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louieloui #255103 04/18/07 12:44 PM
Joined: Sep 2006
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Laura,

I have read enough about the NSD to be convinced that it has helped many people.

But before my onset, I was on a diet where I shunned rice, potatoes, bread, cereal, and pasta - but I ate tons of fatty meat and cheese. I did keep my weight down, but developed symptoms of AS

I am now convinced that a plant based diet, with very little meat, is the way to go. I do eat potatoes, rice, etc. now and I feel good when I do. It seems the cause of AS symptoms can vary from person to person.

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Quote:

Laura,

Do you suffer from Crohn's disease? I have read info sources that say sufferers of Crohn's disease have trouble absorbing Magnesium.

I don't think I have an intestinal disorders except that I used to drink 1/2 gallon of coffee daily. Also, I was once a very heavy drinker, and I would - don't mean to be gross -see mucus in my stools. Also, I was on an extremely high fat/high protein diet.

Now that I am mainly on a plant based diet with just a little meat, I really don't take magnesium citrate to often any more. My stools are already comfortably loose due to all the greens and whole grains that I now consume.

The health industry provides all kinds of disease names for different symptoms. What seems apparent to me is that certain symptoms can have multiple causes. In my case it seemed to be diet and lifestyle that caused me to have the symptoms of AS. I had no symptoms until the age of 43. I am gene negative.

Somewhere I read that health begins in the intestines. Magnesium is a great laxative. Take too much and you will have the runs. But cleaning out my intestines by supplementing with magnesium citrate seems to have been very beneficial to my health. Magnesium relax's muscles and helps you sleep better, among other things.




I've never been diagnosed w/Crohn's and am really hoping I don't have it. However, about the time all of this started I took Calcium to help regulate my intestines. It worked for awhile, then it stopped--I think mainly due to stress. I do know that I had to take a Calcium tab that had low magnesium in it as I had read that it can work the other way (give you the runs), and that's what I was trying to avoid.

Now I have to be on Questran due to having my gall bladder removed last year. Too much bile. My diet has always been decent to good. Not great--I don't always eat a balanced diet yet I am not a junk food junkie, only have 1 cup of cappuccino a day, don't smoke, barely eat fast food, and rarely drink (especially now that I'm on painkillers in the evenings).

Having the runs when I have to go somewhere used to give me panic attacks, so there is no way I would ever purposefully put myself on something that very well may cause me to get that way. Not worth the stress and anxiety. I wish it were the opposite though. I'm willing to try just about anything once.


~Laura~
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Laura,

If you have been taking calcium supplements - you very well might have been agravating your condition.

Too much calcium will aggravate a "calcification of soft tissue" condition

Please read the above link - and understand that both AS & DISH involve calcification of soft tissue (ossification)

Last edited by layer3guy; 04/19/07 04:26 AM.
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I haven't been taking calcium for awhile now. Over a year and a half or so. But that's interesting to know because I was taking it when all of my symptoms started. They figured I had/have IBS, and I had never mentioned the popping/catching in my pelvis as I was more concerned w/the stomach issues.

Not having a diagnosis of anything is very frustrating as you never know what's "safe" to take, or do, or anything.


~Laura~
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Laura,

Where intestinal issues are concerned, do some google research on coconut oil. I have read some real intersting things.

Here is a link that my interest you.

Coconut Oil as a remedy for Crohn's disease

louieloui #255108 04/18/07 08:21 PM
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there are exercises that you can do in the water that wont hurt you but doing nothing only makes you fuse faster keeping as mobile as you can is the best thing you can do....ask mannatee she has some water exercises that aint dangerous and are made for us who have AS....oak



my little angels
louieloui #255109 04/19/07 12:19 AM
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I was in the same situation about a yr ago. What I have learned about exercise is if is causes pain don't do it. For us no pain no gain theory does not apply. I know how you feel about the belly. I have a belly from steroids and IBD along with not being able to work on abs. I have cut carbs and watch snacks. I was able to loose some weight. It is frustrating to not be able to do the physicial activity. My advice; listen to your Dr. The only other thing that I can tell you from personal experience is to do light streches when lying in bed. That will keep you from getting "rusty". Best of luck. Kathy @ moose57

louieloui #255110 04/19/07 01:52 PM
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I hear ya,

When things were bad I hated looking at my self in the mirror. I felt like I was being destroyed. Everything bounced when I walked and everything I did hurt. Getting up off the floor hurt, let alone trying to exercise. My doctors promised the meds would help and that doing exercise during a flare was not a good idea as it promoted damage to the tissue instead of healing. So I waited until my body felt capable of exercise.

Try not to think of the things you can't do. Remember you have a disease, it's not your fault and anyone who laughs at you clearly has no idea what you are going through. My girlfriend broke up with me, my boss treated me poorly and even my doctor seemed to think I was over reating (or so I imagined). Rest is a very good thing to do while you have a flare, ya your gut gets bigger and everything gets flabby, but it's the only thing you can do. Keep your chin up, stay as active as you can without pain, focus on healing (meds and diet...then drop the meds - they are hard on the system)

I tried to keep as active as possible when I first got diagnosed. I kept walking with knee braces, I rode a motorcycle (ya I bought a little 125cc bike to get me around, that's pretty much it. Bowling hurt my arm alot, dancing in small doses was OK, team sports were out, and I suppose doing lite aerobics or yoga would have been good (but I didn't do them). Swimming is really good. Basicly you need to do things in a safe environment where you can call it quits whenever you feel you've had enough, where you can control exactly how much you have to put out.

When you're finished exercising, ice your joints and make sure you eat a really healthy diet with plenty of protiens (see the No starch diet NSD). Take suppliments to help you heal. I take multi vitamins, calcium and magnesium (helps reduce cramping), cod liver oil and glucosamine (helps repair joints). Make sure you sleep enough, you need your sleep so your body can heal properly over night. I also tried to stay warm alot, I kept my house really warm in the winter (cost me a fortune).

With the NSD I was able to do more and more activities, I have started skiing again, riding my bicycle, and travelling around with my camera (my hobby, it gets me out an about). I feel great these days and I hope to get back into hiking, running and mountain biking. I've even bought a nice new Motorcycle which takes alot more muscle to handle.

Other activities you can do are resistance training with surgical tubing, exercise in water, skating (gliding along is easy on the joints), or tai chi.

hope it helps
kris

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