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  1. blank Lisa Willis says:

    I have Graves Disease and my thyroid was irradiated 14 years ago. Thus I am now in the hypothyroid category. I have had depression since I was a teenager and the anxiety began occurring after the radiation. I’m wondering if I too could fit into this category although I do not have Hashimotos. Thanks!

  2. Flouride causes hypothyroidism also!

  3. blank Priscilla says:

    I too can relate to this I’m one that is nonthyroid, due to radioactive iodine treatment twice I was diagnosed with graves decease ,sory short too many DRS. without studies about Thyroid even some of the ENDOCRINE DRS. ,IVE HAD some Drs. To tell me depression as nothing to do with thyroid, and patients suffer from misdiagnose, we put our lives in someone elses hands ,so Drs. can take our money, ins., money,is this ok ,?NO! MY HEART TREMBLES, It took me 6yrs. to get in to a Endo.
    I feel like I’m dying because of This kind of life we live now days ! BUT WHO CARES AS LONG AS THEY GET THE ALL MIGHTY $$$$$”.
    HOW SAD,GOD WILL HOLD THEM ACCOUNTABLE!
    JESUS HELP ME HELP US!
    PRISCILLA

  4. blank Mary L Radloff says:

    I am hypothyroid but my GYN did the blood work to diagnose me. I’d been to several GP’s but they never even took my pulse! Told me to just stop eating (I was gaining weight). Didn’t know how they figured that out because all I was doing was sleeping all day (NOT eating). I told the GP’s that but they were just lazy and incompetent. Fortunately for me, my health was important enough for me to keep looking for a “good” doctor. When my GYN diagnosed me, he asked me how I had gotten to his office (he was 20 miles away), I told him I drove. He told me he didn’t even know how I got up the stairs to his office as my pulse was at 40 beats per minute!!! He was disgusted to learn how those GP’s treated me!!! He started me on Synthroid but it didn’t work for me, so he switched me to Armour Thyroid. What a difference!!! I finally had my life back after 4 years of putting up with QUACKS!!! They were licensed doctors but obviously LAZY!!! My health insurance refuses to pay for my Armour Thyroid medication (but will pay for Synthroid). Armour Thyroid is made from pig thyroid (and a few other things), Synthroid is a man-made, synthetic pill. We pay “out-of-pocket” for my Armour Thyroid medication just so I can live a “normal” life. I’m interested in how you are doing, so please let us know.

  5. blank Emma Leir says:

    I have a 14 year old with Hashimotos, caught early last September so actually hyper, not yet hypo, who was also thinking they were ADD, definitely depressed and with high anxiety. The endocrinologist was impressed I’d got a diagnosis so early and said most kids ‘go down the mental health route first.’ The T3, T4 and TSH are now all in normal range but the depression is still so bad that they have tried to kill themselves. In fact we are just out of hospital today after a suicide attempt. So what to do? The poor kid has psychiatrist after psychiatrist saying there must be a reason for their behaviour and my kid says ‘I don’t know why I feel this way.’ How can I help? What research can I show the psychiatrist? How can I get the psychiatrist and endocrinologist to work together? I could really do with some answers if anyone has any.

  6. Please look into sunflower lecithin capsules. My families Drs have started suggesting them to their patients. My mom took them for 3 weeks & all of her bloodwork came back improved or perfect including thyroid levels. The same thing happened with her sister & I’m waiting to hear back about others I’ve suggested it to. This stuff is gold, worth a shot & I’d really love to see more people healed from these issues. I’m a hypothyroid mom myself as well as T1D & they help me too. Good luck 🥰

  7. What good is any of this information if you can’t find anyone to effectively treat you? Ive taken thyroid medication for years with the influence of varying doctors to no avail.

    1. blank Natasha Let Roux says:

      I just went for 2 biopsy’s and saw a head and neck surgeon because my biopsy showed my left thyroid gland had nodules and in those nodules there are traces of CANCER Leukaemia cells growing. I thought I was going to die but I’m still here I had my left thyroid gland removed on the 21st January 2021 and I’m home now and it’s the 27th. So I’m waiting to heal. It takes 6 week’s or months I can’t remember now🤣

  8. Fascinating. In my second year of college, I was hospitalized for depression: I was basically nonfunctional and a kind and wonderful professor made sure I got some help. He also made sure I did NOT have electroshock treatments (this was mid-1980s). I was diagnosed bipolar and given lithium. Three years later I had radioactive iodine treatment for nodules on my thyroid. Two years after that I stopped taking lithium while undergoing therapy for depression. The fog lifted and I went about my life. Fast forward about 20 years: post-partum hormone tests show a thyroid deficiency. Temporary post-partum Hashimoto’s is not uncommon, but with my history the docs were not sure if that was the case. I started levothyroxine and it took about 3-4 years to stabilize the dosage. Since becoming a mother, I’ve watched my immune system go crazy: developed seasonal allergies, soft tissue inflammation (spondlyarthritis), and rheumatoid arthritis. My very smart, opinionated, and nonconformist son was diagnosed with ADD at age 10. He’s now 13 – and after reading this story that rang so many bells, I think we’ll have a thyroid workup done for him.

  9. Ok. So. When I saw this article I was immediately drawn in. This is my story. And this, is my story; my first child was born and she was what you would call “strong willed” or “spirited” from the start. Beautiful and brilliant, but definitely not easy going. From the time she was two I just felt like something was not right. She would get into these modes where it was like a tantrum with no return. At all. She was unreachable. No amount of talking or coaxing or bribing would bring her back. You just had to wait these explosions out. As she got older I experimented with her diet and found that if she ate a high amount of protein, for the most part we could keep most of these episodes at bay. Once she started school, her teachers worked with us to make sure she ate protein every 3 hours, and that worked. Until it didn’t. In second grade her episodes became more frequent and more violent. One day she became upset and threw a chair in the classroom. At that point I remember thinking to myself “either she is bipolar OR she has something physiologically wrong”. I knew I had to figure out what was going on. As much as she was strong willed she was a very rational child and so very self aware. I took her into our favorite doctor. He is very intuitive and even though she DID NOT HAVE 1 SYMPTOM of low thyroid he tested it, after my explanation of her outbursts, and how I had put her on a strict diet. Sure enough, through testing (I don’t remember her numbers) we found that she has Hashimotos.
    I’m not a doctor, but I feel like her outbursts came from extreme exhaustion that she couldn’t express. She was an active kid, I mean the kind that stops napping at 18 months, so it wasn’t obvious that she was tired. I think the high protein diet was a good band aid for a while because it gave her the energy boost that she needed. Once we got her thyroid medication she was a completely different child. Not one outburst since and she is 13. It pains me to think that there are other kids out there that could have this problem and that it’s being labeled otherwise. I am so glad to see some awareness being spread! I just love it.
    Keep on, keeping on! You are right on the money!

    1. Wow! Her symptoms as a baby also sound likeAsperger’s syndrome.

    2. blank Natasha Let Roux says:

      Absolutely agree with you

  10. I understand that this is an old post but I’m reaching out to see if anyone replies. I guess I’m confused. I have been diagnosed with bipolar myself a few years back. Depression since my teen years. My mother has told me for years she thinks my symptoms (too long to list) are related to thyroid. I have never considered that my mental health could be the result of this as well. My question is – there has been a connection made but what has that actually done. Just inform us or is this allowing people to come off of the bipolar medicines and get back to a normal life. Please let me know how this info has improved your symptoms and not just your knowledge. Thanks

    1. blank Natasha Let Roux says:

      It’s your hormones that is un balanced. Go for a blood test to check you thyroid levels. The thyroid itself gives all these problems.

  11. blank Tina manfredo says:

    Hello i have most of these symptoms and been on synthroid for past 20 yrs. Im visiting a Dr next week who is into integrated medicine and HRT(hormone replacement). I have to get my self back. I hope this works. Fingers crossed. Tina M

    1. Tina,

      I’m so very interested in your story. Please reply back here on what happened after your Integrated Medicine Doctor visit and possible changed in your medicine / symptoms.

    2. blank Natasha Let Roux says:

      Sending prayers.

  12. blank Donna M Moore says:

    I’m so Proud to have Re Read This again because I have HOPE and Yes advocatey for Our Children because This is Happening as This that is happening is Doctors Putting Innocent People on Psychiatric medicine before checking out Their blood work and Then that Life being lost in a system set to fail

    1. blank Tammy Redrow says:

      Hello I just wanted to add this is so very true. I was u diagnosed for over 4 years my fam Dr kept putting me on nerve meds and antidepressants (1997) I was not diagnosed until an ENT send a bulge in my neck and stated I needed to get bloodwork done immediately. Since then I have learned my entire family has thyroid and diabetes issues. I have been on all kinds of meds. Gained over 100lbs since my early 20’s and have never had my numbers balanced also A1C is about 6.9. I have a preteen took her to the ped Dr because she is 40lbs over weight, was very concerned. We have BCBS and it took over 9mo to get the 900$ lab bill covered because they argued it is not normal for a child of her age to get the test done that were done. So I would stress that the Ins companies need to be educated as well as Dr.s because it is a grueling battle and just because your number may be level one moment the next day they can be off again. Leading to memory fog memory loss hair loss irritably body temp issues eye sight issues and a slew of other things.
      Thank you for your time

  13. blank REBECCA RYAN-HIGDEN says:

    The mental and emotional disorders in people with thyroid diseases are not exclusive to hypothyroidism. I have Graves. Before my tt I was hyperthyroid. I went into thyroid storm. I was cautioned by my doctor not to sign any legal documents or make any big changes in my life. I was absolutely manic. I also had fears that kept me from fully enjoying my life. Not even 50 years ago, people with Graves disease were committed to asylums. Tied to their beds. Cruel treatments. Graves disease attacks the brain and that brain stays under attack even after the thyroid is removed, but now in a completely different way. The hypothyroid way, even when meds are optimal. Exactly as you’ve mentioned. We need to re-classify autoimmune disorders that affect the thyroid. They should be classified as autoimmune disorders that use hormones, specifically thyroid hormones, to attack potentially every cell in the body. They only become visible after they begin the attack on the thyroid My Graves has taken 1st my tonsils then my reproductive system, eyes, brain, thyroid, skin, and now my cardiovascular system. Plus a whole lotta other crap in between. Every single cell and organ, just like hashi’s. I’m not complaining about my health here. I’ve accepted me. I’m complaining about the fact that no real further studies about autoimmune thyroid disorders have been done since it was named more than a hundred years ago, and doctors then had zero idea about the autoimmune response involved. The focus has been one one aspect and that’s the thyroid. Then doctors dismiss us if we bring up very real and debilitating symptoms. They say its not related to thyroid disease. Well, no kidding. It IS related to the way our bodies are using those hormones. We need to change this. I have no idea where to begin when no one even listens..

    1. Thank you for sharing your story Rebecca. Absolutely all forms of thyroid disease including Graves’ disease can affect the entire body including the brain. I’ve had on my mind to write another mental health article about all forms of thyroid disease at Hypothyroid Mom so thank you for the reminder.

  14. I study and research as much as I can. I have Hashimoto’s hypothyroidism. I’ve been told I have to learn to live with my brain fog. I keep being put off regarding my weight (was 130 when I got sick, now tipping 200 pounds). I just keep gaining. I’m exhausted most of the time. But I dont sleep much. I also have edema in my legs and feet. My doc just tests for TSH. I also suffer from anxiety and migraines. Both got exponentially worse when my thyroid got sick. It’s so frustrating. My family has asked me to stop reading up on thyroid issues because they can’t understand that so many things are directly affected by the thyroid. Thank you for this article and being an advocate for us. I am learning that I must be an informed advocate for myself. No one else has as much at stake as I do.

    1. Kelly from July 17 2018-
      Omg ! I could have written the post you just did. I have been steadily worse within the last 4-5 years. I’ve had every symptom and then some, but was told repeatedly it was not my thyroid. I’ve gained nearly 100 or more pounds since 2014. My hair is balding. I have days where all I can do is sleep. I’ve been diagnosed with fibromyalgia , anxiety, auto immune alopecia ariata …I have wicked migraines and nausea. I haven’t been able to work and quality of life has suffered immensely. I just want to feel better again! Any advice is appreciated.

  15. I have identical mirror image twin daughters. Both have always been extremely physical and active in sports an in life. Three years ago the rug came out from under my oldest. In the course of six months she went from running a sub 5 minute mile to struggling to post a seven minute mile. She saw her doctor repeatedly during that time frame and was diagnosed with everything from anxiety, depression to asthma. The medication she was given just made matters worse. If I didn’t know my daughter better I may have misinterpreted her rages, mood swings etc to drug use. A family acquaintance pointed out the goiter on her throat at a cross country race. After the observation we demanded a full blood workup. She was diagnosed with hyperthyroidism due to graves disease. She opted for full thyroid removal. She is on a daily synthetic now and maintaining. Her identical twin however has taken a nosedive ever since her sister’s surgery. She battles with anxiety, depression, binge eating disorder etc. We have had her TSH levels tested a couple of times and she is “within range”. I am so lost and so frustrated that these girls have lost so much to this damn gland. We are dealing with two extremely intelligent individuals who have researched this disease themselves. Any further suggestions would be appreciated. I am at a cross roads: has one twin stayed strong to support her sister and just gone into an emotional two year tailspin or does she have an underlying thyroid/health issue that has gone undiagnosed?
    any guidance or ideas are greatly appreciated!

    1. Have her get the FULL panel! Not just TSH! And if she’s even CLOSE to either high or low on their range ask them to treat it. If they won’t, see someone else! I have also found that not every doctor/lab have the same “normal” range! So they may say normal but another doctor may say it’s not normal?!

  16. Would you like to be enlightened? I have been battling bipolar symptoms my whole life. My mothers family ALL have it and my father’s side many as well. Last year my wife took me to a counselor whom referred me to a psychiatrist, so I could try medication.. Well, I told her of my food allergies which she totally ignored, prescribed me depakote. I went frickin nuts asap!! When I came to I looked up depakote, its bound with lactose. Milk causes my manic episodes, gluten causes me to be hostile. I saw the client lists of this counselor, he had about 100 or so bipolar patients, literally ALL were in jails.. He told me most lost it when they drink.. Alcohol is grain, mostly wheat so draw your own conclusions.. There is NO help out there if the doctor is part of the AMA, they have a protocol they must follow no matter what your symptoms are.. I could write their manuals..lol.. What if you have graves but seem to have hashimotos also?? The meds I took made me worse actually.. Have battled this so long I am on the verge of giving up.. My 5 year old daughter keeps me from hanging myself honestly.. Met 1 true doctor, he had same issues as me, got sick had to retire before he was done heloing me.. Feel like a Tuskegee Airman.. I don’t mean that disrespectfully at all..
    Excuse my hyper rant..:)
    Blessings

  17. blank Christine says:

    PLEASE Contact me As Soon As You possibly can!! Please. I have hypothyroidism Hashimotoes, and have been diagnosed with bi Polar yrs back. i am in a crisis situation trying to decide if this is physical or mental. I have questions that you may be able to help me answer. My name is Christine

    1. blank Donna M Moore says:

      Please help Me as I’ve been taking levoxyl 100mg
      For many years for hypothyroidism and a host of meds for Bipolar 1 rapid cycling.
      This above bipolar diagnosis was made back in 2000 after I went to a hospital because I wasn’t able to sleep, at times I was bouncing off the walls etc.
      These symptoms along with weight gain inspire of not eating began after I had to have a partial hysterectomy not long after giving birth to my daughter. My hormones had always been a mess as I have my ovaries but throughout the years I’ve had many laparoscopic surgery’s for endometriosis and polycystic ovaries but I still have both of them and they are still actively producing hormones anyway
      Before this crisis I was a nurse working, wife, mother, Daughter, Sister And student.
      Like I said I got slapped with the bipolar diagnosis
      Put on so many different psychiatric medications that completely rendered me Incapable of full filling Anything.
      I kept seeking help and it got worse and worse.
      I finally went into a Thyroid storm as I put on so much water weight that I also experienced congestive heart failure as I ended up in a coma at Baylor all Saints in Fort Worth Texas.
      Finally I got a diagnosis of hypothyroidism and
      Eventually I started coming back.
      I never received the initial somatic testing, like blood work to rule out endocrine diseases especially Hypothyroidism that the DSM recquirs before a bipolar diagnosis can even be made.
      I’m angry As to why didn’t The Doctors missed this. Why didn’t They do blood work???
      I had and still have insurance.
      This ruined my marriage, my career but mostly My abilities to be a mommy to my small children so long back.
      Now my kids are grown and my husband passed away although We stayed married He and I never recovered from the trauma that All of Us endured .
      Now that I’m realizing this to be true I want off of these bipolar meds that I still take to this day along with My Levoxyl. I also have my thyroid levels checked every 3 months and have sense this date.
      I’ve raised suspicions about this over 5 years ago to My Psychiarist and even went to an endocrinologist
      To have Them collaborate together about this issue and They blew me off.
      Because I got so sick I applied for SSD and I got it as I had already paid enough in working as a nurse
      I should’ve been able to continue with my career as I’m willing to give up my SSD and to have my diagnosis of bipolar type 1 rapid cycling reversed to only Hypothyroidism.
      I take medicine for this and I have all documentation through out these years
      I’m going to attempt to come out of this foggy place I’m in and have been in by getting off these bipolar medicines with help from my Doctors as I’m so down about loosing so much time to this but as with any hardship if this Tragedy can help one person than it will make sense to me.
      Please get in touch with Me.

      1. I can relate with your story. My boys are 13 and 16. They have grown up seeing me exhausted all the time. I have spent many years laying on my bed…tired. If they wanted something they knew where to find me. I take Adderall just so I can make it to work. Then Xanax to help with my anxiety. I have not had much of a life for many years. Even though I have 90% of the symptoms for hypothyroid my TSH is always normal. So I get depression and anxiety meds for 2 symptoms but nothing for weight gain, hair falling out, no eyebrows, dry hair and the list goes on. So when your doctor doesn’t help you who will?

        1. You could have been me. My story is very similar. Numbers always “normal” because traditional doctors don’t test everything. Exhaustion. Hair falling out. Anxiety. Etc. find yourself a FUNCTIONAL MEDICINE doctor and get some real answers. Mine sent me to get an extensive workup. The test was called “Boston heart diagnostic” and has answered MANY questions for me. Please. I encourage you to do this. Traditional doctors are just not going to do what’s in your best interest.

        2. blank Donna M Whitwell says:

          Continuing reading and researching and Being Your own advocate as well learning through social media reputable sources and get to a integrated Doctor as soon as possible are My suggestions.

      2. blank Donna M Moore says:

        Update as I Went for More Testing To try to see if I have An Auto immune Hashimoto’s and I have My Blood result which state that I’m Normal so I’m like Okay as I take 100 Mcg levothyroxine along with a water pill etc. so I go back for a test for my Cortisol levels and those were slightly low but I was told that I just needed to stay on my Levothyroxine as I continued to talk to this Endocronologist She descided To try Me on Cytomel 5 mcg (Liothyronine ) and also lowered my Levothyroxine to 88mcg and since my original
        Post on hypothyroid mom I’ve not had to take my water pill every day and My Kidneys are starting to function, so My Questions are mounting and so is a lot of other Stuff.
        I’m literally fighting for My Life as I’m My Own advocate and this is all documented.
        18 teen years of chasing this cycle of a host of medicine and two meds T3-T4 Could have fixed My Brain and body ( extreme edema) .
        Why? I’m not at all sure as I know that I’m not alone in this Life and that More needs to be done to Help so Much so 🙏

    2. blank Donna M Moore says:

      Hello Please Know That Your not alone as I’ve found HOPE in all Of Everyone’s Stories and at the same time I find FEAR Too but We are All going to be Okay No Matter What as I’ve been battling this for sometime and I know that We are all Miracles

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