My Hashimoto's Story

I just got diagnosed yesterday and started medication this morning. THANK YOU for this video. I can not tell you how much this makes me feel better.

I fell into Hashimoto in 2017, like you, and I've met SIX doctors without finding an answer to my encreasing problems. After a year of struggles, I found this illness and asked for exams. And here I am, with a medicine, a scrumbled life and little more. This is our battle, we can do it! Thank you for sharing your experience!

I just found this. My cousin has this and hearing your story has given me a new understanding of how she is. This is also helping with a project I'm doing for my graphic design degree. We're supposed to come up with a health awareness ad campaign, and this is what I've chosen to do. I see the struggle my cousin and others who have it go through every day and it sucks, but she's a pretty strong person. To all who have it, stay strong and know that you got a support system from those who don't have it. 🙂♥

Thank you for this! I feel so alone as none of my friends or family have this issue and going to uni full time is hard sometimes. I’m 20 and got diagnosed in August and am currently still figuring it all out but this has been really helpful. Stay strong!

I was diagnosed almost 4 yrs ago with hashimotos. It took 1 yr 1/2 of going back and forth to many Dr's to get diagnosed . Just keep learning. I have educated myself. I have gone gluten, soy, whey & dairy free which has helped a lot. They keep telling me no meds because my levels are "normal".

Im with you...dr didnt find out..till my tsh was 150.. almost stopped me completely..so now im battling, going on...thank you for your story. Love to all of you guys🥰😇

I'm so happy with my new functional medicine doctors. They are so awesome. Does anyone else often feel run down and almost "flu like" sick? I will go from feeling great most of the day to all the sudden feeling sick and fatigued. Then back to feeling fine all in one day. It's annoying. I also get a lot of headaches and when I do I basically ache everywhere. I am improving though a lot after finding my new doctors.

My endocrinologist (not holistic), said food has no impact. 🤨 Thanks for sharing your story!!! I’ve had It since my mid 20’s and I’m 32 now, and It’s a lot of trial an error for me. Paleo style eating definitely has been the most helpful. And I totally get your brain going blank!! When my eating isn’t on point, I lose my train of thought a lot and it’s so weird and frustrating!!!! Hahaha but anyways...loved the video

Thank you for sharing your story. I am suspecting I have this condition. Just had blood work done today and nervously awaiting the results but I’ve had a lot of the symptoms you experienced.

I have had hashimoto's for 3 years now and I'm glad i'm not alone❤️

I've had hypotyroidism as a child. There were many times I was seen for constipation, frequent bloody nose, weight gain, sore throat etc... Doctors never diagnosed me despite so many blood tests. As I got older things got worse. I had panic attacks, heart palpitations, anxiety through the roof, chest pain, shortnes of breath and the list goes on. I felt like a walking dead corpse and I almost was...The worse part about it was that although I tried to eat right I was bullied in every single grade and it felt like it was out of my control. I have the worse depression and I remember as a child having insomnia not being able to sleep at all I would break night and try and get myself to sleep. This really does something to you its terrible. Now even though I am on pills and my blood test looks "fine" I still feel like craaaap. I have very bad fatigue and now also have anemia and a whole grocery lists of other things I never tested positive for. I am very weak and struggle to get up in the mornings just to use the bathroom i have to drag myself its so hard on me. Im only 30 and wonder how much more can i take? I just want to throw in the towel.

I have had this disease since I was 9, although no one believed I was sick until I was 13. I hadn’t grown in four years, I lost hair, was always tired, sick, and fatigued. I still have joint pain and overall fatigue, as well as brain fog and depression. About a year and a half ago, I was diagnosed with Gastroparesis (caused by Hashimotos), which basically means my stomach can’t digest most food. I’m doing so much better now, but it really affects so much of your life. Thank you for this video, I hope you’re doing well.

Thank you! I was diagnosed a few days ago with Hashimoto’s and I’ve been going through everything you’re talking about.

Love this video! I have Hashimotos - I've had it for years and years, but it's still a consistent journey. Loved watching your story - thank you for sharing! ❤️

Thank you for this video I just got diagnosed couple months ago😥 I'm hopeful that I can beat this because I believe in the greater power who created natural substance that can help heal our body! With lots of prayers and self-awareness and much education🤗 I know I can beat this and also stories like yours are so encouraging thanks again for sharing❤🙏🏼

So glad you made this video and I hope you keep making these because I also was just diagnosed with hashi and I have to make changes to my diet as well thank you

This was so helpful. I am under diagnostic for Hashimotos now, and I am 100% positive I have had it for many years. Tested tsh, anti-tpo, ft3+4 this week. In 2019 my anti tpo was 530. It explain the sudden pain in my hands and fingers, extreme fatigue, depressions, extreme muscle pain, forgetfulness, dry skin, crisp nails and hair. And hair that just won’t grow long ++++ Waiting for the results this week, and hopefully I will get levothyroxine 🙏🏻

Thank you for the video. Hashimoto's runs in my family. My mother and I have it; three of my female first cousins have it too. Diet plays a huge role indeed. I was able to reduce my TPO antibody count from 528 to 404 and TSH from 2.5 to 0.81 in 2 months by following a modified AIP diet (Wahls Protocol), intermittent fasting (14-16 hours) and by taking supplements (Vitamins D & C, NAC+Se+Mo, CINA 200, Coriander seed water and Milk Thistle). I don't know which of the supplements helped. But I lost 7 kgs in the process. My endocrinologist reduced my Thyroxine from 50 mcg to 37.5 mcg after seeing my test results. So, there is hope.

i’ve had hashimotos since 4th grade and it’s honestly sucked but having it for 5 years it’s honestly just gets better and i sometimes totally forget i have it. hope you see this and i love you so much!!💓💓

Everything is just SO familiar. Been watching a lot of these videos and I just relate SO much. It’s been over 4 years of trying to figure out what is the heck is going on with me. And now I’m almost certain I have this. Or at least SOME type of auto immune disease. Thank you 🙏