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#1 | |||
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Junior Member
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I am a new member, but wanted to post a question. Does anyone know the amount of steroids in mg's one person can have during a year?
I am having a relapse at the moment, the first in 14 years, and have MS in a very mild form. However, my exacerbation has already started subsiding some, but I know it is going to take time, so was hoping I could move it along. The reason I am asking about the quantity of steriods in mg's, is because in less than a year, I have had steroids injected in my spine for my spinal stenosis and wondered if there is a limit. Thank you for any responses. Cathy |
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#2 | |||
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Wisest Elder Ever
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What symptoms is your exacerbation presenting? I've heard that some symptoms are not helped by steroids.
Personally, I won't do the steroids. My flare ups generally resolve themselves anywhere from 6-12 weeks. I'm not working any longer so I guess I tend to just wait them out versus speed them along. But everyone's different and chooses different ways to help them through the crisis. I'd check with the Neuro and see if he/she thinks it will help your particular case. I do know that too much can cause your bones to weaken so that's a downside you have to think about and weigh the benefits vs. the consequences. Good luck whichever path you choose! ![]()
__________________
These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here. |
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#3 | |||
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Junior Member
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Hi,
Thanks for your response. The only symptoms I have is it feels lke I have tight shoes on all the time, and a little numbness in the leg and buttocks. It doesn 't prevent me from doing anything, just feels uncomfortable. It was worse a few weeks ago. I am home all the time so my time is my own, except that I have three Bichon's who get me up every morning at 5 and they have a lot of appointments coming up, 3 vet appt and 3 grooming appt. It just seems odd to have a relapse after 14 years and I have forgotten a lot of what I once knew. Cathy |
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#4 | |||
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Elder
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I try very hard to avoid the steroids unless it affects my vision or my ability to express my own words.
I hope you feel better quickly. ![]()
__________________
RRMS 3/26/07 . Betaseron 5/18/07 . Elevated LFTs Beta DC 7/07 Copaxone 8/7/07 . . |
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#5 | |||
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Elder
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I was told that steroids dont do much for numbness. I did steroids once for numbness, didnt do anything for me. So, I kind of agree a little bit with that statement.
If it's just numbness, which is a fairly harmless symptom, even tho it's really really really really really annoying, I would skip the steroids and wait it out. If things have been improving for you, just have a little patience and wait a little longer. Just be careful around anything hot so you dont burn yourself. I know numbness is really uncomfortable. It's been one of the more bothersome symptoms for me. I really really really hate numbness.
__________________
~ Never do anything that you wouldn't want to explain to the paramedics. ~ Author Unknown ~ ~ "Animals have two functions in society. To taste good and to fit well." ~ Greg Proops, actor ~ |
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#6 | |||
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Senior Member
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Three Bichons!!!! Mine is pictured here.....she's not a purebred, but so lovable as they all are. You must have lots of energy around there with three of them! Hope your MS symptoms are subsiding without steroids. They never seemed to do much for me..........just time. All the best whatever you decide.
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_____________________________________________ .....Judy SPMS -- FIBROMYALGIA -- Ouch! and Ouch! . |
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"Thanks for this!" says: | SallyC (07-25-2011) |
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#7 | |||
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Junior Member
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Quote:
I will e-mail my neuro about it though. Cathy |
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#8 | |||
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Junior Member
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Quote:
Cathy |
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"Thanks for this!" says: | SallyC (07-25-2011) |
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