Thyroid :: Natural Treatments For Primary Hyperparathyroidism?
Nov 23, 2015
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 just wondered if anyone has any idea how common it is to have primary hyperparathyroidism?
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After a very painful kidney stone problem and thus being told I have Bilateral kidney stones; I have just been diagnosed with Primary hyperparathyroidism. The docs want to operate to remove the faulty gland(s) but I am very concerned about the procedure in the UK which does not seem to include the mini op or MIRP operation. Has anyone had this type of surgery in UK(either mini or other) and what were your experiences? I am wondering if I should travel to Florida for it?? I also have low vit D and they want me to take vit d supplements. I think this is dangerous to elevate my calcium level even more?
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I have recently been diagnosed as having hyperparathyroidism and I am currently on the waiting list to have two nodules removed. On reading up on the condition sickness is a symptom but for some reason my consultant wouldn't say that my continued sickness for the last 18 months is being caused by my overactive glands. I am getting desperate now so is there anyone on the Forum who is suffering / suffered the same problem and after having the op felt human again ?.
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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 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 have 3 thyroid nodules and 1 cyst. I have been advised to have a thyroidectomy. I do not want to go this route yet and am searching for some natural remedies. I have heard of using iodine but to be careful do to the fact that that might enlarge the nodules. I recently found out that I am very iodine deficient from a lab result. I have heard of iodine trapping, whereby the iodine taken in when their is a severe deficiency is immediately 'trapped' and held in the gland in order to preserve some iodine for the use of the thyroid. I would like to proceed with caution and try the iodine therapy.
Does anyone on this board have any experience with successfully dissolving or at least reducing the nodules/cysts?
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I was diagnosed with this some years ago after suffering for years with kidney stones, they did try and remove my parathyroid glands but couldn't find them, mine aren't where they should be and further tests have come up blank as to where they might be in my body (looking for a needle in a haystack was the term used!) I take Bendroflumethiazide (sp) alternate days to alter the acid in my urine. I'm constantly tired and fed up being told i need to watch my weight and i should exercise more, i'd love to exercise more but some days it's all i can do to get my head off the pillow. I could go on and on here just wanted to know if there was any sufferers out there and wondered how they cope with this condition?
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I have Hashimoto's disease. Over the last year or so I have really started to experience some of the symptoms of hyperparathyroidism such as super bad fatigue, LOTS of pain in my bones, etc. Are the two connected?
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I noticed before I had surgery I would have red, irritated and swollen bumps that would turn into nothing short of a raised mass on my inner thighs. It really hurt! After the surgery they all left. Well it's been since October 26th 2015 that I hadn't seen them until today. I have them again which leads me to believe that the hyperparathyroidism was not completely cured. They took one adenoma but left a complex nodule. I ask the surgeon to look at all of my parathyroid hormones and he flat out told me no. I'm concerned that when I go back to the doctor that my levels will be back up. If not then there is another issue I don't know about. However, I still believe my skin irritations are from nodule he refused to look at. I'm no doctor though. But if anybody is having this issue and still feels really weak in their muscles I could use some advise as to how I can help myself feel better. I still ache.
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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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At the age of 79 I became aware that the pads on the balls of both feet felt tight and a bit puffy and hardish. Then gradually I experienced a sensation in my toes which I can describe as tingly. This area of both feet became susceptible to cold and required contact with heat pads to feel more comfortable. No pain is experienced. Walking seems to alleviate the tingling sensation. After a visit to a G.P. Raynauds Syndrome was confirmed and keeping the feet warm at all times was advised.
Although I live in a well heated bungalow I take heat-pads to bed at night.
In the morning my toes feel quite warm and look rather pinkish red. This condition doesn't affect my normal activities in any way after a year of beginning. 8)
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Are there treatments/medications that work?
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My daughter is taking hydrocortisone for primary Addison's due to Pheochromocytoma. Does anybody know if she should be taking something to help prevent osteoporosis??
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I've been suffering from these for some time and they've recently become worse. I also had migraine headaches in my youth and now occasionally have silent migraines - aura, but no headache. I've recently been diagnosed with fibromyalgia and I understand that this type of headache is common with fibro. I wondered if others have suffered from this and what, if any, medication has been tried.
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I kissed and had sex with a female partner with unknown std status 6 weeks ago I have not had any symptoms but I'm scared il have a recurrent outbreak. The sex was protected. What are the chances that I had an asymptomatic outbreak and it's only a matter of time for a recurrence to happen. I'm still terrified please help
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I have been feeling really bad about the facial hair that I have. I am a young woman with black hair, and so the hair I have in my moustache area is also black and very noticeable. I do wax it but it always returns, and the waxing also leaves a red and bumpy area. I love the idea of getting laser hair removal. Does this procedure have any side effects?
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I'd like to get laser hair removal on my armpits, but I've heard several scary stories that this procedure may cause breast cancer because it uses a light form of radiation and because it blocks lymph nodes. Is this true?
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I've been suffering from this type of headache for some time and they've recently become worse. I also had migraine headaches in my youth and now occasionally have silent migraines - aura, but no headache. I've recently been diagnosed with fibromyalgia and I understand that this type of headache is common with fibro. I wondered if others have suffered from this and what, if any, medication has been tried.
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