Has anyone noticed having dry eye, dry mouth and dry skin since being diagnosed with Parkinson’s? Just wondering as I never had this issue until my Parkinson’s diagnosis.
Dry mouth, dry eyes and dry skin - Cure Parkinson's
Dry mouth, dry eyes and dry skin
Yes I have dry mouth feels like sand papers at night
Prescription medicine cevimeline plus sugar-free lozenges for the dry mouth. Important to take measures to relieve it.
Definitely dry skin is new for me. As for dry eyes I’ve read that PD slows the number of times you blink causing dry eyes. I saw my ophthalmologist who put plugs in my eyes (painless) that help with the dryness. Completely made a big difference . No dry mouth.
Yes, dry eyes then skin then itchy flaky dry skin started for me about 2 years after PD diagnosis.It turns out to be caused by food allergies (never had any in my life before that.) Strongly suspect PD and food allergies are related somehow
Interesting. I may look into allergies myself. Thank you.
freefallmode,
One common denominator for food allergies and PD is dysbiosis of the gut microbiome. In PwP, correcting the dysbiosis can improve symptoms by over 50%. Correcting the dysbiosis in cases of allergies looks like it is likely to be helpful based only on animal studies, but it does resolve the issue in animals.
Art
Yes to all those particularly dry eyes for some time before being diagnosed i use Hico eye drops which help....then had a dreadful frozen shoulder for 18 months and eventualy after seeing 5 GPs a consultant diagnosed PD ....
I use Blink eyedrops once a day..no DX needed. I do think the meds have some diuretic effect and dry out nasal passages, skin, eyes...and are the major contributor to constipation. Drink lots of water and try to avoid other food/drink that is also diuretic.
Thanks for a tip. I will definitely get some auger free.
Hmmm...I now have dry mouth as well. I'm only on Rytary and Rasagiline. I noticed some of my pills had expiration date 10/21 which is NOW so perhaps that is the explanation. The dry mouth also makes me speak with a slur..my doctor friend was afraid I might have had a stroke cause it showed up after a nap initially and today. It seemed like it had gone away for a while. Appreciate any advice ...I notice it is in the Rytary side-effect list.
Thanks.