Vasectomy :: Beware Of The Side Effects
Dec 24, 2014
Don't do it. The operation went as expected. The side effects were not explained at all. First it does change sex. The tingling feeling that occurs when achieving orgasm will never happen again. Not what was stated by the nurses who obviously were fed a lie, how would a female know? The second thing was urinating problems. Don't be in a hurry because gravity is the master now. The day I went home I found out that pushing only made the flow stop. That was only part of the problem since I now could not hold as much as could previously. It will be that way forever. So now how to I get it reversed at the cost of the insurance? I have been to a urologist but cannot get them to admit that those are serious problem. The year I got my vasectomy I was told I have Multiple Sclerosis.
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Am planning on making a Dr appointment after the holidays but wanted to check in and get some feedback from others to see if anyone has had any similar situations or remedies.
I had the scalpel vasectomy done 1 yr ago. Initially no major complications. Like most the typical soreness that accompanied it. After a few weeks that seemed to go away and life returned to normal.
However, periodically I would have issues where I would get a dull 'ache' in my testicles that might last a day or two. Nothing severe enough to go to the doctor but painful. This has cropped up multiple times over the past several months. The pain is still with me whether I'm standing or lying down and ibuprofen does little to help.
And twice now - once probably six months ago and again last night I had blood in my semen. Not a lot but noticeable. The blood isn't appearing when I urinate.
I know this is more of a Dr related question but I guess I'm just looking for feedback from anyone that might have ran into similar problems. I never had either prior to a year ago and the surgery so that is the obvious culprit.
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Just wanted to get a feeling for how other people progressed after surgery. Had mine 5 days ago and have experience no pain at all really. I have no trouble walking or sitting or anything.
There does seem to be a little swelling on the left side, which is a little sensitive, just wondered if anyone else had this and whether it will reduce over time.
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34 years male, had a vasectomy a week ago, the left side was quite painful during the op to the point it made me loudly say OW during the procedure. They gave more anaesthetic and carried on. The right side, no issue or pain.
A week on and I am still finding the left side rather painful, there is small swelling above the testicle and its still sore to touch, and aches, especially if i have been on my feet for a bit, which will cause pain when i walk too. I know timescales for healing is different for everyone, but I was hoping that by now I would not feel restricted on my daily activities. I have been fortunate that I have been on leave from work and due back in friday, I have an active job, and really not sure how i will cope with being on my feet for hours and possibly taking a knock to my testicles.
Just wondering really what others experiences are to do with recovery.
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I had my vasectomy 3 weeks ago and the left side has healed beautifully. The right side however has a donut shaped wound and string has come out and is hanging.
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I'm writing this post because my father has passed away from methotrexate toxicity in February. This cause of death has been officially confirmed. I'm in a state of shock and I really don't believe that the general public understand the severity or danger of this drug.
As I've read here many MTX patients have been on this drug for months if not years. My Dad was on this drug for only five days.
Here is some advice for everyone on this drug:
> Please everyone always ask for a consumer information pamphlet and be aware of the side effects.
> Even if you feel fine don't ignore any side effects
> Hospitals don't check for MTX levels in the blood - if you find yourself in Hospital ask them to test the levels.
> Be aware of leucovorin therapy ; known as 'rescue therapy' (this is administered if you have suspected MXT poisoning)
> Always follow the directions from a rheumatoid arthritis specialist or dermatologist or oncologist - not a general practitioner
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I just was wondering who has suffered the same and it's actually got better!? I suffer no pain ok maybe a slight ache if my testicle is squeezed/squashed but it's very hard to touch, I'm 10 days in post op and it's pretty much been ok had swelling that's gone down, I'm just concerned about the hardness of my testicle and the cause!? I'm seeing my GP in the morning and gonna book an ultrasound to check over my jewels.
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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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I am a 47 year old male (right weight for height) and reasonably fit running three times a week who has recently had to visit the doctor (first time in years) for severe neck pain caused by strenuous gardening work -so called leisure.
However my blood pressure was checked over the past few weeks and has found to be continuously very high ranging 190/115 to 150/90. My GP has decided to put me on ramipril starting with 2.5mg increasing to 5 mg and then 10mg over six weeks. On reading the comments about side effects I am really concerned which has now possibly increased my blood pressure further - really concerned on what to do, should I get a second opinion through my private medical before starting this treatment?
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I'm looking to start orlistat this week but after reading over everyone's experiences I'm a bit nervous to start. Are the side effects really that bad as I don't want to make a fool out of myself at work!
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I have just been put on nortriptyline for my pain has anyone else had this and did it work was there any side effects.
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I am about to use Viagra and I am a lot scared. I have never needed it but I guess I do now. So who knows about this drug, are there serious side effects. I do not want to trade one problem for another due to the drug itself.
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I used the tablets for 5 months and a bit, should be taking it for 6 months but i decide to give into not taking them due to really bad side effects.
When i started, i took 2 TWICE a day for 4 months but, rashes appeared on my cheeks, completely red and skin dried also on my nose. I couldn't bear the suffering, i applied creams like E45 (made things worse for me) then i switched to sudocrem, applying it to my face where the rashes were. this seemed to help stop the rash from getting any worse. I went to see the doctor who said i should cut down on the tabs to 1 Twice a day so i finally started to heal from the rashes. I carried on using the tabs this way until the rashes appeared on my nose again, it was really bad.
To those who suffer from Eczema, be warned as this course may effect it, making it really bad. This is the reason why i have to quit from this 6 month course (am finishing on 5 and a bit months) As for acne, it helped clear it up nicely even old scars until a point where my skin could heal no further ( i stayed the same after the 3rd month) so hopefully, changes are permanent and my side effects will go away from stopping this course.
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Put on this drug for HBP 2.5mg then 5 mgs had various problematic side effects went to doctor to advise him of my problems with this drug. He then increased the dosage to 10 mgs which I have taken now for 2 months and the problems have multiplied to a point when I have become so ill with all the problems highlighted in these messages that I stopped taking the drug and started to feel better within 3 days. I wonder now what the reaction will be from my GP when I tell him that I want to try an alternative drug. Having high blood pressure I could do without worrying about his comments which other people have endured when they have asked to have an alternative drug.
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I have found reading the posts about PA very helpful, i was diagnosed early last year with PA and have injections every 3 months they have helped enormously with my symptoms, please could any one tell me about the side effects of the B12 injection, i have had various syptoms which i have just put down to the whole PA thing, but would like to know....
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I'm on week 7 of 10 mg, and am pleased to say that my pounding heart, dry mouth and nausea have disappeared, I've only had a couple of headaches, my jaw clenching and tensing up have almost gone. I'm still struggling sleeping but I've never been good at that anyway, so I'll just see how that goes. I don't feel like skipping through life every day, but I certainly don't feel really low any more, I just feel 'steady'. Stick with it everyone, and thank you for your support.
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I'm on my 12th week. I've been diagnosed before with GERD. Now due to the pregnancy, it seemed to worsen as I experience painful heartburns. My doctor recommends I take omeprazole along with antacids. I've been taking antacids because I know they don't bare side effects on pregnancy. I am not sure though with omeprazole. I'm scared. I am afraid it might harm the baby. Anyone here experienced the same?
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I've been on Amitriptyline for 6 months for pain management - lowest dose 10 mg in evening and I am getting on fine after the side effects at the start!
This week I've been started on fluoxetine 20 mg per day for other issues. GP said it might interact with the Amitriptyline but might not so give it a go.
Has anyone else taken these two medicines at the same time? How did you feel?
I've taken fluoxetine before so I'm ready for the crazy initial side effects (off work for 4 weeks so I can get through it!)
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Has anyone had luck with Zoloft ? Any bad side effects ?
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Just in case that side effect sets in - does anyone know the effect of taking sildenafil citrate (viagra) when on ramipril??
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Anyone out there use metformin if so what side effects r u feeling currently taking metformin 1000 mg once a day
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