Rezultati pretraživanja
  1. 29. sij

    “Because the body’s nerves are constantly firing they never get a rest, so when they get triggered by “smaller” things, they will hurt more than a “regular” person.” Please Don't Confuse My With 'Low Pain Tolerance'

  2. 2. velj

    “In all my years as a doctor treating patients with , I never saw a patient who enjoyed feeling ill. I saw the opposite, patients who were once very active, desperately trying to find answers and treatment for their overwhelming symptoms.”

  3. 2. velj

    If you have a you will definitely understand how this feels.. Getting the energy to go for a shower. Having a shower. Having to lay down or nap after a shower because it was so exhausting and used up all of your energy.

  4. "I have come to realize that the words I say out loud and in my head end up defining me. " Thoughts on self-identity with . | Those Are Fighting Words! Metaphors Make Meaning by

  5. tears the minute I got home. PLEASE to all my fellow warriors out there: if TMS is recommended to you, please be sure you are well enough to attend the sessions—don’t be sold on the idea that you might feel too sick/weak now but the TMS will make these 3/

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  6. Getting a massage later today for my broken down immunosuppressed ass 😂😂😂 Self care party of 1 💃👌

  7. prije 2 sata
  8. When the weather changes every inch of the body knows before the meteorologist. It is a war of body and mind. Depression, pain, multiple illness symptoms, and extreme tiredness is the everyday war battling behind a mask every chronic warrior faces.

  9. prije 4 sata

    My illness may be invisible. I am not.

  10. prije 4 sata

    I also currently cant do any of this because a) money b) chronic pain and fatigue and c) I'm too tired to do anything but unbelievably bored because I cant do anything Oh and d) I dont have the space for all that stuff

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  11. prije 5 sati

    I am an educated biochemist from one of the best universities but I can't help in the fight against ME/CFS. Just laying in the dark. I want to help, give my skills to research teams to end this devastating illness. :(

  12. prije 7 sati
  13. You don't look disabled You don't look ill Old people get arthritis We all get tired I'm in pain too You can't show weakness Many are worse off I swear by Glucosamine You can't give in

  14. 2. velj

    really be like that, especially in winter!

  15. 2. velj

    My Mother is my hero. Dealing with a child with a cold is a lot. I will never know how she made with a chronically ill child. She’s entitled to any imperfections people may dislike about her.

  16. 2. velj

    life: In tonight's adventure, I'm lying in bed, about to watch my beloved fiancé in The Curse of the Midas Box. Suddenly, I feel the eminent need of the trash can. You know what I mean. I dive for it; the remote to my fire stick goes flying & shatters.

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  17. 2. velj
  18. 1. velj

    & friends, similar to my "Have you tried...?" thread, what comment do you receive from ableds that drives you up the wall? What's the phrase they all think they are completely unique in sharing w/ you? Give me your worst, weirdest, & most annoying!

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  19. 1. velj

    “It can be easy to become lost within chronic illness itself and begin to see that it is all we are. And so becomes a wave of grief and loss. The loss of yourself.  The loss of that which defines you, as well, you.” via

  20. 1. velj

    Dear , we are looking for someone with a blog about M.E. / Chronic Illness that would be prepared to blog about . We would love to hear from you if you feel you can help.

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