Instability when walking
Posted , 14 users are following.
PMR diagnosed 1 year 9 months.
Actually was on 1 mg for months, then had flare up, which I blame on stress.
Am currently on 3, using A modified version of Eileen's method.
i have noticed since the diagnosis, that I am not as stable on my feet, which is more prevalent after reductions.
I don't have pain..... Just a little less motivated and a bit more tired.
Does anyone recognize this symptom, or is it something from another one of my medical challenges?
Happy Holidays to all, and a Healthy, New year.
Barb
0 likes, 30 replies
EileenH barb30898
Posted
Some years ago some ladies in the north of England attended a Nordic Walking course aimed at seniors - from AgeUK I think - and found using the pair of poles helped their balance a lot. One even was able to stop using her zimmer/rollator altogether after a few months. Tai chi is also said by quite a few to help with balance.
If you are more tired after a reduction at this stage it may be your adrenal glands aren't quite keeping up with the lower dose of pred. And being tired doesn't help balance. Now you are at such a low dose consider slowing even my reduction down even further - and stay at each dose for a few months in between reduction. These are really low doses, there is no rush.
Elijo barb30898
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gail2910-US-MI barb30898
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EileenH gail2910-US-MI
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Anhaga gail2910-US-MI
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EileenH Anhaga
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caroline83483 barb30898
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started at 15mgms, now on 8mgms . The strange sensation I have is that I feel I am walking on a trampoline. This improves as the day progresses. I do get tired and then balance is worse. However I am sure that I am generally improving with a little light at the end of the tunnel.
Happy Christmas everyone and a Guid New Year.
Caroline
EileenH caroline83483
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It is a lot better now though.
Silver49 EileenH
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EileenH Silver49
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barb30898 EileenH
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The idea of going back to exercise, as a regular routine sounds like a good start.
I have played sports, all my life, and the lack of good balance concerns me.
First things first!!
Interesting, Eileen, that you mention bladder problems. I just saw rheumatologist, this afternoon and he claims bladder problems and balance problems are 'probably not related to PMR but did admit hair loss could be connected.
I will slow down on pred reduction and keep putting one foot in front of the other.
Thanks to all
Elijo EileenH
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EileenH barb30898
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Overnight frequency (as opposed to urgency) probably IS due to pred, that is something I have never had any bother with. I would wake about 4am, if I lay there hoping to go back to sleep - I wouldn't. If I summoned up the enthusiasm to get up and go to the toilet even if I wasn't really sure I needed to, I would fall back to sleep in minutes! But during the day if I needed to go, I needed to go - whichever reason.
Balance - of course it can be related to PMR. Your muscles are severely affected by PMR and it is your muscles in coordination that keep you upright! My legs didn't always do what I wanted them to do - same with hands sometimes. They just didn't seem to be working properly! Silly things like changing bedding or trying to open something. When I'm on a higher dose of pred it is much better, when I get below 4mg it returns and has always been the sign of a flare for me.
linda17563 EileenH
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EileenH linda17563
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linda17563 EileenH
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EileenH linda17563
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In my experience feeling drained and extra sweats very often means a bit of a flare going on - the activity of the underlying autoimmune disorder probably waxes and wanes, so you may reduce while it is realtively quiet but then it wakes up again. And of course it is heading for xmas - and lots more to do for anyone who isn't "Bah Humbug" like me. So are you overdoing things? Might it be worth a mg more pred for a few days?
linda17563 EileenH
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Hope it`s as mild where you are as it is here this December....only Scotland has it cold/snowy...not that I`m complaining!
Silver49 linda17563
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linda17563 Silver49
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EileenH linda17563
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EileenH
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linda17563 EileenH
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Silver49 linda17563
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