all of your symptoms sound like a decrease in hormone which in turn could be auto immune deficency this is what causes arthritis lupus hypoand hyper thyroid as well as a large variety of other diseases and the doctors will give you as much medicine as you allow however those cause more side effects and problems I highly recommend seeing a homiopathic doctor drink herbal tea and look on herbal index they have everyday herbs like garlic clove thyme oregano etc. and it tells you what it helps with garlic and ginger are two specific ones I can think of that will help
I, like many of you, have had an array of symptoms. I'm 23 years old, female. Tired all the time, headaches, cold sensitivity, muscle aches, mood swings, weight trouble, and within the last month hair loss. I've been to many drs and no answers. This morning I came across a website that could possibly, hopefully, have the answer for many of us. For all of you out there that had a normal thyroid levels, but many of the symptoms read this document.
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have u had ur thyroid tested... that is what it sounds like to me.. i was having the same problems and i was told that there wasnt anything wrong for the longest time but i was persistant. i made the doctors do tests on me and it turned out i was right that it was my thyroid but they misdiagnosed me for what kind of thyroid disorder it was so i refused the meds. it sounds to me like your thyroid is malfunctioning again.
I am turning 23 in october and for 7 years I have have suffered major weight gain, I have done everything possible and it doesn't come off, I suffer from depression, severe fatigue and daily pain in my joints and muscles. I have to fight to get up everyday and help with my nephews. several times a day I will fall asleep just sitting in a chair, even if I'm talking to someone. for days at a time I will sit and cry, and drive people away. years ago my aunt and cousin told me it might be my thyroid, I was tested and nothing came up. That was 6 years ago, I wonder now if maybe it is my thyroid, and if I should get a more complex test to find out. Because of the weight my family is afraid I will die, and often wonder why I sit hold my body and crying. Saying it hurts makes them upset, they think I am being lazy. I truly wish I was normal, I exercise as I can, even if it hurts. I can't sleep at night, I toss and turn most of the night. Can anyone give me ideas? Going to see my doctor soon and with my mom's help try to find out why this happened to me and if I can be like I use to be, active and sleeping, not always in pain and crying.
i would like an answer to my problem.
Do you know which Homepathic doctor she went too , Can you share some more information. I have been dealing with Hypothyroidism since 2006 ,still have symptoms of fatigue , exercise intolerance , weight gain around 30 , premature grey hairs, muscles aches and joint pain, low motivation. My doctor says mu numbers good but my symptoms doesn't say that . I heard lot of success on Homepathic , please advice.
I came across this blog comply by accident while once again searching for answers to my health issues.
Two years ago my children and I were accidently poisoned by contaminated water from our well (it was a bored well common in 1970's and we had unprecedented rains that allowed farm pesticides as well as other ugly things seep into the water supply). At one point, I had my daughter (21) in one hospital for a week and my son (17) in another hospital - all while I was so sick myself I was barely functional. It was my daughter who figured the poisoning out. I have been hospitalized like 4 times in a year. I have been seen at the Mayo Clinic at Rochester. While now I can drive myself, brain function, ability to speak a coherent sentence seems to have returned, I am left with: chronic fatigue, difficulty sleeping even though I am exhausted, annoying headaches but not migraines that I previously had, chronic diarrhea, joint pain, my feet are ultra sensitive to anything touching them, uncontrollable sweating, I cannot control my body temperature, depressed because I feel so bad, White Blood Cell Count is elevated and the higher it goes the more fatigued and worse body pain gets, weight gain of 40 lbs, edema to the point I can only wear sandals.
I am 49 with a Master's Degree and own a healthcare technology company for 20 years. I am normally the person everyone depends upon. But now, I wonder if I will feel this physically bad the rest of my life and that thought is very depressing.
I have been seen by so many doctors and while I am relieved to be able to get out of bed now, I still am plagued by chronic fatigue, joint pain, chronic diarrhea, weight gain, and no desire to do much of anything but sleep.
One avenue I have not thought to check into is homeopathic. I will look into this. I can't believe that this is all that I have to look to for the rest of my life. There has to be an answer.
You are constipated... it can cause all of those symptoms. You can still poo and be constipated and not realize it. You should be having minimum 2 good bowel movements a day, 24 grams of fiber a day minimum and half your weight in oz of water a day.
Two words: LYME DISEASE. I have had all of the symptoms you have been describing (plus and minus a few) and went to doctor after doctor after doctor. I have seen every kind of '____ologist' under the sun, tried massage, acupuncture, cranio-sacral work, chiropractic, infrared saunas, electric stimulation, etc etc etc. the list goes on and on. I know many of you have been tested for Lyme with the conventional Western Blot and ELISA blood tests. This is NOT enough. I tested negative 6 times. The conventional tests are very out-dated and do not include many types/strains for the bacteria. In addition the bacteria are corkscrew shaped, and after just a few weeks they burrow into your tissues (all of them, and sometimes even your brain). So, the bacteria are hiding and cannot be detected in the regular blood test. Bottom line, you need to research Lyme yourself ('Under Our Skin' is a great documentary) and find a 'Lyme Literate M.D. (LLMD) in your area to go over your symptoms and help with the testing process. Many primary care and infectious disease docs don't believe in Chronic Lyme Disease (the call it Post Lyme Syndrome) and may not take you seriously or know which tests to order and they certainly don't know how to treat it properly. The CDC released a statement a few months ago that their initial estimate of 30,000 new cases per year was wrong... It's closer to 300,000 cases. And it's not isolated to the northeast. It has been found everywhere. Chronic Lyme Disease has caused me to miss out on too much of life. Please, please, please consider this as a possibility, do some research, see a LLMD and have the proper tests and treatments!!! P.S. Lyme is nicknamed 'the great imitator' and was found in the spinal fluid of 80% of MS patients in one study. It was also found in 90% of the brains of people who had passed away with the diagnosis of Alzheimers. Many people with Parkinson's, fibromyalgia, chronic fatigue, Lou Gehrigs Disease, lupus, and so on have been re-diagnosed with Lyme and made full recoveries.
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This sounds like like me, did you ever find out any information.?