When
the Cystic Fibrosis Foundation was established in 1955, children with cystic
fibrosis (CF) rarely lived long enough to attend elementary school. Due in
large part to the CF Foundation's aggressive investments in innovative research
and comprehensive care, many people with the disease can now expect to live
into their 30s, 40s and beyond.
Karin was the Support Group leader in Edmonds, WA until she moved out of the country. She indicates the Association was very helpful when she was first diagnosed with endometriosis. At that time she bought one of our books and found it immensely valuable. She enjoyed the support group meetings, "It was so special to have a group of women who truly understood what I was going through and could empathize with my situation".
Karin was the Support Group leader in Edmonds, WA until she moved out of the country. She indicates the Association was very helpful when she was first diagnosed with endometriosis. At that time she bought one of our books and found it immensely valuable. She enjoyed the support group meetings, "It was so special to have a group of women who truly understood what I was going through and could empathize with my situation".
Largest, national, advocate for dying patients and their families. Dedicated to increasing awareness of, and access to, quality hospice care and palliative care.
When
the Cystic Fibrosis Foundation was established in 1955, children with cystic
fibrosis (CF) rarely lived long enough to attend elementary school. Due in
large part to the CF Foundation's aggressive investments in innovative research
and comprehensive care, many people with the disease can now expect to live
into their 30s, 40s and beyond.
