Fibromyalgia: Numbness, Tingling, Pins and Needles

” The world is full of suffering, it is also full of overcoming it”, Helen Keller

A condition called paresthesia results in numbness, tingling and pins and needles in the limbs, due to disturbances in the nerve pathways. For me it is much worse at night and in my arms, rather than the legs. However, I also have many twitiching new sensations in my legs as well, but the arms right now are worse. The result  is that I wake up several times during the night when an arm is ‘asleep’, numb with cold and actually hurting. When I am up for awhile moving about the feeling comes back in my arm and I fall back asleep on the other side only to wake up an hour or two later with it on the other side. My sleep is very disturbed by this relatively new symptom. But, then I have developed pains in the knees this summer, another new symptom. Just as I think I have had them all, something new crops up. How discouraging. Like other sufferers of pain I live in fear that this new symptom will not disappear.0060723122 While I am a great fan of Harriet Lerner it is this particular book which helps me the most.

I am very sleep deprived of late yet I dread going to bed knowing that a few hours later I will awaken with hurting arms. I do all the suggested right things: I take cal/mag supplements, a B12 supplement  under my tongue, and rub my arms with a camphor cream. I take an epsom salts bath before going to bed and apply heat and/or cold to my neck during the day. I put a small pillow under my neck to support the area that is not on a pillow and I have the right pillow for my  upper body. I try to discipline myself to meditate each day and I also do some gentle movements of my arms often during the day. One particular stretch which does help somewhat is standing against the wall with my arms outstretched against the wall and my head against the surface with gaze forward but not jutting my chin outward, for one minute. I try not to struggle against the pain. QiGong is supposed to be good for this condition. Yet, in spite of all my good intentions the demon usually persists. It isn’t often I write a blog with such whining but to-day after very little sleep and cold, wet, snowy weather (gasp! it isn’t even officially winter yet!), I feel entitled. Forgive me folks! The women in my book speak often about feeling guilty about complaining, but since our symptoms are so diverse and frequent, it isn’t easy to ignore them. So this is a blog about my newest struggle!

4 Responses to “Fibromyalgia: Numbness, Tingling, Pins and Needles”

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  2. December 9/09
    I just watched another PBS documentary on positive neuroplasticity (changing the brain) and now trying to figure out how to use this information to give messages to the brain that will allow me a better sleep! I do so envy people who say they ’slept like a log’ (does a log sleep?!) since I don’t know what that feels like. I think in 10 years from now the neuroscience community working with plasticity will have so many answers for us. In the meantime…here’s wishing for some better nights!
    Barbara Keddy

  3. Diane says:

    I have had this same problem off and on for years. (23 yrs) I have CFS/FM and Hashimoto’s thyroiditis.
    It’s all so very frustrating for sure. Did physical therapy for awhile and learned some stretching exercises which helped.

    I am on day 2 of Metanx that my doc gave me for my numb feet. It’s by prescription and is a very high powered vitamin containing folic acid, B12 (equivalent to several shots) and other B vitamins that helps with blood flow to the nerve endings. It is being used with some success for peripheral neuropathy in diabetic patients. I have read of FM patients that are also being helped.

    So, I hope it will help my tingly arms that fall asleep as well as the numb toes. You might want to ask your dr about it.

    Hope this passes for you soon!

  4. Dear Diane: Thanks for the tip. Keep in touch and let us know if Metanx works for you! I am happy to know that this problem for you has been “off and on” and hope it is “off ” for me sometime soon! You are right…stretching is necessary, but only gentle stretches because anything too dramatic causes a flare-up!
    Kind regards, Barbara

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