FYBROMYALGIA and CFS: New to this , I have had... - EDMESH

EDMESH

2,035 members349 posts

FYBROMYALGIA and CFS

rumblebum profile image
8 Replies

New to this , I have had Fybromyalgia since the days when it wasn't generally recognised by the NHS and there was only one FMG association support office in the North of the UK. Decades later I am still working despite having Prostate kidney and Liver problems and arthritis related to the FMG . Most of the posts I have read seem to be from young whingers that don't want to work but are seeking assistance in getting benefits. Get some moral fibre and go and DO a JOB you CAN DO

Written by
rumblebum profile image
rumblebum
To view profiles and participate in discussions please or .
8 Replies
Jazifox profile image
Jazifox

I find this post quite offensive.

rumblebum profile image
rumblebum in reply toJazifox

Not trying to be offensive, read some posts like I have and come back to me with something more constructive.

edmeshscot profile image
edmeshscotEDMESH

Hi, rumblebum. Welcome to the edmesh HealthUnlocked group.

I’m very sorry to hear about your health problems but please try to be respectful of the other members of the group.

myhealthneeds profile image
myhealthneeds

Many people would love to work but cannot find a way to do so because of their health. You have been fortunate to be able to work but some people are in too much pain in order to hold down a job.

msBrightside profile image
msBrightside

How can you post such a thing? surely knowing the scrutiny we are all already up against. It is severely offensive! My career was taken from me with this illness and I came off benefits to go back to college after being bound to the house for over a year which had me almost to the point of a break down. Many of us long to work I personally envy those who do have the privilege of working and I still strive to get back to it. Though the bleak possiblity is I may not ever have the opportunity.

Whingeing is better than criticising what you clearly do not understand!

ALKT profile image
ALKT

i do not think it is whingeing to print your personal and in many cases painful life experiences with others in order to give comfort to the many people who feel isolated by their ill health. perhaps rumblebum is one of the lucky people to of had pain meds without horrendous side effects. unfortunately near fourty percent of the population are not so lucky.

ukmsmi4 profile image
ukmsmi4

A very offensive and extremely unhelpful remark. This is supposed to be a forum for support not criticism.

Like many others I DID work for 30 years but had my ability to do so eroded over many of the latter years and finally taken away from me as a result of a big breakdown at work over four years ago. My husband also struggles with his own health issues and between us we are struggling to simply exist. This debilitating condition affects all aspects of your ability to simply function on a daily basis, including your self-esteem which is severely degraded by being unable to work.

We would both dearly love to be able to support ourselves properly again like any normal person but are UNABLE to work not unwilling.

Why did you bother joining a friendly helpful forum like this if that is your attitude? Please try and be more supportive. I'm sure everybody here would dearly love to be well and working again.

myhealthneeds profile image
myhealthneeds

I am visiting one woman who is in severe pain all day and every day. She can't hold things securely and she can't feel the soles of her feet so stumbles and falls. She spends most days on her bed with a blanket and hot water bottle trying to get some relief from her pain. She cannot sleep because of the pain. There is no-one who could employ her as she can rarely go out and cannot sit up for very long. If she could work she'd be very happy. Just be very happy that you have the ability to work and that you are not totally disabled by it.

Not what you're looking for?

You may also like...

Cfs and full time work

Hi. I am feeling a bit lost. Last month my gp casually told me most likely i have cfs. I have been...
Suzlj profile image

CFS and shingles link?

Hi, I have had chronic fatigue/ME for four years now, but I am concerned that my mother may also...
Caroljm28 profile image

Possible CFS

Hi all, I'm a 37 yr old and was an active woman. I have been suffering with tiredness/exhaustion on...
Welshiegirl profile image

Daughter with CFS

Hi my daughter who is now 15 years old was diagnosed with CFS in January 2013. It all started after...
ali46 profile image

CFS = me losing my mind.

I just found this website tonight, I'm a noob...so not sure where to start. I turned 43 this past...
Sybariss 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.