FacebookTwitterLinkedinYoutube
Short Bowel Foundation Short Bowel Foundation Short Bowel Foundation Short Bowel Foundation
  • Home
  • About SBSF
    • SBSF Privacy Policy
    • Our Mission, Vision, & Values
    • SBSF Staff & Volunteers
      • Andrew Jablonski
      • Candy Wolfe-Johnson
      • Stephanie Dolak
      • Pamela Mason
    • Become a Volunteer with SBSF
    • Board of Directors
  • Educational Hub
    • SBS Info
      • About Short Bowel Syndrome
      • Intestinal & Multivesicular Transplants
      • GATTEX®(Teduglutide)
      • Parenteral Nutrition
      • Nutrition & Dietary
      • Digestive System
      • Symptoms
      • Causes & Conditions
      • Management of Care
        • Navigating Short Bowel Syndrome
        • Parenteral Nutrition
        • Mental Health & Short Bowel Syndrome
        • Laboratory and Imaging
        • Common Medications & Uses
      • Complications of Short Bowel
    • Infographic Booklets
    • Beyond The Gut: Living with SBS & IF
    • SBSF Cares
    • G.U.T. Program
    • GATTEX®
  • Finding Care
    • Intestinal Rehabilitation
    • Centers of Excellence
    • Directory of Infusion Pharmacies
  • For Clinicians
    • Clinical Inquiries
  • Donate
    • Corporate Sponsors
    • Partners
  • SBS Support
    • SBSF Support Groups
    • Our Stories – Our Strength
    • Intestinal Failure Support
    • Transplant Support
    • Sepsis Support Groups
    • SSDI
    • Videos
  • Research
  • Contact Us
    • Register
    • FAQ

7 Life Lessons I Learned From Parenting My Toddler With Special Needs

Home/Featured Stories, News/7 Life Lessons I Learned From Parenting My Toddler With Special Needs

7 Life Lessons I Learned From Parenting My Toddler With Special Needs

Authored by: Brianne Coffey Contributor for The Mighty
I found the light when I recognized the important life lessons my 2-year-old with short gut syndrome (also called short bowel syndrome) was trying to teach me. There are seven lessons I carry with me that I’d like to share with you:
Read more on Brianne’s Journey on The Mighty!
Brianne Coffey is a stay-at-home mom of a very energetic and charming little boy, Liam, who was born with gastroschisis and now has short gut syndrome (also called short bowel syndrome). With her partner, Mark, they’re committed to creating awareness of rare diseases that affect children.
Ajablonski23 2016-11-15T09:45:57-06:00

Share This Story, Choose Your Platform!

FacebookTwitterLinkedinRedditTumblrGoogle+PinterestEmail

Categories

  • Chronic Illness (15)
  • Disability (12)
  • Featured Stories (59)
  • Fundraisers (3)
  • Gutsy Tales (12)
  • Mental Illness (5)
  • News (54)
  • Parenting Articles (9)
  • Rare Disease (8)
  • SBS Foundation Notification (5)
  • SBSF Member's Authored Articles (1)
  • Uncategorized (14)

Online Support Groups

Short Gut Syndrome Parents Support Group: On Facebook

Short Gut Syndrome Parents Support Group

Short Bowel Syndrome Foundation, Inc: On Facebook

Short Bowel Syndrome Adult Support Group: On Facebook

Short Bowel Support (Shire Website)

Contact Us

Andrew Jablonski
Executive Director
3440 L Street
Lincoln, NE 68510

Phone Contact (402) 429-8119
Email Contact: ajablonski@shortbowelfoundation.org

Featured Links

  • Understanding Short Bowel Syndrome
  • Donate
  • Centers of Excellence

Review us on YELP!

Copyright 2024 | Short Bowel Syndrome Foundation, Inc.
FacebookTwitterLinkedinYoutube