV meds, for migranes and nausea. Tomorrow is my last day, and it will b 6 hours. As I am in the middle of the infusion, my PCP calls, and tells me my chest xray from yesterday shows pnemonia. Ok, so solumedrol with pnemonia.. I am no doc, but pretty sure that is not a good mix. I started with this chest infection about 5 days ago. Always something. I need to sleep, that might help.

ve had a horrible experience with Solumedrol as well.....Back in March I had extreme leg and groin numbness and went on IV Solumedrol for 3 days....I had a nasty reaction to it, but it DID take away the numbness and vision problems almost immediately....Well, within 48 hours anyway..... In May the left side of my head and face went numb and because I was visiting the MS Clinic at that time, I declined the Solumedrol treatment.....That numbness didn't go away for 20 days.....

This concern has been posted awhile back, but wanted to reintroduce it. I had a solumedrol treatment about 4 weeks ago. About 2 weeks later i got chills and my hands started to itch uncontrollably followed later by hives in random places (no pattern to where they were) but mainly arms, stomach, and scalp. Called my neurologist, heard back from his nurse who said there was no way it was related to solumedrol.

At one point this was happening about 15 times per day. I took a round of Solumedrol (3 days) and began taking 300 mg of Lyrica per day. It now happens 4 or 5 times per week. My doctor prescribed another round of Solumedrol which is scheduled for next week (30 days from the first one). I am trying to decide whether I want to do the 2nd round of Solumedrol. It made me feel horrible and was a miserable 4 or 5 days.

Thank you all for your comments and the push that I needed. I called the doctor and went to the hospital. They have me on 5 days of Solumedrol IV 1gram each day. After today's long ordeal it will be out patient and won't be so bad. Does anyone know if that is a big dose? The doctor's made such a big deal about the dose being "huge" that I got a little paranoid until they got my neuro on the phone.

I had a 4 day Solumedrol drip and then step down pack in February and it made me worse. All my muscles tightened up and I have more pain than I did before. Call it a major fibromyalgia attack. Even now in May, I am still as stiff and woozy as i was after the glucocorticoid therapy. Sigh. Did nothing for me that I can tell. I did sweat a lot during the treatment so maybe i lost a few toxins?

t help, so I had the 3 day mega dose IV solumedrol. I did not do the tapering off pills, because I was having a reaction to the medicine. Since the end of February my ankles are swollen everyday, all day. I asked my neurologist, and she said it is a side effect of the solumedrol. Any one else experience this.....swollen ankles for so long? When will they return to normal? Help please. Thank you.

She told me that she had taken the steroid 3 different times for life or death situations and saved her life every time but left her with this crazy side effects. She told me every time she took it, the side effects left her within 32 days exactly but for me it didn't go away for months, and I sometimes still feel weird like the side effects but my aunt said this could just be stress or my mind playing tricks but either way I don't like it.

Technically, any neurological symptom lasting more than 24 hours is considered an exacerbation. Solu-Medrol has proven to shorten the lengths of exacerbations, but has not shown to alter disease course in any way. With that in mind, steroids are completely optional unless there is something life-threatening happening that the steroids may possibly put a halt to. What is life-threatening? Good question, the opinion varies from Doctor to Doctor and patient to patient.

Hello everyone! Sorry it's been a few days, but I can barely remember what has happened.....I just wanted to make the wonderful announcement that I was finally able to have a shower today!! YAHOO!! ***CLAP CLAP CLAP*** I vow, before all you wonderful people, that I will never EVER again take for granted the "small" things in life that people do every single day without a second thought....(ie: showers, walking, brushing my teeth, going to bathroom, etc...

Hello I am a 25 year old female and four weeks ago I was diagnosed with optic neuritis, I was admitted to the hospital for 5 days of IV solumedrol therapy (1000 mg a day). After the treatment my vision mostly came back and the eye pain was completely gone. At the same time I also had a burning arm pain in my right arm with numbness and tingling into my fingers. During my hospital stay I had an MRI of my head, which was normal.

his office just called and wants me to take 1 IV treatment of solumedrol - equivalent to 1 gram of the medication. they said if my symptoms improve, this could be more evidence of MS....if they do not improve, then maybe not MS. my concern is that my symptoms aren't very strong and i don't know if i would really notice a difference...or maybe i would? geez, can you tell i am a mess about almost everything! so, have you done this?

I started rebif and solumedrol at the same time in July, but call your doctor.. Are call the MS lifelines??

I had my first course of solumedrol Friday-Tuesday. Last night (Thursday night) I began needing to urinate every 30-60 minutes. Not like tons and tons. But also not my bladder fooling me. And it continues today! I can't get a hold of my @$&#%& neurologist. So of course my question is whether this happens with steroids. Anybody?

t used it for MS patients for quite a while because most or all tolerate the solumedrol fairly well. Wish me luck. If insurance accepts it I will start the end of this month. I'd love any feed back you guys may have on it...don't know what to expect.

My understanding is (and hopefully someone will correct me if I'm wrong) that IV solumedrol is of the most use within the first weeks of a relapse. In the area where I live, steroid use for relapse is waning. There is quite a bit of research showing the in most cases, the relapse length is only marginally shortened. Given the risks (blood sugar issues, bone density changes), steroids are no longer given automatically. I would consider it if I lost vision.

I am 24 and I have MS since 08 (was on solumedrol, I always lose my vision during ms attacks ) and I have been constipation and with nonstop gas for 6 months, I have tried lots of water, fruit, fiber, vitamins, and most recently miralax which worked at first but then caused lots of blood and pain. Any suggestions on how I can stop this cycle before going to another specialist? My neuro, gyno and primary drs haven’t been helpful on this topic yet.

Hi Everyone I start on my IV treatment for 5 days this Thursday, with 500mg of Solumedrol, I am worried about it, can anyone tell me what side affects i may experience, and how to prepare for it, and can i go to work right after the Treatment, thanks Tyler

I just finished a course of 5 days of IV solumedrol for my MS. I am very concerned about the severe depression I am experiencing. Any information?

Solumedrol life

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