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Re: Desperate in Ottawa with UTI symptoms
From: anonymous@obgyn.net
Thu Dec 29 12:38:19 2005
Look on the Web and find out about Interstitial Cystitis. It might help
you to have the test done for this. My advise if you have the test make
sure your not awake for it. It is extreamely painful. I was alseep but
when i woke up and had to pee was in horrible pain. Also your pelvic
pain can be adhesions. If you have any kind of sugery using C02 that
can also cause adhesions and pain. Depending on your stage of endo ,
endo can also cause adhesions. it usually does for stage 3&4. Good
luck
Vicki
At Thu, 29 Dec 2005, anonymous@obgyn.net wrote:
>
>If you are in that much pain I would go to ER and demand to see someone
>who will take you seriously. As people with an illness, we are our best
>advocates and need to take responsibility for our health. Sometimes a
>doctor dismissing our concerns is legit, but you know when something
>major is wrong with your body. I would not take no for an answer.
>
>Alexis.
>At Thu, 29 Dec 2005, Michelle wrote:
>>
>>I am desperate and hope someone out there might have some answers. I am
>>34 and was diagnosed with endo 7 years ago. I had tremendous lower left
>>pelvic pain that occurred quite regularly. I had the laser surgery to
>>remove any lesions and was put on Depo. Surprisingly enough within a
>>couple of months I forgot all about the whole endo ordeal and was pretty
>>much symptom free. I went off of Depo. around four years ago.
>>
>>During the last couple of years I have had tons of "UTIs". I usually
>>ran to a clinic (as I no longer had a regular physician), they did the
>>dip stick thing, told me I had an infection and gave me antibiotics. In
>>March I had yet another infection. It did not respond to 2 sets of
>>antibiotics. I ended up going to the emerge with extreme flank, pelvic
>>and lower back pain along with lots of blood (could see for myself) in
>>my urine. To sum up the last 10 months since then, I simply will say
>>it's been hell. I have had every test possible, (ultrasounds, cat
>>scans, IVP, tons and tons of urinalyses). Every test comes back normal.
>>Even the cultures from the urinalysis came back normal. My symptoms
>>have been getting more intense and frequent. I have recently started
>>seeing a new doctor. We have tried just about everything. She said
>>that all that was really left to explore is the endo. I never really
>>even thought about endo. since 2001. I did some research on the
>>internet and I was surprised at the symptoms for endo and the urinary
>>track. They listed all the symptoms I have been dealing with (Flank
>>pain, rib pain, pelvic pain, UTI symptoms, FREQUENCY and BURNING when
>>urinating, blood in urine). AWESOME!!! BINGO!! That is it I thought! My
>>doctor sent me to a uroguyneclogists. She told me it was extremely
>>unlikely that I could have endo on the kidney. She said I would be a
>>case study if it was so. She told me to go back on the pill and wished
>>me a good day. I went home EXTREMELY depressed. I don't feel I can
>>take much more. I have missed tons of work, social events and am simply
>>miserable.
>>
>>Yesterday, I expressed my frustration to a friend in the medical
>>profession. She explained that pain can radiate and although it may not
>>be on the kidney I can still feel as though it is.
>>
>>My family doctor is gone for two more weeks, I have no more narcotics
>>left, and I hurt and have to urinate all the time. Does anyone have any
>>suggestions????? I desperately need help!
>>
>>Michelle
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