Thyroid :: Choking Feeling - Gluten Free Helps?
Jan 11, 2015
I am increasing slowly my Synthroid to .112 This week, I am developing a choking feeling in my throat so its swelling. My MD wants me to be 100% gluten free. First of all, FinnMaid, can you help me with this or Anyone out there. How common is the throat swelling when you are increasing meds and do you increase or decrease to make it go away. Also have you truly found that going gluten free does help? I have Hashimotos and am in my 70's.
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Basically I am 25 years old and as i've grown up I've noticed more and more that I was getting stomach cramps and bloating more and more often. It is very sporadic and I couldn't really say exactly what was causing it but I just thought it was normal. This was until the last 12 months when I started to think a bit more about it. I do a lot of exercise and play a lot of football. I was finding that I would get some form of cramp during a football game. Usually quite mild but sometimes worse. I also like to run and when training for a half marathon found that after a certain distance I would get pains. Almost every time after about 30-40 minutes running. It would normally be worse when running in the evenings. I started thinking about it and tried taking several things out of my diet. I am 95% certain I have a lactose intolerance as since cutting that out around 6 months ago I have seen an improvement. But I would still get pains.
This all resulted in me going Gluten Free and I finally experienced what it feels like to have a normal stomach. I was relaxed and could do whatever I wanted without any fear. So I decided for my own health I should get tested for celiacs disease and after 7 weeks of eating gluten again had the blood tests. Today I had the results and they have come back negative. I feel so deflated and just angry. What do I do now? I just feel like going back to Gluten Free and living like that self diagnosed. The weird thing I find with my disorder is it seems to be worse when i'm up and about. If me and my fiancee have gone out around town and have lunch it is often worse when walking around afterwards. I don't always get blinding pains either. It is often just severe constipation or stomach cramps just making me feel uncomfortable.
Really disheartening now and just want to know but can't carry on for much longer and really don't want to keep eating Gluten when I know I feel good when I don't. Any advise?
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I have had choking feeling for the last 2 months. It is now almost everyday. I sleep very well and do not wake up with it. I start getting it by the afternoon until bedtime. It is really bothering me. I have had hypothyroidism for 12 years but my tests are fine and my ultra sound is good too. The ENT doctor says it is stress related but I think there is more to it than stress. It is really bothering me and I do not know what to do?
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Over the past one-two years I have been getting stressed about school work, my appearance, my friends etc. and I had a conversation with some of my friends and they thought I may have had anxiety. I thought nothing of it because it wasn't much at the time but lately it's been getting worse. I feel sick all the time and the most common thing is the choking part. I feel like someone is trying to choke me, but obviously no one is. I have trouble breathing when this happens and my throat closes up and I kind of feel a bit dizzy. I have looked at some websites and they all say it may be a certain infection or something but I want to know if this has anything to do with anxiety? I still have not told anyone about the choking thing except my mum because I want to be sure I am getting this right before I start seeking help.
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I have seen some videos that support a gluten free diet and an end to Hashimoto's.
Has anyone tried going completely gluten free and had an improvement in their symptoms or even and reduction or end to their meds?
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I am a 51 year old female and had a physical last week with my general practitioner because it has been a long time. It included blood tests. One test was about the thyroid and I've got conflicting information about the result.
The report says:
TSH Reflex to Free T4
TSH RFLX is 8.25 - and is high, the normal range is shown as 0.40-4.50
T4, FREE
Thyroxine, Free, Direct - 0.8 - and is in range, range is shown as 0.8-1.8
I've done some research and it looks like this combination falls in the hypothyroidism range. However, my doctor says it is fine because the T4 FREE number is in range. There is no family history of thyroid problems. I'm concerned because I have some of the symptoms of hypothyroidism (fatigue, depression, feeling cold).
Does this sound right to those of you who have experience with thyroid disease? Should I see an endocrinologist?
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Not to go into too much detail, but I was diagnosed with Hashimoto's last Dec (2012). I have seen MANY docs that have no idea what they are talking about. I have finally found a good Endocrinologist who understands hypo-thyroid....but she just wants to treat with synthetic T4 meds. I have also found a Great Holistic doc, that happens to also be a certified nutritionist as well....who understands for every action, there is a reaction. I use both of these docs to collaborate on my health and lab results...to decide how I WANT to treat my self so I can get back to optimum health.
Ready anything you can get your hands on...I repeat! Read anything you can get your hands on! Turn off the TV....and start researching your own health. It's worth it.
I am finding that docs just "treat" the already diseased body, rather than looking for the underlying cause of the disease. Your body is more than capable of taking care of itself if you have the right balance of vitamin/nutrients/minerals. It's when these levels get deficient...that's when you open the door for disease. Once that starts, your health will spiral out of control.
Find out what your deficient in and you can fix your health issues!
So, keep reading and learning. Hashi's patients....look for gluten free, fluoride free...look up iodine and it's effect on your thyroid health. (Dr. Brownstein-Iodine Loading test) Try to get back to the basics....rather than eating frozen foods and processed foods. Check into organic food (Dirty Dozen and the Clean 15). Do a Saliva test to check your adrenal hormones, check your Neurotransmitter levels too (Pharmasan Labs-run it thru your insurance). Read, "Stop the Thyroid Madness" to understand treating thyroid disease with natural desiccated thyroid, rather than just synthetic T4 medication.
There are people out there that understand how to read these results. All of the "goofy" people that tell you not to eat this, take this supplement, etc...may not be as crazy as you think. Look for a holistic, natural doc. Some are better than others...try a couple and see who you are comfortable with.
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My 12 yr old son is experiencing no BM after 4 days of switching him to this GFDF diet ... Before he was IBS .... Not sure what to do
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Here are my lab results from 2/7/14:
tsh- .028 range- .45-4.5
t4 free direct- 1.86 range-.82-1.77
t3 free serum- 3.2 range- 2.0- 4.4
Last year:
lab results from 3/26/13:
tsh- .096 range- .45- 4.5
t4 free direct- 1.53 range- .82- 1.77
t3 free serum- 3.1 range- 2.0-4.4
It looks like I might benefit with the addition of t3 meds. (cytomel) to lower my free t4 and raise my free t3. I feel fine, and anytime I've tried to lower my dose of levothyroxine (.125) even a little bit (.112), I get brain fog, lethargy and GI symptoms. I've been on the same dose for 13 years and my tsh has been low since I started medication. I've only recently requested the free t3 & free t4. My main concern with adding cytomel is that it will further reduce my tsh & the dr will be concerned. This is my 3rd dr in the 7 years since I moved south & every one has been concerned about bone density & heart issues. Any suggestions when I talk to the dr? btw- no hyper symptoms :-) Thanks!
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I have recently "not quite" been diagnosed yet with Lupus however I have certain signs not yet enough for an official diagnosis. High ANA is one, pericardial effusion (mild), no inflammation or symptoms yet. Would have never known I had a problem until the Dr. told me I did!! I used to have severe stomach problems for years, cramps, diarrhea after eating a meal. For hours I would suffer. But for the past 4 or so years it has stopped completely and I am wondering if that is when my immune system started to go overactive due to a possible gluten allergy and now turning into an auto immune disease as a result. I am starting a gluten free diet, today is only day 3, i want to suppress and relax my immune system by not giving it so much work to do!! Unconfuse it and calm it down by eating gluten free and healthier. So nutrients can get absorbed better? Add probiotics, making sure to get Vitamin K...D, B12 etc. (I know K is a big one for Lupus) Does anyone have any views on this or have tried diets like this?
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I hear these go hand in hand and wondered if anyone who is following a gluten free diet has actually gotten better thyroid results without the meds?
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Has anyone tried the new range of gluten free food Udi's?
I saw them in Tesco the other day on 3 for 2 and tried the bagels, muffins and crisps. They all taste just like the real thing! I've really missed bagels since I was diagnosed at 18 so it was great to eat them again.
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I am mid process during the diagnosis (I've had the MRI with and without contrast and get results Monday. I'm currently refusing LP and have the evoked potentials scheduled). If I were to be diagnosed (still hoping not) I have read a lot about being gluten free and that helping with symptoms. As a matter of fact, I may try it regardless of diagnosis to see if it helps. But, has anyone with MS tried it? Did it help?
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I'm going to a party tomorrow night and of course I want to be safe about the drinks I'm choosing to have. I have been doing research on gluten free drinks, but I haven't been able to find anything on Sourpuss! Has anyone given it a go?
Also, what are some good gluten free coolers I could pick up?
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I have had two positive blood tests for celiac disease but a negative biopsy. However, my doctor and I decided it was best to go gluten free as a trial. I am on Day 4 and I have increased fibro pain. Has anyone else experienced this?
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I am also coping with hypothyroidism and I've been searching for the best possible ways to get my health (and life) back. The doctor I have been working with has made the suggestion to go on a gluten free diet. She didn't go into great detail about it, but mentioned that she'd like for me to nix the gluten. I have also read numerous times on the internet about how gluten is a thyroid destroyer. I have tried countless times to go GF, but boy is it hard. I tested negative for gluten and dairy allergies but my doc (a naturopath) was still adamant that I give up the gluten. I feel like such a failure because I only manage to stay gluten free for about 2 weeks at a time until I cave and have something like a slice of pizza or some pasta or bread. There are gluten free alternatives to these items but sometimes they are hard to obtain or are a pain to cook. I have a very healthy diet for the most part but I've found that removing gluten entirely isn't easy. I've also lost weight while going gluten free, which I did NOT want to do. I'm actually already a little bit underweight.
Does anyone have any tips for me? Has anyone out there successfully gone gluten free long-term, and did it affect your condition in a positive way? I feel like a failure because I keep trying to give it up but it never works out in the long run. I always slip up.
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I am coeliac and my GP would like me to try Lisinopril for my unacceptably high blood pressure. However neither he, the pharmacist nor myself have been able to discover if the drug is gluten free. We are also concerned that I have had severe allergic reactions (SJS) to ACE inhibitors in the past.
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I'm gluten-intolerant. Does anyone know if glucose syrup is gluten-free?
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I've made an appt with a naturopath next week as I'm having an increase in bad symptoms since starting levothyroxine 4mths ago and cannot stand it any longer.
I'm expecting to be told to go gluten free. However there's corn/maize starch (contains gluten) in the meds so I'm wondering about those of you who are gluten free - what type of meds are you on?
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I've just been prescribed orlistat completely out of the blue by my GP... And I'm also gluten free as I have a very high intolerance now. So its quite difficult planning meals but think I'm doing ok!
My breakfasts and lunches seem to be between 5 and 10g fat then main meals are nearer to 15g. Is this ok?
What if I want a skinny latte outside of mealtimes, these work out at 2.2g fat... would that make me poorly?
Also am I able to drink wine? I appreciate the calorific issues with wine but I'd still like to enjoy a few glasses on the weekends, I'm more concerned about an orange explosion if I do?
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I am a fellow celiac who dreams of having more gluten-free beer options that taste good and are proven safe. Maybe one day in the future I'll be pushing beer companies to develop such methods. But for the moment I want to know if anyone out there shares my sentiments.
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