Find out how to let us know if you're concerned about another member's safety.
It takes guts

Adrian_Scope
Posts: 8,589
Scope community team
Our very own @Sam_Scope is taking part in the fantastic #ItTakesGuts campaign for Crohn's & Colitis UK and urging those living with Crohn's and Colitis to break the silence and talk about what can be an invisible but very painful struggle.
Telling people about your condition might help change your life, but if you're having trouble finding the words, Crohn's & Colitis UK will do their best to help you speak up and break down the stigma through the #ItTakesGuts movement. Are you living with Crohn's & Colitis? Do you find it difficult to talk about your condition? We'd love to hear from you.

Telling people about your condition might help change your life, but if you're having trouble finding the words, Crohn's & Colitis UK will do their best to help you speak up and break down the stigma through the #ItTakesGuts movement. Are you living with Crohn's & Colitis? Do you find it difficult to talk about your condition? We'd love to hear from you.
Comments
-
Brilliant campaign, well done @Sam_Scope
You never know what people are going through. I am hoping this gives people some inspiration to talk about their condition.
-
I agree.
I was diagnosed with a SpLD a few years ago when I was a full time college student. It is nothing to feel ashamed of. My SpLD only affects my ability to work with numbers and money independently. When I was diagnosed I wrote about my feelings in a letter which I keep on my bookshelf. I always read it on my bad days as soon as I get up in the morning it helps lift my spirits.
Try writing about your emotions or talk about your feelings with someone you trust. You could always try keeping a diary. It definitely helps to talk about disability honestly too. Raising awareness is so important for society.
-
I have coeliac disease as well as my CP I have days when all I want to do is sleep xxx
-
One of my wonderful carers suffers with bowel problems. She was diagnosed with ulcerative colitis some years ago, only to have a change of consultants and was told she `only` has IBS.
She is having a 2nd opinion soon.
It is a very debilitating condition.
love to all xx
Brightness
Categories
- 53.9K All Categories
- 10.6K Start here and say hello!
- 5K Coffee lounge
- 4K Disability rights and campaigning
- 1.5K Research and opportunities to get involved in
- 153 Community updates
- 12.1K Talk about your situation
- 1.8K Children, parents, and families
- 791 Work and employment
- 588 Education
- 1.2K Housing, transport, and independent living
- 1K Aids, adaptations, and equipment
- 290 Dating, sex, and relationships
- 265 Exercise and accessible facilities
- 21.6K Talk about money
- 2.1K Benefits and financial support
- 4.4K Employment and Support Allowance (ESA)
- 12.5K PIP, DLA, and AA
- 2.6K Universal Credit (UC)
- 4.1K Talk about your impairment
- 1.3K Cerebral palsy
- 686 Chronic pain and pain management
- 704 Rare, invisible, and undiagnosed conditions
- 759 Autism and neurodiversity
- 937 Mental health and wellbeing
- 311 Sensory impairments
Complete our feedback form and tell us how we can make the community better.
Disclaimer
Our website contains links to third parties’ websites for your information only.
We have no control over the content of those sites or resources and we don’t endorse or accept liability for the content of them.
Read the full Terms and Conditions and our Community Guidelines.