Dipen's Story for Mental Health Awareness Week

You might have heard that last week was Mental Health Awareness Week. A valuable time when we focus on the importance of mental well-being and learn how to be more understanding and compassionate towards people facing mental health challenges.

We know that a diagnosis of Crohn's or Colitis can be life changing, often impacting a person's mental health. One of our incredible supporters, Dipen, has experienced this impact first hand, after being diagnosed with Ulcerative Colitis in 2013. Read on as Dipen shares his story of enduring persistent flare-ups and navigating the challenging balance between remission and seeking additional treatment, all while trying to make the most of his twenties.


How did you feel after receiving your diagnosis?

I was relieved after I received my diagnosis as it took almost 6 months to be diagnosed with Ulcerative Colitis. At first I was incredibly concerned when I was told by a gastroenterologist that I either had cancer or something called IBD (Inflammatory Bowel Disease). So initially, I found myself at a high point as I thought at least it's not cancer and I can move on with my life. Sadly it did not take long for the lows to hit, within a week I was in the midst of my first major flare up, an experience I eventually learned to live with/through.


Can you describe your experience with mental health and your condition?

I was always on edge prior to having surgery. Every time I went out, I would go to the toilet to make sure I wouldn't need to go on my journey or whilst out (hopefully). Even when I was out of the house, I was always thinking about: 

- Where the nearest toilet is

- The best way to get to the toilets on the journey home or to my destination 

- What time I should be home by 

I would say the condition was controlling my way of living and my quality of life was affected. With having so may flare ups, it was a constant battle to stay fit and healthy, as I would lose a large amount of weight during a flare and then unhealthily put this back on whilst trying to regain some form of fitness.

I was tired of living the same cycle for 4-5 years and wanted change - which came in the form of my stoma bag - 'Mike'.


What do you wish people were more aware of when it comes to IBD and mental health?

I wish people knew that with most invisible illnesses, just because one day I am able to do normal day-to-day tasks, it does not mean I am always at the same energy level, or have the capabilities to achieve what I may have done previously. Also being told the pain 'cannot be that bad' when the pain of the condition on my body and mind is only something that I can experience and live through.


What advice would you give to someone who's in a similar position to you, and struggling with their mental health?

Talk to a family member, friend or confidant, someone who you feel safe to open up with. 

“”

Don't let it all build up inside you, as you can be your own worst enemy by neglecting to see the good things you have achieved. Take time to reflect on how far you've come and the progress you've made. 


What do you find helps on those particularly bad days?

As I mentioned above, talking to family and friends really helps me. Isolating yourself sometimes feels like the easier option, but it can make you feel like you have to do this on your own, when you don't. There are people out there who want to help. I also often find simple things such as listening to my favourite music and reminiscing on better times helps me tremendously. Especially when you're in a bad flare up, reflecting on better times helps you to realise it isn't going to last forever. 


Want to share your story?

We hear from people every day who rely on the Crohn’s and Colitis community for help and support. Sharing your experience can be helpful and inspiring.


Page
saved

This page has been saved in your personal space. Go to “My Page” to view all saved pages.

Helpline service

Helpline Service

We know it can be difficult to live with, or support someone living with these conditions. But you’re not alone. We provide up-to-date, evidence-based information and can support you to live well with Crohn’s or Colitis.

Our helpline team can help by:

  • Providing information about Crohn’s and Colitis.

  • Listening and talking through your situation.

  • Helping you to find support from others in the Crohn’s and Colitis community.

  • Providing details of other specialist organisations.

Please be aware we’re not medically or legally trained. We cannot provide detailed financial or benefits advice or specialist emotional support.

Please contact us via telephone, email or LiveChat - 10am to 3pm, Monday to Friday (except English bank holidays).

Live chat

If you need specific medical advice about your condition, your GP or IBD team will be best placed to help.

Would you like to save the changes made to this page?