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Post by bannanny on Jul 21, 2008 15:55:50 GMT -5
Sorry about the content here, but you know the bladder infection I have? Well, at least now it's not a dribble anymore, but a normal feeling urination. The wierd thing is that every time I go (which is alot) I poop at the same time ....... every single time. What might that mean, if anything? Anybody know? I can't get to town yet to go to the dr....... actually I have to find another new dr. and I hate doing that. So I thought I'd ask you guys first. love ~~ bannannas
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Post by toni on Jul 21, 2008 17:06:00 GMT -5
I knew someone that told me she experienced the same thing you're describing. She said it was "irritable bowel syndrome". I don't really know anything about IBS. Has this been going on for awhile? And do you get cramping at all, or not.
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Post by ctbarb on Jul 21, 2008 18:51:05 GMT -5
Bannanny......Oh yes! I have IBS and that happens to me too. It has slacked off a bit, but there is usually no warning either! I'm buying stock in Depends.....
ctbarb
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Post by bessie on Jul 21, 2008 19:03:07 GMT -5
Bannanny - Do you use a lot of Happy Tummy? Bessie
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Post by bannanny on Jul 22, 2008 15:09:53 GMT -5
Ok, thanks guys....... I'll check out the IBS symptoms. I haven't been using the happy tummy for awhile now Bess. I have to go off it every now and then or there wouldn't be nothin left of me! It's been steady for 4 days now toni, but only occasionally do I get sharp pains in my tum. I'll just hope that it starts to slack up, at least for awhile anyways. It's gettin to be a real pain in the a*s, literally!
love ya's ~~ bannanny
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Post by Deleted on Jul 24, 2008 2:16:37 GMT -5
Okay, since it's you... I'll tell.
I had those symptoms during 2002 - 2003. Was hell on my love life!
Seems to me that Tam tam reffered to an IBS type symptom for the bladder in a post somewhere.
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Post by toni on Jul 24, 2008 8:13:25 GMT -5
Bannanny,
I sure hope your tummy feels better soon.
I know I've got my own "thing" I do, so I'm sharing what I do. But anytime for instance a couple of times in the last 3 years, I've had (something wrong with my stomach) where I had pains on and off, I'll treat myself with an antibiotic for 5 days, then I stop.
I don't know if it's the right thing to do (because of having Morgellons) but "just personally"...I feel it is, and that 5 days on antibiotics has taken care of any "extra problem" or pain I've experienced in the gut area.
I figure (in normal life) that's what I'd do if I happen to have eaten something that "wasn't right" or whatever was causing a new pain, and because I'm not on daily meds at all, that a 5 day course isn't going to hurt anything. A couple of months ago, my stomach didn't feel right, not that I had to be going to the bathroom alot or anything like that, but, I could tell it didn't feel right.
So I did a 5 day course of antibiotics (Levaquin) and by day 3 I felt fine. I just make sure I do enough days to knock out whatever bacteria might be in there that was causing a new "pain".
And daily (no matter what) I take an acidopholus and milk thistle to try and maintain "bacteria balance", and try and keep the liver supported with the milk thistle.
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Post by felixwillford on Jul 28, 2008 12:41:10 GMT -5
IBS was ONLY a way to make money for the Pharm companies. IBS does not exist. Nervous stomach does during stressful times of your life. IBS without stress or worry or a life change...............is simple intestinal parasites. The County Coroner states in all 30 years of performing autopsies (sp?), EVERYONE had a parasite in their intestines that should NOT have been there! Your diet can help with bowel problems. Anyone remember? ?, or ask your grandmother about the homemade brews that were given to children and adults long long ago before Pharm companies .... these home remedies were to clear people of parasites. THen the US decided we were too good for parasites and declared us parasite free. When I wanted an intestinal parasite test, the lab tech and I talked and he said in all honesty..................I don't know how to do it and needed to look up the procedure on the internet. I was negative from him, but he was so unsure of himself and doing that particular test that he told me it does not at all mean that I don't have a parasite. and Because the test at a HUMAN lab was negative, I could not be treated by a Human doctor for what a vet tech already identified without a doubt as HOOKWORM caught from the sewage exposure in the apartment that flooded. I was treated by myself and www.vetamerica.com and orderd Pyrantel Paomate. It's used for both humans and dogs. (same stuff given per weight) By the way, it was THE CDC doctor who recommened that I go to a vet. I never took her name, only know she was a woman in the parasite division and didn't doubt for one minute that I caught a parasite and that many people have them here in the US. That was in 2005.
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Post by felixwillford on Jul 28, 2008 12:45:56 GMT -5
Also, I worked for a drug research company for one year, during that year, we had the contract for the IBS Study.
What a farce!
Anyway, that new drug for IBS, now I think was taken off the market or is going to be.
I've seen the commercials from the Lawyers...................
Have you taken Zelnorm? If so, call us and we can help.................bla bla bla
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Post by felixwillford on Jul 28, 2008 12:47:09 GMT -5
It does boil down to money and who gets the money.
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Post by scrambo on Jul 28, 2008 13:36:45 GMT -5
I do think that Lyme Disease does infect the bladder and gut. I think Lyme may be transmitted in certain dairy foods and that maybe where some are getting it.
When I was first diagnosed, I had early morning, run-you-out-of-bed diarrhea and a lot of urinary incontinence. My urine was very cloudy and had fibers and other weird stuff.
You may need to address a Lyme infection.
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Post by felixwillford on Jul 28, 2008 13:41:36 GMT -5
good thought scrambo.............. lyme can affect the heart too.
Wonder what makes it affect certain parts of some people and not others?
For instance, my neuropathy in my feet? no where else, just my feet and lower legs.
Yet, I don't have the bowel problems.
We are all affected so differently.
What determines what part of a person Lyme chooses to destroy?
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Post by bannanny on Jul 29, 2008 19:46:41 GMT -5
Wow, I thought this thread had gone to morgland!
I tested negative for Lyme Disease, but I have the feet problems big time just like you Kmarie....... that I believe has got to be morgs. I take milk thistle everyday too toni, along with everything else, including lecithin. I just added wormwood to my collection too.
This thing is still goin on with me, but I have to go into town on the first and I'll stop at the lab and get my jug for the 24 hr. urine test that Dr. Hildy has me do, along with more bloodwork. Then I'm going back down to the beach again and I'll see her when I'm there....... gonna stay a few days this time.
The thing that's tickin me off are these pains in my gut, just below the rib cage and mostly on my right side. It's a dull aching kind of pain with a sharper pain every now and then and it hurts if I push on it at all. Any ideas Kmarie?
love ~~ bannanny
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Post by bannanny on Jul 29, 2008 19:47:55 GMT -5
P.S. What's a love life theunknowncat??? ;D ;D ;D
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Post by cyn on Jul 29, 2008 21:21:26 GMT -5
Bannanny, I have been waiting for someone to mention this pain that comes from directly under rib cage, just below right breast. In the past six months it has steadily grown stronger. My hope is that what is causing the pain, is not growing in size the way the pain is. Sorry to hear you have that too, I feel your pain. As I know you will do, tell us immediately when it pops out!!!
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Post by morgie on Jul 29, 2008 22:00:36 GMT -5
I have the pain to but under the left breast. Both areas are swelled but the left side is alot bigger. Doc says costochondritis i only h ope he's right. I also have lumps in uper stomach but these are size of walnuts, much smaller than under the areas under breasts that are big. Maybe swollen ribs is correct as the doc told me and its part of lyme symptoms he says.
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Post by cyn on Jul 30, 2008 13:04:33 GMT -5
Hey Morgie,
I was diagnosed in my twenties with Costochondritis. The explanation I received was that we have hundreds of nerve endings in the chest. Costochondritis means that most of your nerve endings are inflamed. That started me on a never ending cycle of Ibuprophen for the inflammation. Recently, I was unable to take my Ibuprophen for 10 days and still my UPPER CHEST hurts to touch. Let alone the tiny stinging jolts. This is not what I was talking about when responding to Bannannys' pain.
It's been so long, I am not sure how they diagnosed me. But remember them showing me the X Rays taken of my spine, and their diagnosis of arthritis in every disc that same day. Perhaps they run hand in hand.
Shoudn't take much research to solve your quiry. But chosto and your lower pain don't match my history with it. Just my opinion though.
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Post by morgie on Jul 30, 2008 14:39:33 GMT -5
It sounds like yuo've had this long as me Cyn, not very fun and extremely painful, I could write a paper on it from all the years I studied it and what I learn from specalists. I wanted Bananny to know there is a connecton to costo and Lyme since she talked about Lyme in her post. Alot of these symtoms differ but go hand in hand including bladder ones.
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