After the periodontist I just got worse and worse. But it was also up and down, so I kept waiting to see if I would get better. But I didn't. It got really bad. I was barely able to do anything. And everything I did was major stress. Finally, I went to my primary care physician. That was two days ago. I expected him to just try to pass me off to my lung doctor but he surprised me. He gave me an injection of a powerful antibiotic and another one of the anti-inflammatory. I'm also on oral anti-inflammatory and an antibiotic. And so now I just wait and see. I'll know in two weeks. I'm also supposed to follow up with him.
I'm so glad you sought medical care and that your doctor is following up with you in 2 weeks.
I am curious to know if you mentioned the periodontal care to your doctor as a possible inciting event?
I DON'T mean in terms of "post exertional malaise," but rather as the opportunity for an infection to find it's way into your body and lodge itself somewhere or disseminate into bacteremia.
For example, the connection between periodontal disease, dental work, and endocarditis is well-established. Some folks with underlying conditions take antibiotic before and after such procedures prophylactically.
In any case, it sounds like you are in good hands, just want to make sure your physician is aware of your trip to the periodontist in case it's relevant to your current state of health.
P.S. This thread is about you, not me, but I wanted to share that I also had a positive experience with my primary care physician just two days ago. I showed up at his office in person, so he could really "see" me and examine me. I let him know that 12 days ago, out of seemingly nowhere, my baseline level of symptoms and functioning had dropped to a new low that was frightening to me. I gave him my 3 top symptoms/concerns and I was surprised when he postulated that I either picked up a virus or possibly an occult infection of some sort. I have lab work to complete and a follow up appointment in a few weeks. I really appreciate that he took my concerns seriously and did not immediately assume it was "just" dysautonomia or "just" ME/CFS, etc.