Could PD flare up be caused by dysautonomia?
Question for fellow sufferers of PD! I have never dealt with PD before, and have always had fairly smooth skin, however for the past two months, I have had the worst skin flare up ever, and I was completely stuck until I found this subreddit and connected the dots.
Ironically enough, I was also just diagnosed with POTS, though I’ve been feeling the symptoms for about six months now. Does anyone else have dysauto dysfunctions? If so, have you ever noticed a relationship between the two? Are there specific things you watch out for that trigger your PD?
Honestly, the POTS is making my life hell enough. I’ve had to cut back my work availability because I can’t be on my feet for very long. My job is very customer facing, so the days I am there, I have to wear makeup. I have a dermatologist appointment scheduled, but it’s a month out 🥲 Any advice is appreciated, I just want to feel pretty again.