I unfortunately write this issue in the midst of a particularly bad flare up. After hitting too many flare up triggers in one day at the weekend, I was left sofa-bound, crying and in a heap of a mess. When will I learn that I can't do absolutely everything?

I shared a photo depicting my struggle on Sunday morning, on both Facebook and Instagram and was truly touched by how many of you reached out. Some sent me well wishes for a speedy recovery, some shared that they knew all too well how bad the flare ups are and perhaps most surprisingly, some thanked me for sharing my own experiences of living with hypothyroidism and Hashimoto's so honestly.

I very aptly wrote a blog a few months ago (scheduled to go on my website soon) about how I worry that by sharing my own personal journey of living with a thyroid condition, it might make people think I'm not in a position to advocate for others. But as one person commented: “Thank you for being real. I become bored when I read articles from experts that look a picture of wonderful health and only talk about their past experience. But you show how hard it is for you too.”

I don’t sugarcoat living with the health conditions I have and I always promise to be authentic and honest. Although sometimes I second guess whether to post the bad parts of my health experience, I just want to show that I’m like every other thyroid patient; I have ups and downs in my health too. I don’t know many other thyroid advocates who share their own experiences so honestly and show the blips in their health as well as the successes. As well as us all aiming for optimal health, I want to also tell you that it's OK to have less than perfect health days. In fact, it's completely human.

So by meshing the knowledge I have gained through my own thyroid journey, with my own, personal experiences, I try to create something authentic and genuine with The Invisible Hypothyroidism. Informational posts mixed with personal blogs; a place that people know they are understood and made to realise that they are not alone in what they experience. And as a patient advocate, I'm not only responsible for equipping you with the tools and knowledge to get back to good health, but I'm also responsible for giving an honest and authentic experience of living with thyroid conditions.

Since day one of The Invisible Hypothyroidism, I have meshed together being a knowledgable advocate and someone still going through the journey, because it's ongoing. It's always ongoing.

Also, don't forget to enter my competition giveaway if you haven't already!

Thyroid love x

Rachel, The Invisible Hypothyroidism


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Stay in Touch!

As always, you can find my articles, blogs and work on TheInvisibleHypothyroidism.com but keeping in touch via my Facebook page, Instagram, Twitter, Pinterest and Google+ ensures you'll never miss any exciting news or crucial information on managing your hypothyroidism.

That’s all for this issue but look out for the next one in two weeks’ time. If there’s anything you think I should specifically mention, please let me know.

Please Note: None of the statements in this publication should be taken as an official endorsement of any particular product, including sponsored content. I strongly suggest consulting your doctor before making any changes to your lifestyle or health regime. The information included in this publication is not meant to substitute the clinical guidance provided by a healthcare professional.

This newsletter may also use affiliate links where I earn a small commission if you purchase through it. This does not change the way I work or the products I link to, and it doesn’t change your user experience.

Rachel, The Invisible Hypothyroidism