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  1. Mij

    Abnormalities in the urine of people with ME/CFS? A clinician asks for feedback

    I had an OAT. RBC Fatty acid and Amino Acid test done 2 days after exercise and they were all abnormal. One thing that was normal though was Lactate. I don't experience pain. I wonder if that could be why my lactate was normal?
  2. Mij

    Abnormalities in the urine of people with ME/CFS? A clinician asks for feedback

    Tight fitting heavy spandex clothing will do that.
  3. Mij

    B12/Folic Acid and D3/K2 Supplementation

    Sorry the B12 shots are causing you to feel sick. I have issues with my B12 getting low too and find supplementation via pill works just as well as injections without the hurt or distressing symptoms.
  4. Mij

    Abnormalities in the urine of people with ME/CFS? A clinician asks for feedback

    My urine had an ammonia smell when I had h pylori infection years ago, so did my breath.
  5. Mij

    Abnormalities in the urine of people with ME/CFS? A clinician asks for feedback

    @Louie41 let's just say the fruit flies no longer come around :D
  6. Mij

    Abnormalities in the urine of people with ME/CFS? A clinician asks for feedback

    It could be hormonal for some. Since menopause my whole body smells like vinegar.
  7. Mij

    Abnormalities in the urine of people with ME/CFS? A clinician asks for feedback

    Well I do feel very dehydrated when in PEM, but I don't notice any difference in odour or colour.
  8. Mij

    Very quick survey on anti inflammatories

    I take the raw root and grate it to make golden milk. I find it reduces stiffness/achiness in my hands. I enjoy the drink.
  9. Mij

    Something in the Man's Bed Was Making Him Sick

    This story resonates with me. Years ago I finally threw out all my feather bedding to discover that I could breathe easier, and my eyes were no longer itchy/red. Feather duvet lung is a small subset of lung diseases called bird fancier’s lung, which is triggered by frequent exposure to bird...
  10. Mij

    The science of craniocervical instability and other spinal issues and their possible connection with ME/CFS - discussion thread

    @JenB I was reflecting on my own personal experience when I wrote that I was thankful that I was not referred to a spine/neck specialist. I was a gymnast when I was younger and the radiographs might have indicated an 'abnormality' when in fact it might have been normal in my case.
  11. Mij

    The science of craniocervical instability and other spinal issues and their possible connection with ME/CFS - discussion thread

    @JenB I think the big difference was that I was referred to the neurologist by an ME specialist who had 20 years experience and highly recommended him.
  12. Mij

    The science of craniocervical instability and other spinal issues and their possible connection with ME/CFS - discussion thread

    My experience with a neurologist back in 1992 was positive. He ordered a lot of blood work to r/o other illnesses and sent to the hospital for various tests for vertigo. I was never sent to a spine specialist/surgeon, thank goodness.
  13. Mij

    PEM for those who are, or were, mild sufferers, how would you describe it?

    That's right. During my onset I had extremely elevated antithyroid antibodies, vertigo, mild sore throat/sore ear for months, but never a fever.
  14. Mij

    PEM for those who are, or were, mild sufferers, how would you describe it?

    @Subtropical Island thanks for your explanation. Do you have autonomic issues?
  15. Mij

    PEM for those who are, or were, mild sufferers, how would you describe it?

    @Subtropical Island when you start feeling PEM coming on, can you stop the progression by resting? For me, no amount of rest can stop it when it starts, it has to take its course of 48-72 hrs.
  16. Mij

    PEM for those who are, or were, mild sufferers, how would you describe it?

    Interesting. I have never experienced mild PEM. It's always severe when it hits and I can not push through. I have to full stop everything.
  17. Mij

    PEM for those who are, or were, mild sufferers, how would you describe it?

    I didn't experience PEM for the first 7 years of illness. When my health improved and I started running again was when PEM set in.
  18. Mij

    PEM for those who are, or were, mild sufferers, how would you describe it?

    I deleted my original posts. To add . . . PEM symptoms will intensify over the years if you continue to push yourself.
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