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Awesome Ollie the Ostomy Bear

Posted By Jenna A. Bertini, Thursday, January 5, 2017
Updated: Friday, January 6, 2017

The Society does not endorse or support products or services. This is a guest blog post written by ostomy patient and advocate, Dawnette Meredith.

If you have a story you would like to share, please email

Awesome Ollie the Ostomy Bear


This is me, a 50-year-old woman completely thrilled about a very expensive stuffed bunny from overseas. Ridiculous you say? Well, this is a very special bunny. It has an ostomy just like me! I underwent ostomy surgery in December of 2016 after battling severe colonic-inertia for 49 years, 9 months and 15 days. My bunny was a bright spot in my recovery. It was a daily reminder to smile and laugh at an otherwise less than ideal situation. For heaven’s sake, I’m a grown woman, but there I was showing off my stuffed bunny to family and friends! It somehow made it easier to talk about my illness and recent surgery.


This little bunny sparked in me a hope to pass along positivity to other ostomates, and a dream to give children in the United States who undergo ostomy surgery a teddy bear with an ostomy. I designed a Teddy bear with a red button for a stoma and a removable Velcro ostomy pouch. Awesome Ollie the Ostomy Bear was born.

Rady_Nurses_BearsThere’s no better place to start than in your own back yard. Rady Children’s Hospital, near my home in San Diego, which performs roughly 120 ostomy surgeries per year, was the perfect place to begin. I know from personal experience that ostomy nurses are essential to helping patients recover and cope after ostomy surgery. My husband and I sponsored eight Awesome Ollie Ostomy Bears and delivered them to the ostomy nurses at Rady Children’s Hospital. The ostomy nurses were given the joyful task of handing out the bears to their ostomy patients. The response was overwhelmingly positive, and soon Rady Children’s Hospital called for more bears! Soon, other children’s hospitals wanted to acquire the bears for their ostomy patients. I quickly needed to find a way to get bears sponsored in time for the holidays!

Rady_Hospital_BearsI approached my ostomy support group and its members with the possibility of sponsoring the bears for Rady Children’s Hospital. Within 20 minutes, over 30 bears were sponsored! Wow! I hurried to prepare the bears before Christmas-time. I like to think of myself as “The Ostomy Elf” busily working in my teddy bear workshop. In a flurry of fabric and thread, the bears were ready. The second batch of sponsored bears was joyfully delivered to Rady Children’s Hospital in December 2016.

It’s a new year and Awesome Ollie the Ostomy bear has BIG plans! The goal is to secure funding and provide free Awesome Ollie Ostomy Bears to children’s hospitals all across the United States.

If you or your organization would like to sponsor Awesome Ollie Ostomy Bears at a hospital in your area or purchase a bear for yourself, please contact me at or 858-336-4418. Awesome Ollie sponsorship costs $20/per bear. Find Awesome Ostomy on Facebook to keep up on all the Ostomy Bear news.

Tags:  advocate  bear  cope  experience  hospital  nurse  ostomate  ostomy  positivity  sponsor  surgery 

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10 Things I Didn't Know Before I Had My Ostomy

Posted By Jenna A. Bertini, Tuesday, December 20, 2016

When I first got my ostomy, I felt very alone. I felt self-conscious of the smell and sound, and sometimes I longed for my old body. When I couldn’t take self-loathing anymore, I decided to make friends with my ostomy. I reached out. I inquired about support groups in my area and realized there are many people like me. I realized my ostomy is a beautiful thing and has enabled me to do all the things I’ve been able to accomplish over the years. It is my uniqueness.

These are 10 things I would have liked to tell myself when I first had an ostomy — 10 things I didn’t know but eventually learned, which I am so grateful for today:

1. What it was.

I had no idea what an ostomy was before I had one. But I have a confession: I didn’t realize exactly what it was until a year later! Coming out of multiple surgeries, I had so many bags and new anatomical surprises to think about that a little pink bulge on my belly seemed to be the least of my problems!

I’ve learned things in the past 10 years that have shocked, scared and relieved me, such as: You can’t actually feel your stoma — no nerve endings! I’ve had three ostomies and four ileostomies over the years. I didn’t realize how different they were. Once I learned about the differences and functions of each, I was better able to take care of them.

2. What my limits were.

When I saw that I’d have to live life with a bag stuck to my side, I assumed I’d be “fragile” for the rest of my life. But believe it or not, there are so many activities for ostomates out there! Swimming, karate, ballet, yoga — I’ve done everything I did before my ostomy and more.

3. There are so many strong ostomates.

I was privileged to be the Eastern regional recipient of the Great Comebacks award and meet five other amazing ostomates doing incredible things. There is a huge, supportive ostomy community, including celebrities! Did you know Great Comebacks was founded by a former NFL linebacker?

4. Ostomates excel at innovation and inventiveness.

It turned out I was able to do all the things I thought I couldn’t — but that didn’t mean it was easy. Some of the best things in life take hard work, and that makes you appreciate them even more. Let’s just say that plastic wrap, Pepto-Bismol, waterproof tape and wet suits have become good friends of mine. I’ve even made a creative workshop for ostomy patients and healthcare professionals. The “Renegades” music video by X Ambassadors features a blind man who says it best: “It’s not a matter of enjoying it more or less; it’s about enjoying it differently.”

5. How amazing my body is.

I have a new respect for my body and the way it can function now.

6. Judgment hurts, but fear hurts more.

Stay informed and know the facts. The more I actually understood how an ostomy worked, the more I realized how wonderful it was. After that, I took it as my responsibility to educate others.

Instead of wondering if I was being “judged” by others, I took it as a privilege to inform them.

7. Everything is connected.

Take care of your full selfemotional, spiritual, mental and physical.

If you’re stressed you might get physical side effects, such as being bloated or feeling pain and discomfort. Remember to take deep breaths in difficult times.

8. The people who love you, love you.

If you’re just getting comfortable with your ostomy, remember that your support system loves you for who you are. You are more than your ostomy.

Reach out to the ones you love when you feel alone, and never forget how loved you are.

9. Eat fresh.

You are what you eat, so eat whole and nourishing foods. Your ostomy will thank you, and so will you!

10. Life can go on.

Throughout these years, I’ve been strong, determined and willing to do whatever it took to stay alive. I’ve dealt with tubes, bags, poles, you name it. And if this ostomy is all that I’m left with after everything, then I am truly grateful. More than that, I thank my ostomy for enabling me to live life to the fullest, to my fullest. I call it my Harry Potter thunderbolt scar: a symbol of strength, courage, individuality and life.

There are a few things I didn’t know before my ostomy. But what I look forward to most is everything left to learn. Thank you, ostomy, for making the world a wide open door once again.

Follow my journey.

About the author:

Amy OestreicherAmy Oestreicher is a PTSD peer-to-peer specialist, artist, author, writer for Huffington Post, speaker for TEDx and RAINN, health advocate, survivor, award-winning actress and playwright who is sharing the lessons learned from trauma through her writing, mixed media art, performance and inspirational speaking.

As the creator of the Gutless & Grateful, a one-woman autobiographical musical, Amy has toured theaters nationwide, along with a program combining mental health advocacy, sexual assault awareness and Broadway Theatre for college campuses and international conferences. Her original, full-length drama, Imprints, premiered at the NYC Producer's Club in May 2016, exploring how trauma affects family as well as the individual.

To celebrate her own “beautiful detour,” Amy created the #LoveMyDetour social media campaign, to help others cope in the face of unexpected events. "Detourism" is the subject of her TEDx talk and upcoming book, My Beautiful Detour, available December 2017. As Eastern Regional Recipient of Convatec’s Great Comebacks Award, Amy has contributed to over 70 notable online and print publications, and her story has appeared on NBC's TODAY, CBS and Cosmopolitan, among others. She has devised workshops for conferences nationwide and presented at the 2016 Northeast Region WOCN Conference, and is the 2016 keynote speaker for the Hawaii Pacific Rim International Conference on Diversity and Disability. To learn about the art of navigating beautiful detours and to sign up for updates visit

Tags:  advice  advocate  disability  educate  Great Comebacks  ileostomy  inform  learn  life lessons  ostomate  ostomy  resilient  stoma  strong  support  surgery  tips 

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Dealing With Life As A Double Ostomate

Posted By Jenna A. Bertini, Friday, December 9, 2016
Updated: Friday, December 9, 2016

taylor baby picture

How my journey as a double ostomate began:

I grew up in a loving family with five siblings. At the age of three, along with being a twin, I was developing my personality while enjoying time with my siblings, getting ready to start pre-school and feeling filled with joy. I had no worries in the world. I never imagined that one day playing in the backyard my clothing would start to fill with blood.

My parents rushed me to the University Of Maryland Medical Center (UMMC) in Baltimore. After several days of testing, the diagnosis was a rare form of vaginal cancer called Rhabdomyosarcoma. After receiving advice from medical physicians, my parents decided to transfer me to a hospital that specialized in this rare type of cancer.

taylor surgery in hospital

My childhood, and most of my adolescent years, was spent at Memorial Sloan-Kettering Cancer Center (MSKCC) in New York. Along with chemotherapy, radiation and too many surgeries to count, I was faced with having two ostomies (a colostomy & urostomy) for rest of my life. The doctors, surgeons, social workers, medical staff and ostomy nurses made my life as normal as possible. The care they showed was beyond their medical titles and duties. My family is ever so grateful to everyone at MSKCC for their care.

After the age of 12, I was able to do my follow up visit back in Baltimore under the care of Dr. Fromm at UMMC. Since 1995, I have been under the care of Dr. Faud Abbas at the Sinai Hospital of Baltimore. I look forward to my doctor visits. When you find a doctor like Dr. Abbas, you feel comfortable knowing your health is in good hands.

Since having two ostomies from the age of three, my life has proven to be a journey of unexpected challenges. While others appeared to be living a “normal life,” I struggled with self-pity, unhappiness, depression and low self-esteem. I found it hard, embarrassing and painful to be considered “different.”

How I dealt with what life had dealt me:

taylor ostomy awaress I Can shirtMy parents taught me to love myself and to know that my medical circumstance does not dictate my future. Their faith in God helped me to know I was going to be alright.

The support from my family and friends made my life feel normal again. I contacted my local United Ostomy Associations of America, Inc. (UOAA) chapter for support. I discussed different ostomy products to try with ostomy nurses. If a product worked for me, I stuck with that. I dealt with leaks and blowouts by keeping extra clothes and products in my car, at work and at friends’ houses. I still do not dwell on leaks; I clean up and keep moving. When you accept being an ostomate, others will. It is what it is and no one is to blame. If you lived your life before you had an ostomy there is no reason why you cannot live your life with one. Love the essence of who you are.

taylor woke up like thisWhat helped me to accept my ostomies:

The mantra LIVE FOR TODAY - don’t dwell on what happened yesterday and enjoy the moment is what helped me to learn that I am more than my ostomies.

Advice for my fellow ostomates:

taylor fashion gold dressI encourage other ostomates to get out and try activities and hobbies such as sports, reading, having fun, laughing, attending support groups, leaning on family for support and seeking out to the WOCN Society for additional support. And do not let your ostomy pouches stop your fashion style! Try different styles of clothing to see what makes you feel confident - the best fashion style we have is our inner beauty.

I am blessed to have my desires, passions and dreams come true. I am a double ostomate and have been a fashion model for over 17 years. Through my career, I am helping cancer survivors, encouraging ostomy patients, guiding aspiring fashion models and inspiring those suffering with low self-esteem. Just by looking at my outer appearance, no one could ever tell I live with these medical adversities and what I deal with 24 hours/7 days a week.

taylor fashion black dress

We all have the ability to make a difference, to change lives, to be a role model and be all that we can be as an ostomate.

I know am beautiful from the inside out, despite my life being a journey of unexpected challenges. I am trying to change the lives of others by telling my story through my book, Pretty Girl Blues: An Autobiography, my intimate journey of being a survivor. The adversities and obstacles that I overcame allow me to encourage, inspire and motivate others to “live their life on purpose with a purpose for a purpose.”


About the Author:
Jearlean Alston-Taylor was born and raised in Southwest Baltimore, MD. She grew up in a happy home with five siblings, including her twin sister. At the age of three, Taylor was diagnosed with a rare form of cancer. Doctors thought she would not live to see four. Today, Taylor has beaten all odds and uses writing and modeling as an outlet and a way to connect with other ostomates. Taylor is the CEO of J & Company Christian Modeling and Osto Beauties.

Tags:  cancer  chemotherapy  colostomy  double  fashion  inspire  journey  model  motivate  nurses  ostomate  ostomy  p  radiation  Rhabdomyosarcoma  specialized care  struggle  support  surgery  survivor  urostomy 

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A New Beginning

Posted By Jenna A. Bertini, Wednesday, September 21, 2016
Updated: Wednesday, September 21, 2016

Society member Ann-Marie Waechter, BSN, RN, CWCN, MS-BC, is a wound care nurse and volunteer with the global charity Mercy Ships on board the world’s largest private hospital ship, the Africa Mercy. Ann-Marie is writing a series of blogs for the Society and its members to share her experiences on the Africa Mercy and to inspire other nurses. You can read Ann-Marie's first story below.


If you have a story you would like to share, please email us at


A New Beginning

     After a full life of school, study, marriage and raising children, my childhood dream is realized. My husband, Tom, took early retirement two years ago and asked, “How about looking into volunteering for Mercy Ships?” From the age of 10, after reading about the hospital ship, SS Hope, I knew I wanted to be a nurse and someday work on a hospital ship. Maybe because patience is not one of my virtues, I never imagined I would live so much life and see my dream realized at the age of 60! In the fall of 2014, after applying and waiting 18 months for a position to become available, Tom and I reported to Mercy Ships headquarters in Texas for our “Onboarding Training.” We spent five weeks in Texas and then our onboarding group headed for Madagascar for two weeks of required field training. There we began to learn the realities of living and working as a community.


Tom and Ann-Marie Waechter volunteer with Mercy Ships onboard the world’s largest private hospital ship, the Africa Mercy. ©Mercy Ships


     When we were first contacted with the news that, finally, there were positions for both of us on the ship, we were asked if it mattered to us where the ship was going – it struck me as an odd question. However, for the first time ever, the Africa Mercy sat out in the water with nowhere to go. Originally scheduled to head for Benin, Ebola had broken out in West Africa, leaving the ship unable to fulfill its promise to the government of Benin to spend 10 months in the port of Cotonou. Although the Africa Mercy successfully completes thousands of specialized surgeries each year, we are not equipped to effectively address infectious diseases such as Ebola.

     After a lot of prayers, miracles opened doors and in what would normally take six to 18 months to sign agreements and protocols with a receiving government, Mercy Ships was able to do in five days. The way was open for the Africa Mercy to be welcomed into Toamasina, Madagascar.

     After an amazing 18 months and two field services in Madagascar, we have finally arrived in Benin to fulfill our promise from two years ago. Back in West Africa, where the work of the Africa Mercy has been focused over the years, the crew that has been here before were beaming with excitement as we sailed into the port and capital city of Cotonou – our new home for the next 10 months.


The Africa Mercy sails into Cotonou, Benin where the Mercy Ships volunteer crew will provide free surgeries, healthcare training and other services for the next 10 months. ©Mercy Ships / credit: Katie Keegan


     Our advance team, already here for three months, and an African band were here to welcome us. Before the end of the day, we will have been welcomed by the First Lady of the country and top officials in a formal ceremony.


     And so we begin again… the Africa Mercy, the flagship of Mercy Ships, following the “2,000 year old model of Jesus, to provide hope and healing to the world’s forgotten poor” will stay in Benin for the next 10 months providing specialized surgery to the poorest of the poor, those who would have no other access to the surgical care we provide. The Lancet Commission on Global Surgery published a report in 2015 stating that there are four times as many deaths worldwide resulting from lack of access to safe, affordable surgical and anesthetic care than from malaria, TB and HIV combined. Mercy Ships works to fill that gap.


The advance team for Mercy Ships worked in Benin prior to the ship’s arrival to prepare arrangements for the Africa Mercy’s field service. They greet the floating hospital in matching African dress as the vessel sails in to dock in Cotonou. ©Mercy Ships / credit: Katie Keegan

     We docked on a Thursday and by Friday there was a flurry of activity on and off the ship. The five hospital wards, along with the OR complex, with everything secured for sail, have to be unpacked, cleaned, sterilized and setup. The nurses that were already onboard cleaned everything twice with Tristel – and I mean everything. Every wall, ceiling, floor, cabinet, counter, piece of equipment, cord, mattress, bed frame, bin, trash receptacle, bio-waste container and more, was deep cleaned by the nurses who will use these wards to care for the approximate 1,700 patients who will receive surgery on this field service. The pharmacy was opened, cleaned and shipping containers organized with the medications for the field service, for patients and crew alike, along with the lab and radiology.

Our Beninoise crew member, Bio-med technician Emmanuel Essah, presents the Benin Flag to the First Lady of Benin who came to meet the Mercy Ship upon arrival in her country. ©Mercy Ships / credit : Tim Baskerville


     A team of people from the United States helped set up all the facilities off the ship, which includes huge tents on the dock housing our admissions, rehab, ponseti and screening teams, as well as our infant feeding program and outpatient clinic. The outpatient clinic is where all our wound care is done and it will by my “home” until June. In town, we have facilities loaned to us by the government for the duration of our stay, which will house the dental clinic, eye clinic and the Hospital Outpatient Extension (H.O.P.E.) Center.

     The flurry of activities included the beginning of screening. For the next three weeks, our team of nurses will pre-screen as many people as they can, who line up outside the screening center to see if their condition fits the criteria of the surgeons who will soon arrive. It is a difficult and emotionally challenging job; possibly the most difficult on the ship. We have a limited number of surgical slots for each surgical specialty: plastics, orthopedics, maxillofacial, general and women’s health.

     Although many people come with surgical conditions, much more come with non-surgical conditions hoping for help. Some are palliative and are followed by our Palliative Care team. Others need surgeries that we are unable to provide. Of the several thousand people waiting in line this first week of screening, 355 were given appointments to be seen by the surgeons. Every person we have to turn away is gut-wrenching. The screening team, along with the entire Africa Mercy community, reminds each other of the lives we have seen changed from the surgeries we are able to provide. The joy we see on the faces of those we are able to serve make it all worthwhile.


The dockside tents serve as an extension of the Mercy Ship and will house the outpatient clinic where I will work for the next 10 months. ©Mercy Ships


     During the first field service in Madagascar, I served as the Crew Nurse in the Crew Clinic, sharing the same hallway as the hospital. It was a wonderful opportunity to serve and get to know the approximate 400 crew onboard, but my heart longed to work with the patients I saw daily walking the halls, experiencing the miraculous surgeries done by the surgeons who volunteer their time here.

     Thanks to Emory University’s Long Distance Learning Program, and a generous donor who provided enough bandwidth so we could download video on the ship, I was able to begin their Wound Care Program in January 2015. In June when the ship left Madagascar for its two month shipyard period, I headed to Atlanta to do Emory’s Wound Care “Bridge Week.” I am so grateful that the staff at Emory designed a program that made it possible for me to fulfill my second dream – becoming a wound care nurse. Less than a week before we had to return to the ship, I took and passed my certification exam. I became a CWCN!

     During our second field service in Madagascar, I transferred to the outpatient clinic and I love it. It’s the best nursing job I’ve ever had! After all this time, I feel as if I’ve found my place in nursing. Our first surgeries in Benin begin in September and the outpatient clinic will open soon after. Benin is a new beginning – who will we see, what will we see that’s never been seen before, what patients will we come to love, what will cause us struggles, what will bring us joy, what miracles will we see? For now they are only questions, but the entire Africa Mercy crew works with anticipation for the answers soon to come.


     For more information about Mercy Ships please go to

Tags:  advance  Africa  Africa Mercy  anesthetic  care  conditions  CWCN  hospital ship  laboratory  medication  Mercy Ships  palliative  patients  pharmacy  radiology  screening  service  surgery  team  woc nurse 

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