Vesicare cut in half

Common Questions and Answers about Vesicare cut in half

vesicare

I don't have allergies of any kind and I'm in excellent health and I can learn to live with the smell of fresh baked bread in my nostrils.. I mean it could be owrse.. still I think I should get someone to check this out especially as I read about Phantom smells being a possible side efect of brain tumors...
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. More fuel for the fire, but 2 32oz bottles a day or you will get dehydrated on the medicine I am about to recommend. For me, Detrol LA, Vesicare, Enablex didn't do anything for me.
i was loosely diagnosed with overactive bladder and i am on Detrol La, which i think has at least cut the number of times i go in half. i think that this condition is a result of two things: long term anti-depressant/anxiety medication and over use of caffeine(mainly soda). if i do not drink caffeinated soda, i do notice that i go less. it is still however a disruption of my daily life.
I had my TT Friday, and so far I feel great (well as great as I can expect..more on that in a bit). My voice was only hoarse for a few hours after surgery, and even shocked both my endo and my ENT surgeon that is back like nothing has happened. My surgery was suppose to be 2 hrs, but ran into 4 hrs. I don't know the results of the pathology yet..
I don't feel I need it at the moment but I don't understand why I am getting spasms again after all these years of not having them, I thought perhaps it's not neurological and maybe I have over exercised my muscles, the spasms in my butt are more in the back of my leg near my but (bit of both). I will cut my exercise back a bit as I have been going over the top lately with my exercise routine.
i refused to look that way.. as much as it sucked i cut my dose in half.(slowly) also drink tons of water, eat well and LOTS of exercise. I am now 165lbs and i'm ok with that i'm working on getting off of the methadone clinic. It's been a long road, don't listen to what anyone says about how high your dose is or how long you have been taking it. It is NONE of their business it's an individual choice and lets face it it's better than using and all the risks involved and .
Hello, Within the last two and a half months I have been diagnosed with RRMS. I have been taking copaxone now for about a month and a half. My nuerologist set me up with some solu-medrol and prednisone taper to deal with my symtoms. Shortly after this, my MS flared up again. I was set up with another round of solu-medrol and a longer prednisone taper. I have been done with steroids now for two weeks and it seems to be flaring up again.
I read somewhere (I wish I'd kept it) that pills like Vesicare, etc. can cause memory loss. I usually wake up and must rush to pee in morning (sometimes not making it) so I sleep with a light pad and cut out the pills altogether. But then again- I've had MS for about 17 years, and try to avoid meds. I know the drug companies probably don't agree with me but I'm doing ok. I take classes/ stay involved/ depend on the LORD and keep my mind going.
Tonight, I reached SLIGHTLY, not even my full arm extended and had sharp pain that was so bad it literally made me scream like I was in a bad horror movie. It only lasted a secondary and of course caused me to freeze in p,ace when it happened. When I went to move again, it happened again, another high pitched girly scream and this time, I went instantly into tingles from waste to knees. Again, only happened for a second. Tingles went away. Pain is still there but at a much lower level.
I still managed to function and maintain a pretty normal, healthy lifestyle after that surgery, which was in Nov. 04. Then in June 06, I began having muscle pain all over, bone pain in my shoulders/elbow and was diagnosed with fibro. was tested for RA, my factor was elevated but RA was ruled out. Then my mental health began to suffer and I began to experience anxiety attacks, couldn't deal with any stressors in my life. It got to where I couldn't leave my house, paranoia.
I wrote about my journey in a series of Health Pages. About one half of people with MS and Overactive Bladder will be helped by Physical Therapy. There is a neurological problem, but there are also techniques to enhance our ability to overcome it. I found the experience to be empowering and self-affirming. "I" myself, was able to fight back against the torrent of problems causing me to be tossed around like a wreck against the rocks.
She was admitted in the hospital and Dr Hibner @ St.Joesph's IN Arizona said he diagnosis I.C. in a different way than the radioligst do. He is a pelvic pain specialist and inserted sodium pottasium into the bladder and told my daug if it brings on the same type of pain pressure than thats how they diagnosos I.C. and said she had it.Her symptoms are a feeling like she has to urinate and even when she does she still feels like she has a full bladder.
I'm a 20 year old girl. One year ago today...I was wearing a size 5 jeans/shorts....5'8" & 135-140 lbs (depending on how much taco bell i ate on the weekends! =P). I've always been very active, played softball and volleyball throughout my childhood and high school, and was supposed to play in college...but go a shoulder injury last minute. Anywho, around March I began eating even healthier and working out almost everyday still...just out of habit...I feel like..weird if i don't. Then..
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