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This website should be considered general information only and should not be considered medical guidance or professional advice. Always direct any questions concerning your personal health to your doctor or another appropriate health care professional.

WOULD YOU LIKE TO HELP RESEARCH?

Do you hope to have doctors understand this disease better?

Please help by doing the things listed here, it would greatly help LHON PLUS 

JOIN NAMDC AND THE UMDF REGISTRY AND HELP RESEARCHERS LEARN  HOW  LHON PLUS AFFECTS YOU. 

THE MORE PATIENTS WHO PARTICIPATE, THE MORE DOCTORS WILL BE ABLE TO STUDY THIS DISEASE.  PLEASE TAKE THE TIME TO SIGN UP FOR BOTH OF THESE REGISTRIES, IT IS A VERY EFFICIENT WAY TO LEARN MORE ABOUT LHON PLUS PATIENTS.

JOIN OUR PATIENT DATABASE SO THAT WE CAN CONTACT YOU FOR IMPORTANT CONFERENCES, UPCOMING CLINICAL TRIALS AND ADVANCES.   HELP US TO CREATE A GLOBAL COMMUNITY

SET UP A FUNDRAISER LINKED TO THE UMDF "LHON PLUS PROJECT"  SO WE CAN HELP FUND RESEARCH FOR LHON PLUS (PLEASE CONTACT US FOR DETAILS)