- Home
- Share
- Forum
- Fibromyalgia Forum
- Living with fibromyalgia
- Is fibromyalgia 'only in your head'?
Patients Fibromyalgia
Is fibromyalgia 'only in your head'?
- 200 views
- 35 times supported
- 16 comments
All comments
Go to the last comment
Suzhannah
Good advisor
Suzhannah
Last activity on 19/02/2023 at 17:04
Joined in 2016
56 comments posted | 16 in the Fibromyalgia Forum
1 of their responses was helpful to members
Rewards
-
Good Advisor
-
Contributor
-
Committed
-
Explorer
-
Friend
-
Newsfeeder
Sadly this is just one cause psychiatrists have hung onto And then passed as an option to medical people. There is actually no evidence to back up this claim...I suppose doctors dont like to admit they dont know stuff
Other reasons put forward by some specialists are
Bank on head / shock or long illness in childhood
IBS disorder
Poor immune system
Different Virus's like scarlett fever
A car accident
Drinking & smoking, drug taking
The actual truth is:
We as patients and them as doctors dont know the reason for ME/cfs or Fibro. If they did then there would be a clear cause & a clear effective treatment Which there is not
Both illnesses have about 60 overlapping symptoms and sadley Neither leading consultants or scientists or retro-virologists or neurologists or rheumatologists or psychiatrists know how ME & Fibro are caused
It would be a huge discovery A world wide announcement if they did
Take care
You take whatever safe prescribed meds help you And rest a lot Close curtains Reduce noise Use tens machines and or gentle stretching or yoga or maybe reduce glutton in your diet and remove seeds from foods like cucumber & tomatoes etc ...not cures by any means just helpful tools that may aid your symptoms a little
Take care of you xx
See the signature
Suzanne
Rozanne
Good advisor
Rozanne
Last activity on 28/08/2021 at 00:24
Joined in 2020
13 comments posted | 6 in the Fibromyalgia Forum
1 of their responses was helpful to members
Rewards
-
Good Advisor
-
Contributor
-
Committed
-
Explorer
-
Newsfeeder
@Suzhannah thank you so much for this. Most especially grateful for your advice.
Take care of yourself as well🌹
See the signature
Rose
pinsnneedles
Good advisor
pinsnneedles
Last activity on 05/04/2023 at 14:34
Joined in 2020
10 comments posted | 7 in the Fibromyalgia Forum
Rewards
-
Good Advisor
-
Contributor
-
Messenger
-
Explorer
Reading this thread is so interesting, it's shocking to read about the reactions of some people! There's the saying that you can never know what is going on in someone else's life - it's even more true for fibro! You never know if tomorrow is going to be a good day or bad.
Courtney_J
Community managerGood advisor
Courtney_J
Community manager
Last activity on 13/10/2022 at 16:47
Joined in 2020
1,280 comments posted | 32 in the Fibromyalgia Forum
10 of their responses were helpful to members
Rewards
-
Good Advisor
-
Contributor
-
Messenger
-
Committed
-
Explorer
-
Evaluator
Hello everyone,
Thank you for sharing in this discussion! If you haven't seen it already, we just published an article on this topic that you may find interesting. You can read it here: Why do some still believe that fibromyalgia is a psychosomatic illness?
What do you think? Have you ever been told that your fibro is "in your head"? Do others around you understand what you're going through?
@Suzy1243 @Wibblewobble @Suzanne37 @Triciajean @JoannieP @Nicnac2020 @Sarahbubbles @Ttotty @Carolinem @Calia160 @Cookie 321 @Smiler383 @gertyb @Linda456123 @Kimmy64 @Hursttracey @Saskia
Feel free to share your thoughts with us here!
Take care,
Courtney
See the signature
Courtney_J, Community Manager, Carenity UK
MariaB
Good advisor
MariaB
Last activity on 14/02/2024 at 13:17
Joined in 2020
25 comments posted | 19 in the Fibromyalgia Forum
2 of their responses were helpful to members
Rewards
-
Good Advisor
-
Contributor
-
Messenger
-
Explorer
-
Friend
It's good reading everyone and hearing that it's not just me! I ended up finding a new GP in the end. I'll give the article a read, I think doctors need more education about fibro!
Pippadog
AmbassadorGood advisor
Pippadog
Ambassador
Last activity on 21/07/2024 at 22:45
Joined in 2016
190 comments posted | 17 in the Fibromyalgia Forum
25 of their responses were helpful to members
Rewards
-
Good Advisor
-
Contributor
-
Messenger
-
Committed
-
Explorer
-
Evaluator
Your experience with your new GP was an unnecessary outcome. It is not a psychological condition although I did think I was going crazy at one point. I understand it's a neurological condition ( the signals from the brain to parts of the body are malfunctioning hence different activities all over the body eg pain, tingling, stinging and more. As to why the brain is acting this way the Medics are not sure but they feel it is Triggered by a shock to our system eg an acute illness or an accident or something similar. I hope this is helpful, maybe views could change in time.
Give your opinion
Members are also commenting on...
Articles to discover...
23/10/2024 | Procedures & paperwork
06/09/2024 | Advice
04/09/2024 | Testimonial
Fibromyalgia: "If you fight against the illness, you'll never move forward."
11/05/2018 | Advice
18/10/2018 | Advice
18/06/2021 | News
Why do some still believe that fibromyalgia is a psychosomatic illness?
03/05/2019 | Testimonial
The testimonial of Natacha Waking up with fibromyalgia and non-disabling arthritis
Subscribe
You wish to be notified of new comments
Your subscription has been taken into account
MariaB
Good advisor
MariaB
Last activity on 14/02/2024 at 13:17
Joined in 2020
25 comments posted | 19 in the Fibromyalgia Forum
2 of their responses were helpful to members
Rewards
Good Advisor
Contributor
Messenger
Explorer
Friend
Hello all, I just had the strangest experience and I had to come on here to see what you all think.
We just moved house this month so I went to see my new GP in our new area. I told him that I had fibromyalgia and he went off on a long thing saying that fibromyalgia is purely psychological and that it is due to psychological shock or trauma experienced in life.
I have never heard that in my life and needless to say I will be changing GPs! Have any of you ever heard anything like that? I know from my experience it took me a while to get diagnosed and to get my doctors to really look at my symptoms but I've never been told that fibro isn't real! 😱
What do you all think?