Hyperthyroidism :: Natural Treatments For Graves Disease Patient?
Aug 23, 2014
I have posted to this Board before about what has made a difference to my recovery from Graves. In addition to the medication Methimazole, I started on Regular L-Carnitine and then later Acetyl-L-Carnitine and vitamin D supplementation. Others on the Board have posted about the addition of selenium as well as other natural herbs such as Melissa and Bugleweed. I saw this posting on another Hyperthyroid Board and the author has given me permission to copy it to this Board as follows:
I am shocked that our doctor's don't know more about the thyroid, autoimmune disease and its connection to the gut. I went to a naturopath when I was first diagnosed in 2012 because my husband and I didn't like what the endo suggested. After seeing the naturopath we made a connection between my occasional IBS type symptoms, bloating and my thyroid. We started a probiotic and immune support vitamin called Moducare. Then she ran food sensitivity testing through All Tests labs (some MDs are skeptical about this but it worked for my stomach). I had all four antibodies for graves and Hashimoto's and I had symptoms from both and almost undetectable TSH levels. She removed gluten and dairy from my diet and pulled out foods I tested sensitive to like yeast. Then added Lycopus Virginicus and lemon balm tincture to my routine along with vitamin D, B complex and CoQ10. I finally figured out though that the real cure for me was going gluten free and dairy free. No more bloating, no stomach cramps, gas or the big D. Then I found out there is a link between Celiac disease, gluten sensitivity, leaky gut and Thyroid disease. There is a natural graves treatment FB page I am on and a lot of us have cured ourselves of Graves using dietary modifications. I went into remission within 3 months of this diet. I have been normal for over a year now. You really need to be tested for celiac before you start the diet. If you don't have it (it can lead to thyroid disease and then other autoimmune disease when left untreated) then you are sensitive to something you are eating and are most likely dealing with leaky gut. Someday the MDs will catch up with what is really going on here. Our pediatrician is so progressive and knows all this stuff but warned us that a lot of her colleagues are not there yet when it comes to medicine."
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I'm wondering if anyone has any advice regarding diagnosing graves and thyroid eye disease in pregnancy. Having never had any problems until being pregnant I'm very confused as to why I've suddenly got it? At around 12 weeks into my pregnancy I noticed a change in my eyes (one was protruding), after seeing an eye dr, he advised I'd be tested for hyperthyroidism and following his advice the bloods came back as a positive for hyperthyroidism. I was put on PTU by an endocrinologist for the rest of my pregnancy and at week 39 I noticed a yellowing in the White of my eyes and admitted myself to the maternity unit for blood tests following speaking with a midwife. It turned out I had developed severe jaundice (Which I now have learnt through research to be a severe side effect to PTU) and that my liver was failing; I had to have an emergency c section that night. I am pleased to say I have a had a healthy baby boy but I'm so anxious as to whether these conditions will worsen post pregnancy.
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Is there anyone out there that eats gluten free and any evidence to say that it will help with Graves or Hyperthyroidism?
Just exploring my diet as I'm on 30mg of Carbimazole daily and have put on weight. I normally have low fat, high protein, low carb, veggies, fruit and lots of water, but still putting on weight.
Weight gain is this because I'm going back to being hypothyroid or the Carbimazole? Back at the doctors next week for a blood test.
Just wondered whether to try gluten free, although at the most I only eat 2 slices of bread a week and my diet is quite healthy apart from the occasional glass of wine.
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I've been diagnosed with hyperparathyroidism on Thursday 5th of November, I was wondering if anybody has had natural treatment for this please?
In the meantime I'm going ahead with being put on the waiting list for an operation, I have my ultrasound scan tomorrow, Tuesday the 24th of November .
It would be good to hear from those members who have used natural treatment for primary hyperparathyroidism and to find out how you are getting on now please ?
I have had "M.E. " for 19 years , I'm being treated naturally, this helps with my weight and also some of the other symptoms , however I'm still not well enough to work and need help at home etc
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I'm suffering from alopecia areata since I was 6 (I'm 23 years old now). I was prescribed with Rogaine, but I didn't see much of improvement. I also tried applying Aloe Vera gel but also without success.
Could you recommend me some more efficient home treatment for hair loss?
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I have just been diagnosed with graves disease (and overactive thyroid as a result) and prescribed 3 5mg carbimazole pills a day whilst i wait to see a specialist and have an ECG so i can also be prescribed beta blockers.
My doctor said to take all 3 pills at once but i have read that the effects don't last 24 hours and its better to spread them through the day. Does anyone else take 15mg and do you take them all at once or spread out? In your experience when is the best time(s) of day to take them?
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Say you have been treated for Graves Disease with RAI and that deals with the hyperthyroidism (not so much with the eyes though!), what happens to the antibodies that were attacking you thyroid with such vigour and verve? Do they just go home because there's nothing left to attack? Are they always in your system waiting to attack public enemy number 2? And why do these things decide to attack the very thing they are meant to be protecting? Is it genetics? Childhood illness (whooping cough, measles and mumps in my case.) Environmental factors? Stress? Diet?
I am sure there are many schools of thought and theories to all of these questions but I am curious still about where these wee anti-bodies go after the illness (or symptom of your illness) has been irradiated in my case.
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I Am wondering if someone can help me out with what my blood results mean . ok so i went to a walk in clinic because i was having a laundry list of stuff going on with my health . asked doc to do some blood work and see if he could find what might be wrong .
blood work came back showing some thyroid issues . my TSH was .16 my T4 free was 18 free T3 was 6.1 and my TPO was 102
the doc said i have Hashimoto's thyroiditis and referred me to endocrinologist which im waiting for appointment .
so my question is after doing some googling im wondering if the doc might have meant to say graves disease rather than hashimoto's . it was very busy in the office and maybe he just mixed the two up ? the reason im thinking this is because when i look at what my blood work results are they point to hyperthyroid rather than hypo . can anybody tell from my numbers i really would like to know and its a bit of a wait till my appointment with the specialist.
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I am very new to this site and extremely grateful that I found it. I was diagnosed with inappropriate sinus tachycardia almost three years ago. I am taking 350 milligrams of metoprolol. My primary doctor ordered new labs since my cardiologist has not requested any in the last 2.5 years. My results are as follows:
TSH - 0.01
Vitamin D - 26
Carbon Dioxide - 18
Free T4 - 1.3
Thyroglobulin Antibodies <1
Thyroid Peroxidase Ab 421
Primary doc originally thought I graves or Hashimoto's, but now wants me to follow up with an endocrinologist. Of course that appointment is 2 months away.
I do not have many symptoms. I do have the feeling of warmth in my shins, but that comes and goes. I have a little muscle weakness. I have been having trouble sleeping through the night, but 2 glasses of wine have been helping.
If I do have either Graves or Hashimoto's is waiting 2 months for a doctor appointment ok? I would think that I need some type of medicine.
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I've been taking carbimazole 20 for 2 months now as i have graves i had a uptake scan which shows its my whole thyroid gland is playing up .up and down so my specialist had gave me carbimazole to block my thyroid hormones and replacing them back with thyroxine 50 i feel so terrible sickley cant eat well also headace i believe the carbimazole is causing all the trouble.with side effects.
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I've just been diagnosed with Graves disease. I am taking Carbimazole 40mg daily now, for 8 days. I have the dreaded 24hr sweats - aching leg muscles - sleeplessness - no energy and lie on bed for most of each day!
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I am just curious to know how many types of colon treatments are available in USA.
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My husband and I have been trying to conceive for the last five years now. We have an eleven year old daughter, and we have had one miscarriage since she was born as well. Can you tell me anything about homeopathic fertility treatments? Does any of that really work?
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I'm a 36 year old mum of 5... 8 years ago after our 4th child I needed an operation to strip varicose veins on both legs as they were problematic.. Living abroad flights are needed to visit family etc.
We went on to have our 5th child 4 years ago and over the last year they have returned twice as bad as before. They are painful and very ugly.... Starting from my ankles right up to the back of my knees. I'm a fit person, train every day and not over weight. What options do I have other than heading down the surgery route again!! It's starting to affect me as I want to not feel conscious living in a warm country and wanting to spend time with our children in swimwear and shorts.
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After a period of much indulgence at the end of 2015 I am pleased to say I can touch my toes. Having suffered a ruptured soleus on one foot followed by achilles tendonitis on the other, the biggest problem I faced was not being able to run; ironic considering this is how I caused the injuries. Now in the recovery period I have clocked up some distance walking, but have learnt some valuable lessons. Before doing any walking, stretch thoroughly the affected area. On days that you don't walk, stretch as if you were going to walk anyway. Finally, rest. Muscle-tendon units are essentially springs. They work better when they have warmed up, so bouncing or ballistic stretching is counterproductive. Whilst a common problem found during recovery is underestimating the amount of static stretching that is required before exercise, the long period of recovery also leads to side effects of under- and over-using other muscles leading to compensation problems. Stretching therefore needs to be comprehensive and include all muscles in the legs to ensure the recovery process is not a step backwards. Happy New Year to all.
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Are there treatments/medications that work?
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i had intercourse with my girlfriend. she's a SLE patient and v had protected sex. but it got torn and later i had to give her unwanted 72 !! will this effect her health in any way and is this SO contagious that i will also be affected??
and that night she complain of a bit bleeding!!! is this any way normal?
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total thyroidectomy 2 months ago due to Graves disease, 3x since, I have experienced, edema of both eyelids, itching and redness, I am on Synthroid 0.1mg po/daily. The symptoms dissipate after about 2 days.Anyone post Thyroid removal ever have this happen?
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My aunt is diabetic and she is on Novartis for years. However, she has been lately experiencing some heart problems and this worries me. I would like to know if diabetics with heart problems take Novartis or not.
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Regular Hiccups in Diabetic Patient. suddenly start from before some time.
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A few days ago I had a hyperglycemia attack. I am not diabetic and had a good health throughout my life. The attack lasted for several hours. after two days i had an headache and it still persists. Can hyperglycemia cause brain damage ?
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