My husband suffers terribly with dry eyes. He uses Hylo Forte and Poly Visc which help, but at the end of the day his eyes are very sore. Our Eye Specialist is advertising a new treatment (at least for the east coast of Australia) called Lipiflow. I was wondering if anyone has tried this and has it been successful? It costs $600 with no guarantees and I am not able to claim it through my private health insurance., so I would like to know if it helps for PSP.
Many thanks. I have found this site to be an amazing help as I don’t know of anyone in our area with PSP. We spend quite a bit of time at ED with Johns numerous falls and we haven’t discovered any doctors who have ever heard of this disease. We feel very alone.