Guest guest Posted November 21, 2005 Report Share Posted November 21, 2005 Hi Terri & Everyone, I was wondering if you might share what worked for you in curing your CFS. I don't have as severe symptoms as you described but do notice the deep fatigue, dry skin, forgetfulness, disturbed sleep, weight gain etc., some of which I attribute to hypothyroid. What started you turning this thing around? Thanks much, Shelley in Alberta Message: 17 Mon, 21 Nov 2005 07:39:47 -0600 maddress Re: Early onset alzheimers/dementia--warning, long post! I just mentioned in a previous post that I was ill with Chronic Fatigue Syndrome (CFS) for 11 years. MUCH of what you describe your partner experiencing is consistent with CFS: headaches, nausea, memory and cognition difficulties, speech difficulties. I even experienced thinning hair, cracking cuticles and dry skin. In addition, there was bone-deep exhaustion, transitory muscle and joint pain, dizziness, sore throats, swollen glands, low-grade fevers, massive swings in my sleep cycle (from insomnia to hypersomnia). But not every person with CFS experiences every one of these symptoms. And not everyone experiencing these symptoms has CFS. It's just something for you to investigate. I will tell you that when I was first ill, my test results came back normal, normal, normal. My doctor would say stuff like, you're so healthy it's disgusting (attempting to make a joke). My response was, then why do I feel so sick? As bad as the exhaustion was, I think the memory and cognition problems were the worst. Until I found out that they are very common for people with CFS, I thought I was losing my mind. I would be in a store, and suddenly not know where I was. It wasn't that I didn't know which store I was in. I didn't know which CITY I was in...or even which STATE! I eventually stopped driving for awhile because of the memory problems. It would start with me just suddenly not knowing where I was or where I was going. It got so bad that I would sometimes pull out onto a highway, and I wouldn't be able to remember if I had looked for traffic. It was terrifying. We finally decided that I just wasn't safe to drive. But it's a close tie with the speech problems. It's so frustrating to know what you want to say, but to be unable to form the words. Or to get the words half out, then have no idea what you were trying to say. Or even worse, to get the words out only to find out that the wrong words came out. Thanksfully, my family handled this with a good sense of humor. The day I handed a book to my daughter and told her to put it in the " oven " (I was thinking " bookcase " ) is a day we laugh about frequently. It was frustrating, but a sense of humor helped. I'm SO glad those days are over! Terri Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 21, 2005 Report Share Posted November 21, 2005 Terri, I too, would like to hear what you did to treat CFS. I have been going through much of the same thing for 3 years and each doctor tells me they can do nothing for me. It's all so frustrating. So, I've decided to start researching and taking things into my own hands. TIA, DonnaLike a quilt, grace wraps us in comfort allowing us to daily rest in the goodness of the Lord. ~Roy Lessin Donna H in OR http://community.webshots.com/user/dohernandez2000 Researching the family name Monfette PUNISH THE DEED, NOT THE BREED (Responsible pitbull owner) FareChase - Search multiple travel sites in one click. Quote Link to comment Share on other sites More sharing options...
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