Guest guest Posted January 6, 2008 Report Share Posted January 6, 2008 I read some of the postsd and wonder about this? deLadyBex Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 6, 2008 Report Share Posted January 6, 2008 I do. Barth --- c> I read some of the postsd and wonder about this? c> deLadyBex Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 7, 2008 Report Share Posted January 7, 2008 I have also been diagnosed with Fibromyalgia and Chronic Fatigue some years back and had suffered from the maladies for many years before diagnosis. I used to love massages and that part of a pedicure when your feet and legs get massaged. At some point, I just started going through the roof when anyone came near me for massage and had no idea what was going on. This continues to this day. On the issue of chronic fatigue, when I worked in Boston City Hall, I used to go down to the nurse's office in the basement to lie down on the cot to sleep or I would just close the door to the inner office and go down on the rug to sleep. Little did I know that under that carpet was an entire biology lab of micro-organisms there growing with impunity because of the chronic leaking in the office. So many times I would drive to the supermarket after work and just turn around and go home because I couldn't find the energy to get out of the car. On many occasions, I would sit in my car outside the house because I just couldn't get out of the car because of the crushing fatigue. Mulvey son **************Start the year off right. Easy ways to stay in shape. http://body.aol.com/fitness/winter-exercise?NCID=aolcmp00300000002489 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 7, 2008 Report Share Posted January 7, 2008 I was diagnosed with it recently... which I might add I DID NOT have it untill AFTER my ongoing chronic exposure to MOLD! --- In , " ccgardenlady " <ccgardenlady@...> wrote: > > I read some of the postsd and wonder about this? > deLadyBex > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 7, 2008 Report Share Posted January 7, 2008 Good description: crushing fatigue. There was a time when I could barely do my grocery shopping in one store. Now I'm able to go to a few stores, but it's still difficult to get through it all. So hard to explain to friends and family. Barth Mac> On the issue of chronic fatigue, when I worked in Boston City Hall, I used Mac> to go down to the nurse's office in the basement to lie down on the cot to Mac> sleep or I would just close the door to the inner office and go down on the rug Mac> to sleep. Little did I know that under that carpet was an entire biology lab Mac> of micro-organisms there growing with impunity because of the chronic Mac> leaking in the office. So many times I would drive to the supermarket after work Mac> and just turn around and go home because I couldn't find the energy to get out Mac> of the car. On many occasions, I would sit in my car outside the house Mac> because I just couldn't get out of the car because of the crushing fatigue. Mac> Mulvey son Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 7, 2008 Report Share Posted January 7, 2008 I have had chronic fatigue syndrome since 1983 even before much was know about it. My college roommate smoked like a chimney in my dorm room and as a result, I ended up getting bacterial pneumonia. I remember all my neighbors spraying lysol every where I went because they know I was contagious. It was a few months later, I was diagnosed with chronic fatigue syndrome. From there as the years went by I had relapses. The first about 2 years after the first episode. I was fine one day and the next could not go up a flight of stairs. The nurse about fainted when my blood pressure was 45 over 60. She tooks it 2 times and then the doc came in and took it -- they were shocked to see that I could even move let alone get myself to the student health center. As I am sure some of you are aware...they now believe there is a close relationship between PTSD and chronic fatigue syndome and fibromyalgia. I had been diagnosed with PTSD after an emotional trauma and physical trauma of a car accident. I recently had an extreme chemical exposure and have symptoms of chronic fatigue and PTSD. However, my diagnosis of multiple chemical sensitivities did not develop until after I was put on Lexipro and then Effexor ---both of which are mood-altering drugs. And yes, they did alter my mood and my body's tolerance for anything else. If I could tell or warn you about anything, if you have been diagnosed with any of the above, note how your body reacts to mood altering drugs like Paxil, Prozac, Lexipro, Effexor, Wellbutrin. Most of them are being used off-label and please read the lessor known side effects that are listed in lessor known published data. Incidentally, the symptoms for which the drugs were described to me including PTSD, nightmares and insomnia got worse the longer I took them. After 8 months of continuing to tell my doctor something was wrong, I begin to have peripheral neuropathy and blood sugar regulation issues and I am now border-line diabetic. I then then started turning yellow from liver jaundice and again knew something was wrong. After my doctor brushed the " turning yellow " part aside, I changed doctors. Before that, I finally figured out it was the Effexor that was inciting very harmful liver activity. The only other time I experienced the neuropathy is when I was being exposed (and I mean up close and personal ) to the dangerous chemicals that I was inhaling but mostly could not smell. I am now so sensitive that even the slightest esposure to VOCs in the air, chemicals in the water, etc. makes me react. So yes, I have chronic fatigue syndrome, PTSD and multiple chemical sensitivities. I probably have fibromyalgia too considering the joint pain and the muscle tension, but have never gotten the specific diagnosis. Sincerely, Kramer kkramer@... Health Education Information and Resource Services > > > > I read some of the postsd and wonder about this? > > deLadyBex > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2008 Report Share Posted January 8, 2008 Yes, I have been diagnosed with Chronic Fatigue Syndrome, PTSD and Fibromyalgia, many years ago as well, before I had a serious exposure to mold (that I know of), but had been exposed to many dangerous chemilcals while working at Aircraft. I probably developed those illnesses because of the chemicals that I was exposed to (one of them was Methelethel Ketones " MEK " ). I wonder if maybe those of us whom have these illnesses also have more of a propensity to develope sensitivities to mold and mycotoxins???? So, that when we are around mold/mycotoxins we are more suseptable to it than the general public. Oh, and I too have been having problems with UTI's and bladder infections... and my stomach is very swollen. Just a thought.... On Jan 6, 2008 3:50 PM, ccgardenlady <ccgardenlady@...> wrote: > I read some of the postsd and wonder about this? > deLadyBex > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 9, 2008 Report Share Posted January 9, 2008 a toxin is a toxin. these are all regulated by brain effects. a mold spore without myco's inside or attached is probably pretty harmless. I really dought that a mold spore would even be pathogenic without those myco's envolved or other toxins in a DMB. we live are life around mold, our mucus systems are designed to protect us. it is the constant insult of toxins that get us in trouble. without the toxins involved, none of us would be here. if you are hyper-reactive to mold it's the toxins that your reactive to. not the mold spore itself. a toxin is a toxin. once you get olfactory,neuron transmission defects,ect. and brain damage from toxins, you react to toxins. once those pathways have been made and become fibrotic, they are pathways for other toxins to follow. thus, affecting many of the same organs that were damaged during exposure and depending on the type of toxin and it's effects and dosage. that's why with mcs you can hace a range of effects depending on all these things.plus effects from other things that are just irritants to damaged airways.like dust,cat hair,pollen,ect. doesn't mean your allergic to it. > > > I read some of the postsd and wonder about this? > > deLadyBex > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
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