Welcome to Living with JHS; a blog about chronic illness, lifestyle and wellbeing.
“Sharing my story, to support others and raise awareness”
If I can help just one person living with this condition, or one similar, then I have accomplished what I set out to do. Most importantly, I want you to know that YOU ARE NOT ALONE.
Through my weekly posts, I share thoughts and ideas, tips and tricks while discussing what it’s like to live with a chronic illness. Although I suffer from JHS, my blog can apply to those with other illnesses and conditions too. We’re all in this together, and together we can get through this!
My name is Abbie and I possess an “invisible” illness, known as JHS (Joint Hypermobility Syndrome) and it is this that has inspired me to create this blog. When I was first diagnosed back in February 2013, there wasn’t much information available on JHS (or similar illnesses)!, and, although there’s more now, there still isn’t much, especially like this! By sharing my story, I believe that it will help others living with these conditions to understand what’s going on, gain more information and, also, learn more about what it’s like to live with an invisible illness.
At the bottom of this page, and along the side, there is an option to follow my blog. This allows you to get regular updates and ensure you never miss a post! You can also find my social networks there too, or on the contact tab on the menu above. If you would like to contact me, whether it be to chat or ask questions, you’re very welcome!
I guess that’s all for now, time to go and explore! I hope you enjoy, my lovelies!
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