can someone please tell that which medicine works best for OAB ........VESICARE,ENABLEX OR DETROL LA..........I m male and 29 yrs old ,can i also take detrol la.....Any response should be highly appreciated..........
Acai berry is really no use, if you want an anti-oxidant, go for blueberry just, it's cheap and does the same thing. There is no proven double blind studies showing any use as a therapy.
On celexa, tried oxybutinin and myrbetriq. Gave me anxiety. Is enablex a good choice? Side effect of celexa was frequent urination. Eneblex only one that didn't cause anxiety, but side effects are bad. Anybody?
I'm not sure how to describe what I'm feeling or even if it's real or imagined from nervousness. My left side only...leg from about knee down, not feet and my left lower arm/hand feels "weird"...mostly at night when I get in bed and lay to watch t.v. I think my left hand feels weird when I'm typing, not fingers. I have no "pain" , numbness, tingling...just a weird, mild feeling. Sometimes a small shakiness.
this when I had my post op Appt I never truely got an answer then I went back to her she gave me some Enablex that never truely help with the no sensation to urinate nor the having feeling when having sex can some one tell me what is going on?
I have had several episodes of not being able to make it to the bathroom and have also wet the bed several times. My doctor gave me Enablex and the episodes stopped. I stopped taking Enablex and the bedwetting and not making it to the bathroom happened again. The doctor started me on Vesicore and again the episodes stopped. Have you ever heard of this happening after TUMT? I had the TUMT so that I could stop taking Flomax.
he has done urodynamics and also looked into my bladder through scope and said that nothing is wrong with my bladder and urthera,he first gave me vesicare for a month than enablex but condition still remains the same ,then i went to another general phyisican he sent me for x-ray of my lower back,results came out negative.my urlogist told me to go to neurolgist...
Hello Chiari world!
I was diagnosed with Chiari in May. Now two of my cousins, my mom and brother have all be diagnosed with it as well. We are joining a genetics study and are curious if any of you others out there have joined any studies. We would like to know what the Pro's and Con's were/are. We feel that since so many of us have been diagnosed in the last three months that our family may be able to help future families and our future generations by joining the study.
I was wondering if anyone knows of any free syringoma studies being conducted in southern california. Your help is greatly appreciated.
It remains unclear whether hepatitis B virus (HBV) genotype has an influence on treatment response -- as is the case for hepatitis C virus (HCV) -- due to inconsistencies across studies and failure to account for differences in race/ethnicity, according to a report in the March 2010 Journal of Hepatology.
It is well known that viral genotype has a major impact on response to interferon-based therapy for hepatitis C, but it is unclear whether this is also true for hepatitis B.
I have been recently working on some clinical studies on anxiety and I was wondering if anybody knew of any clinical support services? I have looked into a few and came across some that sound pretty good. I was wondering if anybody has ever worked with TransPerfect Trial Interactive before? I checked out their website, TrialInteractive, and they seem pretty solid but I would like to hear other people's take on it. What do you guys think? or does anybody have any other suggestions?
Hi, I'm in Knoxville Tn, and I'm looking for information on the trail studies for Hep C treatment for my mom. Does anyone have any suggestions on where to start?
Does anyone have any information on current or recent studies on this disease? I was recently diagnosed and would welcome any information. My T3 and T4 are normal but microsomal antibodies are 192(high). Thinning hair and weight gain are my concerns.
Elmiron is the only FDA approved drug to treat IC. It rebuilds the mucus layer of the bladder. I also take Enablex for frequency that is pronounced at night! If you think this sounds like you, ask to see a urologist...there are treatments that will make it better...
My doctor did a urinalysis and it came back negative. He put me on Enablex which has yet to help at all (2 wks. ago). I am at my wits end trying to find a solution for what is going on. In addition to the urination problem, I also have tingling in the scrotum and trouble with the head of the penis retracting inward in an uncomfortable manner.
Prior to the surgery, I was totally healthy and had no urological issues. I would be very appreciative for any help. I am getting desperate!
The uroligist put me on Enablex which has been working, and I am due to go back in two weeks......yesterday, I started feeling almost swelled up at the opening of the bladder.....I am embaressed to ask, is it possible that my bladder is dropping....it just doesn't feel right, and I don't know if I should just wait for the appointment at the uroligist, or call the gynecoligist?
She put me on antibiotics and gave me enablex and detrol (neither which have worked). I went back in for a recheck and the repeat urinalysis was exactly the same as before. Doctor sent the sample out to a lab to see if it was bacterial related and I was told that I did not have an infection. She set me up with a ultrasound of the right kidney and it came back normal. OKay so now (as in the past) I have had intermittent right flank pain.
I sent you an e-mail today hopefully you got it. I would encourage you though if not to go to our MOARK IC website and get the article on the vaginal suppositories etc.
If you need the direct link please pm me if I have not already sent it to you!
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