HELP US GET THE WORD OUT ABOUT WORLD LYMPHEDEMA DAY ON MARCH 6th
BCLA is all of us that have chosen to be members and it serves our vision, mission and goals if everyone gets on board to help bring education and awareness about lymphedema anywhere that we can.
BCLA founding member, Lynn Holloway, has written a press release and encourages every member to use the sample provided as a template. This press release has portions of it that relate only to her personal story. So in those areas of the press release, delete her information and insert your own story to entice your local newspaper to have a write-up. Papers always prefer a local 'angle' to a story.
It would be useful to include a picture or two of yourself that shows your lymphedema as a picture is worth a thousand words. It is time for us to stop hiding and let the world know we're here. You never know who may be reading your story and may be touched to find help for themselves.
Please register your name so that we know how many of our members participated in this. Thank you for your consideration!
LAD Walk Press Release.doc