Re: CFS, Fibromyalgia, .....Hypothyroidism T3/T4 ??

From: Robin M (rmasse2333@aol.com)
Sun Apr 27 09:05:55 2003


Dear Angel, I don't really have any answers for you, but I know about canker sores and cold sores/fever blisters. To help heal them afer they come out, take a vitamine suplement called L-Lysine 500 mg. It can be bought at most stores that sell vitamins. I got mine at Wal Mart. They come in a couple of different pill forms. The instructions will say take 1 up to 2 times a day on empty stomach. I take 2 every morning while having a sore & for a couple of days after it is gone. The sooner you start taking them, the better. If it seems like stress causes them to come out, start taking them at stressful times to prevent them. As a sore sufferer, I have found this is the best thing to use. I hope this will help ease a little of you pain as I know how painful the sores are. You can ask more questions if you need to. robin M

At Sat, 26 Apr 2003, Angel wrote: >
>To whom it may concern, my name is Angel [Male - 06/26/63].
>
>Yes, I know this is very long but please read on. THANX!!!
>I have a Hiatle Hernia with G.E.Reflux, am ADD, had my tonsils and
>adnoids removed [because I couldn't and still can't seem to breathe
>through my nose], since I was 2 Yrs. old [I swallowed a whole peanut -
>it was stuck in my lung] result - Pneumonia and Bronchitis - when
>younger I almost died many times - I'm still prone to these ailments on
>a yearly basis, I've had my appendix removed, and I've had multiple
>stitiches ...other than those things... I've never been diagnosed with
>any particular dysfunction and or disease. However, I feel that
>[mainly] for the last 16 years my body has been falling apart.
>
>~Whew, got that out of the way~ The basic part of my problems started
>when I was young, I can't remember exactly when ...maybe 12 or 13 Yrs.
>old, but I remember when it got worse.
>
>January 1992, I awoke in the middle of the night gasping for air. I
>ended up in the ER. This happened to me for what seems like months. Was
>it sleep apnea? An ENT said no way!!! Was it my Hernia and reflux? Hmmm!
>At one point I wore a heart monitor with alarm - for a month, I set that
>off almost every night because my heart would be pounding - as I awoke
>from a lack of oxygen. The doctor's said ...that it was okay [because]
>it was within a normal range for someone in my shape and condition. They
>went on to assume ...I was stressed and depressed! I told them this
>couldn't be, as it was happening only while I was sleeping. I then told
>them my problems up to that point [major symptoms to follow].
>
>*My Uncle and Mother have been diagnosed with Fibromyalgia, they
>[uncle/mom] continually tell me I too have it. Doctor's seems
>reluctant!!!
>
>Anyway, I have pursued many avenues to lessen my discomforts; this has
>come at a great price. My self-esteem has gone down and I feel as
>though I've been a guinea pig both physically and physiologically.
>Doctor's have given me most of the anti-depressant drugs available and I
>~personally~ have pursued therapy, even went as far as to try an commit
>myself, as I had pains and much more that multiple Doctor's said
>couldn't be real!!! The results? I take their meds and then get doped up
>usually ending up in the ER. It seems as though I have a low tolerance
>for most med's. Or is that physiological as well? ~Yes, I do have a
>slight attitude!!!~ Depression seems to be my end result. Imagine
>that!! How much can someone take being told that it's "ALL IN THEIR
>MIND!" I could only take the doctor's pill pushing for 3 - 4 years. I
>have been "grinning and bearing it" on my own for what seems to be a 100
>years now, trying Vitamins, and Alternative Med's [herbs, acupuncture,
>etc], 85% of the time I do very well.
>
>So what are my systems? I ache [everywhere] almost all the time -
>degrees of pain are variable as well as where the pain is located. I
>have migraines that stop me dead in my tracks, lower back pain
>accompanied usually with hip, knee, and foot problems, heart
>palputations, breathing difficlties - sudden and usually out of nowhere,
>canker sores from hell, ringing in my ears, body parts [mainly while
>resting] get numb and tingly, my endurance in most cases is nil - there
>are times I surprise myself ...but if I do exert myself, within usually
>a hour, the payoff is a migraine, neck and or lower body breakdown,
>especially the next day, I'm always tired when I have to be awake and
>awake when I should be tired ...blah blah!!! ...I think you get the
>point.
>
>Here's the weird part: I use to be a very athletic guy, ...Cross
>Country, Track, Swim, Basketball, Cycling, etc... I used to run a
>minimum of 2,000 miles a year for 6 years straight, not to mention my
>other sport activities - the running has stopped but the other
>activities are going as long as I can maintain (Last 14 years? - 95%
>Alcohol free).
>
>Another important part of my problems: In the latter time frame I
>crashed my vehicle [Jan. 1993] ...surprisingly I didn't even get a
>scratch. I flipped 14 times according to eyewitnesses. I didn't even
>get a ticket!!! I to this day don't know what happened but the police
>blamed it on obscure occurrences - a very strong wind gust was
>mentioned. Anyway, I mention this crash because this is where my
>problems took yet another turn. Among all the other problems I had been
>dealing with, now I acquired a new bizarre feature. I thought at first
>I was claustrophobic but this new problem is very selective. Put me
>in/on a plane, bus, a place where no "easy access out" is available, any
>situation ...and then tell me or at best make me feel as though I can't
>leave ...whoa, I want out!!! I've embarrassed myself many times. I have
>been trying to attack these situations straight on, especially when
>challenged by my girlfriend. 90% of the time I manage, 10% I'm gone,
>avoid it, or stay as long as I can stand it.
>
>Summary:
>
>I've done well these last 10+ years, but it appears when I think of who
>I was and who I now am ...I've been slowly giving into the pain and fear
>things. So in closing, I guess I'd be interested in what you think and
>or what some of your colleagues may think. Thanks .....ANGEL
>
>--
>Lots of info/messageboards: http://www.fibromyalgiachat.com/forums/
>


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