Posts Tagged ‘research’

h1

Support Take Steps for Crohn’s and Colitis!

February 8, 2012

This year, The United Colon Vlog is participating in the Dallas Take Steps walk for the Crohn’s and Colitis Foundation of America! Events like these happen all over the country to raise money for the CCFA, which funds research into the causes and cure for inflammatory bowel disease, as well as patient education. The CCFA also supports a program near and dear to my heart, Camp Oasis, which is a summer camp for children with IBD.

A couple years ago Team UCVlog.com raised over $2,000–this year we’ve set the goal even higher–$3,500! We have until May 19 to get there, and with your help, we know we will. No donation is too large!

Donate to your favorite UCVlog star today! It doesn’t matter who you donate to: whether it’s Nadia, Hannah, or Dennis, all money goes to the same place.

Donate to: Dennis

Donate to: Nadia

Donate to: Hannah

Thanks for all your help!
~Team UCVlog.com

h1

C3Life Blog: What is health communication research?

February 2, 2012

Last week I talked about what it means to be a PhD student in the social sciences, and what this stage of schooling looks like. I’ve mentioned before that I am studying health communication, but I find that this term is incredibly vague. Today I will talk about what health communication research is, and what it means to me.

Read more

Keep fighting,
~Dennis

h1

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?

h1

C3Life Blog: What does a PhD student in communication do?

January 25, 2012

My second semester of my doctorate program recently began, but instead of talking vaguely about how school is going, and I want to get specific. What exactly is involved with getting a PhD, especially in something as nebulous as communication? When I tell my friends or coworkers or family or people I meet that I’m working on a PhD, I usually get three responses: slight awe for earning an advanced degree, followed closely by thinly veiled revulsion that I actually chose to go to more school, and then confusion: what does a person do to get a PhD.

Read more

Keep fighting,
~Dennis

h1

What a difference a day can make

December 11, 2011

There is a quote: “it doesn’t matter how slowly you go as long as you do not stop”…sage words from my daddy on the day I ran my first 5K. Not just any 5K, but a 5K with a 14 obstacle course and a mud pit to run through. Yes, a grueling sequence of obstacles set along a 5K path that I decided to challenge myself to do, while I was in recovery from my ostomy surgery back in September.

When I had surgery back in September, I decided at that time, that I needed to set goals to try to get my life back on track. I was a wreck. Emotional and physical mess. I had to try to find ways to restore myself back to “me,” so to speak. The old “me” never really ran a 5K, but whatever…ha! I wanted to try, and I think it helps too, toward building my self-esteem which was damaged quite a bit. My confidence needed some repair as well. Setting goals and achieving them seemed like the best plan to accomplish this.

The best laid plans

It starts out small, setting goals to walk 10 steps from the hospital bed to the door. Then down the hospital corridor or around the nurses’ station until I was finally able to walk out the door of the hospital to the car to go home. Small victories. When I felt that my recovery was on par, I decided that I would start setting goals further out, ones to work toward. The idea of a 5K run came to mind. Upon researching, I found the Survival Race in Texas being held in December – exactly 3 months post-surgery. My first thought, “where do I sign up?” I figured 3 months would be an acceptable amount of time for recovery.

I bought a pedometer shortly after and started tracking how much walking distance I could put on in a day. Later on, I started shopping for an elliptical machine. Then, I began stretching and trying to condition myself to some level of fitness in order to get through this. I had a few setbacks along the way that started to concern me. I kept getting ill with so many infections, flu, colds, I had an abdominal abscess, and I kept having setbacks. I was worried that I would not be well enough to achieve this goal. But harder yet, only a few short weeks before the challenge, I was injured in a car accident. I was about to give up on the idea of doing this 5K. My body hurt so much, and I couldn’t imagine trying to go through this and make it to the finish line. I began to think that this was too soon after surgery, then having so many setbacks; I should probably bail out and quit.

But slowly, I began to improve. I started walking a course outside my house and kept going until I reached the 5K mark. I would jam to my tunes, and the time flew by. Then, I started to jog and my endurance built up and I felt confident that I could do this. I was just going into it thinking all I have to do is make it to the finish line. Don’t worry about the time, just finish. JUST CROSS THAT FINISH LINE!!

Race Day

The night before the race I was so nervous; I didn’t sleep well. I kept thinking about the day ahead and worrying about the obstacles; I researched all 14 and pinpointed the ones that I knew I could easily do and the ones that would be a bigger challenge for me. I kept thinking all along the way how this race is a metaphor for my life. There are all these obstacles, all these challenges, and I have to figure out how to navigate through them. I am not fortunate enough in life however, to know in advance what obstacles are ahead, but I think you get what I mean.

In this particular event there were tires to run through, a mucky river knee deep, muddy hills to climb, walls to leap, crawling under barbed wire through a pond, crawling through wet and muddy tunnels, climbing over wooden and metal structures, a rope wall I had to get over, a pit of paint balls I had to go through on my tummy, barrels to jump over, and a fire pit to jump across. Many times along the way I thought I wasn’t going to make it. I hurt myself, got afraid that I couldn’t do something, or that I would fall from the top of the rope wall—I sat at the top of the wall contemplating my descent. I got tired, cold, my asthma was making it a challenge to breathe, but at each challenge, I faced it, did it, and overcame it until finally, I came to the mud pit–the most difficult challenge of the entire course. It was a lake bed of pure mud that was waist deep. It felt and smelled like poo-(haha one must admit this really was the perfect metaphor for IBD!)

The mud pit was the hardest to overcome. Here, I struggled the most, I didn’t think I could get through, I lost my shoes and went through it with nothing to protect me, I got stuck and could not move, it was the part that slowed me down the most, and for a split second I stopped, looked up, and thought to myself, “I’m done-I can’t do this anymore.” This was the perfect analogy for fighting IBD. Still, I kept on going, and once I was able to make it out, I was still carrying the weight of 20lbs of mud on me through the rest of the course. Kind of like, how making it past the biggest hurdles, one still carries along residual weight of this illness. It doesn’t completely go away–sad but true. I have an ostomy appliance attached to my abdomen as proof and scars that will never heal.

Champion for a day

Finally after a little over an hour, covered in mud, blood running down my hand, and bruises on my body, I crossed the Finish line. I was never as physically thrilled to finish something in my life as I was to finish this. I.DID.IT…ME! It was my glorious, feel good, moment. I sank to my knees to thank God for carrying me to the finish line.

This race was tough, but then again, life is tough. Some of us learn this the hard way, but this challenge taught me something about life and about myself. I believe that no matter how hard something is, you eventually get through it. Unlike this race that ended in an hour, so many challenges in the path we walk through IBD take years to overcome if at all, but we celebrate small victories, good days, and overcoming the challenges. Sometimes we get to the end of a struggle and feel victorious. I also learned that even if I am afraid of the unknown or afraid of the challenge of what I am facing, if I have enough faith in myself to believe I can make it, I can, and most of all, I learned to not give up. I never gave up-I never quit. Even if it was only for a moment or a day that I could feel high on life for crossing that finish-line, to me, that moment was priceless. It took a long time to capture that feeling-I got to have it, and I earned it.

“Satisfaction lies in the effort, not in the attainment. Full effort is full victory.” ~Mahatma Gandhi

~Nadia

h1

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.

h1

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

h1

Pre-surgery testing

August 31, 2011

Yesterday I talked about the tissue bank donation of my J-Pouch that they will collect after surgery. In preparation for surgery, one must undergo pre-surgery testing. In pre-surgery testing, there are steps that have to be done prior to any surgery. In most cases you will meet with a nurse, a pharmacist, and a pre-surgery physician to cover all aspects of your surgery. You will also have to do blood work and additional scans or tests as noted by your doctor.

This is done in preparation for any upcoming procedure to give the best result as a patient heads into their surgery. This testing leads the patient to surgery in the best possible way so that the surgeon and his staff are best prepared for your surgery. It also helps you know what to expect as much as possible. In my case, having gone through these steps, put some of my anxieties and worries at ease.

“Failing to prepare is preparing to fail.” ~Benjamin Franklin

~Nadia

h1

Donating tissues and organs for research

August 30, 2011

Prior to my surgery, I received a phone call from the Tissue Bank. I was asked to donate my J-pouch for research. The research helps in evaluation, diagnosis, or treatment of future patients. Once the surgeon removes my J-pouch, he will be doing biopsies, and instead of discarding the remaining tissue, it will be sent to the tissue bank, where it will be stored in a facility to be accessed at any time for research. This research does not benefit me directly but will be an overall benefit to any patients suffering from this disease.

Researchers may learn from using my specimen but none of my personal information will be attached to the organ. More specifically, it will have a vague description, such as 20-year-old female with Crohn’s disease. The risks are very low and the hospital is required by law to protect my health information.

I hope that because I have to go through all this, this donation of my body part will benefit other people. With any luck, something good can come out of this mess. So I will send off my J-pouch with a small prayer that it brings some answers to others.

“Research is creating new knowledge.” ~Neil Armstrong

~Nadia

h1

Extraordinary living with an ostomy: Episode 4: Riding a bicycle

August 6, 2011

An ostomy should not hold you back from anything. Your life does not have to change after ostomy surgery. If you enjoy certain activities before having an ostomy, there is no reason you cannot enjoy them now that you have one. I demonstrate in this video a couple of tips on riding a bicycle. It’s not really different other than a few minor adjustments. Make sure the most important thing is that an ostomy can cause dehydration very quickly, so when participating in any physical activity, always keep hydrated. Also, an important tip is to keep your ostomy bag close to your body by the type of clothing or wrap you wear. This will avoid a lot of shifting with your ostomy bag, keeping everything confined close to the body. Lastly, when you perspire, it can cause sweat to make the flange wet and detach from the skin. Just dry the area and try to stick it back on if it happens by reinforcing it with some tape, or if necessary, change your appliance.

“If you worried about falling off the bike, you’d never get on.” ~Lance Armstrong

~Nadia

Follow

Get every new post delivered to your Inbox.

Join 53 other followers