IC Awareness Daily Fact #7 - The Impact of IC & Pelvic Pain on Families & Friends

IC Awareness Daily Fact #7 – The Impact of IC & Pelvic Pain on Families & Friends

IC affects not only the patient but also the extended family. Parents with IC worry about their ability to support their family. Children wonder why their parent cannot attend normal daily functions, like baseball games, and often mistakenly assume that a parent is dying. The ICN has written a children’s book “My Mom Has IC: A Painful Bladder Story” that can help! It’s ideal for children in elementary school!

Tragically, some family members and friends may not believe that IC is a real condition and/or that the patient needs support and encouragement. Research presented at AUA 2010 demonstrated that patients with a spouse who was not supportive had a poorer outcome. The ICN has some great videos that can help educate family members. Find them at: https://www.ic-network.com/videos/

How has your family been impacted by your struggles with pelvic pain? Share your story!

By Jill Osborne|2017-01-31T12:30:33-08:00September 7th, 2014|Awareness, Our Blog|Comments Off

About the Author: Jill Osborne

My Google Profile+ Jill Heidi Osborne is the president and founder of the Interstitial Cystitis Network, a health education company dedicated to interstitial cystitis, bladder pain syndrome and other pelvic pain disorders. As the editor and lead author of the ICN and the IC Optimist magazine, Jill is proud of the academic recognition that her website has achieved. The University of London rated the ICN as the top IC website for accuracy, credibility, readability and quality. (Int Urogynecol J - April 2013). Harvard Medical School rated both Medscape and the ICN as the top two websites dedicated to IC. (Urology - Sept 11). For many years, Jill served on the Congressionally Directed Medical Research Panel (US Army) where she collaborated with researchers to evaluate new IC research studies for possible funding. Jill has conducted and/or collaborates on a variety of IC research studies on new therapeutics, pain care, sexuality, the use of medical marijuana, menopause and the cost of treatments, shining a light on issues that influence patient quality of life. An IC support group leader and national spokesperson for the past 20 years, she has represented the IC community on radio, TV shows, at medical conferences. She has written hundreds of articles on IC and its related conditions. Jill has a Bachelors Degree in Pharmacology and a Masters in Psychology, Jill was named Presidential Management Intern (aka Fellowship) while in graduate school. (She was unable to earn her PhD due to the onset of her IC.) She spends the majority of her time providing WELLNESS COACHING for patients in need and developing new, internet based educational and support tools for IC patients, including new live IC Support Group Meetings via Youtube and the “Living with IC” video series. Jill was diagnosed with IC at the age of 32 but first showed symptoms at the age of 12.