Crohn's Disease Forum » Your Story » Success Stories » Any Success Stories?

04-22-2010, 06:01 PM   #1
Join Date: Feb 2010
Any Success Stories?

I know people do not come on the forums to talk about how awesome they are doing. But these forums are sometimes pretty negative. All I read about is fistula after abscess, followed by obstruction and surgery.
Anyone on here (or anyone know someone) that is doing or has been doing fairly well? How about some success stories? Thanks.
04-22-2010, 06:30 PM   #2
Skinny Dub
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Join Date: Aug 2009
My success story would be that I had surgery back in November and have been doing great ever since and hope I still feel this way years from now.
04-22-2010, 06:50 PM   #3
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*jumps up and down waving arms madly* I'm doing fantastically since my colostomy in December Pooping in a bag is pretty great!

Crohn's Diagnosis: May 2006
Current meds: none
Surgeries: Colostomy, December 2009

"Never trust a fart." Jack Nicholson, The Bucket List

Oscar is awesome! Loving my life with my stoma (with a hint of poo)!!

04-22-2010, 07:26 PM   #4
My Butt Hurts
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OOO!OOOOO!!! I have one!!
I have been in remission for a year and a 1/2, thanks to remicade. I've done very well on all of my meds actually, until they quit working and I have to try something else. Though I have been in and out of remission, I've only had 2 bad flares since my initial diagnosis.
So yeah - it IS possible to live a somewhat normal life if you can somehow get your symptoms under control. I was a 96 pound skeleton in July 2008. I am now 146 =)
04-22-2010, 07:38 PM   #5
Passionate Dreamer
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Join Date: Feb 2009
Location: Buenos Aires, Argentina
It depends on what do you think about yourself being successful.

Treatments work with more or less rate of success and you can also adjust your life a little bit according to the ups and downs of this illness.

I managed to study at the university, to play some sports, to have a family, to have a job and to make ends meet in a crazy 3rd word country. All this things having crohn disease, I donít think I am successful, I think I am a super hero

I understand your feelings this can be very depressing, but you could get some relief if any of the available treatments suits to you.
04-22-2010, 07:40 PM   #6
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It does kind of make you worry, doesn't it?

Well,I don't know if I can claim a success story, but I had fistula surgery in October and have been doing much better in that department. Things with the tummy still aren't perfect, but I feel like I'm moving in the right direction, so that's encouraging, isn't it?
04-23-2010, 06:36 AM   #7
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I'm like the others. I had an ileo-cecal resection in January and now feeling much better than before. Not 100%, but at least no more pain and fatigue all the time. What I learned with this disease is you have to think positive, else the negativity will drive to a worse and worse cycle till you have a full blown flair. Try to adjust your diet, reduce stress, take meds or have surgery when needed and have faith that things can get better..... This forum is excellent since you can talk with people in the same situation as you, who understand you like nobody else can, and are here to support you when needed, and have a laugh about it along the way
04-23-2010, 07:43 AM   #8
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Location: New York

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I've had crohn's/colitis since I was 7 years old...managed to avoid surgeries - been in the hospital multiple times.....

But, worked full time, went to school, had pretty active social life.....then met my husband - we have a beautiful (5 y/o) daughter - I have been on Remicade for over 4 years now - need to LOSE some weight!.....still active with my horses, full time work, motherhood.....

So, I guess a success..... :-)

30 plus years and counting with UC/Crohn's!
on remicade since 11/05

While my experiences may not be what everyone has had- I feel it is worthwhile to share any and all experiences that may be beneficial to others.
04-23-2010, 08:52 AM   #9
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I think I'm in remission, but we'll soon see in a few weeks time!
My major flare was blitzed with Pred 4 months ago, and I feel fab! Only on Pentasa now (Humira is waiting for me tho, just in case)
and going back to work on Monday, been off since January, so I think that's a success story!


Dx Crohn's in TI 2005 symptoms for 15 years prior

BEEN ON -Azathioprine, 6MP, Prednisolone, Pentasa, Budesonide, Metronidazole, Humira, Methotrexate,

NOW ON -Amitriptyline 25mg
21/02/14 Right hemicolectomy surgery!/profile.p...4208290&ref=ts

No-one should make you feel inferior without your consent!

04-23-2010, 10:02 AM   #10
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Join Date: Mar 2010
I had 4 years of remission before coming to the board. Then I had a really nasty flare with fistulas. I was scared to try the remicade but it healed my fistula within days and when I saw my GI 4 weeks later we both agreed that I am likely in remission again. I went from being really close to needing surgery, to remission in a matter of 2 weeks. During my last remission I met my hubby got married, bought a home and had a child. We hiked, camped, and snowboarded. We lived it up. With crohns I finished college and made a nice career for myself in the pharmaceutical industry.

Last edited by Lydia; 04-23-2010 at 10:04 AM.
04-23-2010, 10:52 AM   #11
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Location: San Diego, California
I had close to seven years remission before coming back to the board.

After a bad year last year I am currently feeling great on my current med regiment.
Diagnosed in 1996
Currently on: Filgotinib clinical trial, Prednisone, Imuran
Colostomy surgery 4/24/12
Prone to skin infection, abcess, fistula, pyoderma, erathema

Past Failed Treatments:
6 MP
04-23-2010, 01:08 PM   #12
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Join Date: Dec 2008
I'm not feeling too bad at the moment either - I'm relatively stable, have a job for the first time in a long time, have cut my painkillers, now have a great GI team.

I wouldn't be classed as in remission but hopefully with a medication change now in the pipeline things are certainly looking up.
04-23-2010, 01:18 PM   #13
D Bergy
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Join Date: Apr 2007
I have been symptom free for well over two years, and truthfully, I am in better shape overall than I have been in years. Even prior to my official diagnosis.

I had depression all my adult life, and accidentally found out that was related to inflammation form Crohn's. I got rid of it by reducing the inflammation. I am probably the only person in the world, who is glad they were diagnosed with Crohn's, because it led to me resolving the depression problem.

How long will it last? I am not 100% sure of anything, but I think I know enough to keep the disease in a small corner of my life indefinitely. I have more research to do, but I have other stuff going on now that I have to take care of first.

04-23-2010, 04:18 PM   #14
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Join Date: Mar 2009
Location: 60115, Illinois
I can't speak for everyone here. But, I tend to frequent the site much more often when I am flaring or having some other Crohn's related frustration. During my good periods though, I have managed to forget about having Crohn's and thus posted less.

If this is true of others too, maybe this creates a distortion and makes things seem more negative than they actually are. Just a guess.

Anyhow, I have had Crohn's for 5 years. I have never had surgery, but have been hospitalized a few times and I have been to the ER countless times. It has been a roller coaster over the years, but when I have not been flaring, I have felt great. I have traveled out of the country, worked in remote mountain regions of Utah as an archeologist, went camping, ate whatever (except a few of my trigger foods), hung out with friends, dated, etc.
04-23-2010, 04:49 PM   #15
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I think it's understandable that people use the forum more when they're going through a hard time with the disease. It's great to read about the positive stuff here though, especially for someone like me who's newly diagnosed!

Dan - I was wondering in what way Crohn's inflammation is connected to depression. It's just I had thought there was a connection myself so I was wondering if you'd read something or it was just your own experience?

The fox knows many things but the hedgehog knows one big thing. Archilochus

Diagnosed March 1st 2010


Calcium supplement
Fish oil supplement
04-23-2010, 08:36 PM   #16
D Bergy
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Join Date: Apr 2007
After I was diagnosed with Crohn's and had a stricture removed, the doctor recommended Imuran as a treatment. I have had some negative experiences with doctors in the past, and while he was a very good diagnostician, I was not about to take anything until I knew all of my options.

What I needed was some time to investigate this further. I was flared at the time, and needed to get a grip on that right off. I started taking larger doses of Turmeric, Ginger and also Krill Oil. This did quell the inflammation quite a bit, but was not 100% effective. What my wife noticed, before I did, was I no longer was having bouts of depression. She was right, I had not had any depression since I started taking the big doses of anti-inflammatory supplements.

I had used Turmeric and Ginger prior to my diagnosis, but only minimal amounts. I was taking six times as much and that resolved the problem.
I was not expecting that as a result, so placebo effect was not involved.

After deciding on Low Dose Naltrexone as a treatment, I again lowered my dose of Turmeric and Ginger. It did not change anything, but now the LDN is keeping my inflammation down. I also do eat anti-inflammatory foods, and that may also help a little bit.

That is how I accidentally found the cause of my depression. It was a physical problem causing a mental problem.

04-23-2010, 11:59 PM   #17
David in Seattle
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Dan - I'd like to hear more details of the Turmeric, Ginger and also Krill Oil.

04-24-2010, 02:01 AM   #18
D Bergy
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Join Date: Apr 2007
I took Turmeric and Ginger prior to my Crohn's diagnosis. Not for very long before, but from my investigation into Lyme Disease, I found out how beneficial these two spices were to health, and the anti-inflammatory, and decoagulation effect they could have. My wife had undiagnosed Lyme Disease from a Deer Tick bite, and I was the one who would end up treating her. I did not plan on doing this, but could not get any doctor to treat her since she would not produce a positive test.

Now it is well known that those tests are not accurate, but many of our doctors are about ten years behind the science behind many diseases. That is another story, and I am still treating her disease, but she is doing much better now. Enough about that.

I was well aware of the properties of these two plants, and it was natural for me to use them to knock down my own inflammation. I took 1500 Mg two or three times a day of both Turmeric and Ginger. I also added a double dose of Krill Oil that I used to both balance my cholesterol and help with inflammation.

This did help calm down my inflammation, and my lack of D most of the time was one of my indicators. It was not perfect as a Crohn's treatment, but I did not think of it as my solution, it was to buy me time to figure out the disease. Like the Lyme I was already treating, I needed some idea of what caused the problem in order to treat it in a manner that made some sense.

It was at this time my wife noticed I was not going into any depressive funks any longer. I thought it could be coincidence, but it stayed that way for months and now years. I have had a couple of one or two day relapses, but these are from viral infections, or some other direct cause of inflammation. They go away as soon as the illness is gone.

I have not figured out everything about the disease, but I think I know enough to keep it under wraps. I do have a treatment plan that makes sense based on what I understand to be some of the causes of the disease.
I am not completely satisfied that I know as much as I should, but it is good enough to keep me well. At least so far.

That is the short version. I did try several other things in between, and most did not work or were inconclusive. I also found at least one important treatment product that brought me 100% out of my flare and that was Miracle Mineral Solution or MMS. There is lots of uses for this alternative medical product, but it kills acidic bacteria exceptionally well. This was how I killed off most of the bad bacteria in my intestinal tract prior to using LDN as a main treatment. Once that bacteria was reduced, I had no more inflammation problems. LDN and MMS are the back bone of my treatment.

I should mention that just prior to my bad Crohn's symptoms I had several stressful events going on around me.

1) My wife was fairly ill with Lyme Disease.

2) I had recently came close to being layed off from my job permanently.

3) I was taking online classes that were very difficult given our busy schedule and other problems at the time.

4) One of my children was becoming a Meth Head at that time. He is fine now. This one alone was harder on me than anything else by far.

5) Of course, my on and off again depression was not any better either. I could deal with it, but it did not help.

5) I was overweight, smoking more than ever due to the other problems. I felt sick just from the situation. I had never had to deal with so much, at one time.

That was the scenario I was in, just prior to getting really sick with Crohn's.
Stress finally broke the Camels back, unfortunately, I was the Camel.

That is probably the most complete explanation of my situation I have ever given, but I do think the circumstances had much to do with the timing of my illness. I am glad those days are behind me. They really sucked.

04-24-2010, 03:24 AM   #19
One Badass Dude
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Location: Calgary, Alberta
I'm in a manageable state. A few ongoing symptoms (related to diarrhea and frequency), but for the most part the gut pain is gone. I have to be careful what I eat, though.

Still having other autoimmune issues. Right now they're probably bigger than the Crohn's.

Hang in there ibdoer. There are indeed ebbs and flows, Those of us doing better need to continue to contribute. Very important component of any support group.
04-24-2010, 11:54 AM   #20
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Thanks lots for the info Dan; really helpful and interesting. I'm going to do a bit of research myself. I do think depression is often physiological. It seems obvious to me but it goes against the mainstream view.
04-24-2010, 12:23 PM   #21
D Bergy
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Join Date: Apr 2007
There may very well be more than one cause of depression, but if you have an inflammatory disease, the inflammation may be the cause.

Doctors have noticed that patients with Arthritis, Lupus, MS have often have personalities associated with other patients with the same disease. It is sometimes thought that the pain they are in accounts for their less than desirable personality traits, but it often may be the direct mental effects of the inflammation from the disease.

Here is an interesting article related to this subject.

04-24-2010, 05:45 PM   #22
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Join Date: Aug 2009
Had a resection last fall and I am fully recovered, eat a wide variety of healthy foods and am back at work full time with no issues causing problems there. What more can I ask for?

I think it worked out well for me so far

Oh Dan you are not the only one happy. I have been bleeding out my arse for the past decade and thinking it was my fault for eating too much crap and not taking care of myself. It is a HUGE relief to get some understanding of my situation and a chance to make it better
Rectum? Damn near Killed'em

Diagnosed July of 2009 / Surgery Oct 2009 / 175mg Imuran since Jan 2010

Last edited by kenny; 04-24-2010 at 05:52 PM.
04-24-2010, 06:38 PM   #23
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OMG, Dan that article is sooooo interesting. I've noticed the link in myself between mood and inflammation (I've had a range of inflammatory disorders, mostly not serious apart from the Crohn's). I mentioned it to my GP but he scoffed.
Thanks for posting.
04-24-2010, 08:40 PM   #24
David in Seattle
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D Bergy said:
I took Turmeric and Ginger prior to my Crohn's diagnosis...

Thanks for the details, Dan. Wow, you certainly have been through a lot. I'm very glad to hear that you, your wife & son are doing so much better. Like so many of the stories of courage in the face of adversity I read on this site, it's very inspirational, as I climb my own personal mountain.

In terms of the ginger & turmeric, where you simple using the powdered forms generally available at the grocery? Or (in the case of the ginger) where you using the root? Fresh ginger root is fairly spicy, I used to have a terrific chicken recipe I put a ton of it in, I think now it would upset my gut.
04-24-2010, 10:31 PM   #25
D Bergy
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Join Date: Apr 2007
I did use some raw Ginger root or to be technically correct Rhizome, but it is rather harsh to eat that way. I switched to capsules of both Turmeric and Ginger. You can buy it from anyplace that sells supplements.

There are some confusing forms of Turmeric that you kind of have to know a little about. The cheapest form is pure Turmeric, which is just the plant. Other forms contain processed and concentrated Curcuminoids, which are the main active ingredient that has the anti-inflammatory properties. This form is more expensive, but also is better at controlling inflammation. this form is often called Curcummin.

I used the more expensive Curcummin fortified type for controlling inflammation. I now use just plain old Turmeric because I do not need all that potency. I am pretty much taking it for my original intent of getting the other benefits from the plant. The list is huge, and I cannot even begin to list all of the benefits, but here is just one example. There are hundreds of potential health benefits just from Turmeric, and Ginger has its own long list of benefits also.

Study Shows Ingredient in Curry Spice May Reduce Fatty Deposits in Arteries

July 20, 2009 -- The compound that gives curry spice powder its yellowish color may protect arteries from fatty buildup, new research in mice shows.

Curcumin, the main ingredient in the curry spice turmeric, is a naturally occurring antioxidant known as a polyphenol. Polyphenols are found in plants that have anti-inflammatory and other protective properties.

Previous studies in rats showed that curcumin had the power to prevent heart failure. Turmeric-based compounds have also been touted as potential treatments for Alzheimer's, arthritis, and breast cancer.

The current study suggests curcumin may thwart the development of atherosclerosis, or clogged arteries, a key risk factor for heart attacks and strokes.

Researchers in France fed 20 mice a diet supplemented with curcumin or a comparison diet not supplemented with curcumin. After 16 weeks, mice fed on the curcumin-based diet had a 26% reduction in fatty deposits in their arteries compared to mice on the comparison diet.

In addition, curcumin appeared to alter the genetic signaling involved in plaque buildup at the molecular level.

The findings are being presented this week at the American Heart Association's Basic Cardiovascular Sciences Annual Conference in Las Vegas.

05-02-2010, 03:36 PM   #26
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Location: Freeland, Michigan
Success comes in differant forms for differant people. For me it is any time I can get out of a flare with no scars or bags. So over the 24 years my whole crohns disease life has been a success of sorts. A total success would be getting my CD cured but that is a ways off yet, so I'm happy with my little successes.
I'm the Captain of my own pirate ship. You'll find me on the POOP deck!

Greg Yancer
Diagnosed w/ CD Febuary 1986
No surgeries
Current meds:REMICADE (CATS SCARE ME), Pentasa, Nexium, Probonics.
05-02-2010, 04:24 PM   #27
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Since march 10th my life has become a success story, life is soo much better now yes i'm still recovering but I've been so happy, 2 things I thank Crohns for is how much I appreciate the smaller things now, when my friends complain about trivial things I know I'm truly grateful just to be able to eat! Also how close I am with my nan, she traveled 80 miles everyday to come see me in hospital if it wasn't for this it most probably would've been birthdays Christmas and Easter.
Diagnosed Feb 2003
Surgery Apr 2010
05-02-2010, 05:43 PM   #28
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I am doing pretty well at the moment and I've not had any surgery. I was pretty ill when I was younger as well.

There's always hope!
05-03-2010, 01:22 PM   #29
My Butt Hurts
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I didn't want to make a whole new thread for this, and I have been trying to figure out for a week now where it should go.
Since it is a success story, I guess I will just add it here.

My family and I went to Disney World 2 weeks ago. I was so thankful that I am in remission right now. I couldn't imagine needing to find a bathroom 15 times a day in a matter of 20 seconds. I could have never done it. Once while we were there, I had that familiar stomach twinge, and I almost panicked - but it went away in a second. Remicade, I love you.

edit - I ALMOST FORGOT!!!!
I brought my Calmo WITH me in the parks! I folded it up in some toilet paper JUST in case I needed it, which I didn't.
AND - I wore my "DUDE! Where's the bathroom?" t-shirt for all of my Crohnie's!!

(Tee-hee! I changed the sign in the background to say BATHROOM!!!, instead of Epcot.)

Last edited by My Butt Hurts; 05-03-2010 at 01:39 PM.
05-03-2010, 02:35 PM   #30
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Love it!!!
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