solumedrol pulse

t stop ny of the older ones from rising heck. Anyhow, that is one of the ways Pulse Therapy is used. My MS center uses Pulse for most of their IVSM treatments (including when I have had ON.

Hi everyone, just wondering if I should be concerned about my pulse rate. Im taking a 5 day course of high dose steroids for my relapse. I get the dose in the morning and notice my pulse rate slowly rises during the day . At rest it is 95 and I can hear my heart pounding while I am trying to sleep which makes me more anxious. My chest feels sore too. I keep generally very fit and healthy apart from RRMS and my heart rate is only this high normally when I am recovering from exercise.

One can always choose to muscle through relapse, but the Doc needs a good pulse check on your neurologically during attack. Are you on a disease modifier?

From what I have heard, they like to do high dose IV Solumedrol and can only be done in the hospital setting during a MS exacerbation, especially if the MRI shows enhanced lesions. That is my understanding -- I can be wrong. I do not think the medrol dose pack could touch the effects that high doses of Solumedrol IV could do. Your job will not allow you to take care of your health? Are you out of personal time off you can take or sick time? Please let us know!

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?

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.

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.....

After hospitalization on IV Solumedrol, I have had persistent atrial fibrillation and some PVCs and PACs. My blood pressure seems to be under control. The A-Fib goes on for hours and is often a quivering, jiggly sensation and/or accompanied by palpitations...with normal pulse rate due to the Cardizem.

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.

I'm in the middle of 5 monthly IV solumedrol treatments. I get 1 gram one day a month. My first round was 3 days. I am doing so much better than I was 6 months ago. The best effects of the steroids seems to last about 2 1/2 weeks then slowly peters off but still not to the point I was originally. Some symptoms are gone - cramping hands and feet. Fasciculations leave me for only a few days after the infusion but when they come back they are not as intense.

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.

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...

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.

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?

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.

coming with hat in hand is how in te world do ones manage the bizarre psychotic type side effects from the IV solumedrol? I just finished yet another five course today and frankly I had hugs melt down scared my caegiver.. and fnally made th eprimary car e doc understand thath 72 hours of mania, depression, wailing, and all that jazz was no acceptable. This is the first time I have dome them in a home setting versus in patient..could that be afcator? or am I just a little nutty...

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?

i have a PICC line as I have been going through a 2 mnth relapse with my MS and I finally gave in and went to the hospital....of course it is solumedrol pumping through it but its way different than when I had an IV port last year...question though; I feel so dizzy and have feelings l want to pass out at times even though I don't pass out. is it because of the PICC with solumedrol that is giving me a different experience?

Sheesh, this is 2nd exacerbation within 6 months...more solumedrol in 2 weeks.

Had my first dose of IV soluMedrol this a.m. and my tummy is hurting. Anyone else have this problem from it, or is it a fluke. I'll make sure I get some yogurt before my next one and keep pepto handy..

I have had a sore throat for 2 days since ending the solumedrol treatment along with probable thrush. Is this something that should go away or should i get it checked out. Throat is pretty darn sore.

I have only had one experience with the solumedrol and it was like a miracle! I had sudden double vision and trouble walking. I saw the neuro the next day (Friday) and he got me on solumedrol the following Monday. I was on for 5 days in a row. By the end of the third day the double vision was gone and by the end of the fourth day I could read again! I still, two months later, have a little residual nystagmus in my right eye and I need the cane when out and about, but not around the house.

Solumedrol pulse

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