Vasectomy :: 1 In A Thousand Failure - Ridiculous
Dec 27, 2014
They used to say 1 in a thousand went wrong,(when I had mine) then it became 1 in a hundred, now it`s one in 10 with PVPS and a risk of about 4% with other problems. How long before they tell us the truth, some say as high as 30% with problems!!
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The best way about a vasectomy is to NOT have one. Anyone who thinks that they have got away without problems just can not say anything as PVPS can come on at any time until we die I know a friend who is in his mid-seventies and has more pain than in the whole of his life.
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Hi I am looking for help I have just had my second vasectomy done just 2 weeks ago due to a failed vasectomy the first time. I have 2 large lumps 1 at the incision site and 1 and the opposite end of the incision and they are both causing me a lot of pain which runs down my leg I have seen my doctor but has told me to give it a couple of months but I didn't get any pain like this the first time. Can a second vasectomy increase any chances of side effects or chronic pain.
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Okay, so a little over 4 months ago, I donated my left kidney. For the past month, I've been having a slight pressure (not quite pain) in my right lower back area, where my one kidney is. I just had a checkup a few days ago with urine and blood tests, and I have seen the results. There is no indication that anything is wrong though. Maybe they missed something? I forgot to mention this to the kidney doctor during my appointment though.
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I really don't know what to do, i just made another apt for second opinion on hrt. I have alot of symptoms and much anxiety and don't know what to do. Both success and unsuccessful tries of these hormones will be much appreciated.I
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I had microfracture/debridement for an ankle OCD of the medial talar dome of my right ankle at the end of April 2010. Other than my doc having issues with the cartilage flaking off when he tried to clean things out - all went well. At least I thought so at the time.
Went through several months of PT and it seemed pretty good.
About 18 months post surgery, I was having issues with the ankle. My doc at the time suggested a shot of cortisone - which I agreed to - but didn't really help. He then suggested I might look into other options - all of which my insurance considered "experimental" and would not pay for. So I limped along.
Finally, last month, while stretching my ankle gave a loud "pop", hurt like the dickens and swelled up. So, I finally felt "pushed" to go to a new doc my primary highly recommended (and who was covered by my new insurance).
Wonderful new doc. Admitted he felt OATS was not a step for me since my OCD went off the side of the talus. He was going to send me to someone who specialized in cadaver plants - but first - a new MRI.
New MRI was good, but with the high powered system, my ankle was in bad shape - felt like it knocked something loose in the joint. I called the new doc to ask if that was a possibility. He called me back himself and said he already had the results of the MRI and he now felt comfortable recommending re-doing the microfracture/debridement again over the cadaver implant. As he said, if the m/d failed we could still do the other at a later date.
So I have an appointment on Monday to actually SEE the MRI results and discuss/set-up surgery. My biggest challenge - choosing a time frame.
While I would love to do it immediately and be done with it - our county fair is in a month and as a Division Chair, I know I wouldn't be able to do my job in any way (climbing and setting displays) - and my kids are all Division Chairs on their own, so I really don't have any help to rely on. Then there is the wedding of my adopted son five hours away the first weekend in September....My oldest son suggested I wait until after the wedding - which is fine - except for the fact that it's football season and I'm running for public office and have a campaign to very literally run! LOL. Maybe being on crutches for the busiest part of my campaign will get me a few sympathy votes - because I think I will talk to the doc about saving the surgery for early September.....which will put me able to walk somewhat normally maybe by Christmas.
So - I am back to this adventure again. Has anyone had to do it a second time with the same ankle?
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I had an ulnar shortening osteotomy and tfcc debridement on may 24th. I had been misdiagnosed with tendonitis for three years, then an MRI revealed a tear in my tfcc. They cleaned up the tear and then shortened my ulna by 6mm.
So my bone is healing and stable. I have almost all of my range of motion back. But the pain in the soft tissue on the ulnar side of the wrist is worse than before surgery.
I have adjusted my whole life around the pain. I no longer have hobbies, cook my own food, or even pick up my three year old son (which is heartbreaking). The most daunting part of this is that I can not do my job. I can type and email, but I can not use my drawing programs for more than 30 minutes a day without screaming. I have spent my whole life training for this career, and all of a sudden I am no longer able to do the job I am paid to do.
I met with the doctor today and he said there is nothing more he can do for me medically. I don't know if this is a failed surgery or not, but I know that I am no better off than before. I had the surgery because I could no longer do my job, and now I have had the surgery and still can't do my job.
The doctor also said there is nothing he could do for me pain wise.
My questions are:
Is there really nothing they can do for the pain? No shots? Nothing? Am I expected to work in excruciating pain or not at all?
Would I even have a chance at disability? I can work at a computer, I just can't use the skill set I have that makes me employable. I feel like I would have to start from scratch.
Is this considered a failed surgery? Should I get a second opinion? My surgeon is the best in my state and is really nice. I don't know if there is a better surgeon out there.
Do any of you live with chronic pain? How do you do it? Do you have any tips as to where to start?
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I feel such a failure. I'm a trained nurse I give other people advice all the time yet I cannot help myself...let alone others. This is so difficult. I thought I was healthy. I eat well and have a positive disposition...well I used to. Will I ever be the same again?
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currently my creatine 205.
can take enalapril or losartan? will it affect or worsen kidney function.
well, i have been taking enalapril since 2008 . my creatinine was hopping around 150-180 in these 7 years till 2015.
However, due to chronic diarrhea , vomiting. acute renal failure. creatinine shoot up to 400 in Jan and urine infection in march.
creatinine now hopping around 200-250.
doctor stop my enalapril and replace with amlodipine 5mg
once i stop the enalapril , my urine protein is back. from march 0.17g to 0.61g. i am worried.
i didn't have any urine protein over those few years since 2009 to 2015. i guess this is the reason which i can keep well in my condition with creatinine hopping around 150-190.
i am worried that the urine protein my cause my kidney worsen and dialysis may starts soon.
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Joined: Tue Apr 19, 2016 5:03 am
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3 weeks ago, i was admitted in hospital. over my 2 weeks staying in hospital, doctor didn't do anything, didn't on drip . just give me injection of Hydroxychloroquine.and i was diagnosed with urine infection. so creatinine able to goes up from 160-210. but down again to 155.
however, last few days, my creatinine shoot up to 240. such a shocked to me. as i didn expect there is so much shoot in just few weeks time.
doctor has been stop my enalapril, which i used to protect kidney and keep my urine protein negative.
however, there is 1+ urine protein in my urine test. my blood pressure used to below 130/80. now sometime, it can shoot up to 150/95 if i do some physical activity.
i have been worried for my condition. This year, i was admitted twice. Jan admitted due to diarrhea and dehydration. delay the admission. so creatinine shoot up to 400++, nearly need dialysis. however, after drip. then able to drop to 150++
then during march usual check up. my creatinine also shoot up to 240. however, after the hospital stay, it manage to down back to 150++
i wonder is it because i started to work and sometime i worked quite late. then my creatinine shoot up so much?
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I'm 56. Several years ago I was dx with chronic diastolic dysfunction failure. With help from diuretics I lost 100 pounds in fluid. I was stunned when diagnosed. I still am and have trouble believing it. Lately I've had nagging coughs. I'm here to find out if anyone else has experienced this coughing and also had trouble with acceptance.
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My mom is 91. She has CHF and with watching salt, has been controlled quite well. She will get some edema in the both lower legs and ankle and feet but that has in the past gone down. She has developed this ankle / foot fluid edema in the left foot for 2 weeks. Can't get it to go down. Went to her heart doc. Said to begin Lasix 20 mg for 3 days. Its not gone yet...on third day. Urinating a lot. She's watching salt now close. Is it rare for edema and fluid to be in ONE ANKLE/FOOT? She has one kidney. Actually she can get quite dehydrated often.
Kidney is usually ok. She was diagnosed with peripheral artery disease but that hasn't been an issue for quite a while. Can I please get comments on what kind of treatment long term is she looking at. She's only 5 ft tall and not overweight. Should she get the stockings if she also has perph artery disease?
After you start Lasix, will it take a few days to do down?
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Pills for RA are not working for me so rheumatologist is suggesting self-injected Humira or Enbrel. I read the side effects and they are scary. Especially it can cause heart failure even if you don't have a bad heart. I'd like to hear from any of you who are on these drugs and your experience with them.
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I started out watching porn and masturbating when I was 10 or 11 years old. I didn't have a girlfriend until I was 15. The first time we tried to have sex I couldn't get an erection sufficient enough for penetration. The times after that we tried to have sex and I got a weak erection, but managed to penetrate her. I got pretty hard when I was inside but it quickly goes away when I'm not inside her. I realize what the porn and masturbation has done to me all these years so I'm unable to perform in real life situations. After reading many people in similar situations as me, I've decided to give up porn/masturbation forever to be able to perform in real situations with real girls. Summer is coming up when I will be able to go to my girlfriend's house in a little less than two months. I've installed porn blockers and stopped masturbating since about four or five days ago. I feel absolutely no urge to watch porn or masturabte. Do you think I will be healed? I hate living like this and want this to be over with. If you have any questions, just ask.
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I was just wondering if anyone has protein in their urine with Chronic Kidney Disease and what did your doctor do about it if anything. I am trying to keep my GFR stable. The last time it went up a bit but am worried about the protein causing more damage quicker.
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Is it possible to have CKD or kidney failure without protein in urine?
Last week my masseuse found a knot in my back that she suspects could be inflammation in my kidney. I've had some weird symptoms popping up over the last month like foot/ankle swelling, profound fatigue, leg cramps and blurry vision. This last week though I began developing SEVERE flank pain (like 9 on a 10 scale), back pain (started out lower, now entire back), horrible nausea, horrible headaches, shooting pains down my legs, metallic taste in mouth, dizziness and loss of appetite. Not to sound melodramatic but I feel like I'm dying. The pain is constant but the intensity seems to be moving in 24 hour cycles. Today I feel awful but I was able to shower/get dressed. Yesterday I couldn't even get out of bed. I slept for 16 hours. It's been going in that pattern for the last week and a half.
My doc did a urine culture last week, got results today and there was no protein in my urine, but I had 3+ ketones and a large amount of leukocytes. Blood work from a month ago just came in and my kidney numbers were off a month ago: BUN (32), Creatinine (1.8), eGFR (33). Between the symptoms and the blood test I'm thinking it sounds like renal failure, but could it be CKD without protein in the urine?
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Is an enlarged heart classed as heart failure?
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After being all set and really enthusiastic to go get myself a vasectomy and finally get to enjoy no more worries or needing any more birth control, I did a lot of research online and on men's health and forum posts.
The unknown and unpredictable risks of being one of that certain small percentage of all men that will have problems directly from a vasectomy seems too great for the benefits.
A certain percent of all men will get complications and have problems after a vasectomy. As many as 15 percent or more of all vasectomy men can have complications, that's nearly one of every six men with vasectomies !!! The percentage is still being debated but it seems to go higher each year and higher with each new study done. Most seem to be fairly mild problems with fast cures and quick results. But a very small number or smaller percentage have major and long lasting problems. Maybe beginning so many years later that many men will see no connection between later problems in life and his vasectomy done many years or decades earlier.
The cure rate for fixing chronic pain and immune system troubles seems to be very low. Dr.s don't seem able to get any cures to work for the very few men most badly affected by vasectomy complications.
Most men have no big problems at all or just little long term annoyances like slight pain or decreased ejaculation force or intensity that they feel are well worth the birth control results they wanted from a vasectomy. Some have trouble and get cured. The two biggest long term problems with fewer cures are chronic long term pain afterward and immune system problems in men reacting to their own sperm cells.
No one seems to know ahead of time which men will do fine and which men will have big problems from a vasectomy.
Some men have troubles right away and some don't have any troubles until years or even decades later. Some men do great and never have any problems at all.
One big problem a very few men have is from their own sperm trapped and leaking into other unnatural parts of their bodies (body parts not intended to store sperm) every day with no outlet. Then their own immune systems are stuck needing to dissolve and break down hundreds of millions of new sperm produced by a man's testicles every day of his entire life. New daily sperm that all vasectomies totally block from leaving his body at all. His body is forced to break down all that daily production of sperm cells and rid his body of that pent up sperm being manufactured inside his testicles daily.
All sperm have only one half of each man's own genetic materials, the female's egg provides her half of the total chromosomes needed to make a new and unique baby.
All of the cells in a man's body have his full set of chromosomes inside every cell, except his sperms which only have half of his chromosomes. Men's normal body cells are recognized by his own immune system as being his own cells. Sperm have only half of his chromosomes and sperm seem to be seen as invading stranger's cells once they leak into other parts of a man's body after a vasectomy closes the only escape path for all his sperm to leave his body. The pent up sperm leak into the scrotum and get outside of the normally enclosed testicle and vas deferens system that exits his body before a vasectomy. This leaked out and pent up sperm then need to be digested in the scrotum by a man's own immune system to be destroyed and gotten rid of.
It seems for a very few men that the same digestive cells that dispose of pent up sperm inside the scrotum can travel up into and deep inside the two testicles by traveling the same exact exit leaks that the daily production of sperm use to exit out of the testicles. Even vasectomies that completely seal the testicle end of the vas usually form some leaks to relieve the pent up pressure inside the testicle from the never ending production of more sperm daily inside the testicle.
Some men seem to end up being slowly or more quickly castrated as these same immune system digestive cells enter into the deep interior of their two testicles and begin digesting the insides of both testicles and all of the delicate sperm making factories and tissues inside the testicles. Their own immune system digests the inside of their testicles just as it would digest all of the pent up sperms that cannot exit his body after the sperm finish forming and leaving his testicles into the rest of his body.
Long term chronic pain in the testicles after a vasectomy can be a huge problem for some men too. Some have it soon after and some have it years later. No one seems to know why or how to provide a cure for many of these men. It could be obvious pain from having pressure build up from sperm trapped inside the testicles. Or pain from the insides of the testicles and epididymis slowly being destroyed and dissolved by the man's own immune system. Or pain from nerve or tissue damage that occurred during the vasectomy cutting and when closing the ends of the vas.
No one can predict which men will have troubles before they occur.
I'm still holding out for new and better methods of male birth control for myself. Some new ones are in development that sound much better to me.
Just look it up yourselves on line before you take the jump to get your vasectomy. And read men's vasectomy problems on here first and make up your own mind. It sounds like few Dr.s want to tell every patient in detail about these big problems because of the small number of men who will have the biggest long term problems afterward.
But for those unlucky men with major problems there are few cures to get relief or repaired.
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10 days ago I had a vasectomy and I felt pretty good over the weekend, recovery has been fairly easy. We were able to have intercourse which at the time helped the minor pain in my testicles. However this weekend I had to chase my son all over the place at our church because he wouldn't stay out of things lol and I was picking up our baby some too. I over did it because now all the pain is back and I'm swelled up... what should I do? There's one particular area that looks agitated because it is a little red and warm (probably from inflammation).
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Has anyone had a reversal?
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i had vasectomy on nhs and it is well worth it. Very little pain during the operation which took about forty minutes,and the following two weeks were uncomfortable but bearable. I considered going private but braved it on nhs and they were brilliant.No regrets at all and dont listen to your so called friends who fill you with horror stories. It's been ten weeks now and feels no different to before.
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