United Ostomy Associations of America
  • HOME
  • OSTOMY INFORMATION
    • Ostomy Information
      • What Is An Ostomy?
      • Living with an Ostomy: FAQs
      • Diet + Nutrition
      • Ostomy Skin Care
      • Sexuality
      • Bill Of Rights
      • New Ostomy Patient Guide
    • My Ostomy
      • Ileostomy
      • Colostomy
      • Urostomy
      • J-Pouch
      • Continent Diversions + Other Ostomy Types
      • Temporary Ostomy
      • Short Bowel Syndrome
      • Español
    • Children to Young Adults with Ostomies
      • Infant/Toddler (0-3 Years)
      • Preschool (3-5 Years)
      • Elementary School (6-9 Years)
      • Pre-Adolescent (10-13 Years)
      • Adolescent (14-18 Years)
      • Young Adult (18-25 Years)
      • Parents & Clinicians Resources
      • Know Your Rights
      • What To Expect After Surgery
      • Odor Control
      • Fast Facts
      • Ostomy Game
    • Crohn’s Disease & Ulcerative Colitis Information
      • Defining, Caring and Treating
      • Preparing for Ostomy Surgery
      • Common Issues, Managing Diet, Mental Health
      • Intimacy, Fertility and Pregnancy
      • Resources
    • General Information
      • UOAA Ostomy Marketplace
      • Product + Supply Information
      • UOAA Resources Library
      • Resources for Nurses/Home Health
      • Travel Tips + TSA
      • Donate Your Ostomy Supplies
      • Emergency Supplies
      • Related Links
      • UOAA Virtual Ostomy Clinic
      • Outpatient Ostomy Services Locator
  • SUPPORT
      • discussion
        Ostomy 101:
        Easily communicate “What is an ostomy?" with our infographic.

        Read More

    • Find Support
      • Support Group Finder
      • Support Group Websites
      • UOAA Virtual Ostomy Clinic
      • Online Peer and Ostomy Support Programs
      • Outpatient Ostomy Services Locator
      • Find a Mental Health Provider
      • Find an Ostomy Nurse
      • Online Discussion Board
      • Apps for Ostomates
      • Emotional Concerns
    • Connect With Us
      • Start/Affiliate Your Group With UOAA
      • Resources For ASGs
      • National Membership
      • Sign Up for Our E-Newsletter
    • Participate
      • Attend An Event
      • Become An Advocate
      • Join Us for a Conference
      • Make A Donation
      • Become a Member of The Phoenix Society
      • Donate Your Ostomy Supplies
      • Take A Survey
  • ADVOCACY
      • portal
        Roadmap to Establishing Outpatient Ostomy Services
        Documents that are available as PDFs to download and print.

        Read More

    • About
      • Advocacy Program
      • Advocacy Priorities
      • 10 Questions to Help You Speak Up and Self-Advocate
    • Get Involved
      • Understanding the Medicare Competitive Bidding Program 2025 Ruling
      • Take Action
      • Join Advocacy Network
      • How to Be An Ostomy Champion
      • Ostomy Awareness Day
      • Roadmap to Establishing Outpatient Ostomy Services
    • Tools and Resources Library
      • Non-Medical Switching Resources
      • Ostomy and Continent Diversion Patient Bill of Rights
      • Restroom Access Self-Advocacy Tools
      • Travel Tips + TSA Communication Card
      • Swimming with an Ostomy
      • Mythbusters Infographic
      • Workplace Resources
      • Aging with an Ostomy or CD
    • Take Control of your Healthcare
      • UOAA Virtual Ostomy Clinic
      • Know Your Ostomy Checklist
      • Know Your Ostomy Supplies Checklist
      • Physician Visit Checklist
      • Know Your Health Care Insurance
      • Know Your Pouching System
      • Know What’s in Your Medical Record
  • WHO WE ARE
      • Have a Question for Us?
        UOAA is a 501(c)(3) nonprofit organization that supports, empowers, and advocates for people who have had or who will have ostomy or continent diversion surgery.

        Contact Us

    • About Us
      • Our Mission + History
      • Our Leaders
      • National Sponsors + Partners
      • National Membership
      • Contact Us
    • How We Help
      • Advocacy
      • Awareness
      • Support
      • National Conference
      • Ostomy Nurse Scholarship
    • Get Involved
      • Volunteer
      • Become A Leader
      • Join A Committee
      • Career Opportunities
      • Sign Up for Our E-Newsletter
  • LATEST
  • EVENTS
    • Ostomy Awareness Day
    • Run For Resilience 5K
    • Ostomy Academy
    • Educational Webinars
    • 2025 National Conference
    • Calendar
  • GIVE NOW
  • SEARCH
  • Menu Menu

Sixty Years with an Ostomy

IBD, Ileostomy, Patient Stories, Personal, Travel

By Ed Pfueller, UOAA Communications Manager

Beverly Dabliz is ready to celebrate a monumental 60th anniversary but even her closest friends do not all know what it is for. Recently she decided it was finally time to share the news. “Just last week I told a close friend I’ve known for 66 years – I’m the godmother of her twins, but even they did not know I have an ostomy. It was just not something people talked about,” Dabliz says. She adds “People are surprised to learn the news, but it does not matter to them one bit.”

Dabliz had ileostomy surgery in 1962 at Ferguson Hospital in Grand Rapids, Michigan. Ferguson was one of the first clinics in the world to perform such surgeries. By the time she turned twenty she was suffering from ulcerative colitis and by twenty-four ran out of treatment options. “After sixty years I have never regretted it, it has allowed me to live a great life,” Dabliz says.

Almost no one with the exception of her doctor understood the procedure and how to care for it. She knew she was on her own on how to carry on and reach her full potential.
Even if you have a great support network Dabliz recommends, “You have to own it and take care of it.” Ostomy supplies of that time bear little resemblance to the lightweight, contoured appliances of today. “I wore a heavy two-piece rubber appliance held on with an ostomy glue,” she recalls. It was not until the 70s that pouching systems began to evolve into something similar to the one and two-piece systems commonly used today.

“It was just not something people talked about,”

Over the years Dabliz has helped other ostomates in need through the Detroit Metro Ostomy Support Group. While doing hospital visits she would always appear in fitted clothes and enjoyed how grateful the patients were to hear from someone else living with an ostomy. She is happy about the recent return of in-person support group meetings. At meetings, Dabliz is sometimes surprised by some of the concerns new ostomates have regarding things like food, “I just tell them to be sure you chew your food very well, in the beginning, I tried it all without being scared but I’m still often the last one eating. I chew my food so well I’ve worn down teeth.”

Beverly Dabliz, right, works during a mission trip to Costa Rica with her Michigan church group.

Dabliz worked in the accounting department of a computer company in Detroit and Plymouth, Michigan for 45 years before retiring. Her boss was aware of her ostomy and supportive. “I never missed a day of work because of the ostomy,” she says.

Six years ago Dabliz had a fight with kidney cancer and three years ago a shoulder replacement surgery. But she has otherwise been fortunate to live a healthy life since the ostomy surgery six decades ago. She still makes it a point to get out of the house almost every day. “I have always been very active and really have not had any ostomy issues,” Dabliz says. In her eighties now, she still enjoys golfing and was in a bowling league for many years.

Beverly Dabliz working as a volunteer at the Eagle River Methodist Camp in Juneau, Alaska.

Dabliz can also still be found tending to her yard and is reluctant to give up shoveling the Michigan snow – though neighbors have started beating her to it. With the exception of some subtle changes, her ostomy regiment remains routine. She consistently uses the same products.

Dabliz is an active member of her church and has gone on many mission trips over the years in countries such as Jamaica and Costa Rica. “I’ve had to use outhouses in Alaska and done mission work after Hurricane Katrina,” Dabliz says. Even in these tight living quarters, nobody knew she had an ostomy.

An ostomy has never gotten in the way of her passion for traveling and cruising the world with her older sister. The pair have even circumnavigated Australia and New Zealand. Her advice; “I take extra supplies and always bring some on carry-on and have never had any trouble flying. Just do it. Go swimming, do whatever you want to do,” she says.

In celebration of her 60th Stomaversary and 85th Birthday, Dabliz is hoping to take a Holland America cruise around Iceland with her sister. Her minister and family have known of her ostomy but she hopes to tell more friends about what this landmark occasion means to her. Dabliz is confident they will take the news in stride as they help her celebrate a life that could have been cut way too short if not for that long ago ostomy surgery.

Related

March 10, 2022
Tags: active life, bowling, cruise, cruising, golf, ileostomy, long life with an ostomy, longtime ostomy, ostomy, ostomy bag, ostomy history, ostomy pouch, retirement, stoma, stomaversary, Travel, veteran ostomate, work
Share this entry
  • Share on Facebook
  • Share on X
  • Share on WhatsApp
  • Share on Pinterest
  • Share on LinkedIn
  • Share on Tumblr
  • Share on Vk
  • Share on Reddit
  • Share by Mail
https://www.ostomy.org/wp-content/uploads/2022/03/Dabliz-Costa-Rica-2005-2.jpg 530 864 Contributor https://www.ostomy.org/wp-content/uploads/2017/02/UOAAlogofinal2.png Contributor2022-03-10 14:01:242022-03-11 15:19:00Sixty Years with an Ostomy
You might also like
Allison Rosen’s Story: Me, Myself and Fill
Ostomy Output Challenges
stoma, ostomy, stoma photo, colostomy, ileostomy Know Your Ostomy
Ashley and Mariah’s Story: A Young Daughter Inspires her Mom to Break Down Walls When Advocating for Short Bowel Syndrome Care
6 Ways You (Yes, You) Can Make a Difference on Ostomy Awareness Day
Traveling with a service dog Traveling With Your Service Animal
13 replies
  1. Nancy Oleksy
    Nancy Oleksy says:
    April 5, 2022 at 5:47 pm

    I too am a 60th anniversary (stomaversary). I had mine when I was 2 years old. I agree most people don’t know I even have one. I have just lived with it all my life and never even think about it. Glad to see I am not alone. I have a Urostomy by the way. For the younger people or anyone just getting an ostomy you can live a normal life.

  2. John vasu
    John vasu says:
    April 5, 2022 at 6:07 pm

    I have had my colostomy for 70 years. Mine was caused by a birth defect. I have a temporary permanent colostomy. I was teased all the way through school. I am now on the Board of Directors of the Ostomy Association of Metro Denver. I am Vice President. I want to start a support group for children and their parents. Contact me if you want to. I would love to talk to anyone who is having problems or just want to talk. Thank you

    • Deepa Chandhrasekhar
      Deepa Chandhrasekhar says:
      May 28, 2022 at 10:59 am

      Hello,

      My name is Deepa Chandhrasekhar, and I am a fourth-year medical student at Midwestern University in Arizona. I am working with Dr. Michael McGee, a colorectal surgeon at Northwestern University to write a piece on patient perspective on life with a stoma. We are looking for any individuals who are willing to submit a personal letter on their lived experience with an ostomy for publication in the Seminars in Colon and Rectal Surgery. The hope is to bring more awareness to patients who are considering a stoma and dispel rumors and myths about living with one.

      If you are willing to contribute, that would be great! Feel free to email me at dsekhar108@gmail.com for more information.

      Thanks so much for your consideration!

      Sincerely,
      Deepa Chandhrasekhar, MS-IV
      dsekhar108@gmail.com

    • wesley griffith
      wesley griffith says:
      August 19, 2024 at 6:13 am

      Is this offer still available?

  3. Sandy Kay
    Sandy Kay says:
    April 19, 2022 at 3:16 pm

    I would like to hear from Beverly Dabliz. I am a 50 yr. ileostomate. Would love to chat.
    Sandy

  4. Ralph Stasiak
    Ralph Stasiak says:
    November 29, 2022 at 1:59 pm

    I have had my Ostomy, since I was 19 years old and just celebrated 52th anniversary

    I contacted colitis when I was 13 and suffered with it all through High School, which had then gone to ulcerative colitis, and my only choice to live was to have my ileostomy

    Not many people know that I have one other then my family, but as time goes on I’m starting to talk more about it

    Feel free to contact me at rastasiak65@gmail.com

  5. Sarah Bates
    Sarah Bates says:
    June 24, 2023 at 2:05 pm

    I had my ileostomy in 1974 when I was 6.
    That’s 50 years next year?
    Mine was due to ulcerative colitis at the age of 6. My brother had his a year later when he was 5.
    We might be some of the youngest people with long ileostomy, I don know, but great to learn about others with long stomas.

  6. Susan Strauss
    Susan Strauss says:
    September 14, 2023 at 3:48 am

    My mom (90 years old) from South Africa must be one of the oldest people with a permanent stoma bag. It is 56,5 years now that she is wearing it and still handles it on her own

    • Gary
      Gary says:
      August 11, 2025 at 9:32 pm

      I have had a urostomy since I was born 64 years ago. I have lived trying and doing anything I ever wanted and it has not stopped me doing anything, I worked mainly in the building trade but I had to stop when I got to about 40 years old not because of my stoma but I had to have a kidney removed and shortly after trouble stated with the remaining one and this as caused that to be damaged and I suffer with chronic infections . I have lost count how many operations I’ve had through my life but I can honestly say having my stoma as never stopped me trying or doing anything any normal person would

  7. Ashley
    Ashley says:
    September 28, 2023 at 9:57 am

    Dear Susan,
    Thank you for offering this about your mom.
    So great to know she is well and able to manage herself.

    I had to have an emergency surgery end ileostomy last year at 58 that saved my life.
    I’m so grateful for all the comments left today and the story of Beverly Dabliz.
    You all have really eased my thoughts of worrying about age.

    Very grateful.
    Ashley

  8. Mary E Bolton
    Mary E Bolton says:
    April 18, 2025 at 12:17 pm

    I live in FL. Born in PA

    Had ulcerative colitis 2013, had a j-pouch done
    That did not work
    This was done at Shane’s In Gainesville

    I’m having some bleeding Going on

    • Beverly Dabliz
      Beverly Dabliz says:
      May 6, 2025 at 8:07 pm

      Hi Mary E Bolton,
      Sorry, you are having trouble. I am not sure how well people do with j-pouch’s. My traditional ileostomy works fine. I have had no issues for almost 63 years. If you read the article, you can see I have lead a normal life. Sorry, I do not understand bleeding. I am now 87 and try to keep busy everyday. Do you have an ostomy organization near you, sponsored by the United Ostomy Association. They are a group of experienced ostomy folks. Best Wishes

  9. Freya Diamond
    Freya Diamond says:
    May 14, 2025 at 4:45 pm

    I have had my ileostomy since I was 27. I am now 80 and have been leading an energetic life all these years. I taught aerobics for about 15 years. Played tennis on traveling teams. Then I became a race walker and competed and medaled in my state. I have always walked and hiked. Now I’ve been doing yogalates twice a week and walk 3 miles the other 5 days. I hope to continue to be active. I am also a book artist and have made at least 800 books about my dreams. Am I bragging too much?

Comments are closed.

Our Categories

Advocacy (78) Caregivers (18) Colorectal Cancer (19) Colostomy (138) Continent Diversions (8) Digital Sponsor (77) Disaster Preparation (4) Emotional Health (60) Events (32) Exercise/Sports (47) Fashion/Clothing (11) Healthcare (21) IBD (52) Ileostomy (181) J-Pouch (7) jejunostomy (7) Membership (3) Nutrition (19) Ostomy 5k (19) Ostomy 5k (15) Ostomy Awareness (55) Ostomy Basics (55) Ostomy News (94) Ostomy Nurse (13) ostomy reversals (12) Ostomy Supplies (2) Ostomy Tips (93) Ostomy Videos (4) Patient Stories (96) Pediatric Ostomy (4) Personal (63) Research (3) Sexuality (12) Short Bowel Syndrome (16) Skin Care (9) Social Life (4) Support Group News (12) Support Resources (14) Teens (3) Travel (11) UOAA Conference (17) UOAA History (3) UOAA Volunteers (3) Urostomy (110) Young Adult (7)

Support Us:

Your Donation Funds UOAA Educational Programs:

DONATE TODAY
SUSTAINING GIFT
BECOME A MEMBER
UOAA E-NEWS SIGN UP
Get updates on events, national advocacy and important topics in the ostomy and continent diversion community.

Contact Us


United Ostomy Associations of America
P.O. Box 2293
Biddeford, ME 04005-2293

Virtual Ostomy Clinic

Contact UOAA

Donate Your Supplies

Call us toll-free at: 1-800-826-0826.
Our Information Line hours are Monday-Friday, 9am to 3pm EST. If you have an emergency, please dial 911 or contact your local medical professional.

Please understand that UOAA is a private, nonprofit, advocacy and informational organization. We are not a medical facility and we do not have medical or legal professionals on staff. Therefore, UOAA does not provide Medical, Mental Health, Insurance or Legal Advice. Visit UOAA Virtual Ostomy Clinic provided by The Wound Company for non-emergency, virtual ostomy support.

Privacy Policy

Get Involved

UOAA is the leading organization proactively advocating on behalf of the ostomy community. Recognizing that we are always stronger together, we encourage everyone to get involved by joining our Advocacy Network. We’ve also created several Advocacy Tools and Resources to help you successfully advocate on behalf of the ostomy community to ensure every ostomate receives quality care.

UOAA Run for Resilience Logo

UOAA does not and shall not discriminate on the basis of race, color, religion (creed), gender, gender expression, age, national origin (ancestry), disability, marital status, sexual orientation, or military status, in any of its activities or operations.

Digital Health Award
© 2005-2026, UOAA. All Rights Reserved l Design by Tap House Media
  • Link to Facebook
  • Link to X
  • Link to Pinterest
  • Link to LinkedIn
  • Link to Youtube
  • Link to Mail
  • Link to Instagram
Link to: Twists and Turns of J-Pouch Recovery Link to: Twists and Turns of J-Pouch Recovery Twists and Turns of J-Pouch Recoverywinding road Link to: Caring for the Caregiver Link to: Caring for the Caregiver Caring for the Caregiver
Scroll to top Scroll to top Scroll to top