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This doesn't happen very often. I've noticed it usually when I am intoxicated with alcohol and when I have released pre-ejaculatory fluid. I will get a burning sensation along the urethra, and going to urinate seems to help since it clears out the pre-ejaculatory fluid or semen, but even after repeated urinations it can remain for a half hour or so. Is this normal for some people or is it a sign of an illness?

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I got no response at all in the other catigory I put it in, so I will move it here; Hi everyone. this is my first post on the board. First off I am a 24 year old male. I have had a problem with drinking since I started at around 15. I have pretty much been a regular almost every day drinker for the past 6 years. Its been a pretty big problem to say the least. I have since quit drinking and have been sober for 3 weeks now. The reason I am posting, is that probably about 6 months ago I started having trouble getting and keeping an erection. I still have a very high sex drive, and am able to get an erection and orgasm, but it is difficult. ( and the erections I get are no where near as full as they used to be) I am pretty much positive that it is due to the drinking. I am wondering if there is anything I can do at this point to reverse the effects that the alcohol abuse has put on my sex life. This is pretty terrifying to me, especially being my age and not being able to have a normal sex life. I am scared to th

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I am 31 with 3 kids and have had a Neurostimulator for 13 months. It is the BEST thing I have ever done regarding my chronic pain. I was on 40 mg of methadone and 30 mg of hydrocodone daily before my implant. Today, I take one Norco-10 in the morning only because I have to turn the stimulator off at night. My leads are very positional when I am lying down so I can only sleep in one position if I leave the stimulator on at night. This causes my whole body to hurt after a while, so I now turn it off at night and take the Norco in the morning. As far as restrictions, the worst of it is over 8-12 weeks after the implantation of the leads. I really wanted my leads to grow in/scar over correctly the first time, so I was VERY careful and kept the restrictions for a full 12 weeks. Here are the main restrictions I followed then: 1) No lifting over 5 lbs 2) No reaching or putting your arms above your head 3) No driving for the first 2 weeks (with three kids this was as long as I could go without driving) 4) Gradual increases in exercise (no weight training for 3 months) Three months post-implant, the restrictions decreased significantly. Now, my only restrictions are based on my chronic pain.not my stimulator. My Medtronic rep has one client that is over 70 and skydives regularly. His leads have to be replaced about once a year, but he believes it is worth it. I hope this helps!

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In April 2004, my mother suddenly felt achy and decided not to go to a bridal shower with me. Next thing I know she's unable to walk and my dad rushed her to the hospital. For about 2-3 months we went without knowing what was wrong. I think it was U of M who wouldn't let her leave until she was able to walk on her own. Riding in a vehicle shot pain through her body, she could barely stand clothing on her body.one hospital actually said that some event in her past was so traumatic it was causing her to act like this. That we weren't giving her enough love. If you knew my family, you would know that's the complete opposite. Thankfully we have my dad and because of his persistence, we found out what was causing my mother to be in so much pain. I couldn't tell you how much it means to me to see my mom even drive or do things on her own now. She would literally push herself in one day so much that she'd end up in bed for a week after that. I was a senior in high school. By then I still had no idea what I wanted to do with my life. My great grandfather who lived next door to us died not long after my mother got sick. In fact, I remember staying the night in the hospital room along w/ my mother to look over my grandfather. Dying doesn't scare me, but seeing the people I love in pain tears me apart. I'll never forget seeing my mom being pushed in a wheelchair at my graduation. I try not to let her know how much it hurts to see her in pain even now after almost 5 years. My family means the world to me. My mother is my best friend and I'm daddy's little girl. About a year or so ago my dad was getting rashes and really had no positive answers. One Saturday morning I was having a lot of abdominal pain. I was seriously considering going to the hospital. That day I did, but it wasn't for me. My mom was on her way to take my dad to the chiropractor and decided to turn around, stop at the house for something and took him to the hospital. Next thing I know he's being taken to another hospital and things are a lot more serious than I thought. So obviously, I ignored my pains and waited until we had more knowledge of what was going on. It wasn't until the next day after being at the hospital, which was about an hour and a half away, for who knows how long I came home and had my husband take me to a closer hospital. I ended up having my gull bladder removed. Come to find out my dad had went into shock while I was in the hospital. I waited probably a day after I was out of the hospital to go see my dad. They came to the conclusion that he has Lupus and Rheumatoid Arthritis. Some still aren't sure that's completely it. He's still struggling with medications. They had him on such strong steroids it did 1000 a lot of damage. Thankfully he's home and still going to work. But what's insane is.the last thing he remembered was driving home from work the Thursday or Friday (I can't remember which) before going to the hospital. He didn't remember things until maybe 2 days before he left the hospital. That's almost 2 weeks of his life he has no recollection of. I try as much as I can to be there for both of them when they need me. What I'm worried about is driving myself into an even deeper depression that I was in the first place. What should I do to help with all of this? My parents are the kindest, most generous people I've ever known. Why do they need to go through all of this? I'm just thankful they're also very strong or else they wouldn't be here today. I've left lots of chunks out, but as you can see a lot has happened to my family. buy levitra on sale online Tramadol and Lexapro  boots manchester viagra

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Hi Everyone, Just found this board yesterday as I was researching the Viagera that my doctor just prescribed for me. I had discussed with him my erections not being as strong as they were just a year or so ago so he prescribed Viagra for me. I am 45 yeard old, married and in good health. My questions come from my first experience this morning. I tried a small portion of the 100mg pill, about 1/3 size at around 5am. Managed to make use of it around 7am. The result wasn't dramatic but it helped somewhat. I now have a bit of a headache which I usually don't get. Is this a normal experience? Should I have tried the whole 100mg tablet? What might I expect then? Pankow.
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Oldskool47 I saw in the other penile implant thread that you are planning to have the surgery soon. First, congratulations on your decision. I'm sure it was difficult to come to that point.it surely was for me, since there's no going back. Secondly, as you've seen on previous posts, I think you'll be extremely pleased with the outcome. I have been, and it's so nice to no longer have to take pills, injections, and try the VED, which was successful only one time. I look forward to hearing from you in the future as to your progress. I'll be glad to answer whatever questions you may have if I have an answer! Good luck. doj fluconazole side effects in babies treating candidaside effects of lisinopril 5 mg My health plan only provides 4 pills a month. I've asked for 6 at the pharmacy but then they make me pay full price for all of them (no coverage). This is a real problem for me. I'm very active sexually. Without the pills, my performance is not very great. With the Viagra, I'm great. My question is: Is there a way to really order Viagra online at a discounted rate? Of course I mean safely and legally. Like everyone I get the spam emails, but would never want to buy from any of those companies. prescription free viagra I am 61 and been using penis injections the for 3 years. They work very well but I am tired of them. Is the anything else I should try? I have used the "V" and "C" and they work well on an entry stomach.  google groups buy viagra

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Hi Meggs, So sorry to read what you are going through. I agree that you need to find another doc. I also have been told I need a fusion at the same levels as you. Right now I am putting myself through another round of physical therapy and trying some additional nerve blocks, but I am still able to work, and so am doing everything I can to avoid surgery. My ns has left it entirely up to me as to if/when I have surgery. Once he confirmed that my discs are pressing on the sciatic, that was pretty much it. I just have to say the word and surgery will be scheduled. None of the jumping through hoops that you seem to be going through. He did tell me that it was my CT scan, and not the MRI that gave the clearer picture of the disc compression. Both images showed herniated discs, but it was the CT scan that showed that the discs were pressing on the nerve. He then sent me for a guided nerve block to be certain. Don't give up - sounds like you've just seen a couple of not so great docs..
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Hi Meggs, So sorry to read what you are going through. I agree that you need to find another doc. I also have been told I need a fusion at the same levels as you. Right now I am putting myself through another round of physical therapy and trying some additional nerve blocks, but I am still able to work, and so am doing everything I can to avoid surgery. My ns has left it entirely up to me as to if/when I have surgery. Once he confirmed that my discs are pressing on the sciatic, that was pretty much it. I just have to say the word and surgery will be scheduled. None of the jumping through hoops that you seem to be going through. He did tell me that it was my CT scan, and not the MRI that gave the clearer picture of the disc compression. Both images showed herniated discs, but it was the CT scan that showed that the discs were pressing on the nerve. He then sent me for a guided nerve block to be certain. Don't give up - sounds like you've just seen a couple of not so great docs..
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