Hello all - 🤗

Thank you for taking the time to read/follow my story. I did meet with a Rheumatologist back in May about my test results. She said that because I didn’t have many other physical symptoms commonly associated with autoimmune disease (joint pain, hair loss, etc.), that I didn’t necessarily have an autoimmune condition and as a result, she couldn’t diagnose me with anything. She said her approach going forward was a “wait and see” method and that if I developed new symptoms that I could contact the clinic as an existing patient to be seen quickly. So regarding test results, still a mystery. 🤔 In regard to my dry eyes, I was diagnosed with Ocular Rosacea by an Opthamologist and did a six month course of Doxycycline. It improved my symptoms somewhat but I still struggle with dry eyes and mouth, especially at night. I know this part is anecdotal, but I am also getting a bunch of dental work done (one a broken root) that I’ve needed for a while, and sometimes I wonder if there is any link between the inflammation in my eyes and my teeth. That’s pure speculation at this point but I’ve been to countless doctors appointments for this and haven’t had any solid answers as to why this happened. It’s hard not to speculate. From a community standpoint, I appreciate you all in your separate battles. I send you hugs (if you like hugs), and words of encouragement. You are not alone!