My Immune System Hates Me!

I was recently diagnosed with RA August of 2020, almost the exact same time as Chelsey! I have only listened to two full episodes of the podcast and am so thankful to have found it, and super interested in hearing more. Just to hear someone else talk about the things their going through, all the same “crazy” problems, the mysterious aches and pains, very emotionally exhausting. My issues (for lack of a better term) are more like what her mom is going through, for many years. In the short time I’ve listened I don’t feel as alone. Thank you thank you so very much for making this podcast and helping to encourage others to get tested. I haven’t had any success with any treatments I’ve tried in the last year but I will try to stay strong and keep trying. 🥰

I have plaque psoriasis which is unsightly but controllable but having pustular psoriasis…WOW! What both of you had to go through get the proper diagnosises…unreal but not uncommon.

First of all, Chelsey’s open heart and passion to connect with others is the most beautiful and important key to keeping this podcast honest and grounded. I love the guests she brings on. As an autoimmune disease fighter, to be able to listen to the stories of others and know that I’m not alone is most essential. I am constantly inspired by others and always feel comforted.

Thank you for being an advocate for us all and for sharing across the spectrum of autoimmune diseases. Thank you to everyone willing to share their stories. 💜💜💜You are all strong, fierce, and brave.