My Hashie’s Journey

back in October, I went to see the doctor about my hair falling out. Turns out that there was a lot more going on that being folically challenged. The more I chatted with my Doc, Doc M, the more it became apparent something serious was going on:

  • Skin so dry it was cracked and peeling off  
  • I put on 9kg in 6 months after maintaining a stable weight for 5 years
  • A complete loss of control of my brain and speaking mixed up words (nope, not learning a new language)
  • Deep gravelly voice that had gone from Taylor Swift to Aretha Franklin
  • Exhaustion and insomnia
  • Winter was hell, I froze pretty most most of the season – not a usual occurance in sunny Sydney
  • Pain in my shoulder joints that made boxing impossible


So off for. Whole round of blood tests, and I do mean rounds – 4 in total. Doc M also could feel a small lump in my throat. It was a wait and a half for the results but the blood tests painted a picture that maybe all to familiar for some people. My TSH (thyroid simulation hormone) was in the upper range of normal, I was ferric aneamic and my thyroid antibodies were 15 times, yes 15 times the upper normal limits. Doc M’s diagnose was Hashimotos Disease, pending ultrasound confirmation.

And this is where my Hashie’s journey started. It’s a common disease, 1 in 10 women will be diagnosed with Hashimotos, and 1 in 6 women overall will will experience hypothyroidism in their lifetime. So my blog is changing direction, at least for now. Writing is an outlet for me, and I just want to tell my Hashimotos tale. I don’t claim to be an expert, I’m certainly no WebMD on the subject, but I am a suffer imparting what little wisdom I have.

I’d love to hear from other people with Hashie’s, share your story, your advice, you shoulder to someone else who’s just begining their own Hasie’s Journey.