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.
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..........
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 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...
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?
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 have been on this for 6 months without significant change. For two months Detrol LA was added without any change in my symptoms either. Now I have been given Enablex 7.5 mg and after a week I am still waking up every 2 hours with the sensation of pressure in my bladder. I am very frustrated and would appreciate any suggestions.
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...
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 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?
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?
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!
My urine test showed negative for UTI, but he figured he would be safe. After that failed, I went to my second urologist. He listed to my symptoms and started prescribing medications. He did a voiding ultrasound, but it seemed to show nothing. We tried Cipro, Detrol, and Enablex. All seemed to help a little, but nothing really fixed the problem. Each medication was taken for a couple months to see if they worked. The last medication, Sanctura, seemed to work the best.
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.
I am under the care of a urologist. I have tried several medications and have finally settled on Enablex. It helps with the urges but doesn't prevent them. They are just not as strong or as demanding.
There are many options out there. you just have to keep trying until you find what is right for you and the kegal never hurts.
is there anyone out there that may be experiencing the same symptoms ???? Should I go to another type of Dr- I have been to dermatologist but by the time I get an available appointment- I get in there and the redness is not there- they look at me like I am crazy...
. Nine months of overactive bladder. (No infections and ultrasound, CT scans all show normal).
. Tail bone pain and muscle tightness around waist – groin area (hard to explain) but feels worse
when he is sitting or standing for long periods. (Again, ultra sound, CT scan find nothing wrong)
. Slightly enlarged spleen, lymp nodes in neck swell up with no pain a couple different times over
the last few months. (Mono test a couple times over last months are negative).
.
No two Lyme patients have the same presentation of symptoms, and because of the co-infections, symptoms can be all over the place. An LLMD will doubtless run a bunch more blood tests, based on your son's symptoms, but that's about all.
The standard Lyme tests (often through a company like Lab Corp) are used mostly by non-LLMDs. LLMDs on the other hand often use a California lab called IGeneX, which does a more detailed test with more information for the MD to consider.
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