Antibodies symptoms and conditions

My daughter is now 20 years old. she received her 1st gardasil shot in 3/08 and the second in 8/08. She didn't get the last one and will not be getting it. From the day she got the first shot we should have known something. She nearly fainted immediately after both shots and complained of weakness and flu like symptoms. Started feeling poorly in the days and weeks to come. It was the end of her senior year the doctor tested her for mono. and it was negative but she had an extremely heavy schedule at high school. He chalked it up to the stress of that. Between the two shots she started having numbness and pains in her hands,elbows and arms. She continued to feel poorly and terribly irritable in the upcoming months. We saw a orthopedic doctor for her pains in her arms. He referred us to a neurologist. She was beginning her first year of pharmacy school and we put off the neurologist because she didn't have much time until spring break. During her 1st year of school after her 2nd shot. Her personality changed completely. Became insecure, moody, very anxious , constantly complaining of flu symptoms, bladder infections and had a hard time urinating. When my daughter returned home from her first year away at college I knew immediately that she had changed. She had been a very bright, intelligent, independent daughter and came home the daughter from hell. I couldn't believe what I was seeing. She was miserable, disliked pretty much everything. I had been talking with the doctor and friends over the course of the year and they all said that she was in a very stressful field (pharmacy) and college life takes some time to adjust. Then just a few weeks home from college she was complaining of dizziness, light headedness, headaches and saying she was having an episode. I thought maybe low blood sugars.....until I witnessed one. She was having Myoclonic seizures. She could feel them coming on but couldn't move or react. By the time I witness one of them she hadn't slept in 3 days. She was diagnosed within a week seeing a neurologist and having 50 to 60 a day. It took 4-5 weeks to get them under control in and out of the hospital . She has been on many seizure medicines it seemed like if it worked to stop the seizures she had crazy side effects. She was diagnosed with Juvenile myoclonic epilepsy. No one in our family has ever had seizures. I asked about the shot right away everyone said no and it was dropped. Since last July 08 we have been trying to help our daughter get her life back and it has been the worst year of our lives. She was unable to return to pharmacy school. The first fall 08 she was completely disabled. It looked as if she had had a stroke. They were saying it was the meds or maybe she had a breakdown of some kind. I am learning that it was side effects of this horrible shot. This is why I am posting this lengthy message because I wanted to let other people know that you and your daughter are not crazy!! We just started 2 weeks ago investigating the possibility of the gardisil shot being the reason for this madness. We have learned many things and are very sure that it was the shot that change our daughter.. I was contacted by a friend of a friend about a similar girl having the same pains in her arms and the focal seizures. I am learning more and more everyday about similar situations.. If this information can help one person it was well worth the time to jot it down. I will be praying for all of your families out there dealing with side effects from this vaccination.. I will let you know what we hear when we visit the neurologist at the end of the month. Any comments or information that may help us help our daughter can be sent to ******

I was diagnosed on June 13, 2009 with cellulite. I had a bump and rash on my right elbow and was given 2 antibiotics for it. After 3 days and no results form the antibiotics I went to my primary doctor who told me it was lyme disease because with lyme disease the rash goes away from the heart. I had no other symptoms from it and no bulls eye and the blood tests were negative. I was put on dioxycycline for 21 days and on the 19th day I missed a dose and took another one 6 hours later and then another one another 6 hours later and developed itchiness all over my body. I called my dr. who told me that with only 2 pills left and being on for 20 days I can stop the dioxycycline. OK great! a few days later still itching and he told me to take Zyrtec symptomatically as needed. Still no rash anywhere on my body. OK, so I am on Zyrtec and 2 weeks later I develop a tash on my face. I go to dermatologist and he says it is just acne and gives me tetracycline and erythromycin and call him in 2 weeks. I don't know if I am having an allergic reaction or not and decide to go to another dermatologist who tells me it is an allergic reaction and gives me xyzal for itching and corticosteroid for face and tells me I have high histamine levels. I then go to an allergist and he tells me he thinks its just acne from shaving using electric razor and use erythromycin but NOT to take tetracycline just in case I am allergic to antibiotics. I then go a different dermatologist who tells me I have folliculitis/acne and to take Keflax and a sulfate cream to use. A week and 1/2 after my face is OK with the rash down considerable and I am able to shave again. 4 days into the KEflax I develop a rash on both my elbows. I go to my primary and he says it is contact dermatitis but to take blood test and stool sampler to see about possible infection from antibiotics that destroyed good antibodies. It may be that my good antibodies are not strong enough so continue with yogurt and we will see. I am today having a sore throat, diarrhea and little stuffy nose so who knows what is going on. Also, I am 37 year old male who has nt been the same since going on doxycycline for supposed lyme disease-
I will post again when dr. gives me blood results and stool results.

It seems that everyone is having similar symptoms. I have been on Doxy for about 14 days now and I'm feeling worse every day. I am on it because i had been bitten by a tick and contracted Lyme disease. I don't know much about the disease but it has me freaked out. I started taking the antibiotic 2 weeks after being bitten; losing my balance and almost falling to the ground. I also had a couple of dizzy spells after eating. I seemed to feel a little bit better the first week of taking it but started feeling the side effects. It started out with the occasional dizzy spell then came the exhaustion, anxiety, depression, lower back aches, soreness in the back of my eyes, stiff neck, headache in the back of my head, flu like shivers, racing heart, and complete body aches. I also found out the hard way not to go out into the sun while on Doxy. Felt like the tops of my hands were being pricked with a million needles and burning. I wish I could stop taking the drug and be done, but I am already scared about the outcome of the Lyme disease. I hope I can feel normal again soon.

I was diagnosed with Hashimoto's Thyroiditis (hypothyroidism) about 9 years ago. My teenager was diagnosed 2 years ago. I have done a good amount of research and have also learned a lot through experience.
*The most critical thing is to NOT accept a generic brand of thyroid replacement. My GYN, family doctor, and my endo (who specializes in thyroid) have told me that generic pharms are only required to match the original drug's ingredients/strength by 75%. As my GYN said, if you're in the business of making a profit, and you can get away with putting in 25% less of the expensive (and unfortunately, the essential) ingredient, that's what you're going to do!
*Measuring T4 alone may not reveal hypothyroidism in the early stages, and it will probably not show everything that is going with your thyroid. I knew something was not right, but my old GYN (got rid of her) tested T4 only and said I was fine. I went to an endo who measures 1/2 dozen indicators, including antibodies and thyroid uptake, and I was correctly diagnosed. He also diagnosed my son early on, albeit, my son was exhibiting numerous symptoms. Which brings up another point -
*Everyone exhibits a different degree of different symptoms. So don't be surprised if your thyroid levels are higher or lower than you thought they would be based on your symptoms.
*Find a doctor that will work with you. I had a doctor that insisted my dosage was correct, even though I was still feeling very tired, had dry skin, etc. I finally found a doctor that acknowledged that there is a range of "normal" thyroid function. He upped my med a little, and I've felt much better.
*Know the signs of too high of a dosage - restlessness, eye and muscle twitches, trouble sleeping, etc. Our endo has us come in 1 month after prescribing a new dosage to make sure it is enough or not too much. If I was exhibiting hyper symptoms, I would not wait 1 month to be rechecked.
*Hormonal changes of any kind can wreck havoc on your thyroid - whether you're a male teenager or a peri-menopausal woman. Your thyroid levels can change quickly. If my son or I experience any new symptoms - fatigue, rapid weight gain, unusually dry skin, muscle aches/pains, etc. - I make an appointment w/ the endo. My son's thyroid had plummeted the last time I took him in, and the endo adjusted his med. Illnesses (flu, pneumonia, etc.) can effect your thyroid levels, as well as stress, so have your levels checked after going through a serious bout.
*Once you have your dosage correctly set - watch your appetite! Hypothyroidism can reduce your appetite, and once you've got that corrected, your appetite comes back. Keep a food journal to track your calorie intake.
*Have an annual thyroid ultrasound to make sure your thyroid is not enlarged and to look for nodules (very common w/ hypothyroidism.)
*TAKE YOUR THYROID 1ST THING IN THE MORNING BY ITSELF 1 hour before you eat. I had a friend who was taking her calcium supplement along with her thyroid every day and later found out the calcium was basically canceling the thyroid. Her doctor should have warned her about this, but I think they assume we know these things. Vitamins, herbs, cold medicines, certain foods, and other medicines/supplements can greatly interfere with your thyroid replacement.
*Women with hypothyroidism should take a calcium supplement (take one with magnesium for better absorption) because we are at greater risk for osteoporosis. I take mine at night, so it does not interfere w/ my thyroid replacement.

Hello everyone! I just want to thank each and every one of you for your postings. On more than one occasion I would come to this site because without all of you I probably would have truly lost my mind. I just want to give a brief history of what's been going on with me because if it can help one other person then it's all worth it. In 2005, I go vaccinated for chickenpox, I work in health care, never had them, and wanted to start having children since I'm 36. A month after the vaccine I broke out in a horrific rash ALL OVER and had it until April of 2008. I went to the hospital where I had the vaccine, 5 dermatologists, 3 Infectious Disease, various medical doctors and no one knew what it was. This April, I was admitted to the hospital with Autoimmune Hemolytic Anemia. After 3 hematologists, the last one feels the vaccine threw my immune system into a tizzy. I started with 60mg of Prednisone and eventually got down to 2.5mg. The hemolysis(body produces antibodies that attacks it own body) started again so I went to a new Hematologist and was put back up to 30mg and just got put down to 10mg today. Right now my biggest concern is the hair loss. I use to have such thick hair and now I cry almost daily because I loose so much. I am going to try the Ensure like someone posted just to see if that helps. I drink protein shakes, take Silica, multivitamins (Solgar) that have biotin, and going to try Nioxin shampoo. I have terrible mood swings and now I feel like I am going through withdrawal. It's almost like I want to take more just to feel better. I know that sounds crazy. The big fat moon face, my joints feel like they pop out, confused easily, can't sleep, and just can't really leave my house and live a normal life since April. I HATE IT!!! The only thing that helps me feel better when the daily prednisone "kicks in" is walking and exercising. I feel so bad for everyone this drug is just awful. I get angry because not one person told me what life was going to be like on prednisone. I think that is just mean. That's why these postings are so important. I know this is entirely to long but I feel so much better getting my story out there. Did everyone's hair eventually grow back. I don't know if I will have any left next month. Thank you all so much.
GG

I have been on Topamax since Jan of 08 for complex partial seizures. I was very pleased with it at first but started having
some more unpleasant symptoms. My hair recently started falling out about two months ago in massive handfuls! I was
and am very upset about it. I did have the tingling in the hands and feet when I first started taking it and I don't drink sodas
at all which I did all the time before. I did not lose weight at first but did a couple of months ago when I got very ill with a GI
problem. I actually lost about 20 lbs in about a month. This is when my hair started falling out. I have had a lot of labs
drawn and my TSH was undetectable but my thyroid levels (T3 and T4 are normal) and my antibodies are normal as well so,
there is no telling what is going on?? I just want off of this medication before I am bald!!

I started taking thyroxine about 6 weeks ago - i went to the doc with tingling fingers, bloods showed tsh 34 so doc gave me 50mg thyroxine. Felt awful within a few days i was getting palpitations and felt like my skin was crawling. I couldn't bear even the slightest noise. I had diarrhea (cant spell) fast heart rate, the shakes and couldn't handle lots of people in a room. I am a teacher so it became difficult for me to work. I went up to 100 it got worse, until in the end I decided to stop them.
I am going to wait and see but I would rather be hypo than have these symptoms, my doc said you will feel great soon, pah what a load of c%%%

Ive been on synthroid since Saturday august 23rd and I noticed Im more nervous like I want to climb the walls and im sweating profusly. I have lost over 100 lbs since February and I had blood work done on tues august 19th and the doctor put me on 25 mg. Im suppose to go back in 6 weeks and get my level checked again but Im going to call the doctors office tomorrow and tell them what is happening. If this is what is going to happen Im not staying on it. Im only 42 and I am battling deg.disc disease which hurts enough and sciatia.

I already posted about my son's behavioral changes while on the drug from the time he was 4-7. He is now 9 years old and has been back to "normal now for 18 months. BUT- we recently had his immune system checked though a blood test and he does not have sufficient immunity for ANY viruses. My 6 year old could fight 8 out of the 14, but my son who was on Singulair for almost 4 years has a severely depleted immune system. And from what I have read, could clearly be attributed to the drug. BUYER BEWARE~!

I suggest to anyone that has Hashimoto's Thyroiditis (type of Hypothyroidism) to have a blood test done for Celiac Disease. There has been research done linking Celiac Disease and Hashimoto's Thyroiditis. Celiac Disease can be controlled by a gluten-free diet (wheat, rye, and barley free). In the US, not many doctors recognize/know of this link. I have been hypothyroid for 20 years (had Hodgkin's Disease (cancer) - radiation/chemo at age 16) I have 2 sisters with Hashimoto's Thyroiditis and were iron and B12 deficient. I was diagnosed with Hashimoto's Thyroiditis 3 months ago with iron and B12 deficiency. I have been on a gluten-free diet for 2 months now. My dosage of synthroid (levothyroxine) was 175 mcg and now is down to 137 mcg. I hope that I am one of the lucky ones that will have their antibodies to their thyroid normalized (no more synthroid!) I have a couple of days left before my next blood test and I hope that it goes down more. I am feeling better now than I have in a very long time. I have attached a link for those of you interested. It is an endocrine article from Finland outling the link between Celiac Disease and Hashimoto's Thyroiditis (among other things). I hope that this helps some of you. http://edrv.endojournals.org/cgi/content/full/23/4/464

First of all I would like to thank you foe sharing your stories... you have saved my life.

I got Mirena "the monster" in October 2006. For a while I thought it was the best thing ever. In the next few months I gained a few lb, my skin stared to scare after bouts of acne, I did not have the usual energy. I blamed the new job, stress and aging. It seemed like an accelerated aging but I have just accepted it, low metabolism, everyday stress, you name it.

In May 2007 we went for a graduation of a friend. When entering the auditorium I started the feel panicky... it was a weird sensation but I decided not to pay attention to it. I love crowds, I love people. I forgot about it soon afterwards.

During my annual the doctor told me that my thyroid is becoming hypo and I have the elevated number of antibodies.

Then in July 2007 I was returning from Europe I had a full blown panic attack (I know now what it was). I had to be taken to the emergency room where I was treated for tachycardia and ordered to see the cardiologist. The months between July and December I have spend trying to figure out what is wrong with me. I started to have the anxiety attack on the regular basis, insomnia, I lost half of my hair, I was just barely serving, living from day to day, unable to accomplish anything, I was just trying to attend to the basic needs of my family.

I went to the cardiologist, endocrinologist, ob, EarThroots doctor (In September I developed the strange sensation of a foreign object in my throat), my family doctor (several times). I was put on Beta blockers, Xanax , Lexapro. Nothing was helping. I was depressed and absent, could not remember a thing, my mind was under some gaze. I could not understand: I am happily married wife, mother with no worries, great financial situation, job and perspectives. No drama and trauma in the last few years.

But even though it did not make any sense, I started to look for a psychologist/psychiatrist. I hired the private trainer and started the rigorous program of exercising. I learn how to meditate and attended twice a week yoga classes. I read everything in the library on the subject of anxiety, I learned relaxing techniques, bought tapes, music, dvd's. Changed diet. Eliminated alcohol and caffeine. Got massages. Everything provided only a temporary relief.

I started to make notes... the most severe anxiety started every 28 days (for a week) and sometimes in the 14 days. This when I suspected that Mirena may have something with it. Then I found this site and several other sites. In December, after a month of researching I came to the conclusion that it is impossible that thousands women on different continents are hallucinating... and on December 22, 2007 I went to take The Thing out. the best Christmas gift ever!

12 days later I had the famous Mirena crash (thank you again for sharing!), with a mini depression, suicidal thoughts, full blown anxiety and a lot of crying. The period brought a huge relief. The side effects are still present but they are diminishing day by day.

As someone here recommended, just when I was about to start this month "the anxiety period"... I went to acupuncturist. I told him that I need help with anxiety. When on the table he told me that I am having hormonal imbalance, I have a lot of heat (?) inside and that the region that correspond to the liver is pretty swollen. He told me that he is going to help me in 5 session and that I will be able to take off myself and that my body in a few months will return to normal. I have had two sessions, I did not have acute anxiety this months, I almost feel like my old self.

I am off meds, I take occasionally the beta blockers for heart palpitation (one time in January), I started to supplement with vitamin B complex. I drink Sleepy Time Extra -- with Valerian (celestial seasoning) at bed time. If I need to make sure that I will sleep I take the prescription antihistamine (hydroxizinum).

I am sure there is a light in the long tunnel... courtesy of products of Mirena... well ... you could say that I owe them a lot of spiritual growth and learning... at the price of personal hell...

Please know if I can be of any help-- I will gladly answer any questions.

Have hope! Take the damn thing out!!!

I have read a lot of these blogs and I am seeing that many other people have the same side effects. I was diagnosed with hypothyroidism when I was in 6th or 7th grade I think and I am now a high school senior so about 5 years taking Synthroid. the doctors said that my antibodies had completely destroyed my thyroid gland so I wasn't getting any of the hormones I needed which became very noticeable when I started gaining weight and loosing energy in 5th grade. I haven't really seen any weight gain in a while but I still look like I am overweight. I am 5'6 and 130 lbs so I am about average. Side effects that are also occurring are rapid mood changes, one minute I am happy and something sad happens or I think about something and ill be tearing up. I feel depressed a lot. I am currently on 150 mcg. also during 9th and 10th grade I was put on this drug to stop my puberty so that I could grow more while on the Synthroid I guess it helped a little with height but I still look like a freshman. I don't know if I should stop taking it or keep taking it because I stopped for about a month once and started getting really sick, I would get really bad nose bleeds at random, had constant migraines and felt sick to my stomach. I started taking the Synthroid again and felt fine. I really don't know what to do.

I've took a very high dosage of prednisone for 6 years, from the age of ten years old. 17 years later, i still have an extreme moon face. The only thing that has ever helped me was a facial exerciser (a microcurrent devise), but those results can be hard an expensive to maintain. As anyone else ever had a moon face that wouldnt go away even after stopping their prednisone usage after a long period of time? Does anyone have any advice for me, on how i can finally get rid of this horrible extreme moonface? my face and all my facial features are swollen, including my eyelids, this has been goin on for years. I also have suffered for years from severe chronic diarrhea from an illeostomy reversal. Please help me.

I had some signs of a chlamydia infection and tested positive for chlamydia antibodies, so my doctor prescribed a 7 day course with 2 refills (total 21 days) of 100 mg twice a day. Almost immediately (like within a day or two) of beginning the doxy, my testicles swelled up, became painful, my joints began to ache (even though they had already done that to some extent before I started, they got a LOT worse on the doxy). By the time I finished the 21 day course I was a lot sicker than I had been before, I was weak, had a pounding heart, and even though it has now been a month since I stopped, I feel only slightly better, if at all. If someone could email me and give me some hope that this will go away and I will feel better, I will be very grateful.
Thanks.

Please tell me where I can go for help. My mother is having terrible side effects from taking Lipitor a couple years ago. She will need a wheelchair soon. I can't believe so many of her problems are linked to this drug! Her doctors won't even consider the problem being Lipitor. Even though she is off it now, her problems seem to be progressing. Her feet are numb with the numbness moving up her legs. Muscle tone is gone and her left foot hangs. She was diagnosed with dropped foot last year. She also had a pace maker put in after she recovered from pneumonia. She has been told she has spinal stenosis and needs back surgery she probably is too weak to survive. Now she is being treated for neuropathy with no success. Her doctor has done a spinal tap and a nerve biopsy. She has seen a neurologist who sent her to a doctor in Houston. She has had gamma globulin IV's and an IV treatment in the hospital. I don't remember what it was called. Next step is a blood cleansing treatment done in Houston for 2 weeks to remove antibodies attacking the myelin sheath. Her eyes have occasionally hemorrhaged and she faints due to low blood pressure. My mother was very healthy except for slightly elevated cholesterol 3 years ago. What can we do? She is dying.

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.

Side Effects from Advair: Guest #4309 again Also look at response #7070 written on Sept 11 just below.

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.