So todau was the first time that I actually felt heard by a doctor. I went to a specialist for EDS and she totally listened to me! One of the biggest struggles with an invisible illness is feeling ignored by everyone because they just don't understand what pain I'm in as they can't see it. She diagnosed me with hypermobile EDS and said she thinks she can help the crippling pain I've been in. I haven't been able to do any of my daily activities because of the constant pain. She also prescribed me a wheelchair to help me move around better. I'm so thankful. How is everyone else's treatment going???