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'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.
Is so are you still constantly in afib? I am in Randolph NJ. I was at the doctor this morning. He has started me on Metoprolol, just 25mg twice a day to see what happens. My afib seems to be induced (at least lately) during exercise to I have a stress test + echo scheduled for Weds. Does the Metoprolol make you tired? Also do you have PVC's/PVA's? It is unbelievable to me that you can't feel your heart when you are in afib. I know INSTANTLY when it starts and when it finishes.
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.
Could you provide me the list to ?
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...
I'm from East Orange NJ....but moved to Elizabeth NJ about a year ago......Welcome to Jersey!!!!
Can anyone advise of the best medical facilities and doctors in central NJ for treatment of MS? I'm new to all of this and terrified of what the future may bring.
Another AF family!! (although we are now retired) We got stationed at Randolph in San Antonio to be near Wilford Hall, but I hear now that they have pretty much closed down? If you like the place you are at, why not try and stay there? Is your family part of the CHAP program (Children have A Potential) I'm not sure if the AF have stopped that program, but if they haven't, they will send you to the bases that have facilities to take care of your child.
Hi there, I just received a request to participate in a study sponsored by The Cancer Institute of New Jersey & Memorial Sloan-Kettering Cancer Centre. I was contacted because I am on the NJ State Cancer Registry. Wow, how depressing!
Anyway, this research is looking into Diet and Lifestyle links to Ovarian Cancer Risk and includes a genetic test too.
I am going to join up. Hopefully this will help somehow and give a bit more meaning into my having OVCA.
I am currently a 25 year old nurse living in the central NJ area. I have been diagnosed with Hashimoto's disease and RA. It has been a few years with the RA diagnosis and I have seen several Rheumatologists but none of which I like. Being a nurse, I am very selective with who I choose to be part of my medical team so I was wondering if anyone knows of any good Rheumatologists in the NJ area.
Hey ladies just stopping in to say hi!
I'm from Northern NJ! Welcome! You will find many ladies, from the NJ/NY/Conn/RI area! We are all more than happy to help answer any questions you may have.
I have read about prolozone treatment by injections, and Im looking for a professional in the Boston, MA area to ask questions and most likely get treatments. The nearest professional that I have found so far is in NJ about 200 miles from me. I would like to find a professional much closer.
Has anyone had experience with Prolozone injections? Cost? Number of treatments? Location?
Thanks for your input.
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