Open main menu
☰
Health Conditions
Allergies
Alzheimer's Disease
Anxiety & Panic Disorders
Arthritis
Breast Cancer
Chronic Illness
Crohn's Disease
Depression
Diabetes
Fibromyalgia
GERD & Acid Reflux
Irritable Bowel Syndrome
Lupus
Lyme Disease
Migraine Headache
Multiple Sclerosis
Prostate Cancer
Ulcerative Colitis
View Conditions A to Z »
Support Forums
Anxiety & Panic Disorders
Bipolar Disorder
Breast Cancer
Chronic Pain
Crohn's Disease
Depression
Diabetes
Fibromyalgia
GERD & Acid Reflux
Hepatitis
Irritable Bowel Syndrome
Lupus
Lyme Disease
Multiple Sclerosis
Ostomies
Prostate Cancer
Rheumatoid Arthritis
Ulcerative Colitis
View Forums A to Z »
Log In
Join Us
Close main menu
×
Home
Health Conditions
All Conditions
Allergies
Alzheimer's Disease
Anxiety & Panic Disorders
Arthritis
Breast Cancer
Chronic Illness
Crohn's Disease
Depression
Diabetes
Fibromyalgia
GERD & Acid Reflux
Irritable Bowel Syndrome
Lupus
Lyme Disease
Migraine Headache
Multiple Sclerosis
Prostate Cancer
Ulcerative Colitis
Support Forums
All Forums
Anxiety & Panic Disorders
Bipolar Disorder
Breast Cancer
Chronic Pain
Crohn's Disease
Depression
Diabetes
Fibromyalgia
GERD & Acid Reflux
Hepatitis
Irritable Bowel Syndrome
Lupus
Lyme Disease
Multiple Sclerosis
Ostomies
Prostate Cancer
Rheumatoid Arthritis
Ulcerative Colitis
Log In
Join Us
Join Us
☰
Forum Home
|
Forum Rules
|
Moderators
|
Active Topics
|
Help
|
Log In
Alternative Treatments
Support Forums
>
Ulcerative Colitis
✚ New Topic
✚ Reply
❬ ❬ Previous Thread
|
Next Thread ❭ ❭
Jennifer Cuthbertson
New Member
Joined : Jan 2010
Posts : 1
Posted 1/17/2010 1:54 PM (GMT 0)
I got diagnosed with Ulcerative Colitis in 1998 and have been battling it ever since. I take asacol always and use the Rowasa some times. Nothing ever gave me any long term relief. I began using MonaVie in early September. I didn't feel like I saw results right away. They were very gradual. My mid-November, my digestive system seemed to be working "normally." I was very reluctant to say anything to my husband or the rest of my family because I thought that would "jinx" it. But, it has been 2 months since then. My digestive system is working just like it is supposed to. I have 1 bowel movement a day most of the time. The stools are formed and there is NO SIGN OF BLOOD. This is big for me because I have had to have transfusions. I am not off my medicine completely, but I am only taking 3 Asacol a day. What a difference.
Has anyone else had success with **** ***?
Jennifer Cuthbertson
IamCurious
Veteran Member
Joined : Jan 2010
Posts : 3728
Posted 1/19/2010 10:40 PM (GMT 0)
Congratulations! I am not a big believer in meds either because of the side effects. Besides they may not address the problem. If UC is an autoimmune disease then perhaps my body is allergic to something. I was diagnosed two years ago after a routine colonoscopy. I was allergic to the colasol that was prescribed to me. My symptoms were not serious so I ignored it.
Then last summer all hell broke loose. I have since learned I am extremely allergic to carrageenan and to a lesser extent beef, sorbitol and (believe it or not) broccoli. All symptoms aggravated by coffee. I have since avoided carrageenan (ice cream, coffee creamer, or anything made with cream such as chocolate mouse), switched to moderate tea, and my symptoms have only been minor since last September. Ask your doctor for an allergy test to determine which foods are really poison for you. I used to eat broccoli in my salad almost every day.
(I hope these are not just famous last words. If I have a repeat of last summer then I am sure I will probably beg a GI for conventional meds. But so far so good.)
Besides watching what I eat I take DGL before meals (must be chewed but choose brand without fructose or sorbitol e.g.Nature's Plus) at the first sign of stomach discomfort. Along with slippery elm, aloe vera juice (MAKE SURE ALOE DOES NOT HAVE CARRAGEENAN), and assorted vitamins and herbs.
Durango Kid
Regular Member
Joined : Jul 2009
Posts : 330
Posted 1/20/2010 12:38 AM (GMT 0)
No success with MonaVie. Very expensive too! I had some friends that were distributors. They even got out after they lost their faith in it. I do think it has great anti-oxidant qualities, but for $35..00 p/btl nope.
IamCurious
Veteran Member
Joined : Jan 2010
Posts : 3728
Posted 1/20/2010 12:47 AM (GMT 0)
Here is an excellent website for discussing Alternative treatments. Supposedly there are scientific studies that show boswellia to be effective.
http://altmedicine.about
.com/od/digestivedisorders/a/Colitis_Remedy.htm
Also watch carefully which foods cause problems for you. For example, when researchers want to induce UC in test animals, they feed them carrageenan! And unfortunately it works for me too. Most food ingredient labels will not indicate carrageenan directly, but may list heavy cream. Only when you look up the ingredients for heavy cream do you find carrageenan. But everyone's diet is individual and you need to look up on your own.
subdued
Veteran Member
Joined : Dec 2008
Posts : 3231
Posted 1/20/2010 6:12 PM (GMT 0)
That's interesting about
MonaVie. I can't drink juice, because I'm fructose intolerant. I do take acai berry supplements. I don't take them for my colitis though, and I haven't noticed any improvement in my colitis symptoms from them either. I mostly take them, because I don't get enough berries in my diet. I take cranberry supplements too. These I take to prevent bladder infections.
MonaVie is expensive. There are other 100% acai berry juices on the market that are cheaper and readily available in many food stores, and acai berry supplements can be bought at the drug store.
NuffinButtTrouble
Veteran Member
Joined : Mar 2007
Posts : 679
Posted 1/20/2010 6:52 PM (GMT 0)
I applaud your efforts in trying alternative herbal supplements...next week I will begin taking new herbs that I hope will improve my condition further.
JLG45
Regular Member
Joined : Feb 2009
Posts : 114
Posted 1/20/2010 10:30 PM (GMT 0)
I believe Lesnar had diverticulitis. A few friends & co-workers of mine have had it and remedied the problem through diet.
jujub
Elite Member
Joined : Mar 2003
Posts : 10424
Posted 1/20/2010 10:43 PM (GMT 0)
At this point, I think western medicine has become the alternative treatment, judging from reading all the recent posts here.
pb4
Elite Member
Joined : Feb 2004
Posts : 20577
Posted 1/21/2010 12:52 AM (GMT 0)
My sig below is what I use/do, I'm either allergic or non-responsive to oral RX so I had no choice but to put my skeptisism aside and try the natural route, lucky for me it's been helpful more than not....I still have frequcny and urgency issues (still flaring) but it's a heck of alot better than what it was before.
:)
Christine1946
Veteran Member
Joined : Aug 2008
Posts : 5988
Posted 1/21/2010 9:59 PM (GMT 0)
My nutritionist told me to avoid anything ending in "tol"
pb4
Elite Member
Joined : Feb 2004
Posts : 20577
Posted 1/21/2010 10:07 PM (GMT 0)
LookingForTheCure....
The prodiem fibre supplements I take have psyllium in them (yes, it helps), I eat spinach and sunflower seeds along with all other fruits and veggies, seeds/nuts...I've been eating that way long before anyone posted on here specifically about
sunflower seeds and spinach.
:)
pb4
Elite Member
Joined : Feb 2004
Posts : 20577
Posted 1/21/2010 10:09 PM (GMT 0)
Yes Christine, sugar alcohols (which all end in "tol"), sorbitol, malitiol, xylitol, ect can all exacerbate IBD and IBS symptoms and should be avoided.
:)
Lonie
Veteran Member
Joined : Feb 2005
Posts : 6448
Posted 1/21/2010 10:16 PM (GMT 0)
I agree Pb4 and Christine; I've also heard and read that same thing.
✚ New Topic
✚ Reply