4 Comments

Waiting

Most of you are too familiar with waiting. Waiting months to see doctors who show up hours after your appointment time; waiting to see if a new treatment will turn your life around; and most agonizing of all, waiting for the day you can forget about your broken body and just feel normal.

I would like to share some ideas for passing the time and thoughts on my questionable choices because I know how awful waiting can be, and I am willing to bet that some of you have fallen into similar patterns. When you are sick and just waiting to feel better, your family and friends will not understand what you are going through. They just can’t. That is why, dear friends, we must unleash our inner thoughts to strangers who have also felt broken.

Back before a few new conditions arose and I was “just” dealing with severe Crohn’s disease, I had a knack for making good use of waiting time. I did schoolwork and read books in waiting rooms, hospital beds, and even in the bathroom as I waited for my guts to cooperate enough for me to venture out. Nurses and doctors frequently complimented my dedication, but it was all normal for me. I couldn’t move around much, so I figured I might as well read until I got too tired or dopey. My mind thrives on intellectual challenges, but my perfectionism turns my beloved books and schoolwork into stressors. I always felt like I should try to catch up with my extremely intelligent friends, most of whom got consistently better grades while reading more extracurricular books than I ever could. Friends, I can tell you with the utmost confidence that worrying about catching up is a foolish pursuit.

Take life at your own pace.
I hate to break it to you, but you can’t catch up. All you can do is make mindful choices to make the most of each day. Sometimes illness makes us feel like life is passing us by. Joint pain and malnutrition may slow us down and make us feel hopelessly different from our healthy peers, misbehaving guts may drive friends away when we frequently cancel plans, but the emotional impact of chronic illness seems to primarily stem from the fear that our suffering will seize complete control over our lives. We may lose a lot of control, but really good friends will understand and adapt to our limitations, and we can change the course of our lives by learning how to cope with our health issues instead of just wishing things would change. I am still learning, but I have come a long way thanks to the support of a few kind friends and a whole bunch of people with IBD and ostomies.

Back when I had a full set of organs, I waited for treatments to potentially help me achieve remission, school became extremely difficult, but my optimism stayed intact because I didn’t give myself much time to think about anything but my academic goals, and I honestly kept thinking I was only a few months away from feeling great. It turns out I was making a few mistakes. I highly recommend using your time wisely, but I don’t recommend my previous strategy of working to the point of exhaustion. Apparently there is such a thing as too much dedication to schoolwork, and such focused ambition can easily turn destructive when physical trouble demands dramatic lifestyle changes. Depending on your circumstances, you might have to be open to the possibility of finding new hobbies, academic paths and career options. Time away from school or work can be a blessing in disguise for people who end up finding occupations they truly love. While you’re waiting for life to change, you just might be able to figure out some new ways to feel truly fulfilled.

Pain and fatigue are a constant force limiting my physical and mental abilities. I have lost control over so many aspects of my life, and I am here to tell you that no matter how elusive they may seem, hope and joy are within your reach. Sometimes we just have to drag ourselves through rough days and dream of brighter times ahead. In the meantime, here are a few suggestions for passing the time:

Waiting to find the right doctor. Feeling miserable, but enjoying my lap dog, soup, and a cozy blanket from Grandma.

Be a couch potato sometimes if you wish your brain had an “off” switch and it hurts to move.
I watch comedies when I need a distraction and I don’t want to think at all. Since I’m a political science student who doesn’t know much about the world, I also watch documentaries when I feel like learning. They’re also great distractions from my frustration, and I end up with all sorts of random knowledge. I get teased about this habit, but that’s okay. I think everyone can agree that nature shows can be nice for stress relief, but I also watch the occasional show about environmental destruction or human rights abuses. Avoid those if you’re already depressed.

Exercise: start small and respect your limits

Movement can be good, but within reason. If you’re really sick, stretching and walking might be the extent of your workouts. Apparently you should stop before you get dizzy and nauseous. If I’m in enough pain, I’m completely unmotivated to move. As soon as I’m feeling a little better, I tend go out and disrespect my limits. We can all agree that a bit of exercise is great for stress relief, but staying hydrated and maintaining a good electrolyte balance are more difficult with gut issues. If you work out to the point of needing serious recovery time, try not to feel too bad about your condition. When we’re waiting for our bodies to get stronger, it’s easy to get frustrated. I try to remind myself that I have to start somewhere.

Practice gratitude: spend some time thinking about your blessings

Practicing gratitude is different than convincing yourself that your emotions and suffering are invalid just because other people seem to face more difficult circumstances. My mother tells me that just because there are starving refugee children in Africa, that doesn’t mean I’m not allowed to be upset about my condition. I get annoyed with myself for feeling frustrated, impatient, and hopeless because I figure I have no right to be sad. Other people who deal with different challenges have the right to be upset with their lives, but I should be satisfied with my blessings and accept my problems. I currently have very little advice for you if you fall into similar thought patterns. My friends are still trying to break me of this terrible habit.

I can tell you that hearing stories to illustrate the point that “it could be worse” is dreadfully unhelpful. Don’t let others make you feel guilty for feeling awkward and miserable when you’re struggling with transitions and waiting for life to change. It’s easier said than done, but just ignore the “could be worse” stories and change topic of conversation. After hearing similar comments for years, I still don’t know how to gracefully respond to “At least you have all your limbs,” or “At least you don’t have cancer.”


Improve bathroom time:  
IBD flares demand a  lot of time near a toilet, so you might as well find ways to make it less lousy.
It’s an embarrassing topic that is seldom discussed, but some of us have spent an insane amount of time waiting to get away from our bathrooms. Thanks to my rebellious intestines, I used to live in there for at least a few hours every day. Being stuck in that little room while your body turns itself inside out is not fun. I spent a lot of time doubled over with cramping, but I was conscious enough to get bored sometimes. I had books and magazines that had short stories and segments that involved less brainpower, but I also kept a bit of schoolwork in the bathroom. During particularly restricted times, I watched movies on my laptop and kept a little nest of pillows and blankets in near the toilet so I could get a bit of rest between bouts of misery. Eventually I found the perfect brands of various goodies that helped alleviate socially unmentionable skin issues and discovered that heating pads can help with abdominal cramping. Every time I figured out a new trick to make the bathroom more welcoming, I was so delighted. If you’re spending too much time stuck in the bathroom, talk to people about their tricks for feeling better. You won’t regret those awkward discussions!

Some very important people whose love make this blog possible.

Life is better with good company: find some gutsy buddies, read some blogs, and learn from others.

I may be a gimpy weirdo, but gosh darnit, I can still brighten someone’s day. I can reassure my fellow gut buddies that they are not alone, and I can participate in the IBD and ostomy communities. I encourage you to do the same regardless of your current condition. We are in this together, dear friends. Let’s do what we can to help each other out. Whether you’re so sad you can hardly stand it, a little cranky about being sick and different, or generally feeling okay, your contributions to every conversation with fellow gutsy buddies are more valued than you will ever know.

Advertisements

4 comments on “Waiting

  1. You just put into words my feelings! Thanks, it is nice not to feel so alone.

  2. Hi! I just finished reading your post. I found out last fall that I had Ulcerative Colitis. It took all I had not to look at it as a death sentence! I kept reading the “do’s” and “don’ts” for someone with IBD and it seemed even the do’s were no no’s for me. This got discouraging super fast because I LOVE to eat, always have, and was always able to, and now it wasn’t so fun along with all the discomfort and pain. I don’t take medicine because I refuse to be on pills for the rest of my life. I also refuse to see that as my only option. This past week I got to my worst and knew I had to do SOMETHING since nothing else was helping (and again, a life of meds was not for me). So, i started doing my research on natural healing. (yes, sounds super hippy) And I came across juice fasting. Juice fasting has actually been proven to cure and reverse the “unreversible”. I’m not sure if you have ever watched the biography of the guy who started http://www.fatsickandnearlydead.com/, but he had so many problems that were cured from allowing natural fruits and vegetables (juiced) bring to his body what was needed for healing. I actually started a 60 day juice fast blog today and am going to journal through my adventure to seeing just what is on the other side. I’m sure this all sounds crazy, but I am praying God uses my UC/IBD and this challenge of juicing to bring healing that Dr’s say we can’t get and need to spend tons of money on for the rest of our lives, and to encourage other people who suffer from it that it’s not a death sentence or something we just have to deal with, but that it’s an opportunity to step up our game in life and DO what needs to be done! I am so sorry you suffer as badly as you do with it, but know you are not alone- and I don’t believe this has to be the end.

    • Thanks for writing, Ashlie! A lot of us with IBD develop a love/hate relationship with food, and there have been times I avoid eating because of the pain food can cause. I think natural healing should be researched more thoroughly, because I think a lot of people reach desperate points like you did. It can be difficult to find good information, but gosh it’s great when we do! I think a juice fast sounds awful right now, but that’s because I can eat whatever I want and an all-liquid diet would not go well with an ileostomy. My mother would approve of your willpower… I am lazy and weak-willed about some things, and we have a juicer sitting at home that I never use. Please let me know if you find any juices that are really easy to make, and easy on your angry belly. Your attitude is great, and I really look forward to hearing about your adventures!

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s

the crohn's diary

A little diary, all about Crohn's and other form of IBD!

The big stoma bucket list

after a life crippled by Crohn's and Colitis my 101 stoma bag lady challenge

Erica's Tummy Blog

A blog of my life colored with the dealings of Crohn's disease and more

Colitis and Crohn's

Sharing and spreading awareness about Colitis and Crohn's disease.

bringtheshine

connect ~ inspire ~ support

Crohn's Knows

Taking Time To Talk Crohn's and IBD

Companion Magazine for IBD

Bringing the IBD world together, one story at a time

Tranquil Tummy

Blogging my journey to cure myself of Crohn's Disease

autoimmune barbie

Barbie girl living in an Autoimmune world.

hopefaithcurecd12's Blog

My journey, a way of coping with a chronic illness

childgastro

4 out of 5 doctors recommend this WordPress.com site

VeganOstomy

Helping to create happy ostomates.

Crohn's Allogeneic Transplant (Allo HCT)

Allogeneic bone marrow transplant to cure Crohn's disease – also called Allogeneic Hematopoietic Cell Transplantation (Allo HCT)

Itsgutsandglory.co.uk

25 year old Ex- Ostomate, living with Crohn's and writing about it. Advice, Food and IBD Life

The Fight for Health

Journaling my fight with chronic illness through food, fitness, family and a fledgling martial arts journey.

Tree and Leaf: Honesty. Health. Humor.

Let's be real honest about immune/autoimmune diseases for a minute

#purpleproject

running to the bathroom.. my journey with IBD

My IBD Life

Shit happens, Wipe your ass and get over it

skylersthelimit

To live is an act of courage.

The Irrefutable Opinion

Assaults on the Casually Mundane by K. Jean King

The Chronic Adventurer

Finding a silver lining from his IBD

shine & Smile

Inspire. Dream. Love. & Keep Smiling Lovlies

Crohnie Man

Everything IBD and Crohn's

Mind Your Body

encouragement and advice for folks with rebellious intestines

spilling my guts

encouragement and advice for folks with rebellious intestines

Whoops! Thaila has moved!

Go to http://thailaskye.me.uk

talkaboutguts.blogspot.com ….

encouragement and advice for folks with rebellious intestines

THE OSTOMY FACTOR

Living an ostomate's life with humour and inspiration

Living with the Unexpected

There are over 1,000,000 people living with an ostomy in the United States. I am just one.

The FlowryLife

Living mindfully thanks to IBD

Amazing Adventures (ostomy included)

Courage Inspiration Empowerment

The Caged Bird Still Sings

Striving to be content with the life I have been given, instead of the life I had imagined

BedEleven

My disastrous health, weird life and ongoing story of intestinal failure.

Ask Ansley

My Crohn's Story

Tissue Tales

My journey, navigating through life with a Connective Tissue Disorder.

Dr. Abby Caplin's "Permission to Heal"

Practical Loving Ways to Heal through Chronic Illness

jennovafoodblog

Nutrition: a different outlook

Gotta Go: Our IBD Lives

Two Sisters - Two Differnet Lives - One IBD Diagnoses

Hungry Girl Eats

Notes on the care and feeding of body, mind and spirit.

My Cranky Gut

Misadventures with Crohn's Disease and the Specific Carbohydrate Diet

United Ostomy Association of Canada

Live Life to the Fullest!

Evicting My Misbehaving Colon

IBD and J-pouch Adventures

stanleystoma

The tales of Ulcerative Colitis, a stoma & J-Pouch

30 Days with Juice

A fine WordPress.com site

Lauryn and Lulu

My journey with Lulu (my stoma) & battling Crohns Colitis

crohniechaos

My Journey

%d bloggers like this: