Retinitis Pigmentosa and the Usher Syndrome

I was unofficially diagnosed with RP about 7 years ago but my central vision has been minimally affected during that time.  Recently I went to an RP specialist and went thru all the testing but I decided I did not want to return to him since I did not like his holier than thou attitude.  Are there any research studies on RP being cone?  Where can i find a list of RP specialists in the Houston area.  I know what the other mean by floaters, or flashes of color I really think it has to do with the elecromagnetic pulse that the retina cannot disperse.  Any other RP know what i mean?

[Michael J Kutryb, MD]

The foundation fighting blindness is very active in your area of interest.  Web site is www.blindness.org (hate that name.)  RPBUSA.org is another organization (research to prevent blindness) that you should look into.  There are thousands of dedicated scientists working diligently in the area of RP so stay tuned in.  God Bless You.  

MJK MD