I wanted to catch you all up on some research that i been doing for Females that feel that have no sexual drive weather you think it is all physcal or mental. Just kinda catch up to the new people that come to the board since my last post. My Husband and I are haveing sexual disfunction (my end of it) i don't have sex drive period and right now i am in the mitts of finding out if it is a mental or a physcal problem or alittle bit of both. I am on antidepressent (lexapro) ***** i have to say does wonders for the me being depressed. and my no sex drive was well before i was on antidepressents.Well i have some good news for people who are suffering more or less the female gender and to educate the men that read this board. i have been seeing and dealing with a counsiler to help resolve past present issue and well can anyone guess lol. one of them is no sex drive. Well FINALLY someone realizes in the medical world that female gender has the same issues that men do accept men have viagra(waaaa) well ladies ther About viagra buy viagra on line Re: Help with my Dad's Situation, Any alternatives? DRX9000?
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Has anyone had experience with with parnell medical group in minnesota? Recent status of viagra lawsuits 't get an erection. I don't feel i have performance anxiety as I was completely comfortable with being with this person. I would like to overcome this problem naturally, without any type of medication, but I'm sure of how to do so. I feel I may have low sex drive, but then I argue with myself, and get confused about it, and this just adds to the frustration of the whole situation. I've been to 2 urologists, the first really was a waste of time, and the second sent me for blood work to test my testosterone which was "In the high end of normal." I plan on making another Urologist appointment asap, but figured I might as well ask here for any advice or insight you all could give..Hello everyone, i hope everyone is not suffering with pain too bad and that for those that are that you will soon find a doc to provide you with the care that you deserve! i'm alittle frustrated tonight and really need to vent. first off my poor daughter who is 23 and has been a cheerleader all her life recentley had her mri done which showed a ruptured disc as l5 and a herniated disc at l4. she also suffers from scoliosis as well as spina bifida, which we only just discovered she had in nov of 2008 when i took her to see my surgeon about her back pain. we both have appts on monday with the surgeon, they actually fit her in as there is a sense of urgency with what the mri findings were. for the past week she has called me (she attends college) in tears, literally at times unable to talk due to how severe her pain is. i told her last week to call the oncall doc, which she did, however he completely dismissed her pain and told her to take aleve or to go to the er. so since then she has been too afraid to call for anything. so today she called me again in tears and this time i was ped because she didnt want to call the doc's for fear they would tell her the same thing. so i got on the phone and left a message for our surgeon's nurse, basically telling her that my daughter was experiencing intense pain and that when she called in last week she was told to take aleve and therefore she has been too afraid to call in to ask for anything else, so she has been suffering for a week and could they please call something in for her, to get her through until monday's appt. our nurse called me back and unfortunately i missed the call, but she left a message saying that she was soooooo sorry that she was told to take aleve last week, and they would most definatley call something in for her, that they didnt realize how much pain she was in because the oncall doc failed to say anything about her calling in tears last week, that it would be handled and for us to both come at the same time on monday and again she apologized profusely and said she would get in touch with my daughter immedia 1000 tley to get a pharmacy number to call her something in. dont get me wrong i absolutley love my surgeon and his nurse, they are wonderful people, its the other doc's in the practice that i cant stand. they did the same thing to me 5 months post op from my fusion when i had called in one night and i got the same oncall doc, and instead of calling in what i had been taking, he wanted me to stop that med completely and he wanted to switch me to what he wanted. i told him straight up, that i was not his patient, that he knew nothing at all about me or my history and had no right stopping any of my meds and switching them without the consent of my surgeon. i guess i was right, and he realized that and kept me on what i was taking. when i saw my surgeon the next time i had told him about the conversation and he said that it should have never happened, that nothing should be changed without his consent and that if the doc had any concerns, he should have called something in to get me through the night until the next day and then had him handle it from there. he said he was going to discuss it with the other doc, but i guess its still happening, because he dismissed my daughters pain. i explained to my daughter that she should never have to be afraid to ask for something for pain from her doctor's office and that it really ticks me off that patients, including myself are so fearful of being labeled because we do ask. this is really begining to irritate me now. at first i wouldnt say anything and i would suffer through it, then i got to where i would just come out and ask for something, if i was told no, then i would look for another doctor, but then your labeled yet again as doctor shopping. well yes, of course i'm doctor shopping, but its not to get prescribed meds from each and everyone at the same time, it is to find one doctor that is willing to treat my pain with whatever works. this is just getting ridiculous now that patients are really suffering from debilitating pain because there are idiots out there that want to enjoy a night of euphoria, they are taking away from us, the people that truly need the med. its not that we want the med, we need it to function. what they take for granted and dont even think about on a daily basis, we struggle to do, suffering the consequences of pain afterwards. then you have the "good" doctors that are willing to treat patients in pain with strong meds and for long term, and they end up getting locked up because street junkies go in and fake they are sick, or the dea sends in a dummy patient. i would have to say that most of the docs that are treating pain patients now almost 95% of the time want to constantly inject you even after you've been through them and its been found not to work. so once again we agree to be injected, even though for some it causes more pain on top of what we already deal with, just so we can get medication to control our pain. patients will do anything just to get decent care and it sickens me that we have to be subjected to treatments that have failed in the past just to walk about of an office with a 30 day script. i'm seeing this new pm doc now that wants to inject me every which way, and of course i agree'd to it, but i agree'd for two reasons. one was because i want to give him a chance to see if his way works, but i also agree'd to it so that i could get the meds that work for my pain. the truth of the matter is after being injected now for 2 yrs by 2 different docs, this is probably not going to work, although i am really trying to have a positive attitude. i am very thrilled about the aqua-therapy though, which has not been tried yet and i'm anxious to see how that works, but since i've had my fusion several other problems having to deal with pain are now apart of my life, so what was just a lumbar problem, has now turned into sciatic pain, osteopenia, muscle and nerve damage, a failing l4-l5 level, a dragging leg and much more pain than i ever had before 1000 my fusion. i just feel broken and i'm so tired of fighting to get the pain control that i feel i
deserve and that i shouldnt have to be so afraid to ask for and now i'm so worried about my daughter now and her having to go through the same crap. i'm hoping that since she is younger than me that she will heal faster and wont have any other problems afterwards. she has already been told that her only option is surgery, so our appt on monday is simply to go over her mri and to discuss how severe it is and what he would like to do and when. my appt with him, is to set up another discography for the l4-l5 level, to see if we need to fuse that level now as well and to also go over this "partial" fusion word on the report and what does that mean. i live 20 mins outside of dc and i'm just so tempted to take my venting to the "hill" about how its completely ridiculous for us cp patients to have to suffer and be afraid to ask for relief so we can function like normal human's do. to let them know that i find it disgusting that patients with medical records, mri's, ct scans, xrays & discography's, ect that prove that there is a problem that does cause severe pain should have to even be questioned about treating they're pain, the proof is on paper, in pictures and is in black and white, provide this person the pain relief they need and stop treating them like a street junkies. worry about the people that dont have proof there is a problem and treat the people that have proof with some respect. i dont know maybe i'll write a letter to my congressman to let him know how i feel about all this. thanks for letting me vent, lisa
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Electronic stimulation ended weeks of nagging shoulder, back & neck pain Drug levitra new Keep losing erections Levitra boob flash Another thing if your still curious you may want to try is desenstivity creams, you can buy them at any pharmacy over the counter, its nothing more than a little benzocaine in some aloe vera or similar based ointment. maybe sex witha condom may help too, if premature ejactulation continues to be a major problem talking to a doctor may be beneficial. viagra in the waters kareoke How to stop having wet dreams.
My urologist gave me my first injection about 6 weeks ago. i'm not sure of the mix, but it did not work. just a semi-erection. two weeks ago he gave me a a different mix, called a tri-mix. he gave me the prepared needle to bring home. i injected it and it worked great -- in 10 minutes i had a good erection that lasted for almost two hours, gradually going down. he then wrote a prescription for the tri-mix. i tried it two days ago and it did not work at all. just a little increase in size. i'm pretty sure i did the injection correctly. i injected it into the left side. the pharmacist mentioned that it had a shelf life of about 3 months. he called me before he prepared the mix and wanted to know when i was going to pick it up, as he did not want to mix it too early and reduce it's potency. i picked up the prescrip in 2 days and kept in on ice on the way home and it is now in the refrigerator. does anyone have a similiar experience with the first tri-mix shot not working? i'm going to try it again in a day or so
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Hey honey how r you doing, just checking up on my message board sweethearts, seeing how your doing and wishing you all the best and a speedy recovery generic viagra trial pack Small Fiber Neuropathy Gang Levitra painted couches Hey Guys.I'm 50, had a RP 19 months ago. Viagra gives me only a headache. Injection bi-mix works pretty good, but after 7 months of use I now have a curvature problem. Just tried Muse, 1000mg, no luck. Has anyone with same history used Libidus with hard results, pun intented? Anybody using a pump? Thanks for any suggestion & serious repley.
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