If we become concerned about you or anyone else while using one of our services, we will act in line with our safeguarding policy and procedures. This may involve sharing this information with relevant authorities to ensure we comply with our policies and legal obligations.
Find out how to let us know if you're concerned about another member's safety.
Find out how to let us know if you're concerned about another member's safety.
Fibromyalgia and walking aids, do they help ?
Options
radders
Community member Posts: 6 Connected
Good evening.
I was diagnosed almost a year ago with fibro and cfs , since then I have become progressively worse, more so with nighttime pain , restless legs and really bad stiffness in my legs. I work full time (currently on furlough due to covid) . I am unable to take painkillers due to stomach issues , I am on Amatrypaline. My partner thinks I should see my GP about getting a stick or crutches because when my legs are stiff I stumble a lot and struggle to keep my balance , my question is, would they actually help, and would my gp give me one for fibro stiffness? I would like to say I am keeping fairly active during lockdown, doing short walks when possible and gentle stretching along with some low impact exercise when I'm having a good day,Many thanks
I was diagnosed almost a year ago with fibro and cfs , since then I have become progressively worse, more so with nighttime pain , restless legs and really bad stiffness in my legs. I work full time (currently on furlough due to covid) . I am unable to take painkillers due to stomach issues , I am on Amatrypaline. My partner thinks I should see my GP about getting a stick or crutches because when my legs are stiff I stumble a lot and struggle to keep my balance , my question is, would they actually help, and would my gp give me one for fibro stiffness? I would like to say I am keeping fairly active during lockdown, doing short walks when possible and gentle stretching along with some low impact exercise when I'm having a good day,Many thanks
Tagged:
Comments
-
Hello there, I would definitely get in touch with the Gp they can refer you to occupational health. They will do an assessment. In the meantime I would say get a stick off ebay so that you can keep a safe as possible.
I have always had fluctuating neurological symptoms. I got a stick from ebay. When I explained to the doctor the problems I was facing OT did an assessment ( they gave me a proper stick right height)
Took some time for the intial assessment, 5 months (I'm in London). by then I could not walk much,balance issues (many falls and broke coccyx)and was really struggling with everything.
Many adjustments were made to my home ), I got a bathlift, bed rail, stair rail and ramp etc.(waiting for stairlift).
They also referred me to the wheelchair service and other agencies too and I did not know how much help there is. I am now really bad and after an assessment with adult social care, I am finally getting a carer.
My children do nearly everything for me. I can't tolerate being upright always in pain. I actually have around 33 diagnosis"s 4 are neurological.
Please get the help you need.
Sorry to babble on?
Take care.
-
Many thanks for advice, I shall have a chat with the GP x
-
Hi @radders. I know this is an old topic but I have only just seen it. I have ME, fibromyalgia and cervical spondylosis. I am quite unsteady on my feet sometimes and in quite a lot of pain. I do use crutches when I need them. My legs get quite stiff sometimes and I can't walk without the crutches.
-
Hi,
I’m sorry to hear your going through this. I have extremely bad restless leg syndrome which unless you have it could never understand how awful it is. I use a stick to lean on to move around. I brought it when I had my first covid jab as I was really struggling to walk and the closest shop was a pharmacy and they sold walking sticks so I got one and it has helped me loads. I also have house aids to help me when my wrists and arms hurt. It cost me around £20 I think it was just under and it folds away in a bag so I can take it with me all the time. Please see your GP or have a look on Amazon for one as it really does help. -
Hello @radders, I'm sorry you're going through this condition. Perhaps these articles will help you to know about other people's experience with the same situation:
https://www.verywellhealth.com/mobility-aids-with-fibromyalgia-3972938
https://thedisableddivablog.com/2020/09/12/fibromyalgia-and-mobility-problems-how-to-keep-moving/
https://www.walesonline.co.uk/news/wales-news/woman-20s-fed-up-using-16790319
https://www.completecareshop.co.uk/help-loved-ones/family-guide-to-fibromyalgia?__cf_chl_captcha_tk__=pmd_b005e4ca66e31634222af09d3866209942f5da7a-1629124999-0-gqNtZGzNAyKjcnBszQd6
I hope you'll figure it out soon.
Brightness
Categories
- All Categories
- 13K Start here and say hello!
- 6.6K Coffee lounge
- 69 Games lounge
- 385 Cost of living
- 4.3K Disability rights and campaigning
- 1.9K Research and opportunities
- 199 Community updates
- 9.2K Talk about your situation
- 2.1K Children, parents, and families
- 1.6K Work and employment
- 768 Education
- 1.7K Housing and independent living
- 1.4K Aids, adaptations, and equipment
- 586 Dating, sex, and relationships
- 363 Exercise and accessible facilities
- 737 Transport and travel
- 31.7K Talk about money
- 4.4K Benefits and financial support
- 5.2K Employment and Support Allowance (ESA)
- 17.1K PIP, DLA, and AA
- 4.9K Universal Credit (UC)
- 6.2K Talk about your impairment
- 1.8K Cerebral palsy
- 869 Chronic pain and pain management
- 180 Physical and neurological impairments
- 1.1K Autism and neurodiversity
- 1.2K Mental health and wellbeing
- 317 Sensory impairments
- 818 Rare, invisible, and undiagnosed conditions
Complete our feedback form and tell us how we can make the community better.