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Sunday, January 25, 2015

INFORMATION: Little Vitamins for your Brain


As I have stated in previous posts, the most useful source of information about my Crohn's disease, besides my doctors, has been the Internet. Yes, the Internet, in all its spam-filled, keyboard-warrior, opinionated, misguided glory. While the 'Net is rife with misinformation about any-and-every topic known to man (and even some topics that aren't known to man), there are still some dark, quiet corners of the web that harbor endless seas of useful, truthful, and supportive information. And as you will learn, some of these little hidden gems are making a huge impact on the awareness and forward-process of treating and curing Crohn's and Ulcerative Colitis. I'd like to share some of my personal favorites.

THE BASICS: These sites are generally thought of as the leaders in information about CD/UC:

LIVING WITH CD/UC: Useful, applicable, real-life tips, tricks, and stories:
COMMUNITIES: Find other Crohn's and Colitis patients, share experiences, tips, and stories:
  • Facebook Group: Crohn's and Ulcerative Colitis Support Group - You must be approved by the group's owner to join this group; it's a private group, so anything posted here will NOT show up on random friends' Facebook news feeds. I am part of the admin team, and I am very proud to say this is my daily go-to source for information and support. You will likely make new friends and learn about aspects of Crohn's and Colitis you've never heard of. (With all community groups, abide by the house rules at all times to avoid potential conflict!)
  • Reddit Crohn's Disease - beware, Reddit is not for everyone. As with any website that is run by its members, you may find some posts or items disturbing. However, there are far more useful and helpful (and sometimes even funny!) posts here.
  • Crohn's Zone - community forum. Similar to any forum-based support group, you sign up to participate in discussions with other members. I happen to really like this one because they offer useful articles as well as member posts, and even have a Schwag Store.
PARTICIPATION: Take part in clinical studies, fundraiser events, and research opportunities:
  • ClinicalTrials.gov - registry and results datatabase of publicly and privately supported clinical studies of human participants conducted around the world. Search for your condition or location from the main page.
  • World Health Organization (WHO) Clinical Trials Registry - similar to the one above; worldwide.
  • Chronology - A really unique website which gathers and reports user-based data about chronic health conditions. The more information you give them about your personal condition, the more useful the research can be.
  • 23andme DNA IBD Study - as of the date that I'm posting this blog, this study is still accepting new participants. The kit and ancestry info is FREE for participants: you must be diagnosed with a form of IBD, and you must consent to have your DNA information recorded and researched. Even if you don't have IBD, you can still purchase a DNA testing kit and have your ancestral results sent to you. Your DNA may also help guide future genetic studies for countless medical conditions!
  • GYGIG - Get Your Guts in Gear: A non-profit fundraiser for IBD awareness and research through multi-day bicycling events around the U.S. 
SPECIALTY SITES: 
MOBILE APPS: there are lots out there, these are just the ones I am using:
My list of links above is nowhere near exhaustive or complete. These are just some of my favorites that I wanted to share with you. A great source for even more links with a wide range of topics can be found here: HELPFUL LINKS. There are links on that page to direct you to assistance programs, insurance information, medical journals, and much, much more. 

The Internet has become the world's most loved and hated engine for sharing information. Unfortunately, just as in real-life, there are wrong turns you can take online that can lead you to spam, misinformation, or false data. Use the 'Net at your own risk, and be cautious of any information you gather. Always, ALWAYS ask your doctor or other health professional if you are ever unsure!

I hope these links will help you as they have helped me. What are your favorite websites or apps for your Crohn's and Colitis support? Please share in the comments!

3 comments:

  1. Another Facebook group that I find useful is "Life with Inflammatory Bowel Disease." I also belong to "Ibs" but I'm not sure if that applies here. Thank you Jess,as always you are an amazing jem of information and I'm very appreciative,as I'm sure others are too.

    ReplyDelete
  2. Great post!. Thank you for giving us the essential healthy information for brain.

    ReplyDelete

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