Introductions..: So hello! I never... - Myalgic Encephalo...

Myalgic Encephalomyelitis Community

2,086 members651 posts

Introductions..

cfs_warrior4 profile image
4 Replies

So hello! I never properly introduced myself to this community. I was diagnosed with CFS/ME at 19. I am almost 22. It’s been a struggle. I do have it better off than some. I attend university currently (somehow). But that is all I do. No social life period. No extra items. No housework or chores. Just going to class and doing school work. Doing much else makes me crash. Which is good I found a baseline I guess? But also kinda crappy. If I do anything extra at all on the weekends, I most likely crash (80% of the time).

While here, I have a question for everyone. Anyone have trouble with falling? I recently fell again and sprained my ankle. Wearing a boot. My ankle just randomly gives out on me. My ankles are weak and awful. I already have bad balance. I just wonder if this is a hint at something else or part of CFS/ME. All help and comments appreciated. Hope everyone is doing as well as they can at their own pace.

Written by
cfs_warrior4 profile image
cfs_warrior4
To view profiles and participate in discussions please or .
4 Replies
Kitten-kat23 profile image
Kitten-kat23

Hello.

ALKT profile image
ALKT

I struggled just to get one foot in front of the other for the first 3 years. some people with m.e also have problems with balance you might be able to improve your balance with a simple exercise standing near a wall or something you can grab hold off stand on one leg whilst slightly raising the other foot for as long as you can comfortably do so and then change to the other leg. I found after doing this a few times a day my balance improved. you may get better or more informative info regarding m.e on phoenix rising one of a few good and busy sites for people with m.e/c.f.s. best wishes.

Calliepet profile image
Calliepet

For some reason hypermobility (super bendy joints) often goes hand in hand with ME/CFS, this might be why your ankles turn easily. There will be info about how to test yourself etc on the net.

Patdoyle profile image
Patdoyle

Yes I trip up a lot and have balance problems. Don’t know if it’s related to the CFS but I am now very clumsy.

Not what you're looking for?

You may also like...

At my wits end with CFS

I have only had CFS for around 9 months but am already at my wits end. It was bought on by...

ME research of note: Contrasting ME versus CFS or 'CFS/ME' by Leonard A. Jason et al

Hello, Although this study was first published in 2013 i have recently come across it and see it as...
Starbys profile image

What was your experience at the doctor on diagnosis?

Hi all, I was diagnosed with CFS in 2015 - and still have it. I remember maintaining at the time of...
Regalbirdy profile image

Newbie - CFS

Hi everyone, I hope you are all as well as can be. So my GP feels I have CFS on top of everything...
Lynzhoppy1 profile image

CFS in every day living

Hello I am new to your community and hope you are all ok? I was diagnosed with CFS 3 years a go, it...
Trulysad-76 profile image

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.