Prostate :: TURP - Any Experiences?

I am told that I need TURP for my enlarged prostate problem . could anyone recommend a good Urologist in Dallas Metroplex area who has good experience in this procedure

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Thyroid :: Surgery Advice? Pre / Post Operative Experiences?

If anyone has dealt with this or know anyone who has I would love if you would share. I'm just curious about how the operation goes (its preparations, and after). I have 2 thyroid nodules and they are pretty big and is causing phlegm, voice changes and other stuff.

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Prostate Cancer :: Surgery Vs Hormone Therapy/radiation?

I have been diagnosed with Gleason 7 PSA 9 prostate cancer.

Biopsy showed cancer was in entire prostate and towards the edge but no evidence it had gone outside.

Bone scan normal.

Age 60. Generally healthy.

I have been advised surgery or hormone therapy for three years together with radiation.

The surgeon preferred surgery as did the consultant who would have been in charge of hormone therapy.

I think their logic was that surgery gave the greatest chance of 100% cure.

However I am very apprehensive about surgery and really struggling to make up my mind....

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Prostate :: GL Laser Surgery Recovery - Still Pain While Urinating

I am 4 weeks post op and still having frequency issues and pain when urinating. How much longer can this go on?

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Prostate Cancer :: Surgery, Hormone Therapy Or Radiotherapy?

My dad who is a hale and hearty 79yr old who walks 2 to 3 miles most days has just been diagnosed with prostate cancer, he has a PSA of 7, A gleason 7 (which is a 3+4), he has no symptoms. He is seeing a doctor on 1/6/15 to decide on treatment, surgery or hormone therapy with radiotherapy. likely to opt for the hormone therapy with radiotherapy. Both read quite worryingly re side effects. Anyone out there with info/advice re hormone therapy and radiotherapy. Is radiotherapy alone better as Hormone therapy described as chemical castration, sounds scary re side effects. My dad is fit with good quality of life. Any advice from those that have been there..

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Large Prostate - TURP Surgery? Feedback / Reviews - Penile Implant

I'm 48 and would like feedback on the TURP surgery...

I've had issues with my prostate over the past 2 years. Last October it was 3.9 cm x 4.9 cm. An now its measured at 5.9 cm x 5.7 cm during the past year I've noticed I was getting 5-8 times a night and during the having to rush to the restroom with no time spare, in the past 4 months I've had to force my urine out. Called doc he ordered urodynamics test, it showed that my bladder has no reaction when I'm full of urine. Doc said MY prostate is so large it's shutting off my urethra tube. So he said I need the TURP surgery. .

I'm so unsure about this because I've had penile implant surgery this past Jan. and if I have the TURP I'll lose my ejaculation...

I also would like to know how to do all with not being able to cum?

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HOLEP And Having Incontinency/ejaculation Problems Afterwards

I am a bloke of 66 yrs and am having incontinency/ejaculation problems.

In July 2013 I had an operation – (HOLEP) as I had an enlarged prostate, the operation went well and I was back home in a couple of days. But for a while now I get very down and wish I had never had the operation.

After the op, although I tried to do the pelvic floor exercises I found it quite difficult, and eventually stopped, I did buy a pelvic floor stimulator (male type) and used that for a while.

Anyway now the incontinency is not a major problem as it is a stress type and not always. BUT what is a problem is that when I ejaculate I pee as well, just a bit but it is there and consequently this means no sex since the operation.

I knew there was a risk of incontinence and also reverse ejaculation (semen goes into bladder) I used Tena Men for a while but found after a few months did not need them. I can’t remember when I first tried masturbation after the op but I did, and was pleased to discover that there was no reverse ejaculation (well most of the time anyway   but what did concern me was during the act before ejaculation I would pass pee almost like milking. This has gradually got worse and unless I force myself to pee before I masturbate I even pee as I ejaculate.

The consultant did say he had removed most of the prostate, and as it goes through the pelvic floor muscle (I think) is it possible that the muscle is damaged around the urethra.

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Hemorrhoids :: HAL-RAR Procedure Experiences?

I have been suffering from some internal Hemorrhoids that prolapse after a bowel movement for almost a decade. After they prolapse i gently insert them back into where they belong and it has been ok and hasn't affected my life much.

However the past a few days ago after making a bowl movement i noticed when they prolapsed they were very inflamed and large and painful, i couldn't put them back inside me. I waited until the next morning but unfortunately the couldn't go in so i had to go to a hospital. The doctors managed to insert them back in when they applied some gel but it was painful and not easy.

Then 2 days after same problem but they kept on bleeding, had to go back to the Hospital and same thing.

I hope they get better more manageable soon but i doubt it.

Anyway i really want to avoid the traditional Hemorrhoid surgery as i have read the horror stories on here about being in pain for 4-8 weeks, complications and also i can't afford to take so much time off work.

Hence why i am considering the HAL/RAR Procedure, from my research it is less painful and hypothetically you can be off work for only 48 hours.

has anyone experienced this procedure? What was the pain like?

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Pregnancy :: C-section Experiences - Anyone?

I'm scheduled for a c section Wed. due to my little man's position and the doctor said a vaginal birth could be risky due to the size of my birth canal. I'm a ftm and this really dissapointed me. I'm really scared considering i've never had any surgeries before lol. Has anyone else had a c section? what was your experience? what should i expect?

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Hepatitis B :: TDF (viread) Experiences Anyone?

After 1month of viread, my alt increased from 200 to 373.

Before:

Hbv DNA 170 million
As I said my Sgpt 200
Hbeag reactive

After 1 month
Hbv DNA 133,000
Hbeag reactive
Sgpt 373

My alt increasing is this normal?after 2 more months what will be next happen to my sgpt.please share with ur tdf experienced.

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Gastroscopy With Sedation - Mixed Experiences

Over the last 12 months I've had nine or ten endoscopies. The first few were emergencies and I was not very aware of what was happening due to being fully knocked out.

Having survived the initial trauma, I now attend every 1 to 2 months for regular endoscopy checks. I had decided to try without sedation (just the spray) but the consultant virtually insisted that I have sedation. I was a bit annoyed at first at not being given much choice in the matter. They now use the spray and 3 mg of Midazolam each time. In ten seconds, I'm completely out of it and only wake up in recovery. No significant after effects and I'm usually off home in about an hour. Sometimes it goes really easily for the consultant and other times he experiences difficulties with me. Fortunately, the only time I know anything about these difficulties is after the procedure in recovery room.

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Fibromyalgia Syndrome :: Duloxetine Experiences?

i am really struggling with my fibro. The doc has told me to persevere with this tablet. He has also gave me an anti sickness tablet. I would like to know people's experiences with this please.

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Anyone Experiences? Flatfoot Reconstruction - Frightened

I am having serious doubts about going ahead with my surgery, and I'm wondering if anyone else has experienced a tremendous improvement in the pain and functioning of a foot with a ruptured PTT. My rupture occurred in November, and caused me LOTS of pain, limping, and sticking to three inch heels to keep the weight off my arch. I postponed my surgery to May 21 because I was too frightened. I wore an ankle brace that also pulled up my arch while doing whatever I could at the gym. At the end of March I noticed much less pain and walked three miles briskly with some incline on a treadmill. I can even jump rope now a month later and have been for several 4 mile fast walks. In fact today I was up to 4.7 miles/hr. on the treadmill. Tonight I did a single heel raise! I know my arch has flattened and now looks like my worn out flattened left foot, but am I crazy to be going ahead with this major surgery when I'm experiencing less and less pain and my foot is becoming more and more functional?

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Uterine Fibroids :: Esmya Experiences - Anyone?

I went to a gyno last week to discuss treatment for my 5x7 intramural fibroid which causes me heavy bleeding and sometimes a pressure towards my tailbone.

I was curious about having a embolization but my gyno thought that Esmya would be better for me to start with.

I have so many questions that the gyno couldn't answer (!) so I hope that you who have been on Esmya would like to share your experiences and can help me answer some of them. I am mostly scared of side effects, if it will affect my work, libido etc.

The questions I have for you are the following:

After finishing 3 months on Esmya, how was the bleeding? Was it much lighter after that?

How much did your fibroid/fibroids shrink?

What side effects did you have? Were they transient?

Has anyone been on them for longer than 3 months? If so, did the fibroid continue to shrink?

Will the fibroid stay small and bleeding continue to be less after I finish Esmya? Is it worth taking?

Is it safe? Would you recommend it?

I might add that I'm just turning 40, have to kids and want to avoid having a hysterectomy.

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Endometriosis :: Experiences With Depo Provera?

So I'm only new on here but I want to know what your experiences with depo provera are?

I'm 19 I've been experiencing lower pelvic pain and lower back pain for coming up to 10 years, I started my period when I was 10. I was told I had appendicitis and that got removed, though I was still in agony from that (don't know when that was but roughly around 2007) the doctors kept telling me I should have no pain and it was all in my head, a few days later mum was told my appendix was white and there was nothing wrong with it, I had cysts on my ovaries and Fallopian tubes and water in my pelvic cavity. The doctors brushed it off and told me I had IBS and sent me to the bowel specialist (can't think of the name right now)who said its nothing to do with them and sent me to the Gyni, this went on for a few years of bouncing back and forth from one to the other, I finally got a referral from my GP to go to another Gyni who at first wasn't too interested but agreed to a lap and was then finally diagnosed with Endo in roughly early 2010. Since then I had been on almost all of the contraceptive pills and on the marina, I've had 6 months of Zoladex, I've also tried naturopath and diets, Nothing had worked with exception of Zoladex which I got relief for five months.

My Gyni is now wanting me to go to a pain clinic and wanted me to go to my Gp for a referral which we did and he doesn't agree, he said because I've got my period every day we need to get that to stop and then the pain will stop (He's the only one that understands) So he wrote a letter explaining that and also asking if I could go back on the Zoladex, in the meantime I'm on a antidepressant in ways to help mask the pain.

My Gyni who I saw the other day didn't agree and didn't care that I was loosing every day, she doesn't want to see me anymore and to shut myself and my mum up has put me on Depo Provera.

Now I'm wanting to know what your experiences are with it, she reckons it won't work since I've not got any relief from anything else and said for me to go on Zoladex again won't be good since I will have more chance of menopause (right now I don't care as I already get hot flashes)

I've got no life at all, I stopped school in grade 9 and tried studying in TAFE (College) but now I'm unable to since the pain is unbearable and I have no energy. Government is trying to push me into work and I've been seeing a job seeker that is also trying to get me into work and keeps saying to take pain relief to stop the pain.

Does Depo provera work for you? I've heard some bad things about Depo...

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Hepatitis C :: Naturopathy Vs. Harvoni - Experiences?

I'd like to relate our experience with Hep C treatment. My husband got Hep C back before it even had a letter, in the 1970s, and he is now 62. He has never been much of a drinker, which is very fortunate. He has always had a ridiculous amount of energy, and an active occupation. He kept an eye on his liver (don't take that literally!), and the diagnosis never much affected him. But after a divorce about 10 years ago, he began to consume more alcohol than before, and his liver enzymes crept up, and his biopsy in 2009 said he had Stage 4 cirrhosis. Yet function was still fine, and still he did not feel affected by the disease. The doc said, the numbers say it's time for interferon.

The side effects and prognosis for cure were not encouraging, and I contacted naturopaths I know to get a recommendation for someone for him to see. They recommended a doctor at John Bastyr Naturopathic College in WA State, and we went to see her. She specializes in traditional Chinese medicine for cancer, HIV and liver diseases. She prescribed an herbal combination, and some other supplements. And ZERO alcohol. She was the first doctor who actually said NONE. Other doctors would pussyfoot around and say, don't drink a lot, but no one said, don't have any at all. Not even one beer on Friday. Not drinking was not a problem for him, as he had already mostly stopped having any once he got the Stage 4 pronouncement.

The treatment regimen she started him on made him feel worse, so he went back, and she put him on a different formula, something called Livercel, made by Nutricology. It contains a proprietary blend of Patrinia extract, Phellodendron amurense extract, Yi-Chen wormwood extract and Schisandra extract. He also was taking milk thistle and a few other things. This herbal combo reversed the numbers, brought his liver function (alt and ast) down to high normal, whereas they had been going way up.

He kept to this regimen and was going along fine, back to not feeling impacted by the virus, though of course he knew it was still there. However, at his checkup last June, his numbers were starting to go up again, and now that there was a real cure available, his naturopath said, ok, now the new drugs have been proven effective and have minimal side effects, so time to give that a try, if you can afford it. Which of course, hardly anybody can. So then we started on that journey.

Meanwhile, what my husband hadn't mentioned to me was that because he was feeling so unaffected by the disease, he had started being not so diligent about taking the Livercel. Taking it once a day instead of twice, or skipping a day, etc. Once he got the higher numbers in June, he started taking them religiously, never skipping. And you know what? HIS NUMBERS WENT DOWN AGAIN. The RNA quantitation was 15,774,971 in June, and on the 11th January, it had gone down to 6,646,637. Down about 60%. This shows to me that the Livercel was having effect. So look into that while you are waiting for the new medicines to be available at a reasonable price.

Meanwhile, although his allopathic doctor's request for Harvoni was initially denied by the health care insurance company, they approved it when she resubmitted it. And they signed him up for the Harvoni's patient co-pay subsidy. He has been on it for a week, and so far no side effects at all. I asked him if he felt anything at all yet, and he said, "I think they must have given me the placebo.

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Atrial Fibrillation And Warfarin - Experiences?

I was diagnosed with Atrial Fibrillation about a year ago and have been treated with Bisoprolol and Aspirin. This seems to be working for me but have been advised by my doctor to go onto warfarin as I am at medium risk of a stroke. I don't want to change anything at the moment whilst the present medication seems to be working because I have heard some negative reports of warfarin - not only the side effects of hair loss etc. and giving up various foods but also the fact that you have to tell your doctor about practically any changes in what you eat and where you go (holidays etc). This seems very restrictive. Could I please have your experiences of taking Warfarin.

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Novasure And Tubal Ligation - Experiences Anyone?

I am having a tubal ligation and the novasure procedure done on the 31st of aug. and i usually have horrible cramps.  Just wondering just how painful this is gonna be ? and has anyone else had this procedure done?

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Rheumatoid Arthritis :: Enbrel Experiences Anyone ?

I'm hoping to start a clinical trial for Enbrel beginning in May (they need me on MTX for 3 months before I can start the trial) and am wondering if anyone that has used it or is on it currently can tell me how they're doing on it?

I woke up this morning with that heavy duty exhausted, malaise feeling that I felt for so many months before being diagnosed last summer. I had to work a mandatory training 40 hours last week, played catch up over the weekend and worked another 8 hours yesterday. I woke up to that heaviness in the chest; not a sick like heavy as in bronchitis or chest cold, but literally like someone was draining my insides out. I am emotional today and that's what happens when I get these episodes. 

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