Juicing – Good or Bad


Juicing

This morning I was looking at Twitter and I saw a tweet that said that juicing really isn’t good for you and lead me to this article.  I know many an IBD that swear to juicing so of course I had to take a look.

Of course like most click baits these days, the article wasn’t quite what was being described.  It goes on to say that juicing as a form of detoxing the body doesn’t really work.  Of course, this isn’t news to me because if you know anything about nutrition, fruits and vegetables while good for you, can actually be harmful in large quantities.  There is the sugar contents and carbs.  I very rarely touch any juice as it also doesn’t have as much vitamins or fiber then if you eat the actual fruit since most of the nutritional elements are in the skin and the skin a lot of times doesn’t make it into the juice.

The reason behind this post is because when I first saw the whole good or bad, I thought right away to all of my IBDers that juice and to them it is a life saver.  Many people can’t tolerate or digest whole foods.  Juicing is a big way for many of us with digestive issues to get our calories and vitamins.  Of course, those needing this make their own juice and usually will have the skin as apposed to the commercial juices that don’t have them.

I actually got angry over the tweet because it should have been said differently.  To just say it isn’t good is very misleading.  The tweet didn’t mention detoxing.  If it did, I would have ignored it.  Instead, it was something just put on the surface which will somehow eventually be taken out of context.  And then, this will lead to people thinking less of those of you that juice for your health.  And also, if you look really fast at the article, which I just did, the first thing you see is Juicing is Officially Dead.  Well, not for my IBDers, I can tell you that.

The one good thing that they do say in the article is this, and it comes at the very end,

Juice still has its benefits. Juice squeezed from fresh fruits and vegetables is more nutritious than sugary, whipped-cream-topped Frappuccinos. It’s also a convenient way to consume healthy foods on-the-go: I wouldn’t gnaw on a carrot or a beet on my morning commute to work, but I’d certainly sip them through a straw.”

So how many of you juice?  What has been your experience with it?  Why do you juice and what is your favorite recipe?  I would love to hear from you and hear about your experience.

juice

 

 

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Upcoming Blogs


Just a quick update.  I am looking to start writing again and I would love to change my format a little.  I want to get you, my viewers, more involved.  So, here is what I want to do.  I am going to list some things I will be writing about soon and I would love for you to let me know if you have any experience or stories you want to share.  You can email me at aguywithcrohns@gmail.com.  It can be a couple of sentences or a couple of paragraphs.  I will respond to you and if I choose to publish what you wrote, I will get your approval first.  I would never publish anything without permission.

So what will I be talking about.  Well, if you have anything to say about the following, let me know:

IBD and arthritis

IBD and weight loss or gain

IBD and depression

Starting a new job with IBD

For now, that is all I have in the works, but of course, if you have an topics you would like me to talk about, let me know.  I look forward to hearing from everyone with their stories and ideas.  Can’t wait to see what we can all transform this blog into.

Barney

 

2015 Super Bowl Pool ~ for The Intense Intestines Foundation


This is something I have been wanting to do for a while but never seemed to make the time for it.  So, this year I am doing it.  I am holding a pool for the Super Bowl.  50% of the money raised will go to The Intense Intestines Foundation, a charity that helps people with Crohn’s Disease, Ulcerative Colitis, and Ostomies.  The other 50% go to 4 winners.

I am selling boxes for $10 each.  I will pick the box for everyone so it will be random.  There will be a winner for each quarter, so 4 winners.

Super Bowl Pool 2015If you would like to buy a box, or 2 or 10, let me know.  To make payment easy, I am using Paypal.  You can send the money to aguywithcrohns@gmail.com.

If you have any questions about this, please let me know or email me at aguywithcrohns@gmail.com.

We Interrupt Your Regularly Scheduled Programming….


I hadn’t planned on adding anything this month since I am doing the Writers Challenge and posting a post a day.  But I had an idea and I want to put this out there to get some help.

 

This goes out to anyone reading this that has IBD.  If you don’t have IBD, you can ignore this post 🙂

 

Ok….now that the normal people are gone, we can talk about them.  He he. 

 

What I am needing from my IBD community are some photo’s.  I am planning on making a video for World IBD Day and an idea hit.  Since so many of us were upset over CCFA’s handling of our condition in their advertising, I want to do a video to show just what it is truly like to have IBD.  So, I need pictures of you at your worst.  Do you have a bad moon-faced?  Do you have pictures of your hospital stay?  Maybe you have a stoma you want to show off.  I want to make a nice collage of them in a video. 

I will also need some triumph pictures but the majority that I need are the downside pictures.  If you have some you would like to send, please mail them to aguywithcrohns@gmail.com.  If you want yourself mentioned in the picture, please give me your name, twitter handle, website address, blog address, date of diagnoses and what condition you have.

 

Thank you everyone for your help.  I now return you to our regular programming.

Health Activist Writer’s Month Challenge – Day 4 Sharing Resources


 Create a “care page” – a list of your best resources that someone who is newly diagnosed could go to when starting to advocate for themselves or a loved one. Remember to include sites that lead to successful self advocacy!

I won’t say much here today.  I am going to let my fellow activist to all the talking.  So here are some links to some great people and great sites.  Some you might know, others you are finding for the first time.  Enjoy.

Inflamed and Untamed – www.inflamed-and-untamed.com

Blood, Poop & Tears – www.bloodpooptears.com

The Great Bowel Movement – www.thegreatbowelmovement.org

The United Colon Blog – www.ucvlog.com

I Have UC – www.Ihaveuc.com

Girls with Guts – www.girls-with-guts.org

The Crohn’s and Colitis Foundation of America – www.ccfa.org

Love For Mutant Guts – www.loveformutantguts.wordpress.com

Intense Intestines – www.intenseintestines.org

Chronology – www.chrohnolgy.com

Karen Langston – Mind, Body, Soul – www.karenlangston.com

Crohns Disease Warrior Patrol – www.crohnsdiseasewarriorpatrol.org

My Journey With Crohns – http://www.myjourneywithcrohns.com

The Crohn’s Diaries: Living Sick with Inflammatory Bowel Disease – http://livingsick.com/

There are so many more that I could put down, but I would be typing for days.  So go check out these sites and from there you will find many others.  Have fun and let them know how you found them.

Health Activist Writer’s Month Challange – Day 2 Introductions


 

 Introduce your condition(s) to other Health Activists. What are 5 things you want them to know about your condition/your activism?

Hello.  My name is Jeffrey and I am a Crohnie.  Well, that is how I would imagine an introduction would go in an anonymous IBD support group.  Of course, an intro like that kind of has a negative stigmatism to it because it reminds us of intro’s used in AA which, even though it is a good group, you go there because of an addiction.

Well, having IBD is kind of like an addiction.  It is something always on our minds.  We take drugs to forget the pain we are in.  And no matter how much we want to forget about it, we seek out others who have the same so we can relate and fit in.  But, IBD is NOT bad. 

That is #1.  IBD is not something we can control and it is not contagious.   IBD is an auto-immune disease and we have no control over it.  Like many addictions, IBD is condition that happens and we have no control on how it will act.  We can try to manipulate it with medicine, exercise and diet but it will ultimately act however it wants.  It is the body attacking itself so there is nothing that will spread to someone else when you cough, sneeze or bleed.  You can’t give it to someone else.  It is a genetic disorder that needs a lot more understanding.

#2 – People with IBD at times are in a lot of pain.  There are different types of disease under the IBD umbrella.  They all act differently and there are different severities to them.  But over time,  anyone with IBD will experience pain.  The worst thing about this is that the casual observer may not know this as you can’t tell just by looking at someone.   People with IBD get good at hiding their pain so you might not know just how much pain they are experiencing.  But know, it is there.

#3 – A lot of people with IBD feel alone. They don’t know anyone else with the disease and because it isn’t a well-known disease, no one understands what they are going through.   This lead me to my activism.  I grew up alone and in the dark with my Crohn’s.  There was no internet.  It was hard to find information about IBD, let alone meet people who had it.  Now with our global community, I have taken to the web to let as many people with IBD know that You Are Not Alone.  Within the past year I have learned so much about my disease and met so many great people.  This is the main reason I do what I do.  I don’t want anyone to grow up in the dark.  Whether you are 8 or 68, you are not alone with your disease.

#4 – IBD is not a death sentence.  Many people with IBD feel like their life is over.  For some that spend months at a time in a hospital, living a normal life seems impossible.  For some, they have to live with a stoma and feel like they can’t live like that.  From what I have seen and learned this past year, you can live a great life.  IBD does not kill.  I know I can get into a debate over this because IBD can cause other problems, which in turn can kill a person….but IBD alone will not end your life.  You will survive.   I recall words from a fellow activist who is currently struggling herself “You are strong, you can do this.  You are a fighter”.   IBD can and will cause depression but just know that you will live and get on with your life.  Try not to focus on the past and all the problems.  Instead try to look at what you want to do with your life and try to make it happen.  Baby steps.  Don’t try it all at once.  But you will find that if you make the attempt, you just might succeed.  The more you focus on the good, the less you will think about the bad.

#5 – IT IS NOT YOUR FAULT!!!!  I think everyone with IBD at one point in their life looks in a mirror and asks why me.  They try to look at what they did in their life to bring on their disease.  Was it something you ate, or a procedure that you went through.  As I have stated before, this is a genetic disease.  You did nothing but be born with a gene.  Nothing you did brought on the IBD.   It just chose to rear its ugly head when it did.  I have learned that instead of asking the Why Me question, I know ask, what can I do to calm the beast.

IBD really is a bitch of a disease.  It is still largely unknown to the general public and a lot more research is needed.  We need to bring more awareness to this disease.  I speak up now to help educate others.  If you meet someone with IBD, don’t be scared of them.  Don’t ask how they are because odds are they won’t tell the truth.  Deep down, they are probably hurting.  Instead, give them a hug and be there for them.  Listen to their words. No matter the age of the person, I think we are all still a scared little kid just wanting some comfort and to know that everything is alright.