Multiple sclerosis advice
Options
jules5943
Community member Posts: 5 Listener
Hi, I’ve been poorly for over 10 years on and off. Was diagnosed with reactive arthritis, more recently psoriatic arthritis and now fibromyalgia.
It’s got bad now and don’t work anymore. I’m not convinced it’s fibro and I’m starting to wonder if it’s ms.
Had a mri head scan done Thursday last week so waiting on results as I believe if I have ms it will show?
Had a mri head scan done Thursday last week so waiting on results as I believe if I have ms it will show?
You know when somethings really wrong with you and don’t think their diagnosis can be right because of how you feel? I have been feeling that for a while.
I am extremely fatigued. If I do something like I mowed grass, medium garden, been in bed 3 days exhausted and unable to do much at all. Trapped nerve feeling in my hip, bum cheek area for over 6 weeks with no reason why, making it hard to walk. Weak hands, tingling in fingers and feet, vision got worse, unexplained sharp pains over body. Memory is shocking, can’t remember why I walk in room half of time.
I am extremely fatigued. If I do something like I mowed grass, medium garden, been in bed 3 days exhausted and unable to do much at all. Trapped nerve feeling in my hip, bum cheek area for over 6 weeks with no reason why, making it hard to walk. Weak hands, tingling in fingers and feet, vision got worse, unexplained sharp pains over body. Memory is shocking, can’t remember why I walk in room half of time.
I don’t have spasms though.
In a way I’m hoping the mri shows ms so that I get an answer to all this. Especially now I’m not far off house bound.
any advice from sufferers of ms if this could be that disease and will mri scan tell me for sure?
In a way I’m hoping the mri shows ms so that I get an answer to all this. Especially now I’m not far off house bound.
any advice from sufferers of ms if this could be that disease and will mri scan tell me for sure?
Comments
-
This sounds really difficult for you @jules5943 Hopefully, you will receive an answerCommunity Volunteer Adviser with professional knowledge of education, special educational needs and disabilities and EHCP's. Pronouns: She/her.
Please note: if I use the online community outside of its hours of administration, I am doing so in a personal capacity only.
Categories
- All Categories
- 13.1K Start here and say hello!
- 6.7K Coffee lounge
- 69 Games lounge
- 387 Cost of living
- 4.3K Disability rights and campaigning
- 1.9K Research and opportunities
- 202 Community updates
- 9.3K Talk about your situation
- 2.1K Children, parents, and families
- 1.6K Work and employment
- 777 Education
- 1.7K Housing and independent living
- 1.4K Aids, adaptations, and equipment
- 593 Dating, sex, and relationships
- 363 Exercise and accessible facilities
- 741 Transport and travel
- 32K Talk about money
- 4.4K Benefits and financial support
- 5.2K Employment and Support Allowance (ESA)
- 17.3K PIP, DLA, and AA
- 5K Universal Credit (UC)
- 6.3K Talk about your impairment
- 1.8K Cerebral palsy
- 875 Chronic pain and pain management
- 182 Physical and neurological impairments
- 1.1K Autism and neurodiversity
- 1.2K Mental health and wellbeing
- 317 Sensory impairments
- 822 Rare, invisible, and undiagnosed conditions