Guest guest Posted January 1, 2002 Report Share Posted January 1, 2002 Welcome to our list. It is a good one. Loving, caring and supportive. I have a question for you. What is over active spinal nerves? Take care, Irene Books may well be the only true magic Alice Hoffman Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 1, 2002 Report Share Posted January 1, 2002 Age range:32 Male/female: Female What are the symptoms? (A)- I have all over muscular pain as well as some neurological symptoms, tremors, double vision, headaches, unable to sleep because of pain. I have also been diagnosed with over active spinal nerves. Has you illness been diagnosed? (A)- It was suggested by a rheumatologist in march 01 I had fibromyalgia. How long was it that you suffered before you found out what was wrong? (A)- I believe I have had FMS for at least 5 years. If Fibto-CFS How long have you been suffering with it? (A)- N/A Is there a time that you can remember when it started? (A)- My condition has got worse over the past year but it became more noticeable to me sept 00. Some of us have found lack of exercise we are overweight. Have you found this to be a problem also? (A)- I have gained about 1 stone in the past year due to lack of ability to exercise and having no energy. Are you on disability? (A)- No If you are any pointers for others trying to get on disability? What have you found that helps ease the pain, warm baths, medications etc.? (A)- I have been on Tramadol for 18 months. I take 100mg in the morning and 200mg in the evening, I also take 300mg of Quinine to control muscle spasms. I recently attended the Pain Clinic and I have just started on a course of acupunture as well as homeopathic remedies of Bryonia and Rhustox, recommended by consultant at hospital. Other things I have tried is massage', hot baths and gentle stretching to ease muscular pain. Do you have sleep problems? yes How do you deal with it? (A)- I must admit I don't cope with it very well. I can be woken up by the slightest sound and if i'm in pain then I don't sleep at all. Do you have family that understands your illness? (A)- My partner has been brilliant and attends all appointments with me. We had just got together when I had a major attack and ended up in hospital it frightened the life out of him but he then saw how severe FMS could be. The rest of my family are very supportive of my condition. Some have found certain foods causes problems with CFS or Fibor, have you? (A)- I have a found that too much gluten can upset my stomache, so I stay away from gluten based products. What type of Dr have you found that has helped you the most? (A)- The most helpful have been my GP and Pain Clinic consultant. I saw a neurologist who said I was suffering from stress and didnot believe I had the symptoms I was describing. I am currently waiting to see a rheumatologist, so I will leave my verdict until I see them. Over all I get the impression that a lot of doctors do not believe that FMS/CFS are actual illnesses, and I work in a hospital. I hope this has been a help and look forward to hearing from other FMS sufferers. Yours Trish Nicoll __________________________________________________ Quote Link to comment Share on other sites More sharing options...
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