A Thyroid Family

Click here to listen to a reading of this blog:


Exciting news, my book is finally here! New to learning about your thyroid health? Learn why it's important to be your own health advocate in my book now. Available on Amazon

I don’t want anyone to feel like they have to walk on eggshells around here.

No fake smiles or pretending. Sure, try to be positive, but don’t feel like you have to mask how you’re feeling. You don’t have to share every detail with us, but if it helps you, please do. If your day sucks, we want to hear why and all about what happened, so we can try to help you or at least share the burden. Share when you’re happy, sad, frustrated and angry – feel safe here to be in your own skin. Let us unite and support each other. Let’s cry together, but also celebrate success together. We’ll help lift each other up to better days and be there on the not-so-good days.

We are a thyroid family.

This post may contain affiliate links, to find out more information, please read my disclosure statement.
If you found this article beneficial, please take a moment to share it so we can help others get better with hypothyroidism and Hashimoto's, whilst also raising awareness. "Be Your Own Thyroid Advocate."

Written by Rachel, The Invisible Hypothyroidism

Newsletter
Sign up to The Invisible Hypothyroidism's newsletter

You'll get an easy to digest, relevant round up of thyroid news, advice and support to get you feeling better, once every two weeks.

Don’t stay feeling rubbish. Get better.
Social
Get real, helpful advice directly from another thyroid patient. Me!

Give my Facebook page a like, follow me on Instagram, Twitter, Pinterest.

Community
Join My Facebook Support Group for patients

Join My Facebook Support Group for patients Thyroid Family: Hypothyroidism Advice & Support Group


2 thoughts on “A Thyroid Family

  1. I am in the very early stages of even getting a diagnosis. This has been going on for several months and most recently the bone chilling chills began and last for awhile along with the tingling of hands and feet. Is there a mineral or a food group that would help with this? Or will it be a medication? Also, how does one discover doctors who are functioning docs?

    Thanks in advance.

    1. Hi Debra, you can google ‘Functional Doctors’ followed by your city or town to locate some nearest to you, and then email them for more information. Some may also offer long distance options such as using Skype or telephone.

Leave a Reply

Your email address will not be published. Required fields are marked *

This site uses Akismet to reduce spam. Learn how your comment data is processed.