Hi, I have a problem. My husband has a hidden penis, behind a fat pad. He lost a lot of weight, over 100 lbs years ago. but he still has a very large fat pad. I don't think he sees it as a problem, it makes his penis seem extremely small. plus over the years we have been married it seems to be getting smaller? if that is possible. The problem is he has to hold the fat pad back when having sex, and we can only have sex in certain positions. Also, I can hardly feel him anymore. I would like to know, is there anything that can be done about a Hidden Penis, and how do you talk to a man about this problem. Thank you Buy softtabs viagra What should I do, I have to jump the gun! Viagra cof forid 11 Okay I need some advice/opinions here on a major issue im having. It's really important. To make a long story short, i've had this weird back pain for awhile now (been going on for MONTHS) It started as a funny pain i've never felt before, in one area on my upper back on the left. It got worse & I went to see my Dr (A new Dr actually) to see what it could be.Basically I went for a few visits, she gave me licoderm patches (which suck) same thing, no help. Recently I went back again because all of a sudden it's like.ka POW. It seems to have gotten SO much worse. it's constant. Burning, tingling, stabbing, itching, cramping, all in rotation. I've been going out of my mind. Basically she and another Dr took a look @ & felt my back again and diagnosed it as a pinched nerve.She gave me amtytriptaline.which.yeah.suc ks too. I scheduled an MRI for this sat, which can't come soon enough b/c i'm scared about whats going on. NOTHING has helped this pain lately. I'm not a cry baby, or weak or a drug seeker.i can take pain, but this is ridiculous. OTC stuff does NOTHING. Today I tried in a non chalant way to see if she may give me something a bit more appropriate for my levels of pain (Not to mention anxiety b/c of all this.insane heart rate, BP through the roof.I work myself up) No, I got some new piece of crap medication for nerve pain that I refuse to even bother with. I wanted to go in and see her one more time before I resorted to the ER. So I suppose my question is if I go to the ER and be honest with them about how much pain I really am in, tell them my problem and that i'm having an MRI, & my dr won't prescribe me anything that will help or has helped me for my pain, will they be likely to prescribe me some painkillers to just get me through the next few days even or anything? It seems like it would be acceptable, and I have no other options.HELP! Any experiences, advice, input would be helpful, ASAP, because if i'm going to go it is going to be soon. Thank you! softtab cialis
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Hi rod, welcome to the boards, there are some great people here that will be able to help you find what you are looking for, so you've come to the right place, as most of us have been in your position, so we know how others are feeling. your actually only three months out of surgery and typically the recovery time for a fusion is 6 months, on top of that you had a 2 level fusion. i had a one level and the recovery took just over 6 months, so i would expect you to still be fairly painful, however the meds you are taking are very low for pain control and i'm shocked that your othro doc doesnt have you on something stronger. i was on stronger pain control up until about the 6 mo. mark, and then my ortho begain putting me on lower pain control and the weaning off process started. i was never completely able to come off of pain medications and the lower we got the worse my pain was and i realized there was just no way in hthat i could perform simple tasks such as taking a shower, blow drying my hair, sleeping ect with what i was taking. thank god i had a rheumatologist that took over my pain control and she began treating me again with stronger meds, which she did for 2 yrs. dont want to get you nervous but during that 2 yr period i continued to see my ortho doc, as my back surgery only made things worse for me and my pain even on pain meds was nonstop, although controlled with what i was taking. one of the problems i had that was new, was i had severe sciatic pain from where the screws and hardware were, well a year (5/2008) after the fusion we went back into surgery to take those out thinking this was what was still causing my pain. not so! i was still in horrible pain and we did another ct scan, which showed that the level above my fusion had a diffuse disc bulge, so now he wants to do another fusion on that level (l4-l5). my rhuemy referred me out to a pain management specialist to control my pain better and that brings me to the current time of today. its very hard to 1000 find a pm doc. that will only prescribe medications, most will want to perform different types of injections to see if this helps in controlling your pain and many will put you through different types of therapy, even if you've been through all of these procedures before and they are shown as being unsuccessful. every doctor is different and has a way of doing things and they will want to try they're way on you, at the same time they will control your pain with stronger meds but eventually will want to take you off of them. once in a blue moon you might be able to find a doc that does only prescribe meds, unfortunatley in my state at least, those docs ended up loosing they're license and are currently in jail and because of this, many docs no longer will prescribe just meds, they will try other procedures too. as long as my doc is keeping my pain under control to where i have some sort of quality of life, then i personally have no issues with trying other procedures, even though i've been through them all and they have failed to help and at times have made issues worse, i'm hoping that maybe one of them will work and i wont have to rely on medications but the reality of it is, is that most people with back injuries who have had surgeries will always have pain and many of us will have to take medicatons the rest of our lives, the problem there is finding a doc that is willing to prescribe long term. its very hard. my current pm doc does not prescribe long term and i knew that because i was told this before i made the appt by the receptionist, but the pm doc i was seeing was doing some barbaric and unsafe procedures as well as prescribing a total of 11 meds for me to take daily, only 2 of those were actual pain medications. i felt i was in danger of her possibly killing me or causing me to become paralized, so after 2 weeks i left & was referred somewhere else, first by a poster here on the boards and then by my ortho surgeon. right now i'm only taking a total of 4 medications which are oxycontin for long acting control, oxycodone for bt pain, tramadol for my fibromyalgia and soma more or less to help me sleep. my pain levels went from a 7-8 down a 2-3 and have been consistent for almost 3 weeks now. i'm just waiting for my workers comp to approve all the other procedures he wants to do and then we can get started and see what happens. we have a plan in place and goals to meet, so i'm happy with that. depending on what happens in the end though, if everything he has done does not improve my pain to where i wouldnt have to be on pain meds, then i know that i will having to search again for another pm doc that will be willing to treat long term. hopefully it wont get to that, but after two yrs of going through this i have my doubts although i try to remain positive. so not only do you have the task of finding a pm doc, you have the added task of finding one that you can rely on to treat your pain for as long as needed. i would like to add some information to help you on your first appt when you do go. make sure you go in fully armed with information about yourself. go in with copies of your xrays, ct scans, mri's ect. make sure you take your pharmacy history with you, which you can either get online through your workers comp ins. company or you can have your pharmacy print out a copy of your history. its usually better if you get it from the pharmacy because they can print up the medication name, the strength and how you were taking it as well as the qty you were recieving. also take in any medical records you have that shows your history and diagnosis'. keep a pain diary as well, which shows what you did daily and how it effected your pain levels and what you took or did that decreased those levels. i hope this information has helped some. i dont live anywhere near you, so i cant help in that aspect, but im sure many people here will provide you with names of places either they went to or have heard about. best of luck and keep us posted lisa
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Im new to all these message boards i was traumatized at a young age.I was told that my penis ( glands ) would always hurt,,so never touched my penis glands. When i would it would hurt bad,like a stinging pain.Im not circumcised and i never pulled my foreskin back because i was so scared of the pain i would have.I know it the most part its mental but i just wanted to know if anyone had any info on how to lessen the pain if possible.Im trying to get over the pain but its always in my mind. I cant pull my foreskin back flaccid or erect but i've been doing the stretching exercises i've seen in these post. thanks i hope someone can help.Viagra stories real people's experiences |
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