Vesicare and headaches

Common Questions and Answers about Vesicare and headaches

vesicare

Sometimes I feel I have no right to be here, because these docs keep telling me no ms. Anyway, I'm done boohooing, and I have some updates and questions. Okay, since I was dxed with the PsuedoTumor Cerebri, they have me on the diamox 2x a day. Still having pressure headaches from the high spinal pressure anyway. Just don't feel like going back to neuro. My neuro eye doc said the high pressure went down behind my eyes since being on the diamox.
Even though I told the Doc-in-the-Box that the worst pain was on the side of my lower leg up by the knee, she only would x-ray the ankle which was super swollen and four shades of purple. I've been walking around on it for a week. I saw the orthopedist this am. I have a Massionneurve fracture.
TM is like MS you can flare old symptoms up when you are tired, hot, infection and even my headaches could stir up and worsen my TM symptoms but is the burning in a new place mean that there is new damage? Or is is just my old damage and the signals getting jumbled on the way. Or is is migraine, can you get burning sensations with migraine??? Does anyone know?
He ran some blood tests, and a few things showed up that were peculiar but only slightly 1-3 points out of range. My muscle pain and fatigue, headaches and lethargy incressed. My doctor decited to prescripe fentanyl patch at 50mcg/hr, soma, and flexaril. I also have been diagnosed with adhd and take aderall and prozac for bordeline personality disorder. My kidneys dipped low in function several years ago and sense then i have been on vesicare.
My back, hips, neck, I had frequent headaches in the morning, the hot flashes and night sweats were constant, I had intractable heart burn, and had passed 6 kidney stones in 2 years. (I passed them at home-not something I'd recommend...) I was so tired that everything was a chore. The kidney stones gave me UTI's (I learned after the first one to take Uristat (pyridium -urinary tract numbing agent) and Cranberry capsules which kept the infections from starting.
Nausea, loss of appetite, weight loss (10 lbs). He’s now 6’ tall and 135 lbs. . Little bit dizzy and some mild headaches. Up to this past year, son has been extremely high energy, active and athletic. He was a very good soccer player till last summer. Varsity coach (one of first to notice) asked what is going on with his ball control and remarked he wasn’t playing well at all. Son felt like “his brain was not telling feet what to do fast enough”.
Now I do get headaches with this and it does make it worse but I also don't get any headaches and then assume it's the aura. Now this has been going on for months and months and months (daily) and the twitching was driving me insane, I went back on gabapentin for nerve pain and this seemed to help the twitching heaps but I still keep getting it but not as bad as before HOWEVER... when I have a shower, put a warm face washer etc.
I had the LP, 2 weeks ago, had the dreaded headaches for a week and a half, during the LP the litocane needle hit the lumber nerve that gives me a lot of trouble(pinched nerve), I felt it and told him, and ever since then its been hurting. Then it finally eased up, and when I had the cystoscope done, when I bent over to pick up my phone, I got a pain in my lower back so severe, I almost went down. Now I'm in alot of pain from that, more pain I didn't need.
i also have alot of pain under my bellybutton i am not sure if that is the problems with my uterus with the HPV or of its a bladder problem i always have pain there, my doctor put me on vesicare which is suppose to help with frequency it made me very sick to my stomach and gave me headaches, just wondering if you could give some insight or suggest any other rememdies, and vitamins or minerals or juice or tea or anything i can do to help
The insomnia can be best dealt with by taking the drug in the morning and midday. Other common side-effects include loss of concentration, dizziness, headaches, irritability; loss of appetite, nervousness, blotchy rashes especially in the sunlight, constipation, dryness of the mouth and vomiting" I remember telling Phil (pharmacist) that I really don't need any more dizziness or loss of concentration. I wouldn't mind a little loss of appetite, though, ha ha!
Please make yourself at home and snuggle down. It will be a bit bumpy, but worth it!
His symptoms today are tail bone pain when sitting or standing too long. Overactive bladder has improved slightly and he has stopped taking Vesicare. Fatigue and sleeping a lot. Based on his symptoms do you think this could be Lyme Disease? If blood test comes back negative should we pursue more tests? Also, son has been on Amnesteen (a form of Acutane since December) all of his symptoms occured before he started taking.
frequent need to go, developed inability to hold, burning whilst peeing, abdominal pain, ovarian pain, kidney and flank pain, nausea, headaches, and discomfort during intercourse. Initial UTI test was negative (my dr said means nothing) and urine appeared healthy, however I am pending lab results. His best guess was that I have KIDNEY REFLUX (in my case resulting from frequent 'holding on' at work, not being allowed to leave my desk).
I can still function in my daily life, but doing anything that requires real thought (including conversation) is very hard sometimes and it's sort of like my mind and body have been numbed and covered in novocain. I feel stoned and like things just aren't really hitting me so to speak. There are times when it's hard to even focus my eye sight on anything, as all my eyes want to do is drift off and blankly stare in to the middle distance while my head shuts.
He said I may be having a form of migrane headaches and put me on Topamax. It has been 3 weeks and no more smoke smell since I started the pill.
I feel very tired all the time and could sleep day and night if I let myself. I have also been getting headaches....3-4 times per week....and some of them are quite severe. And if that's not enough....all this physical stuff is taking a toll on me emotionally. I feel gross and almost hate leaving the house because nothing seems to fit right and I hate the way I look.
Double vision returned in June 2007, and lasted until August. I also had vertigo and nausea, pretty consistent fatigue, conistent headaches, and lhermitte's sign. How many neuros before diagnosis: Just 1. My MRI radiology report had measurements of some of my lesions, and a pretty good case for MS, which was mentioned several times in the report. My neurologist all but diagnosed me on my first appt., but wanted to run some additional tests (B12 defic., Lyme's).
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