RESOURCES FOR CAREGIVERS
JOIN OUR NEWSLETTER
Receive custom tools to help you manage your condition and get the latest in bladder and bowel health from NAFC!
RESOURCE CENTER FOR CAREGIVERS
Whether you are a professional caregiver or a family caregiver, taking care of someone with incontinence is a demanding job. From the physical tasks to the psychological nurturing, you will be pushed and pulled in a lot of different directions. Yet, your service is invaluable. Taking care of another person shows strength, compassion, and tremendous amounts of character. At the National Association for Continence, we recognize that you are presented with tests each day. This section has been created to provide information about products that caregivers might find helpful in the care of a loved one with bladder or bowel control problems.
We’ve assembled a number of articles and resources to help guide the home caregiver. Whether you’ve just begun caring for a loved one with incontinence or have been at it for a while now, these articles can help dispel some of the myths of incontinence and also provide you with some new tips. Click on any of the boxes below for more information, and don’t forget to check out our blog’s articles on caregiving – click here to search our entire blog for even more helpful information.
RELATED ARTICLES

Kara’s Story: Why I Support Organizations Like NAFC
Having a support system like NAFC to help deal with the emotional and physical setbacks of incontinence makes a huge difference. Read Kara’s Story.

15 Mental Health Tips For People With IBD
If you suffer from Inflammatory Bowel Disease (IBD), you know that it can do a number not only on your physical well-being but also your

NAFC And NorthShore Partner To End Stigma Associated with Incontinence
NAFC is proud to name PMF, a premier medical supply company for the Intellectually/Developmentally Disabled and Aging communities, a 2022 Trusted Partner.

Voices Of Incontinence Personal Story: Incontinence Can Be An Isolating Condition – But Only If You Allow It To Be.
This story is a part of the National Association For Continence’s “Voices Of Incontinence” campaign, which shows, in patient’s own words, what it’s like to