A Thyroid Family

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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 upbeat, but don’t feel like you have to mask how you’re really 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.

Join The Thyroid Family online support group. Run by thyroid patients for thyroid patients. 

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

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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.

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