Vesicare cut in half
Common Questions and Answers about Vesicare cut in half
vesicare
I've been with the same person for a year and a half. I had abstained from sex for the past two months in response to the symptoms. My doctor put me on valacyclovir 1gm/daily after receiving the igM +s. I recently noticed some very small cuts on my vulva. I applied hydrocortisone to the area and it feels slightly better. Doctor put me on Vesicare 10 mg as well, but I still feel the urge to urinate after I void my bladder. He's sending me for a pelvic MRI next.
) ), and I have to take Tums (going to ask if I can change to Caltrate for the chocolate,lol) I am also taking an antibiotic and percocet for pain. My pain is getting better, but it is more of a fear of the cut that just pain (the pulling). I'm not having any "bad" symptoms (only tingling/numbness/muscle twitching from calcium)..but I read that my natural Ts can still be in my body for now..which could be helping me not go "super hypo".
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.
My bladder spasms are the ones that are painful but I have a choice of having 5 or 10mg Vesicare but he gave me the 10mg so I had been cutting the tablet in half as it makes my mouth so dry but I have gone back now to full strength and if this continues I am going to try the Botox as I am desperate.
Sorry Guitar Girl that your having such a hard time with spasms, they are not pleasant if this is what I am having.
I am a 32 year old female. I am pretty healthy. However, about a month and a half ago, I started having very severe urinary frequency and urgency. I had no pain or burning during urination. However, I tested positive for a urinary tract infection and began on pyridium and bactrim. My symptoms did not improve so I began on Levaquin for 10 days. Since then I have had an ultrasound of my kidneys, ovaries, and bladder, and everything was normal. My labwork was also normal.
Basically it is where you get burning and discomfort and it feels like you have a UTI but you don't, I also was getting the urethral spasms that were very painful, I am now on a drug called Vesicare and it has helped, my urologist thinks my problem will eventually go away ( I hope so), he said some of my problems are neurological as well. Vesicare is also used to treat bladder urgency in MS and bladder spasms in MS.
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.
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 .who wants to be an overdose statistic.????NOT ME!!
dx = demylinating disease/white brain matter disease
detrol didn't work so the urologist changed me to vesicare. That seem to be helping. Without the meds I am up every two or three hours without much output.
then people. AND DOCTORS would get it AND all the decisions would be so clear cut,
Sorry for another of my famous novels...
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.
i am 37 . i too have gains weight. i weighed 135 a month and a half ago...today i weigh 173....for a total of 38 lbs!i weigh more now than when i gave birth , all 3 times! i don't understand. tho possible peri-menopause ? i also have had some night sweats . some woke me up w/ horrible electric heat in my back . sometimes i wake up on cold wet sheets.. i am getting pimples , unsightly hair ,and my boobs LITERALLY feel like huge heavy bowling balls.
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