3 Tips for Eating With EDS & Co.
Today we will be addressing the challenges that hypermobile patients can face around food as part of our series on EDS & Co. As a
Today we will be addressing the challenges that hypermobile patients can face around food as part of our series on EDS & Co. As a
In my last blog, I shared about my journey this past year and one of the treatments that have helped me heal – ozone therapy.
Hi Friends in the Fight, Your support during the last few years has been essential to my journey towards feeling Mighty Well for myself. In
Friends in the Fight pictured above: @zebratissues, @bendy.bookworm, @classifiedanomoly If you’ve recently been diagnosed with Ehlers-Danlos Syndrome (EDS) or Hypermobility Spectrum Disorder (HSD), odds are
Any society, or really any group of people, will carry biases. We are taught – subconsciously much of the time – to make assumptions about
If you’ve recently been told that you need a feeding tube, you likely have many emotions and questions. Know that you are not alone and,
Just a couple of years ago, Justin Bieber shared that he was battling Lyme disease. It was rough, but he was able to take the
This week was the start of Disability Pride Month. We’ve loved seeing posts from our Friends in the Fight sharing their own stories of disability,
Featured above: Friends in the Fight celebrating Disability Pride — @survival_of_the_sickest, @maddiexgordon, @taylorthetransgineer, @kristendoornbos, @thedisabledhippie As June winds down, I often feel a twinge of