Posts Tagged ‘Stories’

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The invisible red thread

February 1, 2012

There is an ancient Chinese belief that an invisible red thread connects those who are destined to meet, regardless of time, place, or circumstance. The thread may stretch or tangle, but it will never break. That being said, I believe that everything happens for a reason and I am exactly where I am supposed to be in my life at this moment.

Setting the course

When I moved to Texas, following my permanent ileostomy surgery back in September, I ended back in the hospital within four days of my arrival. I was so sick at the time and did not even have the chance to find new doctors yet. I was overwhelmed with the Texas system along with having to relay all my advanced and extensive medical history to doctors I just met. Having to arrange for medical records from Wisconsin to be faxed here, and make dozens of phone calls with my surgeon in Wisconsin, only to find out there are doctors here unwilling to treat you because you were not in their insurance network. This all made for a very stressful and anxiety ridden 10 day hospital stay. Looking back, it was a strange blessing in disguise because I was forced to expedite everything in such a hurry that in a very short time upon arriving, everything was transferred here.

During the stay at the hospital, I was under the care of a GI doctor by the name of Dr. Rassa Shahidzadeh whom I immediately liked and trusted. During the 10 days, I spent long hours going over my health history and all the background of my illness with him, and and felt very comfortable with how he handled my treatment. When I was discharged from the hospital, I was told to follow-up with Dr. S, but unfortunately he was out of my insurance network and I was told to find another GI. I cannot describe the bitter disappointment. It was so frustrating to find a new doctor, go through all the background on my disease with him only to find that I could not see him post-hospital stay. It was a big letdown to say the least. So the search began to find a new doctor in my network.

When one door closes, another opens

It took some digging but I did find a doctor by the name of Dr. Balachandar. I set up an appointment to meet. Our meeting was very successful and I walked out of her office almost high with excitement and relief. She was wonderful to me; an excellent fit. And suddenly all the worry, all the anxiety and all the frustration led to this one moment and all I felt was an incredible weight lifted off my shoulders. Her demeanor and willingness to want to learn about my condition and history was inviting and open. Her gentle nature was very fitting with my personality, and she is good at explaining things. I ask a lot of questions, and I am grateful that she not only answers them all, but she gives thorough explanations and more than what I even asked for. She didn’t hurry me through the appointment like I have experienced in the past. Since I had to leave such great doctors behind in Wisconsin, it was a big relief to finally call Dr. Balachandar mine.

A lot has happened since I moved to Texas–some good and some not so good. But for the most part my health has improved considerably, and I am grateful that my better days are numbering more and more. Recently I had a small setback and ended up in the ER for a brief stay. My illness flared, and not only did it affect my tummy, it went into my joints. I had a follow-up with Dr. B this past Monday, and when I left her office it occurred to me while walking out to my car, that I had such a peaceful feeling. I always get so worked up about everything and somehow, someway this doctor calmed my fears. I was actually relaxed. Her interesting mix of modern medicine and Ayurveda healing practices are a welcome change to what I was used to before.

This is how it was it was meant to be

It is very difficult to leave trusted physicians who have walked along your path through so many trials of a chronic illness. It is harder yet to find another doctor willing to take on where those doctors left off, someone open to face the challenge of a complicated patient. I am grateful to have found such a doctor. It’s strange how things happen and when you step back you realize that maybe THIS ALL IS EXACTLY the way it was supposed to be, that every step on my path led me to this place, at this time of my life. These are the people I was supposed to meet. These are the people I am supposed to be with. I had to let go of some, but I gained others. It is kind of profound to think about how life leads you to people and places that are meant to come your way and you don’t even know it yet. It’s as if that invisible red thread has already sewn together the people you are meant to meet on this hidden life line, those who pass through your life temporarily and those who stay.

“An invisible red thread connects those who are destined to meet, regardless of time, place, or circumstance. The thread may stretch or tangle, but will never break.” ~An ancient Chinese belief

~Nadia

Question: Have you established a good relationship with your doctor? Have you had to change doctors?

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Keeping stress levels balanced when dealing with IBD

January 22, 2012

Here are some tips on helping deal with stress. Mostly intended to assist in dealing with stress when you have inflammatory bowel disease, but these are good tips for anyone. Although this is a serious subject, it became difficult to film this video at times. Many times I use bullet points on topics I want to cover, but it is difficult to think ahead of all the points I want to make. I show my frustration in the end of this video with a couple of bloopers!

“Give your stress wings and let it fly away.” ~Terri Guillemets

~Nadia

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What’s the difference? Temporary vs. permanent ileostomy

January 8, 2012

Besides the obvious difference–temporary being for short term, and permanent being forever–this video covers the difference between the type of surgery each of these are, as well as, the reasons why a patient may need temporary ileostomy surgery or permanent ileostomy surgery.

In some cases a patient may undergo temporary ileostomy surgery only to later have to undergo permanent ileostomy surgery–as in my case. Despite having two temporary ileostomies, I now live with a permanent ileostomy. In this video I talk about both.

“My life is my message.” ~Ghandi

~Nadia

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Exclusive interview with Ally Bain, creator of Ally’s Law, and her gastroenterologist Dr. Rubin

December 19, 2011

Recently we were contacted by WestGlen Broadcast Public Relations as part of a nationwide campaign to spread awareness in the inflammatory bowel disease community about Ally’s Law (known as the Restroom Access Act). Ally Bain and her gastroenterologist Dr. David Rubin offered us an exclusive video interview to spread awareness about this law. This was a phone interview with Dennis and I because we were all in different locations.

David Rubin is an associate professor of medicine, co-director of the Inflammatory Bowel Disease Center, and director of the Gastroenterology, Hepatology, and Nutrition fellowship program at the University of Chicago (UC).

Ally Bain was diagnosed with Crohn’s disease at age 11 and at age 14, Ally experienced a Crohn’s flare up in a department store and had an accident because she was denied use of the employee-only restroom. Since then, Ally has dedicated herself to raising awareness about Crohn’s disease and the rights of people living with the condition by creating “Ally’s Law.”

There are many resources where you can learn more about getting involved to help legislation pass this law in your state. Check out CrohnsAndMe.com as well as CCFA.org to learn more and find additional information.

We feel very honored to have been given this rare opportunity. We should all do our part and get involved in this movement because “everyone deserves restroom access.”

“Awareness is empowering.” ~Rita Wilson

~Nadia

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Cookin’ With Nadia: Chicken Rice Dish ft. Dennis

November 29, 2011

Dennis visited me in Texas and we cooked this dish:

Ingredients:
Chicken
Rice
Salt
Pepper
Bullion
Celery
Onion

Watch the video to learn how to make this simple dish. A great dish to have when you are not feeling well.

~Nadia

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Words of thanks

November 24, 2011

It generally is my practice to give thanks each day for all my blessings in life. Thanksgiving is a day of reflection on those blessings and a day set aside for recognition. There are days of celebration and recognition all over the world that deserve mention, and I try not to highlight just U.S. holidays or my personal days of celebration. But, today please let me make an exception. This week has been a very dark and sad week. It seems that when one thing goes up something must come down. I have learned my life is a strange wheel turning good and bad at regular intervals and have decided that this is something that I must learn to accept. Good or bad, it is life.

This has been a difficult week for personal reasons. A couple days ago as my parents and I were travelling out of town, we were on the interstate when a utility truck struck a car and smashed into us. I was in the back seat and was thrust into the back of the driver seat. My injuries required me to be rushed to the hospital by ambulance. It was a very frightening and horrifying experience. I suffered a sprained knee, whiplash, an injured shoulder, abdominal trauma and contusions, but I am alive and I am here to write this, here to give thanks.

But more heartbreaking, a good friend was killed in front of campus just crossing the road. She nearly made it to the other-side when she was struck by a car. The driver of the vehicle left the scene and is still at large. My friend was alive but in grave condition and died shortly after. I spent the past couple days in deep reflection over the friendship I shared with her and feel eternally blessed to have known her and shared time with her. I will always remember her non-stop happy personality and her ability to see the good in all. People pass in and out of our lives, and for every person that I met and has touched my life in some way, I will always cherish the moments we shared.

So, I write today to express gratitude toward so much. Always remember: Cherish your family and friends, life is made of years that mean nothing and moments that mean everything. Listen to songs that take you back to a special moment. Sing out loud even if you are off tune. Remember that every new day is another day to change your life for the better. Know that the times in life that seem like the worst, teach us and can give us lessons that can, if we chose, make us stronger and live better. Remember to take chances. Say you are sorry. It’s okay to cry; I do it all the time, both happy and sad tears. Say I love you. Laugh at lame jokes, and laugh until your ribs hurt. Sometimes we can’t solve our problems, that’s reality and sometimes reality is the hardest thing to understand. Make great memories. Take thousands of photos. Make time to do random acts of kindness. Make it come from your heart. Don’t look back and wonder what would have or could have been. Sometimes the smallest gestures change the life of one person and to them it means the world. PRAY-it doesn’t matter what you say or how you say it, just pray. No matter how far you go down the wrong road, know that you can always turn back. There are so many blessings…open your heart.

And it is with deep gratitude that I thank you for all your support.

Love, Nadia

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Nadia in the concrete jungle

November 19, 2011

Looking back over the past 12 months I can honestly say that it has been one of the hardest parts of my journey thus far. It has definitely been a year of loss and tears–feelings of hopelessness came with a resounding blow. I could lament and list all the blows I have taken, but I will spare you and myself from having to go over them again because the place I am heading toward is acceptance, and THAT is not such a bad place to be hiking towards.

September 2nd, 2011, marked a pinnacle point in my journey. It is the day I underwent surgery to receive a permanent ileostomy. Unless one goes through a surgery that physically changes their appearance and anatomy, it is quite difficult to explain the psychological and emotional feelings of what that entails. For someone like me, who has gone through three ostomies: 2 temporary and 1 permanent, it wasn’t something that with which I was unfamiliar with, but it was a trial in letting go of hope; hope for a turn-around in this disease, and a hope that my body will appear as ‘normal’ on the outside. It was a challenge to understand that this will improve my life.

September 2011-Hospital

September 2011-Hospital

The first two weeks following surgery went great, but then complications set in, and once again, I was hospitalized for nine days with a serious infection and abscess from surgery. For some reason, this was a moment of incredible defeat for me. I had undergone this drastic surgery to improve life only to end back in the hospital with more complications. I kept thinking that my whole life will be spent paying a price for everything that happens to me, and no matter what route I take it is still wrought with obstacles. Honestly, it was almost more than I could take. It was then, in the hospital, my mom said there was too much I haven’t done in life, and I have to fight a little harder to get well. She told me that if I could set a goal to work toward getting healthier for my 21st birthday, we would do something exciting.

Setting a Goal to Recover

Two months later, on my 21st birthday I felt well enough. So, we travelled to New York City-even though it was a short trip-it was incredible. For my first time in years, I was able to leave home and travel for vacation purpose and not health or medical related. That is a huge deal. HUGE! I am not sure if many people can understand fully what it means to travel for the sheer enjoyment of it!! For the past 5 years, 98% of the travel has been to visit doctors, hospitals, specialists, to have surgery, special testing, second, third or fourth opinions, but never for the pure sake of enjoyment. Over the years, I watched as both my brothers traveled all the time! Both of them left home to study abroad-one to Spain, and one to Switzerland, while I was too sick to even attend school. But this was my time. New York City, HERE I COME!

New York is Where I’d Rather Be

We arrived early on our first day and had time to see some sights. My adrenaline was pumping off the charts. Fatigue? Forget about it! Low energy? Wha!? That little pain? What pain? My mind was working overtime to tell myself that NOTHING better go wrong. My Health would not ruin this moment for me!

We headed out from the airport to our hotel in a New York taxi to begin my first adventure. Picture me in the back seat of the taxi, beaming from ear to ear, with a camera in hand, shooting a hundred pictures of the sights, from the window, OOOH-ing and AAAHH-ing at everything exciting. I was the epitome of your typical tourist. I was shameless about it! I did not care; nothing and no one would let the wind out of my sails! I was going to soak up every moment: feel, taste, see, hear– to bring to life all my senses to experience all this excitement! It felt so good. NO, not just good, this was amazing! Even when our taxi driver cut someone off in traffic, and we got cursed at, was awesome! We just got yelled at in a taxi driving around in New York City!

Happy New York Birthday

Once we arrived to our hotel, there were more surprises! A birthday cake and candles were in the room waiting for us! Sneaky planning ahead! With a view of the Empire State Building right outside our window, we enjoyed cake and juice, and we started our plans for the five days that we were going to stay there! First on the agenda was to pick up our all-access New York City passes. We headed to Time Square and the Planet Hollywood to do that. Oh my gosh—Time Square! I still can’t believe I stood there in the midst of all the New York chaos! It was almost too overwhelming and over-stimulating to this small town girl that lives on a ranch in Texas!

Birthday Cake

Birthday Cake

We picked up our passes and had a soda at the Planet Hollywood where the staff sang Happy Birthday to me! I was flying high, and then, it hit me for the first time of many during the week—I am on vacation. I am here for fun. No doctors or hospitals. This was just for me. The sting of tears came and went, but for a moment I had to say a prayer of thanks. So this is what it feels like, huh? This is what everyone talks about.

During the entire trip I was Face-booking every moment to share with my daddy, who stayed behind in Texas. I posted tons of photos! (I took over a thousand) I wanted to, not only have a timeline to share with Daddy, but also to have the memories to look back on when this was over!

Our first night was spent in Time Square, seeing the sights and soaking it all up, but we had a long day and ended it early as we were in bed by 11. Before falling asleep, so much was going through my head, but one thing I kept thinking was that travelling to New York with an ostomy was not difficult at all. Although finding a public bathroom was a little bit of an issue, nothing about my ostomy posed a problem. I kept thinking, however, that a few years ago this would have been completely impossible. For another time on this journey toward acceptance I had to say thanks for having the freedom my ostomy has given me to enjoy this moment. I closed my eyes, and I am sure I slept with a smile on my face.

Times Square

Times Square

Where Dreams are Made of

The next several days were a whirlwind of activities. We saw so many exciting places in New York it is hard to believe we did as much as we did. We went to the top of the Empire State building where I promised to call my brothers. Nyle and Nabeel shared my excitement so much! We walked through Manhattan, learned to ride the subway, walk through “Occupy Wall Street,” and then to the 9/11 Memorial at the site of the World Trade Center.

I have to say the 9/11 Memorial was the most heartbreaking, humbling moment of the week. I stood at the memorial site and walked through this serene place and could not help the tears that I shed as I read the names of each victim. I was standing at the fountain watching a gentleman touching a name, I walked a few feet away to give him privacy and felt him staring at me. I looked at him and asked if he knew someone whose name was on here. He pointed to the name of his best friend. I was so deeply moved and so sorry for his loss that I broke down in tears. I could not help myself. Maybe that is normal, maybe not. But suddenly it made so much sense that we are ALL on a journey. We all have obstacles and trials and pain. We all lose. We all suffer blows. Some are so much more devastating than others. Mine pale so very much in comparison. I have so much to be thankful for! (I don’t know who you are; stranger at the WTC site, but you impacted my life in that moment in a very profound way.)

9/11 Memorial--World Trade Center Site

9/11 Memorial--World Trade Center Site

Throughout the week, the list of activities grew: a water taxi down the Hudson River to see the Statue of Liberty and Manhattan from the water, Little Italy, Chinatown, more subway rides, Battery Park, Central Park, The Metropolitan Museum of Art to see Rediscovering Islam through the Arab World (which was amazing and profound), making my 11-11-11 at 11:11 wish in New York was exciting and kind of epic, Museum Of Worship, New York City Library to see the Malcolm X exhibit, Magnolia Bakery for red velvet cupcakes, and Grand Central Station! Through most of it I felt pretty good. I did get seasick on the water taxi and had to take it a little slow. It is like I lived a lifetime in those few days. Toward the end of the trip, we took in a Broadway show. We saw the Lion King in the front row of the balcony, and I was mesmerized. It was an amazing, out of this world experience! This entire trip was off-the-charts special. I was so happy to have friends and family encouraging and joining me on this journey even from a distance. It made sharing it so much more thrilling! I saw so many places just from the suggestions of others that I would not have gone to without their advice!

Statue of Liberty

Statue of Liberty

Be It Ever So Humble, There’s No Place Like Home

Late Saturday night, we arrived back home to Texas. I was ready to come home. I was ready for the trip to be over. Although exciting and adventurous, I am definitely a homebody. After all that adventure and excitement it did take a toll on my body. I used up the last reserves of adrenaline and energy I had to get through it all and it came crashing down as I hit my bed at home. I slept for 14 hours. It took a few days to get back to “normal” after all that experience, but if you ask me if it was worth it, I would give you a loud and resounding–YES!!!

Grand Central Station. I *heart* NY

Grand Central Station. I *heart* NY

“Though we travel the world over to find the beautiful, we must carry it with us or we find it not.” ~Ralph Waldo Emerson

~Nadia

Have you been able to travel? Share with us.

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Life interrupted: Ankit’s story

November 16, 2011

Here is another entry in my series on extraordinary living through IBD.

When I first heard Ankit’s story, he told me there wasn’t much about it that was remarkable. But this 22-year-old graduate student underestimates how much his journey could actually impact so many others. Those that live in an area where Crohn’s disease is virtually unheard of, where most patients are misdiagnosed with abdominal tuberculosis and struggle to find answers and solutions–his story brings us to New Delhi, India.

A Rude Awakening

After beginning flight school in the United Kingdom, Ankit was living high on life. Overcoming his parents’ reluctance to allow him to leave India, as well as a new start after a falling out with a very close friend he began his path toward his life-long dream of becoming a pilot. However, four and a half months into his training and days after receiving his private pilot’s license he began to experience abdominal cramping and serious symptoms that became worse over time. His symptoms included night sweats, vomiting, high fevers, and cramping. He lost an extreme amount of weight in a short period of time. He received antibiotics, fiber supplements, and laxatives for his first course of treatment, but it was unsuccessful. With no insurance and continued problems, Ankit resigned to the fact that he would have to leave flight school and return home to India for treatment.

Initially, upon his return, tests revealed severe inflammation in his intestines. Ankit was diagnosed with abdominal tuberculosis, and the course of treatment for that had begun. His journey through this disease began different than some as he had more issues with constipation. A week would pass with only a single bowel movement. The pain became unbearable for him. After a series of hospitalizations, the doctors then steered their diagnosis toward an intestinal blockage. Surgery was the recommended course of treatment, but thinking ahead, Ankit knew that according to Indian aviation rules, once he got major surgery, he would no longer have the option to become a professional pilot in India. His dream would die, and with that, a part of him as well, so he refused the surgery.

The Harm of Misdiagnosis

He began a liquid diet of Ensure because he could not eat regular food in the hope that the inflammation would reduce. He had low motility in his colon. He could drink as many Ensure as he wanted, but no solid food. Although still very ill, the liquid diet made him feel better, and he decided to re-enroll in college in India and work toward his bachelor’s degree. As he continued the liquid diet for a year, and worked through college, his illness impeded his everyday life. He struggled to pay attention in class because he became so uncomfortable, and because of the weight loss, he was often bullied by other students who had no understanding of what he was going through. He continued to fight strong. Although symptoms continued, not as severe, at this point he was diagnosed with IBS-C (irritable bowel syndrome with predominant constipation). Laxatives stopped working, and he began using suppositories regularly to relieve the pain.

After additional treatment failed, Ankit finally found a doctor that diagnosed him with Crohn’s disease. He was angry that for so long he was misdiagnosed and treated for something other than Crohn’s disease. His fear and frustration hit an all-time high. His research online revealed so many horror stories, telling him life was over because of Crohn’s. He stumbled across websites talking about overcoming Crohn’s disease with no drugs and alternative treatment through diet. He was deeply inspired by Jay from Crohnsboy.com who advocates the Specific Carbohydrate Diet (SCD) as a treatment for ulcerative colitis and Crohn’s disease.

Ankit then took treatment into his own hands, and although not recommended for everyone, he committed himself to a strict dietary regimen after reading the book “Breaking the Vicious Cycle.” Along with some dietary supplements, his journey with SCD began. His progress was slow, and he made many mistakes, but over time he began to see improvement. He learned how to take his physical and emotional pain and channel it into focusing on this new treatment. He focused on making himself well. His determination to heal was so strong. His strength and commitment to this diet began to take shape.

Along with diet, he continued to receive treatment for Crohn’s from his GI doctor. The diet, along with the medication, LDN (Low Dose Naltrexone), provided him very good results. No more pain, bloating, spasms, less constipation, and cramping. He combined the SCD diet with the Paleo diet and was able to come off of all laxatives and Crohn’s medication that he was taking. (Yay for Ankit!)

Taking Back Life

Now he lives his life in India on his own terms. He took his life into his own hands. He went off the beaten path and decided to heal himself because of the lack of understanding about this disease in his country. I quote Ankit: “MY GUT tells me I am doing the right thing and to hell with what others think or believe.”

He has now completed a year on the SCD diet with just a bit of cheating. This illness has made him a more compassionate and a stronger person. He values everything in his life much more. He is feeling “normal” now, and has decided to go back and complete his flight training after completing his master’s degree in software engineering. Even though he is in remission, he recently started being more proactive, and is taking homeopathic medicine to prevent future flares and to stay away as much as he can from conventional drug treatment.

Although we at UCVlog do not advocate for or dismiss any form of treatment, we do understand there are times that we, as the patient, have to take control of our journey. Doctors are human, they make mistakes, and we have to be our own advocate for our healthcare and do what’s best for us. I wish to extend a great cheer to Ankit for overcoming such a debilitating situation through sheer determination to get well on his own. For somebody that did not think he was that remarkable, I believe he should think again. Although life for Ankit was interrupted by Crohn’s disease, he was able to get back on his path to live his life the way he wants. Great job! Here’s to continued good health and happiness. Good luck in flight school, Ankit!

“Courage is not the absence of fear, but rather the judgement that something else is more important than fear.” ~Ambrose Redmoon

~Nadia

Ankit at Maharishi Dayanand University

Ankit at Maharishi Dayanand University

Ankit at Maharishi Dayanand University

Ankit at Maharishi Dayanand University

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Inflammatory Bowel Disease PSA

November 7, 2011

Some time back I had come up with this idea to try to explain to others, what is inflammatory bowel disease, and although I could describe my own situation, I decided to broaden my search in describing IBD by asking others how they would describe it. What words would you use if you were asked by someone that does not have Inflammatory Bowel Disease to make them understand what we really go through? Hence, my idea for this public service announcement was hatched.

This is a compilation of the responses we received on our fan page on Facebook.

Along with our own thoughts and descriptive words, we put it to music: Boyce Avenue–Skyscraper cover. The lyrics are perfect as they talk about how you can be broken down (in this case, by illness), but you can rebuild and come out stronger. That’s what we all hope and strive for. This is a message of HOPE.

Maybe this can be a way for others to have an idea through our words even if they never understand how it feels…

“Never let go of hope. One day you will see that it all has finally come together. What you have always wished for has finally come to be. You will look back in amazement at what you have been through and you will ask yourself… ‘How did I get through it all?” ~Unknown

~Nadia

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Inspired by others—Kate from Australia

November 5, 2011

Since my recent permanent ostomy surgery, I have been thinking a lot about living the rest of my life as a permanent ostomate and how that will impact all the things that I want to do. Honestly, the way I have been doing for these past 2 months since surgery has made me feel that nothing can hold me back now. I believe that having this ostomy gives me the freedom to do so much more than I thought that I ever could, and it poses no interference to all that I can see myself doing. I am very sensitive and tuned in to so many other people that are on a similar journey and have watched as they, too, have made similar improvements with their health since their ostomy surgery or going through the challenges of this disease. Putting myself out there and sharing my story has given me the rare opportunity to meet others and hear their stories as well.

Many people share their history through their illness, accomplishments, challenges, photos, videos, and through all I am inspired by their tenacity and strength as they persevere. Often, I receive something that inspires me to share with others. There are many such stories that need to be told and this is a great arena to share…this is one such story.

Recently, I met Kate (from Australia) through the United Colon Vlog. Kate does not have inflammatory bowel disease, but she has been challenged for more than a decade with a prolapsed bowel or full thickness rectal prolapse at the age of 18. Although not the same, her symptoms very much mirrored that of a person suffering from IBD. After 5 major surgeries, she now has a temporary ileostomy. She told me recently that she will probably face permanent ileostomy surgery in a couple of years, as there is no quick fix, and her surgeons believe that a reversal will probably be unsuccessful.

Kate has not allowed this to hold her back. Not that long ago, she traveled to Canada from Australia with her husband. During her trip, her husband photographed her in various places showing her ostomy. She sent me a message in my inbox with the photo gallery attached, and with every photo, I just kept getting the goosebumps as I saw her accomplishments in every portrait. My heart connected with her immediately and I kept saying to myself “Oh my gosh, Kate, look at you!!” I actually felt the stinging of tears as I was so proud to see this because for some time now, I have been communicating with her, and I know parts of her journey and how hard this has been for her. To see these photos is so incredibly liberating. As much as she says that I inspire her, she inspires me–so much that I wish to share some of her photos and will be displaying additional photos on the United Colon Vlog fan page on Facebook. Her husband did an amazing photographic depiction to give the feel of strength and remarkable accomplishment for someone who has been through so much.

Kudos to you, Kate! May you continue to inspire. Thank you for having the courage to share these photos and your story and allowing me to show them. And thank you for being my friend. I know this may have been difficult, but your willingness to open yourself up to others will touch the hearts and lives of so many people across the world. It did for me! You rock, Kate!!

Instead of saying, “I am woman hear me roar” we can restate it to say “I am ostomate, watch me soar.”

Much love,
Nadia

Kate at the top of Mt Edith Cavell after hiking for almost 3hrs. Her greatest accomplishment so far.

Kate at the top of Mt Edith Cavell after hiking for almost 3hrs. Her greatest accomplishment so far.

If you have photos to share, proud moments of you overcoming the challenge of your disease, a huge accomplishment, please email me (Nadia@UCVlog.com) or message me on Facebook so that I can share your story with others. We can all inspire one another. Let me tell your story.

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