When I was 21, in the matter of one week I received an IBD diagnosis and had my heart broken. My boyfriend from college who had previously treated me like a queen, never visited me in the hospital and broke up with me the day I returned home.
I’ll always remember walking into my parent’s bedroom and telling my mom about the break-up. My body frail. My arms battered with bright purple bruises up and down. The weight of a lifelong disease and 22 pills a day hitting me head-on with every emotion possible. My mom’s response, “Well, you’re not perfect in his eyes anymore.”
From that point forward, I worried about the invisible Scarlet Letter of my illness and how it would impact my love life.
Would a man ever be able to love me, for all of me? Crohn’s and all?
You are not a burden.
The recent advice column shared in the New York Times entitled, “Is it Ok to Dump Him Because of His Medical Condition,” plays into every fear and every worry IBD patients grapple with. While Crohn’s and ulcerative colitis can happen at any age, people are more frequently diagnosed between the ages of 15 and 35. Finding out you have a chronic disease with no cure in those youthful years of life—often prior to finding a life partner or starting a career path, is incredibly overwhelming. The fear of the future and what is to come with your hopes and dreams is nearly debilitating at times.
So, it’s pretty freaking ironic when the author of “The Ethicist” who considers “readers’ ethical quandaries” responds back to this question about breaking up with someone because they have Crohn’s by saying:
“Committing to this person may be committing to a life as a caregiver”… and… “You don’t owe it to anyone to accept that burden.”
You are not a burden.
Referring to people with any chronic illness or disabilities in this way is not only hurtful, but extremely ableist. You can’t assume everyone with IBD is going to need a caregiver in a partner. If the author had any idea about how Crohn’s manifests, he would know that the disease is a rollercoaster…oftentimes years of being able to manage, followed by hardships, setbacks, and flares and back again.
As a 36-year-old married woman and mom of two, I have referred to my husband as a caregiver, but he’s more so my source of support and someone who sees me for much more than my disease. He would never think of me as a burden. He would never have considered breaking up with me because life could get complicated with my disease. He sees my disease as a part of who I am, but recognizes I am so much more.
You are not a burden.
To the 25-year-old single girl with ulcerative colitis reading this. To the parent of the child with IBD worried about whether their little one will ever find love as an adult. To the guy being talked about in the NYT article who most likely was broken up with—believe this:
You will meet people who turn a cheek once they find out you have IBD or suddenly show disinterest. It sucks in the moment. It feels like you’re getting punched in the gut. But use that pain to recognize that type of person isn’t meant to be your person. Take that heartbreak and use it to your advantage. Set you bar high. Settle for no one. Use your disease to shed light on people’s true colors. Who is going to be there when the going gets tough? Who lifts you up when you’re too weak to stand on your own? Who sees strength in your vulnerability with your health and the way you take on life?
You are not a burden.
I’ve had Crohn’s for 15 years (next month!). Last night I needed to take a pain pill to quiet the gnawing pain in my abdomen. This morning I had to make a fast dash to the bathroom multiple times in front of my husband and in-laws while my kids needed tending to. I apologized for needing to go to the bathroom so many times. Even as a veteran patient who’s four years into marriage with a man who loves me unconditionally, the words of that damn article rang out in my mind. I felt the guilt and wonder creep in….am I a burden?!
No matter how long you have IBD, no matter how well you have it managed, there are still moments where you feel less than your peers. There are still moments you can’t keep up. There are still moments if you wonder whether you are enough.
Just remind yourself…and I promise to do the same…YOU ARE NOT A BURDEN. And shame on you New York Times…as a journalist, I expect more. And so do your readers.
You go chica!!!……couldn’t have said it any better!…… that hurts to hear that anyone would look at anyone with an illness as a burden. I was diagnosed 31 years ago 9 months after having my daughter . Those exact fears have crippled me from letting anyone near my heart as much as I’ve yearned for love I could never let anyone all the way in and down played my disease, my aches my pains. I’ve had 2 resections , 1 anal fistula surgery connect to my vaginal wall and multiple other surgeries related. If this disease isn’t hard and embarrassing enough we have journalists in this world writing that were burdens. Makes me ill! I just turned 50 and I struggle daily inside with a huge mask on my face as if I’m conquering the world because of cruel uneducated folks like that. I believe you have just helped me in finding my voice sweeting ………thank you ! Thank you for being brave enough to have a blog about this insidious disease and to just speak our truth ! … my daughter is now 30 and just had her own baby girl and I pray that my grand baby never has this disease but I know between my daughter who was diagnosed 3 years ago and me my grand baby will know WE ARE ENOUGH!! —and we ARE PERFECT!! Thank you thank you thank you for being you , STAY TRUE to you always!!! Your an inspiration!
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THANK YOU, Tracy! What a kind message…you are SO right. Appreciate the love and support!
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Thank you so much for writing this. I just turned 30 in December, I had UC since age 2, underwent j-pouch surgeries starting in 2017 and got my official Crohn’s diagnosis in 2018. These thoughts have plagued me constantly and while I think it will take more time for me to be able to accept this its still so comforting to read from another IBDer.
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