I am currently on my fourth different medication for "hashimoto's" disease and have either had allergic reactions or severe stomach problems as well as insomnia with all of them. Is any type of injection available for someone like me?
View 1 RepliesI have type 1 diabetes and take insulin for this. I have had diabetes for a long time and I am very use to my injection regime. My doctor has now said that I need to take metformin alongside, but I thought metformin was for type 2 diabetes.
View 2 RepliesI was recently referred to an endocrinologist due to 'abnormal' blood test results. The results were not shared with me. The endo gave me a full exam & at the time concluded my thyroid was fine & I was just stressed from work & maybe a psychologist would help. He took a blood test anyways.
A week later I got a call to say a prescription was in the post for 125 mg of Eltroxin!
I've managed to get a copy of the blood test result that the endo took & I'm trying to figure out if it means I have Hashimoto's disease. My endo never mentioned this to me but it seems from what I can find online that might be the case. Any help at all with this is greatly appreciated :
TSH: 13.79
Free T3: 5.2
Free T4: 14.7
ESR: 2
Anti TG: 358.8
Anti TPO: 8.1
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?
View 2 RepliesI'm a 16-year-old female who has been diagnosed with Hashimoto's disease. I was diagnosed in November of 2013, and in December of that year I had the left side of my thyroid removed because of a mass. I am currently taking 88 mcg of Levo. I have struggled with headaches nearly every day for the past year and a half. I've tried everything, I've had blood tests, an MRI, I've tried every OTC pain pill, and I was prescribed Vicodin and Hydrocodone. I have gone to an ophthalmologist as well. I haven't had my levels checked in about 3 months, and my appointment isn't until next month. But I wanted to know if anyone knew if this disease can cause constant headaches, as well as depression.
View 1 RepliesHas anyone read or been told by their doc they should "not" take probiotics if they have Hashimoto's or other autoimmune illness?
I read somewhere that one with autoimmune problems should not take probiotics that it could cause systemic yeast infection. Now I can't find that article. Everything else I read states probiotics good for autoimmune disease.
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.
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.
Over the last year and a half, they have been testing my thyroid as it keeps showing up as underactive (no they have not done anything about it, for some reason they just keep getting more bloods done?). Until 2 years ago, all of my bloods came back perfect, with a high iron count of 148, but the other levels pretty much smack in the middle of normal ranges. This time, My iron came back as 53 - the doc said for me this is quite bad because mine are usually so high. My Thyroid level was 13, and he told me that my Vitamin D was terribly low. Although he did not give me the exact level of Vit D, I can only assume it was rather terrible as that is the only supplement he told me that I need to get onto immediately.
So, I know these levels are not great, but as it was a rushed appointment, he told me those levels, told me that I have Hashimoto's Disease and wrote up another batch of blood tests. So now I am lost.
Can anyone tell me what on earth this all means?
I AM going back to him, but couldn't get an appointment until mid/end next week (which is great because my bloods should be back by then anyway).
This will be the 4th set of bloods I have done in the last 18-20 months, all of which showed an underactive thyroid. I'm just not sure why they are still testing?
Is this normal? And what do those iron and thyroid levels mean? I'm assuming it isn't anything drastic or he would have done more about it?
So I am a type 1 diabetic where I take insulin injectables for my insulin needs. I have taken shots for as long as I remember, well now I am 15 years old and my mom is diabetic. I see that she takes pills for her diabetes. She says she is type 2 diabetic. I want to know why she can take pills and I have to take shots? She is on Metformin so I would like to forego the shots and take the pills.
I would like the effects of the Metformin so I know how it would help me with my diabetes. I want to start on it as soon as I can. I would be able to go places without having to take a shot all the time. I need to go to somewhere private and leave my friends when I do my shot.
With the medication I don't have to do that. Does anyone know about Metformin and can tell me about the side effects and stuff?
I'm 37 and was convinced i couldn't get pregnant because of my Hashimoto's. So it was a quite a surprise when I saw that positive test. Has anyone had any experience with a later in life baby coupled with a thyroid disorder?
View 1 RepliesI had right part of my thyroid removed last year due to the tumor. I didn't get any treatment, doctors were saying that everything is ok, just need to do TSH tests every few months.
During this year I had loads of strange symptoms like hair lose, weight gain, sleeplessness, late periods, itchy and dry skin, cold hands and feet etc. Doctors were saying it's stress, so when I was in Poland for holiday I paid to see specialists: endocrinologist and gynecologist,
I've done TSH test and it came out 5,3.
Endocrinologist said even if it didn't reach the maximum (5.5) my thyroid is on the border of efficiency and I need to start the treatment. He said that healthy person has TSH level between 1 and 1.5. He diagnosed Hashimoto and underactive thyroid.
I am on Euthyrox 50, checked TSH after 2 weeks and it was 2,74, but GP (in England) said that IT'S NORMAL. They were saying it when I was telling them about the symptomes I had and how did I feel.
I also got special diet to help me lose weight (I gained about 2 stones in one year without the reason).
I just want you to keep asking your GP's to send you to specialists, don't let them tell you it's all good when you apparently don't feel good. It's shame that you have to pay to get proper treatment because NHS is saving money and GP's don't want to refer people to hospital.
I'm 23 years old, 5 months ago I got diagnosed with Hashimoto's. I was scared of having to go on meds for the rest of my life at such a young age so I opted for natural route. The homeopathic Dr. I went to see gave me i Throid iodine pills, and had me go on a 2 week liquid diet (I only lasted 4 days) and he wanted me to do a 60-90 smoothie diet. Needless to say I gave up after the 4 days and when I stopped the diet I stopped taking the i Thyroid pills. 2 weeks ago I went to see my endocrinologist who wasn't very happy that I hadn't been taking the Synthroid as she had prescribed and told me the results from my ultra sound to my thyroid looked rough. She went on to stress how important it is that I take it and how my levels are worse off then when I first came to see her. She also told me if I was trying to get pregnant how important it is for the baby to have thyroid. So yesterday I find out I'm pregnant and now I'm freaking out. My natural part of me is screaming don't take it, start the iThroid religiously and stick to it, but I feel like it's too late. At this point it's too late for me to experiment what may/may not work for me in terms of trying out the natural route. I had months to figure that out and I didn't and now I'm pregnant. If my baby needs my thyroid to develop properly then I need to start taking the prescribed synthroid. My endo prescribed me .05 mg I don't know if that's a lot or a little. She also told me if I find out I'm pregnant I need to let her know immediately so she can increase it by 30%. I guess I'm wondering if others who have hashimoto's and those that have gone through pregnancy while taking synthroid can tell me anything. I'm scared my body's going to react weird to it. I'm scared my hairs going to fall out and I'm going to gain weight (currently 5"5 114lbs.) I read those are some of the side effects from Synthroid. I'm scared to have heart palpitations and anxiety) which I already have but I'm scared it'll make my anxiety worse to the point I'm a complete wreck. While having all these fears I'm also scared about what may happen to the baby if I don't take it. So before writing this post I popped my first synthroid pill. Maybe I'll go on it until the baby is born and then come off it and try natural again? Anyone think that's a good idea? I just don't want to be dependent on something big pharma produced in a lab. Maybe it's just a matter of changing my diet and exercising and eating gluten free foods. I'm wondering if anyone with Hashimoto's can tell me about their experience with it and help ease my mind.
View 2 RepliesI just had a AM cortisol lab of 1.1. Over the last 6 months I have been told I have Hashimotos.
What does this mean?
I've been struggling with my Hashimoto's diagnosis. I am actually "alright" at this present moment, but it was a long and rocky road. My Endo is not very informative at all and does not answer my questions. Last time I asked her about taking supplements. She stated she is biased because she practices Western medicine and won't comment on whether or not she thinks it's a good idea to take supplements.
I decided a little over a year ago, to take 200 mg Selenium as an added supplement, because I've been reading on here, that it will help with getting the antibodies down and I must say, I can tell a difference in how I feel today from before.
Now here is where I'm confused: my best friend since Kindergarten got diagnosed with Hashi's last year. She's really been having a hard time with it. Last time she saw her Endo, she asked the Selenium question. Her Endo said don't take it, because your risk of developing diabetes increases! That's something I've never heard about. So all day today I've been reading and researching this and I'm reading either it's so good to take when you have Hashi's and then some study they did that confirms my friends' Drs' point about the increased diabetes risk. Any thoughts?
Wondering if anyone has Hashimoto's disease? I saw a specialist a couple of weeks ago who told me I most likely have this. I went from extreme hyperthyroid to hypothyroid. Skinny and energetic to sluggish and heavy. I'm pretty miserable with it. I've just been sent a letter with my levels:
8 May - TSH .03, free T4 29.3, WBC count 5.1
15 June - TSH 15.95, free T4 9.9
6 July - TSH 12.38, free T4 8.3
I have an important question.
My last blood work from one mouth ago revealed a TSH of - 0.16. (ranges 0.3-4.5)
Though my levels of free T3 & T4 were midrange and maybe even slightly lower than they should be.
FT3: 3.30 (ranges 2.1-4.2)
FT4: 1.02 (ranges 0.7-1.8)
I'm on 112,5 levothyroxine and 12,5 cytomel daily dose.
Is it safe to have a TSH that low?
Can I even upgrade my meds to 125 levo a day? I still feel hypo and under medicated.
I did hear about the 'optimal' values between the ranges were a lot of people are on their best in their 'sweet spots'.
If the rule of thumb is that FT4 has to be 50% of the range and FT3 upper half to upper third, i's logical that I'm still hypo. This all being said, will my TSH drop even more when I go to 125?
I don't understand the link between TSH and the FT3 & FT4 results. How can I have such a low TSH and still not reach the recommended levels?
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.
View 1 RepliesI am a 24 year old who works a 12 hour rotating shift pattern (including night shifts). For the past 6 months or maybe more o have had upper left abdominal pain (cramping/aching) and more recently lower pain (sometimes across lower, sometimes left and sometimes a specific place on the lower right). I put it down to IBS due to shift work. My partner convinced me to see the GP as I have a family history of IBD. Oh and my bowel movements vary from constipated (less than once a week) to lose (not diarrhoea and multiple times per day)
Had stool tests and blood tests. I expected them not to find anything to be honest and just did it to please my boyfriend and put his mind at rest.
Doctor phoned and said that "the stool test shows signs of inflammation indicative of inflammatory bowel disease". I couldn't really ask more questions because of where I was. Phoned in for blood results and told by reception that they were fine.
I have been referred to the gastroenterologist and have an appointment in 2 weeks.
I am tired all the time and find it really difficult to get out of bed, frequently have naps at work but put that down to shift working.
I don't want to take any laxatives because I never know when it will change between constipation and loose stools and when I'm working, I often can't get to the toilet.
I often have joint pain but I also have a knee injury and some hyper mobile joints.
I am so confused as to what is going on and hate not being in control of my body. I know I only have mild symptoms, I feel so alone (shift work doesn't lend itself to meeting people regularly).
I am having an SI joint injection Monday...I have the option of doing it with or without sedation. Thoughts? Experiences?
View 7 RepliesI went onto the injection in 2005 and was on that for 9 years due to migraines etc the doctor advised me to have the nexplanon inserted and i've now been on this a year. Tbh i think i'm lucky i've only ever had one period and that was just after my injection started in 2005 so nothing for 10 years. Before the injection my periods were clockwork every 28 days for 5 days at a time. Just wondered now i'm on the nexplanon how long would it take for everything to come back to normal after i've had it removed. I'm thinking of having it removed late 2016 to try and start my own family.
View 2 Replies