New here, Cfids/CFS for almost 30 years. - Myalgic Encephalo...

Myalgic Encephalomyelitis Community

2,018 members633 posts

New here, Cfids/CFS for almost 30 years.

Overcome_Ails profile image
4 Replies

Learning how to manage symptoms of CFS is equivalent to knowing what the body is saying and then listening to it.

While not necessarily functioning at 100% for the majority of life with a chronic illness, my health journey has definitely improved. Its more about balancing energy levels and reserving my "spoons". (the Spoon Theory) while actually healing in the process.

The impact of CFS has been tough. I'd like to believe that I'm tougher. Looking forward to participating with others who have Cfs and whose lived experiences all matter.

Written by
Overcome_Ails profile image
Overcome_Ails
To view profiles and participate in discussions please or .
4 Replies

Hi Overcome_Ails and welcome. I am a big believer in Spoon Theory, especially if there is a big dollop of Ben & Jerrys on the end :) In all seriousness though, pacing has made a difference and although I still boom and bust I get through it better rationing out my energy.

Good to hear things have improved for you.

Overcome_Ails profile image
Overcome_Ails in reply to

Hi @raffs Haha yep Ben and Jerry's on spoons end! like that idea :)

and absolutely..pacing is crucial to tapping into being well, and I've found that the "boom and bust" times don't last as long as they used to.

Take it easy, and keep some spoons on reserve!

Rose-Rose-Rose- profile image
Rose-Rose-Rose-

Hi there Overcome_Ails, I'm relatively new to this, only started October last year with cfs/me after a bad bout of laryngitis . I'm just beginning to realise that I need to listen to my body, after research and reading people's experiences. It will be lovely to share and chat sometimes with people who understand how dibilitating and isolating this horrible condition is.

Reading 'raffs ' reply has made me crave Ben and Jerrys!!

Overcome_Ails profile image
Overcome_Ails in reply to Rose-Rose-Rose-

Hi Rose, I always crave Ben and Jerry's LOL!

And yes, once the realization that we have to live in these bodies computes...it is only then we can start to let the body, mind, and spirit heal....

This condition is indeed isolating. It is difficult to make plans, to harness energy levels for just about everything, and most of all not having supportive network of people who "do understand".

Instead of letting the condition limit me, I'm learning how to limit my condition by balancing and accepting what I can or cannot do, when I can do or not do, and embracing the things that matter.

Thanks for your reply and hoping we continue to chat here!

You may also like...

Newbie - CFS

feels I have CFS on top of everything else I have going on!! He’s referred me to the CFS clinic,...

CFS in every day living

community and hope you are all ok? I was diagnosed with CFS 3 years a go, it has caused me quite a...

CFS Clinics, Gluten, Thyroid

Hello, my GP is willing to refer me to a CFS clinic in east london. Apparently its a...

Cfs an absolute horrible and wearing disease

Hi my name is Angela I was diagnosed with cfs last year 2016, but have had it at least 6 years and...

The Effect of COVID on ME/CFS

on how COVID affects people who already have ME/CFS before contracting COVID? I'm looking for...