Connect with others who understand.

  • Learn from expert-reviewed resources
  • Real advice from people who’ve been there
  • People who understand what you’re going through
Sign Up Log In
Powered By
Real members of MyFibroTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.

sometimes the world in my head feels unreal like I’m hanging on with my fingernails. Do any of you have this and what do you do for it?

December 29, 2018
 · 
Reactions

Answer Summary

Members deeply connected over the question of managing fibromyalgia alongside costochondritis, anxiety, and depression, with many describing... Read more

Members deeply connected over the question of managing fibromyalgia alongside costochondritis, anxiety, and depression, with many describing the overwhelming sensation of symptoms feeding into each other and feeling like reality is slipping away. Several members shared that Cognitive Behavioral Therapy has been transformative, teaching them to break down spiraling thoughts through grounding techniques like focusing on trees and wind during walks, while others found relief through low-dose Klonopin or Ativan for worst moments, gentle daily exercise like yoga, and prayer. A recurring theme was the isolating nature of fibromyalgia's invisible toll, the frustration with doctors who immediately prescribe medications, and the importance of finding others who truly understand the relentless cycle of anxiety and depression that accompanies chronic pain.

A MyFibroTeam Member

It does and quite frankly, that seems to be the nature of FMS. I tend to have daily mini battles but when I go through something, it tends to be worse for weeks at a time with no real clear sign of letting up. God knows, I have been brought to my knees many times this year and on rare days where I feel like 75% of who I used to be, i praise God and thank him so much bc it’s those days that keep me going. No one understands the toll FMS takes on you until you’re experiencing it for yourself. It’s a hard illness to describe bc it’s always changing but the one thing that seems to remain the same is the anxiety and depression!!!

December 29, 2018
A MyFibroTeam Member

I agree. This latest episode has been like a roller coaster. I do have Ativan which I hoard for the worst times. I just don’t want to do the antidepressant route. I just seems like you get attacked from all sides at once!

December 29, 2018
A MyFibroTeam Member

No drugs. It is a different way of thinking. There are workbooks out there that teach how to breakdown, and challange, what is viewed as reality. Just today i was taking a walk and obsessing about an issue. I stopped and made myself look at the trees, feel the wind...etc. it is not magic but it helps.

December 29, 2018
A MyFibroTeam Member

Cognitive Behavorial Therapy is the one thing that helps. It has saved me by forcing me to break down the swirling in my head.

December 29, 2018
A MyFibroTeam Member

No it’s not only you🙂. I’ve been battling depression and anxiety seems like forever. It’s just this time they all have collided at Christmas ho ho ho. My pain is a generalized ache most everywhere with zingers thrown in from costo and ibs. Yoga poses I used to do easily I can’t even do part way without some pain that stops me. I’m trying to do some gentle exercise each day it seems to help for a few hours. For me it’s the anxiety that makes it worse

December 30, 2018

Related Questions

View All
A MyFibroTeam Member asked a question 💭
Paulding, OH

A MyFibroTeam Member asked a question 💭
Bc