Tissues symptoms and conditions

Severe peripheral lower extremity edema with increased fluid retention in cellular tissues, so far I'm up to 12 pounds of fluid retained in my body.

I started taking Avelox 9 days ago. I was prescribed 14 days of Avelox after a round of Ceftin failed to clear up a sinus infection.
I am an avid tennis player, playing 3-5 times a week. My first bad experience happened yesterday when I went out to play and as soon as I walked outside I had a head to toe tingling feeling. This felt like I had chills but no goosebumps were showing. Over an hour or so later, the goosebumps showed up. This was in 90 degree heat!! I first thought it was dehydration, which it may have been, since I didn't seem to be able to get enough water/Gatorade no matter how much I would drink. This is even at night when I am not in the heat!!
I didn't take the medicine today. Played again this morning. I had the same tingling feeling head to toe, but no chills this time. To explain the tingling, I told a friend my skin felt like it was creepy crawly! It was a horrible feeling again in extreme heat!
I, also, have a hamstring that feels a lil tinge to it. I never have these problems and I am guessing this is due to the medicine, too.
If I walk outside, my body temperature feels like it shoots up! Even though I do not have a fever.
I went to my doctor's office and he is out of town! I asked to see another Dr. and he was "too busy to see me" since he was trying to get to the hospital! I was told to call my family Dr.which I did, only to be told he was also booked and I couldn't be seen. So, I gave up! And, not taking the medicine anymore!! Never again. This will be on my list of 'Allergic to.'
I usually have no side effects from medicines.

I was on Yaz for two years, and gained a total of 17 pounds from the day I went on it, to the day I went off of it. I'm sure some of the weight gain can be attributed to other factors, but I didn't really change my diet or exercise regime at all and the piles still packed on. I also always looked really swollen, almost pregnant, like you could see the water retention in my tissues. I had issues with my hair falling out, too. The plus was that my moods did feel more leveled out, but then the weight gain and hair loss caused other emotional issues so it was a no win situation.

I went off of it about a year ago, I've lost 15 pounds of the weight and my hair loss has pretty much subsided. But now I have very short periods, lasting three days tops. I worry that Yaz did something to my body that may affect my ability to get pregnant long term, as it seems my hormone levels have seriously depleted...

I just went in for my second shot of Lupron (out of a series of 6) for treatment of stage IV endometriosis. The most noticeable side effect I experienced was during my first menstrual cycle after my first dose of Lupron. I had never experienced menstrual pain or cramping (even though I had advanced endometriosis) until after Lupron. I have a fairly high pain tolerance and yet the cramping for the first 2 days of my period were almost debilitating. I had extremely heavy bleeding and have had spotting daily ever since (app.18 days). I have gained about 3 pounds because I have no energy at all. I'm usually active and work out 4-5 times a week but by the time I get off work, I'm too fatigued to do so (hence the weight gain I guess). I have hot flashes and night sweats all the time. The most recent side effect is high blood pressure. I have never had high blood pressure in my life (I'm a healthy 25-year-old woman) and when I went in for my 2nd Lupron shot today, they told me I all of a sudden do. I don't seem to have mood swings but do feel depressed and sometimes more anxious than normal. I have experienced a decreased interest in sex as well.

I have been taking 40mg lipitor for over 9 years now.

I have had back issues since an injury to one disc (L4?), and had microdiscectomy in 2001? Took about two years to actually get close to normal.

The last few years, I have had multiple issues with shoulder pain, wrist pain, elbow pain, lower back pain, Upper rump muscle pain , and now both hips are killing me (the shoulder, upper rump muscles and hips are by far the worst). And I am now so weak in my lower back muscles, that it feels like I will (and do) pull out my back.

I have seen NO many doctors I can't even name them all. I have had operations, multiple injections (cortisone) taken pain meds, etc. Nothing has helped and in the last year and a half, I have gotten steadily worse. To the point where I can't really do much of any activity. Sleeping at night is painful. Can't lie on left shoulder, and can't lie on either hip for more than a few minutes. If I fall asleep on my side, the pain wakes me up. When I try to walk, 80% of the time, I end up with a pain in my upper right rump (sacroiliac area), that I MUST sit down to get the intense pain to go away, which it does. But comes right back when I walk again.

I have had x-rays, MRIs etc, and never reveals all that much. Disc issues, yes. NOt much else.

Recently, I have begun to get a nasty clicking (catching) on my left jaw (joint?). Not really painful, but something definitely wrong. My dentist sent me to his Chiro. I went and liked him right away. I had gone to another chiro for years and I believe in them. But this one is the best I have seen.

Anyway, one of the FIRST things he suggested, was that it was POSSIBLE that the Lipitor is causing all of my problems. Put me on COQ10, and doing multiple adjustments and treatments. I will be seeing my regular doctor 5/26, and my chiro wants me to see if he will take me off lipitor and put me on Niaspan instead.

I guess my question is: Can Lipitor be fine with me for so long, and then in such a short period of time, turn me into a compete wreck from the pain and wasting away of my body/muscles? I've told doctors for over a year now that there is SOME connection as to all these issues and pain. One Doctor, of course, gave me the "you are getting old" bull. Yes, I am 56 yrs old. But I understand the process of getting old, vs the complete failing of ones body.

Also, IF it is the Lipitor, can it possible all go away? Or should I expect some damage forever?

One more thing, the last ortho I went to the other day for a second opinion, wants me to do a EMG, to see if there is muscle damage. I was not planning on doing it, but wonder now, should I? He was not doing it because of lipitor, as he never even talked about that to me. I had shoulder operation and have not had the results I feel I should have had.

DIDN'T WORK AT ALL & HAD BAD SIDE EFFECTS! This didn't help my severe 'painful red bumps' kind of acne. In January 08 the dermatologist put me on solodyn 1x daily, Rosaderm face wash, & Atralin topical gel, both 2x daily. Eventually she switched me from atralin to RetinA, b/c the atralin wasn't strong enough. I have many health problems, but the last few years I have been feeling absolutely awful- constant body & joint aches, constant fatigue, & mood swings due to the pain. It got so much worse in Jan 08. My doctor & I had been talking fibro for a long time, but she diagnosed me in early March 08. She suspected fibro, as well as an autoimmune disease (when your body attacks your own tissues by mistake) due to a massively high ANA (anti-nuclear antibody) count on a blood test, so she referred me to a pediatric rheumatologist (there aren't many) b/c I was under 21 at the time. The rheumatologist diagnosed me with myofascial pain, which is very similar to fibro. She explained, "It's the exact same pain as fibromyalgia, except it moves all around instead of staying in certain points." Then she told me something shocking: SOLODYN CAN CREATE CONSTANT FATIGUE, BODY PAIN, AND OTHER FIBROMYALGIA-LIKE SYMPTOMS!!! IT ALSO MAKES A PERSONS ANA COUNT SOAR, WHICH CAN BE SEEN IN BLOOD TESTS!!! So she told me to go off the Solodyn right away, which I did gladly because it had been weeks & it hadn't helped my acne. She told me to watch for changes in my myofascial pain/fibro symptoms. After about 1 week my muscle & joint aches started to lessen. Obviously the Solodyn had increased this pain. The weird thing is, after about 3 days after stopping Solodyn, my acne improved. It was almost like Solodyn was preventing my acne from going away! When the results from my next blood test came back, my ANA (anti nuclear antibody) count had dropped but it was still high, indicating an autoimmune disease. It appeared Solodyn had raised my ANA count to a level even higher then it normally was!! It turned out I did have an autoimmune disease, but my rheumatologist told me she's seen teens who take Solodyn & have an elevated ANA count b/c of it. Then they have to run hundreds of tests b/c they think they have some disease that they actually don't have. When they stop taking Solodyn, their blood tests normalize, & then it proves don't really have an autoimmune disease. But by that time they've gone thru dozens of unnecessary tests, not to mention the stress & worry of thinking they might have a disease that may potentially be life threatening. They wasted time, money, and sleepless nights, all because solodyn screwed up their blood tests!!

I have been on Lipitor for five weeks. I can't believe how awful I feel. I ache all over. I my arms and elbows are sore; I have had pins and needles in my hands; charley horse like spasms in my calves (mostly at night); sharp knife like pains in my upper thighs; even my teeth hurt. I am a 46 year old female – I can’t believe this. I have made an appointment with my doctor as I have to get off this drug. I have experienced some blurred vision and hearing impairment too. If I hadn’t of found this website – I truly would have thought I was a bit crazy….
I have never had any symptoms like this before and never thought of myself as an old lady - but that is what I feel like. It is unbelievable.
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I have endometriosis and would like anyone with the disease to contact me so that I can find out more information, etc. My email address: ******

Same here. Pretty much like a zombie. Numbness and tingling in hands and feet. Spaced out. Stoned like in high school.

I had Kenalog shots many years ago, beginning in 1969 for the initial onset of terrible hay fever when I was a senior in high school. It was wonderful at the time because the shot cleared up all hay fever symptoms. I probably had the shot, in the hip, once a year for a couple more years. I did not notice any dimple or change in the skin or muscle at the injection site. I stopped getting the shot because I didn't have any medical insurance. Then around 1993, with medical insurance restored, I decided to have a Kenalog shot again when hay fever symptoms kicked in (August). The hay fever symptoms were relieved, but to my surprise, my leg and feet muscles were cramping terribly off and on all day for several weeks. My legs have been very sore to touch now for many years and I wonder if it is a result of the shot. My understanding is the Kenalog medicine is in an oil base and is stored in the fat tissues of the body or the liver for slow release over a period of a few weeks. As with everyone else who has listed here, any potential side effects or instructions to be on the look-out for side effects was not communicated or initiated by my physician.

I had my demon mirena inserted in July 2004 after the birth of my son. Since then my life has been one nightmare after another. I have had body/muscle aches, swelling in ankles and hands. Slight fever all the time, skin rashes, dizziness, depression, my hair texture changed, insomnia, and night sweats. I was so tired I couldn't even do normal daily activities. My mood swings were so severe I began to think I was bipolar. I have been to about 15 different doctors over the past 4 years and I have been diagnosed with everything from Rheumatoid Arthritis to Lupus to Graves Disease and after finding this blog and others I know realize it's my Mirena! I called my doctor and am having it removed ASAP! She agreed that is was more than likely the mirena that has been ruining my life for the past 4 years. I didn't equate my symptoms with the mirena because they didn't start until about 7 months after I had it inserted. It was SO not worth it. I would have MUCH rather had another child than to go through all this misery for four years. I can not wait to get this thing out of my body.

Hi everyone,

i need to tell you about what just happened to me, because it seems most people are definitely not informed of all the possible side effects of prednisone - not only just relating to the dose of prednisone you take but also for how long.

I have been using prednisone for almost 14 years now, the doctors all tell me i'm unlikely to ever get off prednisone now because i've been on it too long. I know all about it's usual side effects (water retention, mood swings, thinning of all tissues including blood, acne, anemia, etc etc).

One side effect i was not advised of, not even in any educational material about prednisone either, was that long-term dependence can lead to Acute Adrenal Crisis. Which is deadly if not diagnosed and treated promptly. Thus i nearly died two weeks ago. I became rapidly ill with vague symptoms that i now know are symptoms of acute adrenal crisis. *THE ONLY REASON THE ACUTE ADRENAL CRISIS OCCURRED WAS BECAUSE OF LONG-TERM USE OF PREDNISONE*. Not many doctors will warn patients in advance of this. It is however, very very important that people are aware that long-term use of prednisone needs to be very carefully weighed with the benefits of using prednisone (i was started on prednisone in 1995 to treat severe Crohn's Disease).

Acute adrenal crisis can happen over weeks, months or years - in other words, it can come on so slowly that by the time you know there's something wrong you're already very very ill and in great danger.

I am very glad to have found this website and i hope you will all refer anyone who has any experience with prednisone to this site - education and knowledge is power - the power to stay alive.

(by the way, the treatment for acute adrenal crisis is to load up on prednisone - seems i'll probably never be free of this drug unless i can get my adrenal glands to begin working again (as prednisone "takes over" for the adrenal glands and they effectively go to sleep, and this is especially true for long-term use)).

My sympathies to everyone who has to go through the many nasty experiences with prednisone, especially the young children (I had to start it when i was 16). It really does mess with your body and mind, and in my case, became lethal.

Please pass on all your information relating to use of prednisone to everyone you can - it really is that important and seems to be the only way to avoid most of the disasters related to prednisone use.

take care everyone,
Linda
(Australia)

Sorry, I can't just walk away.

When you find patents or patent applications for certain purposes, then you know that your ideas are well founded. There are several patents for using an anti-malaria drug for asthma. I would bet that somebody had that idea all the way back to the 1960's. So it is very possibly no coincidence at all that a chloroquinoline or other quinoline ring would be part of montelukast's chemical structure.

Here is one of the patents.

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It is well known that quinoline rings can be toxic to some people even very rapidly. As in this very extreme example.
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PEDIATRICS Vol. 27 No. 1 January 1961, pp. 95-102 This Article

FATAL ACUTE CHLOROQUINE POISONING IN CHILDREN
Howard M. Cann M.D.1 and Henry L. Verhulst M.S.1

1 National Clearinghouse for Poison Control Centers, Accident Prevention Program, Public Health Service, U. S. Department of Health, Education, and Welfare
Four cases of acute chloroquine poisoning in children are presented. In three instances death occurred within 2 hours of ingestion of larger than therapeutic amounts of the drug. The rapid occurrence of death in acute chloroquine poisoning is probably explained by complete and rapid absorption of the drug from the gastrointestinal tract resulting in high blood concentrations which depress vasomotor function and respiration. Cardiac arrest follows and may be caused by the direct myocardial action of chloroquine, to anoxia, or to both. The similarity of the manifestations of acute chloroquine poisoning and those of acute quinine and quinidine poisoning suggests that acute toxicity may be attributed to the quinoline ring portion of these drugs.

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I don't think that we are seeing extreme examples. But we may be seeing less extreme immediate reactions or reactions where the toxicity builds up over time.

Quinoline rings are know to cause neurotoxicity. There are theories about how that happens. One of the theories is about blocking connexins which are gap junction proteins in the brains.

I don't know how montelukast could be breaking up so that it causes toxicity. Or if the problem is the how rapidly the liver enzymes can metabolize it. But there is plenty, plenty, plenty of clinical evidence that there is a quinoline ring culprit somewhere in the picture. Or some by-product of that causing problems.

Somehow it was decided that montelukast did not have the safety issues that the other drugs in the same category have. See this.

"The starting point in the development of montelukast appears to be a quinoline-containing structure, likely identified as a weak random screening lead (Figure 3). The Merck group hypothesized that this molecule was mimicking the olefin backbone of cysLTs, and that the addition of mimics for the acid and peptide regions of LTD4, might improve its potency. As a first step, the dithioacetal linkage first seen in some SmithKline compounds was incorporated; this led to a compound with greatly increased in vitro potency but poor oral bioavailability. When one of the carboxylic acids was replaced by an amide, forming MK-571, the new antagonist had even greater potency and good efficacy following oral administration. The enantiomers were resolved to yield MK-679 (verlukast), a compound with better clinical effects than MK-571, but whose clinical development was stopped for safety reasons. Further structure-activity relationship studies led to the development of montelukast (16), an antagonist that appears free of the safety concerns plaguing earlier members of this series."

If we can find out why the earlier versions were not safe and how they thought fixed it, then maybe we can find out what is going on with the quinoline ring in some people.

I would be very surprised if the FDA will address our concerns. Why does it always seem like they wait for enough people to die like in Vioxx? Wasn't Vioxx responsible for thousands of deaths?

I took my 16 year old child off of singulair 6 weeks ago (3-28-2008). She started taking it 11-17-2003. She became dark, depressed, grades dropped, dropped out of dance and cheerleading, started cutting her legs with razors, stomachaches, headaches, anxiety attacks, trips to the emergency room. 6 months of fluoxetine given by her psychiatrist. Nothing helped her be happy again. Sad and Dark young woman. NOW: She smiles a lot, and is eating diner with the family. No headache or stomachache for a month now. She is sleeping better. Before she said that her mind would not stop thinking. She is taking pictures again and even asked me to order her book called "Understanding Exposure" and is talking about taking a class on digital photography at NMSU branch university to start on her college electives now. She is out more and even has a part time job at an ice cream parlor. Just lately I have stopped checking the trash for waded up tissues with blood (from cutting). Chris, I have had all her medical records sent to her primary Doctor and we are very willing to open them up. You have to have a child suffering to understand where we are coming from. The most dangerous place on earth is standing between a mother and her child. Singulair took our children from us and maybe changed them in some way forever.

I received the Kenalog shot in January. I started feeling tired and muscle aches, which I thought was just a virus. Then a dent appeared on my arm 2 weeks ago, and my muscles surrounding the maroon color dent began to tighten. I now have tendinitis in my shoulder and arm and I have lost all strength. My doctor said it could be from the shot, but stopped seeing me. i am going for an MRI on Monday because of the damage and pain that is non stop, and they are trying to figure out what is wrong. I have had several blood test because they swore I must have Lupus, or Rheumatory arthritis which came back negative.
I am very frustrated. I am a server by trait, I am a mother of 5, and it seems like my life is changed. I can't work, no one can give me answers, and I would like to know if these symptoms will go away or if I am stuck with this arm atrophy forever.

I've had a "dent" for about four years now, and had no idea what it was until now. I'm relieved to find out that it isn't anything like cancer.....but will it ever go away? Are there any known treatments or cures?
I'm very upset that my doctor gave me no warning of side effects of the Kenalog shot. I was only told that it would aid in my relief from allergies. I have now received the shot for five years in a row, and have two "dents" on either side of my lower back. Any advice on legal action?????

I had a Kenalog shot about 6 weeks ago in my face for what my doctor thought was swollen tissue after a surgery, however the Kenalog has eaten away at my tissue creating a "dent" in the side of my face. This has been a really terrible and frightening experience, and I am very concerned that the tissues will not regenerate themselves over time. He has told me that it could take a year for the tissues to regenerate themselves. Please, anyone out there who has had a similar experience with tissue atrophy after a Kenalog shot, please would you let me know if this tissues really ever came back gradually? Thanks so much.

Hello, everyone. I didn't know there was a page like this, but I'm glad there is. I've been on Topamax for 3 weeks because the medicine I was on for 2 years didn't do anything and the headaches weren't going away at all anymore; they were continuous. The first week at 25 mg I had the tingling for a day or two, the involuntary muscle twitches, the terrible mouth taste, and the chest pain. All but the terrible taste went away by the second week at 50 mg but I started getting wobbly legs and dropsy. I read an article somewhere where a person on Tomamax called the drug Stupamax or Dopamax and said anyone on it turned into a box of rocks. The box hit me at 3 weeks and 75 mg. I'm not wobbly anymore, I'm still irritatingly dropsy, and I am doing things that only a person with half a brain would do. Plus, my ears have been ringing for two days, and today I feel like I'm in a tunnel and everything is far away. I'm getting ready to call my doctor. On the OTHER hand, I haven't had a headache that lasted for more than a half hour in 3 weeks. So what's best? Going back to headaches or continue to evolve into a box of rocks?

I was a 2:42 marathoner. I used a synthetic varnish containing isocyanates, pentanedione, organic solvents, in one 7-hour session; the company-recommended respirator did not in fact prevent transmission: Severe chemically- induced asthma, plus neuropathy, plus, plus.

I've used Advair 500/50 for six years. There have been many diverse effects from the chemical exposure; I'd not questioned any being Advair side effects. But the raised blood pressure was not initial, and certainly not a priori. Diminished hearing, diminished eyesight, anxiety. Again, not to lump in, but these questions are new for me. But the point I'd like to bring before this group is this: In August I was diagnosed with ehlichiosis , and was prescribed 28 days on doxycycline. They recommend eliminating many possible antagonists to the doxycycline. My respiratory capacity had been continually diminishing. My ongoing physician said this was to be expected and recommended only the next more powerful steroid. Not a good solution. Before all this I was strong; repaired myself. In the absence of constructive answers, wondering if the Advair was weakening me, making me dependent, I quit the Advair as well on beginning the doxycycline. Today is eleven days post-doxycycline. Eight days ago there began with increasing severity, a terrible wracking deep cough producing dark yellow mucus. Painful. No fever. Grevious throat from the wracking, but I question whether this is a cold or infection. It's just in my lungs. Maybe it's as though I've thrown off an epithelial coating. These past two days the quantity of deep yellow mucus is not as ready, but the wracking and coughing is more severe. And my lung capacity, my respiratory capacity, is frighteningly diminished. Until these past two days I'd considered this an infection, especially post-doxy. But it doesn't feel like an infection. And I'm scared. Is this because I quit the Advair abruptly after long regular use? Have any of you had a similar experience. Can you discuss the effects of abruptly discontinuing Advair. Have you stayed off it. What's happened to your respiratory capacity. Have you any professional studies, trials or experience to recommend. Thanks.

This is a nightmare. I have been on Lamictal 200 mg, tab in morning, for approx. 5 months. About 3 1/2 months ago I started getting muscles aches and weakness, muscle overuse problems, fluid retention ( like 12 pounds), stayed in a trance with very little short term memory. Thought it was everything but this medicine....I am an avid athelite, yes, even at 51. So, I blamed myself for not slowing down. Quick exercising totally, for 2 months, iced 3 times a day on leg muscles. Finally after making it to the summer without a mental breakdown, I went to the emergency room and a new internist to get checked out. Blood work, thyroid, hormones,ok.... Really don't care what they think , I can not walk, it hurts like hell. The Dr. did tell me to get off Lamictal....ok 7th day and I have some relief but it is not complete. Called manufactures, interesting, yes- these are side effects!!! But the studies are limited. Listen , unless you have seizures, get off this medicine... you read the full disclosure of side effects and then search yourself......It can ba a huge FOOOOOPA.....And you are the fool that will end up holdling the bag, not the manufacturer. Hopefully I will get better. Right now , I just trying to stay calm.

My joints all over my body are painful. I don not know if it is a side effect of lithium because I take other medications. The drugs include femara, niravam, cymbalta, famvir, calcium 1000 mg., a multivitamin capsule, glucousimine, echinacea. please give me some advise as to why I get veryt painful joints and the back of my neck pops constantly throughout the day.

We made an entry regarding our then 3 1/2 year old son in Oct, then Dec of last year. It has been approximately 5 months since we removed our son from the use of singulair, after a year of use. He now stammers a bit, as opposed to severe stuttering, and his aggressive behavior is greatly diminished, though he does still have episodes, both noted in particular when he is going through or immediately following growth spurts. I begin to feel that we may never totally regain our little guy as far as his serenity is concerned, but the differences between last fall when we removed him from his medication and now are remarkable. What has totally returned is his ability to concentrate. Any excess energy is now easily channeled into dancing, jumping, wrestling, and playing music. I Thank God that in the last couple of months, he has once again expressed interests on his own accord in regards to wanting to develop friendships and enjoying the playtimes he experiences with other children.
Is there any physician that would be able to state how long singulair remains in the tissues? My concern is in regards to the occassional outbursts of anger or sudden depression. I will be seeing his doctor this month for his annual exam and will be discussing the symptoms I still observe.

there are many adverse effects individuals feel are attributable to statins that do not reverse with stopping the drug--neurological adverse effects from nerve involvement, such as periphral neuropathy. The damage done to the nerves may be permanent damage and not reversible with "tincture of time". In addition, the "tissue half life" of a statin is unknown (amount of time required for half the drug to be out of the tissues)--could be months or even longer. thus even if the symptoms do not disappear within a weeks' time does not exonerate the drug as the cause of the symptom(s)

My legs swelled immediately upon taking Levaquin with pain also in the tissues of my legs and not the joints. Breathing problems also accompanied the leg swelling. 5 months after taking Levaquin my legs are still swollen with pain and I can not take a deep breath. My oxygen level is only 94. Any advice on a cure would be greatly appreciated.

This company who makes Wellbutrin also made a drug called advair (for asthma). This info may help..........

I am not a specialist. All I did was look up as much information as I could after the Medical Doctors told me advair
couldn't cause these side effects and it doesn't cause an auto-immune problem.

YOU ARE EXPERIENCING PROBLEMS OTHERS MAY NOT UNDERSTAND!!!

Candida is always looking for a chance to grow and spread. It can CHANGE ITS FORM in different ways. It can change itself to resist certain substances you take to eliminate it.

Thyroid:

Thyroid gland is located in lower front of your neck. It makes thyroid hormone, which is secreted into the blood and then carried to every tissue in the body. It is essential for helping each cell in each tissue and organ to work right. Thyroid hormone helps the body use energy, stay warm and keep the brain, heart, muscle and other organs working, as they should. A malfunctioning thyroid and a compromised immune system can make you more sensitive to any common allergens. This combination can also produce numerous other harmful side effects including WEIGHT CONTROL.

Fungus:

When antibodies form to attack the pathogens, the pathogens can often take on a similar appearance or likeness to the various tissues they attach themselves to (THYROID tissue, HEART tissue, LUNG tissue, MUSCLE tissue, etc.) When this happens, the antibodies will attack the pathogens along with the tissues of the organ, lining or whatever they attach themselves to. This can lead to various kinds of allergic reactions and medical complications of all kinds. This fungus (candida) can also produce a waste product called acetaldehyde, which produces ethanol. This minimizes your body to assimilate iron. This decreases the amount of oxygen in your blood. This reduces the chances for oxygen to get into your individual cells. Ethanol wipes out enzymes that are necessary for individual cell energy.

Leaky Gut Syndrome:

Hair-like roots tunnel their way through the small intestinal wall, working their way into the blood stream itself. Partially digested food particles can enter the blood stream. After a certain point your liver will no longer be able to filter out these food particles and TOXINS from re-circulating through your body by means of your blood. When food particles travel through your blood, they become like foreign invaders in your body. Your immune system will respond to this attack in various ways. At this time, your body can begin to experience reoccuring complications simply on the foods you eat, things you drink and even supplements you take.

Use the web and do the same. It's amazing how much info you can find. And once again, if you know of anyone who was prescribed advair and you feel the same way as I do about the product, handle it the best way you know possible. I have yet to figure out how to undo the damage.

Best of luck.