Sleep Dysfunction and Myofascial Pain

[@davamckay]

Had debilitating MPS since I was 14, told all my life until I was finally diagnosed at 35 that my symptoms were in my head - pain didn’t work that way. Over 2 years of weekly intense therapeutic treatment (physio/massage/needling) and Cymbalta for pain - helped me regain my life. I’m now almost 50… 15 years of pain usually at 2-4 / 10 which is amazing

[@AndrewHedlund100]

I got diagnosed with MPS. It’s driving me insane the triggerpoints won’t go away It’s like living life with pebbles in your shoes instead they’re in your chest and ribs abdomen And sometimes they’re hot sharp

[@davamckay]

@@AndrewHedlund100 I’m so sorry 😢 I feel your pain. I had to do 2 years of intensive physio therapy, massage therapy, trigger point injections and Cymbalta for relief. Cost a lot of $ but was worth every cent to get my life back. Now I’m off Cymbalta, know my limits but still need regular trigger point massages (every 1-2 months) and Chiro. I hope you can try it.. and you find relief

[@Truerealism747]

@@davamckay do you happen to suffer with hypomobility ßcared to go in cymbalta are side effects ok

[@thetruth4373]

Am 25, having pinched nerves on upper back and it has worsen my insomnia. It's been 3 years now and am miserable because of the pain.

[@Achalakanungo]

Great information. Could you share a link to the hinged mouth piece?

[@asifiqbalraju9824]

Sem problem no sleep nack or Rmbus