Research: Studying the impact of social support on the quality of life of spousal caregivers of patients with Multiple Sclerosis

Hello everybody — I was asked to supply the study showing below, for the Caregivers of those with MS. If you are reading this and you have MS, please ask a caregiver to complete the study. If on- the-other-hand, you are the caregiver, then we hope you will be pro-active and complete the information being asked. — Thank you,

Regards,

Stuart Schlossman

Stu’s Views & MS News

=============================

My name
is Camille Simonetti, and I am currently a doctoral student in the field of
counseling psychology at the State University of New York at Buffalo. I am
studying the impact of social support on the quality of life of spousal
caregivers of patients with Multiple Sclerosis.

 My hope is that my research
will result in an increase in programs dedicated to caregivers of people with
Multiple Sclerosis as well as other support resources for caregivers. I have
created a survey that takes 40 minutes to complete. 

The study has been approved for posting by health policy staff
of the National MS Society and is listed here –

http://www.nationalmssociety.org/research/researchers-need-you/surveys/index.aspx.

I have attached a
paragraph along with the link below. Any help would be much appreciated.

If you
are a caregiver who has a spouse with Multiple Sclerosis, you are invited to
participate in this research study in understanding the factors that contribute
to the quality of life of caregivers who have a family member with Multiple
Sclerosis. 

This study has been approved by the IRB (International Regulatory Board)

Please
click on the link below if you are interested in participating:
http://www.surveymonkey.com/s/K5TBHMN

Sincerely,
Camille Simonetti
Doctoral Student in Counseling Psychology
SUNY Buffalo

Visit our MS Learning Channel on YouTube: http://www.youtube.com/msviewsandnews