Connect with others who understand.

  • Learn from expert-reviewed resources
  • Real advice from people who’ve been there
  • People who understand what you’re going through
Sign Up Log In
Powered By
Real members of MyParkinsonsTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.
May 23
 · 
Reactions

Answer Summary

Members responded to a question about eye symptoms with Parkinson's by sharing a wide range of experiences including dry eyes, double vision,... Read more

Members responded to a question about eye symptoms with Parkinson's by sharing a wide range of experiences including dry eyes, double vision, blurry vision, hallucinations, loss of depth perception, glaucoma, and macular degeneration. Several members offered practical strategies such as using prism lenses, prescription eye drops made from blood serum, cataract surgery, and using a phone camera to magnify small print. A recurring theme was the importance of seeing an eye specialist every six months and always informing doctors about a Parkinson's diagnosis, since some eye issues may be related to the disease while others may not.

A MyParkinsonsTeam Member

I have had Parkinson's 7 years now and my eye doctor sees me every six months instead of every year. He is watching both my diabetes and Parkinson's and every visit has series of tests to see what the change is. In the near future he has advised special eye drops and perhaps visits every 4 months. His first suggestion was bifocal eye glasses as the eyes tire during the day.
My vision has improved but there is a slow decrease everyday which he believes is due to stress. He also agrees on the importance of midday nap. Not laying in bed and reading but sleeping. It gives the body a chance to rebuild the needed strength.

June 28
A MyParkinsonsTeam Member

I've had dbl vision, unable to see anything up close at all, dryness and blurry vision. I went to an opthamologist and learned I had cataracts. When removed, lenses were put in my eyes to correct distance and close up. I couldn't believe how brilliant colors were and could see 20/20. I hope everyone has been checked for cataracts! Still dry at times causing blurs.

May 30
A MyParkinsonsTeam Member

Hi @A MyParkinsonsTeam Member I have never heard that before. Thanks for sharing this!

May 28
A MyParkinsonsTeam Member

I used to see my eye doctor once a year now with Parkinson's I do it every 6 months. He has helped with many various recommendations including eye drops.

June 26
A MyParkinsonsTeam Member

That’s what I do with the small print. My phone is getting a workout!

June 5

Related Questions

View All
A MyParkinsonsTeam Member asked a question 💭
Olive Branch, MS