As more and more people are open about their struggle with IBD, even famous people are joining in. It’s great to see actors, singers, and other famous people being frank about the disease and helping break the stigma. In the last couple of months, we saw these stories:
- Irish magician Dynamo discussed his diagnosis in an interview titled “Magic Won’t Cure Me.” For those us with the disease, he advises:
If you’ve got Crohn’s then you just have to get on with it, deal with the negative things that come with it, and not let it change the happiness in your life. You can’t help it; it’s what it is.
Continue reading “Celebrities… Just Like Us (They Have IBD)”
Inflammatory bowel disease can be embarrassing. Our instinct to hide the disease can be very strong, and might even protect us from discrimination and prejudice. Yet being ‘out’ about IBD can be positive, and even healthier. So — are you out?
Let me say: I didn’t invent the ‘coming out’ analogy for IBD. It’s often used in the medical literature to talk about people with illness, especially people who hide mental illness. There is evidence that hiding an illness is much like hiding sexual orientation or a substance abuse problem. (The term of art in the literature is ‘concealable stigmatized identity‘.)
There are good reasons a person might choose not to be ‘out’ about IBD. Many societies have strong taboos against anything to do with poop. People often react to talk of illnesses like ours with ignorance or disbelief, and it can be hard to find a sympathetic ear. To the extent diseases like IBD are ‘stigmatized’, hiding a diagnosis can be a way to avoid that stigma.
Continue reading “Are You ‘Out’ With IBD?”
Everyone with IBD looks forward to the day a cure is found. But what are you doing to make that happen?
Maybe you’ve done a fundraiser. Maybe you’ve donated money. Maybe you’ve participated in a clinical trial. That’s all important, but there’s an easier way to help fight IBD — and it requires not a single penny, drop of blood, nor sip of prep.
What you can do is join Crohnology — the social network for people with Crohn’s disease, Ulcerative Colitis, and other forms of IBD. Crohnology has more than 8,000 members from 91 countries, who share their experience with the disease to help each other feel better.
Continue reading “There Is No Cure Without U”
(This is a guest post by Laura. She lives in Australia and blogs at Stomalicious; you can follow her blog on Facebook.)
Before my Crohn’s diagnosis at age 30, I was a relatively confident, independent, worldly woman.
Having IBD impacted all of that. As my symptoms worsened, insecurities increased. I became introverted, anxious, and less confident in many ways. Going to work, socialising, even grocery shopping became a struggle.
I became heavily reliant on my family for help and support. There is nothing wrong with this, but after being so independent, it was difficult for me to accept.
Financially, physically, personally, socially … my world changed. My self-esteem plummeted in more ways than one.
Continue reading ““I Am Not Ashamed To Get My Body Out…””
One of the medicines most often prescribed for IBD is prednisone. Most people know it helps reduce inflammation, but there’s lots more to it than that. So how does it work?
Prednisone is in a class of drugs called steroids. ‘Steroid’ is short for ‘steroid hormone’ — ‘steroid’ describes a specific shape of chemical, but ‘hormone’ says more about what the chemical does. A hormone is simply a signal from one part of the body to another, to help regulate various bodily functions.
Steroid hormones come in two kinds, corticosteroids and sex steroids. Sex steroids are produced by reproductive organs, and include testosterone and estrogen. When most people talk about steroids, they mean the synthetic sex hormones that some body-builders use. Prednisone isn’t that kind of steroid, alas.
Continue reading “How Does Prednisone Work?”
Learning to cope with inflammatory bowel disease is crucial to living with the disease — but are some coping strategies better than others? Is there a ‘best’ way to cope with IBD?
It turns out there have been several studies of coping. Not surprisingly, some ways of coping are better than others. The most recent study along these lines was published last year in the Southern Journal of Medicine.*
The authors took 150 patients with IBD and gave them a survey that looked at their coping behaviors. The survey asks patients to note how often they do things like, “prayed or put your trust in God”, “waited to see what would happen”, or “tried to keep a sense of humor”.
Continue reading “How Do You Cope?”
People get inflammatory bowel disease from a combination of genes and environmental triggers. Having the right (i.e. wrong) genes makes a person more likely to develop IBD in the presence of the right (wrong) external factors. In a previous post, we looked at both causes of IBD; this post takes a closer look at the external factors that cause Crohn’s Disease.
In 2013, the journal Gastroenterology and Hepatology published a two-part review* of the known “environmental” factors that can be associated with Crohn’s Disease. Why only CD? The authors don’t say, but some of the studies mention Ulcerative Colitis as well.
‘Environmental’ in this sense means things that are outside the body — even if they can be eaten or absorbed. The study points out that there are three basic ways external factors can contribute to Crohn’s: 1) by making the gut leakier; 2) by changing the immune system in the gut; 3) by changing the gut microbiome.
Continue reading “External Risk Factors For Crohn’s Disease”
For many people with the disease, IBD counts as a disability — at least under the U.S. Americans with Disabilities Act. That means there rules to protect people with IBD from discrimination. One of the places where those rules are most important is work.
People changing jobs or entering the workplace often ask: “do I have to tell my boss?” The answer is ‘no’ — but it’s a little bit complicated. There are two parts to the question: first is when you are applying, second is when you have the job. And, again, this is for U.S. Law
Continue reading “Do I Have To Tell My Boss?”
What if you couldn’t eat for… who knows how long? That’s exactly what happened to Jon Reiner, an author with Crohn’s disease. He tells the story in his memoir, The Man Who Couldn’t Eat.
The book starts with Reiner’s disease in a bad flare — as in, near-death bad. He winds up in the hospital with intestines full of holes, so fragile that one of the holes can’t be closed properly. Reiner’s doctors decide that in order for his guts to heal, he can’t eat or drink anything — not even distilled water — for as long as it takes.
That said, the book is not full of graphic detail about symptoms. Instead, it’s about how the disease changes his relationship to food. What happens after Reiner is told not to eat is hard to explain: first, you have to understand that eating isn’t just a thing you do. It’s a big part of who you are.
Continue reading “The Man Who Couldn’t Eat – a review”
From time to time, the research wranglers at the Crohnology Blog find ourselves lassoing a few stray stories of IBD-related news. Thus we present another Research Roundup, where we bring those stories back to the corral for your perusal…
- Avoiding fiber might make flares more likely in Crohn’s patients. A study of 1619 patients with CD and UC shows that patients with Crohn’s “who reported that they did not avoid high fiber foods were ∼40% less likely to have a disease flare than those who avoided high fiber foods”. This is contrary to conventional wisdom that high-fiber foods can trigger flares, although the study does not show a clear causal relationship.
- Why don’t people take their biologics? A study of people taking anti-TNF medicinines (Remicade, Humira) shows that a quarter of them were ‘non-adherent’ — that is, not taking their meds as prescribed. The main reason was that they were supposed to be taking Humira, which can be injected (or not) at home. Other reasons were shorter disease duration and ’emotional response’. Non-adherence is an important reason why biologic meds stop working over time, so taking the meds as scheduled can help keep them effective.
- Etanercept may trigger IBD. According to FDA records, some 443 cases of IBD may have been triggered by the anti-TNF drug etanercept (brand name: Enbrel). Etanercept is not approved to treat IBD; patients were taking it for conditions like rheumatoid arthritis.
- Stem cell transplant is no better than conventional treatment for Crohn’s. A study of patients with severe Crohn’s showed no statistical difference between stem cell transplant and more conventional treatment. One patient who underwent stem cell transplant died.