June 3, 2010
I was diagnosed with LAM in May of 2010. It was a lonely road. My PCP read 2 pages from a website when LAM was suspected. About 2 weeks later, IT was the diagnosis. At that time I contacted the LAM Foundation and got a call back right away. My mind was eased quite a bit! They were encouraging and knowledgeable. It was suggested I connect other LAM women who further eased my mind. THIS IS SCARY, but with the support of the Foundation it's not so lonely.
I've personally experienced the results of this organization in...
support over the phone, thru email and mail.
How frequently have you been involved with the organization?
About every week
When was your last experience with this nonprofit?
MY ROLE:Client Served & Received support and information.