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  1. Jaclyn

    So exhausted

    Hi there Mrs R - I hear what you are saying about the vaccines. We each have responses to them that are unique to us. My story is that before the covid epidemic I had been diagnosed with CFS/ME in 2015 following a really nasty dose of salmonella, preceded in 2012 by breast cancer, radiation and...
  2. Jaclyn

    Hi New Member, Crying finding out there is a name for this

    You're definitely not alone with the pain. There are no solutions as such for fibro - but there are supportive doctors and you may need to do some online research to find any in your neighbourhood. Yes, doctors can be dismissive, which is incredibly unhelpful. The onus is on us to find what...
  3. Jaclyn

    New to this forum

    I feel a bit weird launching into posting about myself to no particular person, and hope I'm in the rifht part of the forum, but here it is: After reading a few other FM sufferers experiences it's helpful to know I'm not alone. Amongst the hardest thing to understand is the fact that most people...
  4. Jaclyn

    Painful Feet!!

    Yes, I've also found my feet are so painful at times that I hobble around until they warm up a little. But even sitting down for 5 minutes, then getting up again, I find they're back to really painful. I've found this happens more often when my immune system gets another knock from any virus...
  5. Jaclyn

    Amino acids have nearly done away with my fibromyalgia

    Thank you for this post. I've ordered L-Arginine and L-Citrulline from an overseas supplier. I live in New Zealand and the knowledge of alternative treatments from general practitioner doctors seems to be limited. In fact, there are still some doctors over here who don't believe...
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