Wheat symptoms and conditions

I am 26 years old. I've been on warfarin for almost eight years. I wish I had seen a site like this eight years ago when I started on warfarin (after DVT and P.E) I may have had some insight into the hellish two years that were to follow: hair-loss, depression, weight-gain. But I attributed all this to stress (it was pre-med varsity and I was under a lot of pressure academically).
Anyway, now my life is more settled, I eat right, exercise furiously 5 times a week...but I have digestive problems. Bloating, gas, overall discomfort in my stomach almost every night. I've cut out milk, wheat, coffee...nothing.
But tonight I started thinking...could it be the warfarin?
Does anyone experience or know about possible side-effects of warfarin on the digestive system, and does anyone have some useful advice????

I've taken Estrostep for at least 7 years now, and I thought I have been symptom free until just recently I started to question some unusual symptoms and if they were caused from my birth control. I've had terrible bloating and constipation for the past year and I am thinking I might have a bad reaction to eating wheat, but I've never gone off the pill since I was 14 so I don't know. Also I find it IMPOSSIBLE to lose weight. I am a very serious triathlete and I train 12 hours a week, two to three times a day most days and cannot lose even 5 pounds with a perfectly clean low calorie diet. My sex drive is completely in the dumps and has been for years. It causes a lot of problems with my boyfriend and I but I'm afraid to stop taking the pill to see. I've tried Junel Fe and ortho tri-cyclen and felt that each made me gain at least 15 pounds with no diet change.

Not a side effect, but a benefit. I am allergic to gluten.
After continuous migraines when taking natural Vitamin E capsules, my pharmacist told me the gelatin capsules can contain wheat and referred me to the synthetic Vitamin E DL-Alpha. I quit getting the migraines after I switched to the synthetic version.

My son has been on Singulair since the age of 6. He is now 13 years old. He developed seizures 3 weeks ago - temporal lobe aura epilepsy during which he was hearing voices. EEG abnormal, MRI normal. He hasn't started medication for the seizures but I have stopped his Singulair immediately! This was just a hunch - searching the net to see if there is any correlation. I have been to the Pediatrician AND the GP the past 3 weeks and no one said anything. I think a great number of children are on Singulair in SA. Does anyone know about the possibility of this danger?

My husband suffered for a full year with constant burping--not reflux, not heartburn, just air, like colic. He was so bloated that it was painful for him to sit. He went from doctor to doctor, and even to a GI who suspected Celiac's. He also had a feeling that his throat was constricted, and once went to the emergency room, afraid that it might close up. The doctors found nothing.

He has a severe dust allergy (it causes hives, no respiratory symptoms) that was diagnosed last year, at which point he was prescribed Zyrtec and Singulair. He mentioned the prescriptions to every doctor he saw (this is in New York, not the boondocks, btw), and every one said it can't be the Zyrtec or the Singulair. It should be noted that we eat all natural foods, no white flour, no white sugar, so we knew there were no artificial additives that could be causing his reaction. My husband even tried cutting out dairy, then wheat, then all gluten, for over a month.

Finally, about five weeks ago, he told a cousin about his mysterious symptoms, and she asked if he was taking Zyrtec. He said yes, and she said he should try going off it because she'd had a similar problem with that drug. He did, and within four days, the burping and bloating stopped.

Because his itching was uncontrollable with Singulair alone, he decided to try taking one Zyrtec, thinking it might not hurt. Within 24 hours, the burping and throat swelling was back intensely.

The doctor switched him to Allegra. He took one and it helped him. He took a second pill two days later, and the burping reaction started. The allergist confirmed that people who have this "rare" reaction to Zyrtec may also have that reaction to Allegra.

If you are suffering from these symptoms, go off the Zyrtec as soon as you can. I wish someone had told us so that my husband would have saved himself a year of suffering.

My daughter took Lupron as a 14 year old, perfectly normal teenager with the exception of endometriosis. She is now a 33 year old shell of the vibrant teen she was. She is bi-polar, maniac depressive. The changes in her were immediate and startling to say the least. I feel like it ruined her life. I have just started investigating the terrible side effects and was shocked to see so many other people whom lives it destroyed. If anyone has advice, anything to get help, please reply.

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

I have had diarrhoea now for nearly (8) eight weeks.
I am currently trying to get off of a Prednisone prescription that was given to me September 14th, 2007, for Costochondritis/fibromyalgia/ Chest wall pain.

I have been very sick from withdrawals and side effects since Sept 14, 2007. The Doctor I was with at the time was trying to get me off of the Prednisone too fast and making me even sicker! I.E. cutting me one particular week during the end of October from 20 mgs to 10 mgs a day! I have since refused to go to that Doctor because he made me sick.

I stuck with that dosage at the time because the Doctor told me to; ( plus an older Brother who would call me daily and scream at me long distance to be sure I was following 'Doctors orders'!) but I was so 'out-of-it' as a result, that I had items and personal effects stolen from me by the very 'care-givers' I had hired to take care of me and help me around the house? They told me later that I had 'instructed' them to give all my stuff either to them or to the Goodwill.

The entire second floor of my house was cleaned out by the time I started feeling a bit better and the so-called 'Caregivers' abruptly quit and moved out of town! Plus! My paid-for 2002 T-Bird was sold. I vaguely remember my Brother 'ordering' me to sell it. He was jealous and didn't want me to have it. He nearly had my house offered up for sale as well...but I got better just in time. I no longer want to speak to my Brother.


At any rate, I am down to 1.5 mgs Prednisone a day and my head has 'cleared up' substantially; also I still suffer from 'Brain Fog' and other terrible side effects of trying to getting off this poisonous drug.


I am now also suffering from a brand 'new disease' because of this Prednisone.
Doctor #### has diagnosed me with "Leaky Gut Syndrome".


I cannot eat 'normally' anymore since November. All simple crabs, sugars, breads, pastas, eggs, soy, potatoes,creamy salad dressings, potatoes salad, tuna salad, egg salad...a whole plethora of food items I can no longer consume!!! I have a freezer full of food I can't touch! The Holidays were a nightmare! I couldn't eat any of the foods or desserts! No ice cream! After going to one friend's house for Thanksgiving and being unable to eat a morsel, I stopped going anywhere. The torture was too much for me to bear!


I can't eat Chinese, Italian, Mexican, pizza~ any ethnic foods anymore!


P-nut butter,cereals, mushrooms,crackers, meatloaf, etc. Too many to list!! No more sodas, vitamin water, not even gator-aide can I drink. No more teas, coffee, chai-tea, etc. etc. Especially! No 'junk-food' at the usual places. No chocolates, candies, gum, or yogurts, cheese or dairy of any kind. No shellfish either.


If I do 'cheat' and eat the forbidden food (like toast) anyway, it creates more withdrawals and severe 'brain-fog'! I cannot 'cheat' because this body 'knows somehow and I have to 'pay' for it later by means of brain-fog and terrible withdrawals for days on end.


I can't go anywhere and "Do lunch" or "Dinner" with anyone. This simple social pleasure has been stripped away from me! I dwell in a personal living hell here. Isolated from people and social dinner occasions. Depressing.


BUT ! I can drink all the water I want! GRRRR!!!!!! >:oP

...and eat dry or fresh-steamed vegetables, baked chicken and turkey (No gravies) Or baked fish/ Salmon. Or Steak all by itself...but no steak sauce; no katsup either. I can eat salad. No crutons or cherry tomatoes.(withdrawals) Italian-type dressing (vinegar and oil) This is all I have been eating for weeks now and I am sick of eating the same stuff night and day. So I haven't been bothering to even eat anymore because it is sickening to me to eat the same stuff day after day. At least this cuts down on the amount of diaoreaahh I have now.


I have lost weight and feel physically very bad.

I was prescribed to take 30mg/day (Prednisone) to try to reduce the inflammation brought upon by Ulcerative Colitis. I have taken Prednisone before....up to 60mg/day, when I was first diagnosed with UC. I don't really remember all of the side effects I experienced, but I do remember my calves and feet swelling, a bit a of moon face and very little weight gain due to the UC. Does anyone have any suggestions to how/and when I should take the daily dose of Prednisone (early morning, with food...what kind of food)? Also, I would love to hear from anyone with Ulcerative Colitis and how they are coping with the disease. From their diet when in remission to during a flare-up! Thanks...

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.

I have been on mirena now for 10 months. I was on the depo for 10 years prior. I loved my depo adn only went off of it after Kaiser said I could not do it any longer. I was told that mirena was a god send and a lot like my depo. I can say that the combination of depo and mirena I have not had any period at all. but that is where the happiness ends. I have experienced moths of breast pain. it hurt to touch them let alone put anything on them. after about 6 months and numerous trips to the vet it disappeared. then I got a small rash on my neck and by my arms. went to dermatology and since then I have been there, or to my primary or an allergist every week since then. the rough severley itchy skin is constant. remarkably every 29 - 32 days it fades for 2 days or so and just when I am sure it is going away wham back it comes and each time it is getting worse and worse. having never had any skin problems before I believed the doctors tha tit was folliculitus, then they said dermatitus, then they said uticaria and then hives or the last straw i was causing it that it was in my head. i just got a new allergist and while she doesn't knwo if it is my mirena she can tell me I have histamine levels that are off the chart. my husband is allergic to a lot so we already use free & clear everything and my housse is spotless but I am still being told it is soemthing I am doing to myself. I have also been reevaluating my things and I relaize I have been experiencing a lot of numbness and joint pain. so much so that my primary sent me to a rhuematlogist and he ran every test for lupus, and many other diseaeses adn even cancer. I was going crazy. Iwas beginning to think maybe I was mental. I have since been researching mirena and I am finding it so much more than what the pamphlet says. I finally got the nerve to call my ob, adn she ahs since been researching things with me and we know for sure that no matter what next week I get my mirena removed. I am just feeling so alone and depressed. I am 33 years old and instead of enjoying my new marriage I am contemplating a divorce becasue I do not want him to be stuck with soemone who might be crazy. seeking support and anyone else who feels this way.

I am 20 years old and I've been on Yasmin for almost 2 years and off for about 2 weeks. Yasmin gave me an irregular heartbeat, vision problems, severe fatigue, muscle spasms and aching in my joints, and constant cramping in my lower tummy but these have started to slowly die down. My current side effects include severe allergies to foods (milk, wheat, tomatoes, eggs), antihistamines, and chemical sensitivities (perfume, soaps, detergents, cigarrette smoke). Also, I have been struggling to swallow food for 11 weeks now and found out that it may be a nuerological side effect from yasmin. The doctors where I am from don't seem to believe me and they all think I'm crazy so I just don't know how I am going to get help for this. One doctor even told me that I was doing this to myself and that I was anorexic. I'm obviously trying to get help or I wouldn't have been there asking him. I just wish I knew how long it takes to get back to normal or if I am ever going to be normal again.

I am using Advair temporaily. It provides relief when I have a lot of sinus drainage and can't breath well. I am also reading Sally Fallons Nourishing Traditions and cutting out wheat, corn and most dairy. Also, all unnatural food additivesand processing including pesticides. Go to mercola.com to search for info on health and what's in the food we eat. I had no idea what was in stuff I was eating. I was shocked. I am hoping that I can get to a place where I won't need the medicine.

I am taking 25 mg of Toprol XL once a day at bedtime and it is effectively sedating as well as antiarrhythmic. However, I feel tired and I end up taking naps much of the day, which is extremely unusual. Actually, I am getting twice the amount of sleep I have ever gotten.

Some of the side effects and symptoms that others are mentioning on this board are also symptoms of magnesium deficiency, which is the cause of many cardiovascular problems in the US and West due to a naturally magneisum deficient diet based upon refined wheat. ******

I have been on yasmin for nearly year with a break of 2 months. I was on spironolactone for a year but my periods became erratic so I went on yasmin to try and control my acne. In the last 6 months I have started to become bloated and get stomach pain and be really gassy.This is quite constant but especially after I eat. I have a really good diet, no wheat,dairy or sugar or fizzy dronks, but still I experience pain. My skin is clearer than when I am not on it but i don't think I want to be in constant pain.
I also feel lethargic and get tired easily and have put on a bit of weight, but that's quite normal as I have PCOS, so my weight fluctuates constantly.

I have only managed to take Siomvastatin tablets (1 x 10mg) per day for 5 weeks. the headaches have been terrible.
I already suffer from stomach problems (intolerance to wheat, corn, maize starch etc..) and I cannot say this medication has made it worse, as I would not know.
Stopped medication for a week and then startedagain today--within 2 hours a headache, slight dizziness and nausea.