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..........
I used it. I went up to 20 mg and still didn't help. I think I have tried everything out there. Enablex seems to help me the most. I never had any side effects from any of them.
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...
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!
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.
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?
It's unbelievable that I made so many mistakes just writing down my problems, the worst is I forgot I entered this and entered again tonight. I've been having problems for 7 years until diagnosed. I'm not sure how this site works. This cognitive problems is not good. Questions is this a problem of MG, drugs, alzheimer's, a stroke or depression. I haven't called the my nerulogist yet. He said to call if I saw double. Concerning county mental health, why county?
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!
Hi there. Sorry that you are going through this. I cannot advice on hyst.or not but I can tell you that I had severe endometriosis and had a complete hyst.2 yrs ago due to the pain and risk of organs twisting. I am currently taking 1mg of estradiol and Praise God it is working for me. My bladder is fine but the endo caused issues with urythra "not sure on spelling sorry" so I have to take enablex to avoid accidents. My doc told me before surgery that this was a possibilty.
Definitely get your bladder checked for a urinary track infection. I doubt that's the case. What you are describing is exactly how I felt. Peeing once if not more an hour. Pee, stand up, feel like I have more. Incredible urgency to pee. You give in to go and your lucky to pee half a teaspoon, but it felt like you are holding back niagra falls. I have an overactive bladder. You need to cut down all your coffee, pop, tea, alcohol, and spicy food. Drink plenty of water. I know I know.
It is equally unknown whether MG can cause silent PID or only with symptoms like low abdominal pain. Regardless of cause, for most PID the symptoms are mild, not sufficiento to be any kind of "medical emergency".
I continue to have burning at the base of my scrotum and penis 9 months after contact. I thought that MG could spread to other parts of the body especially through oral sex.
But my problem is some of my other symptoms are not related to MG. I have problems walking, my giat is wide, I have a Babinski reflex, I have horrible involuntary muscle movements in my legs at night and problems with disfunctional bowel and bladder problems. My doctor ran another blood test and it showed twice a very high fatty acid level or VLCFA. But DNA test did not show ALD. My doctor started me on Zanaflex for the leg muscle problems when she thought I had ALD.
Hi there. Ocular MG is a disease of the neuromuscular junction resulting in muscle weakness and fatigability. This is an autoimmune disease where anomalous antibodies are produced against the acetylcholine receptors in voluntary muscles. The most common presentation is double vision and eyelid drooping or ptosis wherea the pupil is spared. Diplopia is seen when MG affects a single extraocular muscle in one eye, limiting eye movement and leading to double vision.
the urologist also said i have a high-pressure bladder and put me on enablex. unfortunately i still get infections. my urine gets a musty, strong smell and a cloudy color to it -thats when i know an infection is coming. the urologist says i might have a burning bladder. what is that? and how is it different to an infection? he does not believe that i have infections -but then what is it? and why does my urine burn like it does? i also suffer from candida albicans. could this be related?
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