Suggest Best Treatment For Lewy Body Dementia
We retired to a small town in East XXXXXXX with little in the way of medical research facilities. Due to my wife's condition and need for her care -I am her principal caregiver- I am unable to travel to areas with such research resources (before moving here in 2004 I was a research librarian at the Library of Congress and had direct access to the National Library of Medicine).
My question: who is doing the most active work in LBD? What progress are they making? How best can I keep up with their work?
How might I best contact them?
Any leads will be appreciated.
See Lewy Body Dementia Association website.
Detailed Answer:
I am so very sorry that your wife is dealing with this disease. I have an aunt who has LBD as well so I have seen it's effects in someone I care much about.
I think your best bet for finding the information you are looking for is with the Lewy Body Dementia Association website:
http://www.lbda.org
On this site under "Research" you can find abstracts and information about clinical trials.
On their home page there is a list of conferences. I understand you probably cannot get away to go to these, but sometimes there are collections of papers that are presented at these that you might be able to get ahold of afterwards.
Various disease associations are good places to find what the current standard of care is and most current data.
I don't know if this applies with the LBD Association, but with some disease associations, one of the people who work there can suggest to you who the prominent doctors or researchers are for this particular disease. So you may want to call them to see: National Office (Atlanta, GA): 404.935.6444
I hope this information helps. Best wishes to you and to your wife.