Mesothelioma Support Group Offers Hope and Encouragement
Request Mesothelioma Information
Terms & Conditions
I have read the legal disclaimer and agree that submitting this form does not create an attorney-client relationship. The Simmons firm lawyers are licensed in Illinois and a limited number of other jurisdictions. They and the Firm cannot file actions in all states without associating locally licensed attorneys and/or becoming admitted in that jurisdiction for a limited purpose. The only way to become a Simmons firm client is through a mutual agreement in a formal letter. I understand the Simmons firm must check for conflicts of interest before assisting me with my legal inquiry.
(or press ESC or click the overlay)
Description:
Since 1998, Shelly Kozicki has helped care for her husband Craig throughout his fight against peritoneal mesothelioma. She offers advice and comfort to others facing this type of mesothelioma and she also talks about the importance of a mesothelioma support group.
The Simmons Mesothelioma Foundation is a type of mesothelioma support group that offers support for families of those who are fighting peritoneal mesothelioma.
Rate, comment and share this mesothelioma support video on YouTube.
Topic:
Coping with Mesothelioma , Peritoneal Mesothelioma , Mesothelioma Applied Research Foundation
Click any of these mesothelioma & asbestos topics to see videos, read articles, and hear real life stories.
Category:
Featured:
Keywords:
Quickly find related asbestos & mesothelioma videos by selecting from the following keywords.
peritoneal mesothelioma , peritoneal mesothelioma treatment , mesothelioma treatment , malignant mesothelioma treatment , mesothelioma cancer treatment , asbestos cancer , asbestos related disease , mesothelioma diagnosis , mesothelioma prognosis , mesothelioma support , mesothelioma support group , mesothelioma victim
Length:
1:26
Views:
457
Video Transcript: Mesothelioma Support Group Offers Hope and Encouragement
So the Meso Foundation is curemeso.org. I would go there and get the information off of that website. There are volunteers there, which I happen to be one of them, who are a patient advocate. I talk to people. I don’t give medical advice, I am not a doctor. But I am listener, and ear. I am hope at the end of the line. I have lived it, I have been there. So, that is all I can offer you is an ear. I just wish there was someone like me out there nine years ago. Just to bounce something off of. Just to say what am I facing? What is ahead of me? What do I have to look forward to? What is it like? What dot he ports feel like? That would be my biggest words of advice, is to start by calling the meso foundation or getting on the website.
