Removal Of The Prostate By Robotic Arm? Any Information?
Jan 7, 2015
I am in a bit of a quandary is there anyone out there that has had their prostrate removed with the use of a robotic arm,I need to find out as much information as possible as I am thinking this may be the lesser of the two evils that they say I need. I would like to find out everything about the op and how it impacts on your life after, how long does it take to heal, how long do you wear a bag, how long before you can have sex or is that part of your life just a memory
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24 year old and yesterday my hysterectomy has been agreed by two gynecology professionals one of them being the surgeon
And I have also had my pre-op assessment and am now just waiting for a date however the surgeon has said he will perform the surgery by robotic assisted key hole surgery.
And I was wondering if anyone else has had this type of hysterectomy and any I formation....
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Just got Gleason score 4+3
PSA risen from 17.8 to 20
plan for robotic radical prostatectomy in 3 weeks - has anyone else had this surgery?
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My 73 yo father had a radical surgery 5 years ago (prostate removal) due to the cancer. To date, he is suffering from urinary incontinence. He is also taking "Cymbalta" as a medication but no relief has been granted. I was wondering if anyone could let me know about a new medication in the market that would work better than "Cymbalta" ?
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I had a total robotic hysterectomy on 11/17/14. after my 6wk ok for sex, it was very painful, bleeding,watery dishcharge, felt something inside my vag. I went to dr. an he said I had scar tissue and possibly didn't get all my cervix(how is that poss)so he put silver nitrate on it and I went back 4wks. said I still had some so put more silver nitrate on.. went back 2 wks later, said it was all gone and didn't see cervix & I didn't feel anything either (was ok for sex)we had sex 1x and very easy. was painful but not horrible. haven't since until 4/28/15. it was horrible, bleeding, cramps, excruciating pain. deep thrusts especially. since ive had watery yellow discharge (some odor)again -so much its like I pee myself-not pee, and feel a hard, thin something inside vag. (tongue shaped)when i touch it or move it, I instantly cramp bad. I need to know what is going on, y I cant have sex (never had prob presurgery)could it be torn cuff? is that my cervix still left?
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I had a robotic hysterectomy Jan. 2010. I have had pain ever since. I have recently been diagnosed with nerve damage. Has anyone else had any kind of problems after the robotic surgery?
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I had a month ago, a robotic assisted partial hysto, I have only my left ovary. I chose to keep in, being 39, I was not ready for hormone replacement therapy. So, I feel pain so bad, and a warm burning sensation in my pelvic area. I was feeling better a week ago, Now, back to the pain before, I had Endometriosis removed during my hysterectomy, and two loose staples (internal) from my surgery in 12-14-15 (appendicitis/Fallopian right tube removal). I was wondering is there anyone else having pain? I was told Oh you'll feel so good in a month after the surgery.....
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I am having a da vinci robotic laparoscopic myomectomy on Tuesday and I am really scared. I am scared of the general anesthesia, I am scared of the pain meds and recovery. I am scared of not being able to do things. I am even scared of being scared. Anybody else go through this surgery that could ease my mind...only positive stories please I can't take anything negative.
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I had a total robotic hysterectomy 5 weeks ago. Sunday night had unplanned sex. It was not painful, I'd say uncomfortable. When my husband ejaculated, it burned!
Today, Wed. Still burning, uncomfortable and frequent urination.
Does this sound like an infection? Or irritation because it was too soon.
I even resorted to using hydrocortisone last night because it was driving me crazy and I could not sleep.
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I and other volunteers see a lot of posts regarding symptoms after an exposure. Some are minor such as a rash or a swollen node to "HIV like" such as a cluster of fever, sore throat, sores and body aches. Keep this in mind that as humans we are covered or exposed to germs, common viruses, and fungus which we all carry. This is called the "the biome" which is the invisible part of our environment. When we have sexual contact with somebody or their body fluids we expose each other to these organisms and our body reacts accordingly to fend off these invaders sometimes making us feel ill or display manifestations of symptoms. Stress and anxiety post exposure contribute to this since chronic stress decreases the immune system and makes us more susceptible to common infections. But what about the rashes? One may ask. Stress and anxiety causes the "fight or flight" response in our bodies causing release of cortisol which causes itchy rashes on the skin. Cortisol rashes are also called "hives" can be be similar to rashes found in STDs and can be frightening when they occur, (Ive been there). Allergic reactions also play a part. Also, sometimes the timing of exposure and illness is purely coincedental. Finally, if you have had a high risk exposure- when in doubt, test out.
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I was on Nortriptyline for a year for migraine prevention. I found it was making me extremely tired and my heart race. I unfortunately stopped it two weeks ago abruptly. Does anyone know how long withdrawal symptoms last for. Still feel jumpy, brain zaps, insomnia and headache.
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I had a doctor appointment today and I tested over so I might have gestational diabetes I have to go into another clinic to get a 3 hour test for it..it makes me nervous but my mom is a nurse and says you mainly just have to maintain your sugar levels...does anyone have information on gestational diabetes?
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Anyone out there have any information on central pontine myelinolysis , my 26yr old son has been diagnosed with this condition. He has been in hospital for 6 weeks and spent the last 4 weeks in intensive care, he went into hospital on Christmas eve after having seizures to do with alcohol withdrawal the first couple of days he was doing fine then things started to go wrong. He started to loose his balance he started slurring his speech and was getting very confused. He then lost his ability to swallow then started to slip into a coma at which point intensive care induced him into a coma and we were told not to expect him to survive. A week later he started to come round and could breath for himself but could only use his eyes,3 weeks later and he can communicate by blinking his eyes can squeeze my hand with both hands can wiggle his toes and can understand everything we say to him. We know we have a long way to go and don't know what the long term recovery is but would be grateful for any info from anyone who has come through this condition.
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Just wondered if anyone has had these injections, can't seem to find out any information about them. Already had tvt surgery which was unsuccessful so really want more information before I have another procedure.
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I’m trying to find any information about Hedge apple use for treating cancer patients. So far it's really hard to decide whether to try this or not mainly because most information I found were more focused on discussing if you can eat the plant or not, then on the issue of it being used for treating cancer. Basically it seems like it wouldn't do any harm to try this, but I don't know how long or even how should Hedge apple be used for cancer treatment. Some people say they just eat it, but also, I didn't see any rel info on how effective this plant be in either preventing remissions (which I hope), or cancer.
Please, if anyone has any info on Hedge apple use for cancer treatment, especially breast cancer treatment, share.
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I am looking to have a left flat foot reconstruction in The Fall of 2014 at HSS.
I am trying to get as much information as I can in regards to making the right decision. Currently I can still exercise but have pain when walking a distance or being on my feet all day. Also my foot is starting to turn in and affecting my knee.
I want to hear how did you know when it was time for you to get this surgery done. How bad was your foot before you considered this surgery. Could you walk at in orthotics without pain or were you in constant pain all the time.
From what I hear this is a horrible surgery and I don't want to be worse off than I am now. I have already had 4 opinions with different OS and they all recommend close to the same thing just different ways of doing it.
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I had my bladder repair just under 3 weeks ago and found these weeks to be a lot worse than when I had a repair 5 years ago. That was done with stitches,this has been a mesh repair. I think the shock of the op and being discharged too early,I think, has added to worry. I still feel smelly due to discharge or blood and worry when I open my bowels ( never been constipated before!) Felt really low and tearful this time as well. BUT...I have felt much better for the last 2 days and feel more positive...I feel for everyone on here. We really should be given more info when we leave hospital...
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I work for a Software company since last 15 years. I suffer from Computer RSI which makes it very painful to use mouse/keyboard, hold a pen and such things. Nothing has been revealed in my MRI or nerve conduction studies which is making it very challenging to convince people at work, who are not very aware of RSI.
Can you point out to any resources at Internet to show that RSI can be a severe problem even when nothing shows up in your investigations?
Has Computer RSI been formally accepted by medical science as a diseases?
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I had a colonoscopy with sedation (midazolam and fentanyl) in Chorley Hospital a few days ago and I still feel as if I had a PTSD. I read the information sheet and expected to be relaxed after sedation, with maybe some discomfort. When I was injected with the drugs (midazolam and fentanyl), I suddenly felt very anxious. I tried to seek reassurance, but the physician was talking to somebody else, busy preparing for gastroscopy. I think it could have helped if somebody asked me how I was at that point. I also had some trouble speaking – I think I was able to speak, but I could not hear myself so it made me feel very strange. Later on I read that difficulty speaking is a side-effect of midazolam. I felt quite intense pain during colonoscopy and the kind student nurse was talking me through it. I recovered well, I think, but I remember the whole procedure (so the amnesia that the leaflet talks about obviously doesn’t happen in every case). Next day I was very irritable and anxious and sick later on.
My main grievance is about lack of information beforehand concerning pain and the nasty side effects of the sedation. The leaflet mentions that you might feel ‘discomfort’. Of course you will feel discomfort – you will have a camera up your bum, what are supposed to feel? There is no ‘may’ about it. However, there is a difference between ‘discomfort’ and ‘pain’ and these words should not be used interchangeably. The leaflet and what you are told by the medical staff makes you believe that you will be drowsy and relaxed while medication works, and then back to normal after. I got quite a shock when I had the anxiety attack after the drug was injected and realized how vulnerable and helpless I was. I was also very unpleasantly surprised at how awful I felt the next day. Had I known this could happen I would have opted for entonox. Unless something changes dramatically in the way they perform colonoscopies, there is no way I’m having another one any time soon.
I would not like to discourage those for whom colonoscopy could be beneficial from having it. However traumatic it is, it is preferable to dying from cancer. However, I think that medical staff are not well trained in empathy (only student nurses seem to have it) and you have to be very assertive with them in order to receive honest information. If you are unlucky enough not to experience post-colonoscopy amnesia, the feeling of being at the mercy of medical people who are inflicting pain on you can be disturbing. It might be preferable to experience the pain whilst being alert and able to speak, and thus having some degree of control.
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As far as I know, there is not ETD cure, yet. I am interested in finding one. I am a Caucasian 34 year old man living in Santa Clara, CA. I have a BA in Psychology and work in a Neuroscience Lab. I was diagnosed with ETD a year ago. I have been suffering from it for 17 years. 13 years ago I had a bought of Bulimia that lasted for about a year. I had Anorexia Nervosa as an adolescent. I was given the maximum dose of testosterone to boost me through puberty since Anorexia was preventing it. Soon after I abused alcohol, marijuana, tobacco, and various other drugs until 2005. I believe all these factors have contributed to my ETD. I was diagnosed with OCD and Generalized Anxiety Disorder two years ago and have been taking Effexor (Venlafaxine) to cope. An Ear, Nose, Throat doctor (currently called Head and Neck surgeon in US) prescribed me Flunisolide (corticosteroid) to reduce ETD inflammation. It seems to help a little, but it is certainly not a cure, even when used for a significant period of time (i.e. 3 weeks).
My ETD has been recently aggravated by my attempts to remove pimples and skin tags, which may be a symptom of OCD. Has anyone else experienced this situation? Numerous doctors say there is no connection between the skin abrasions and ETD, but they obviously don't have ETD.
Primarily, I am asking for information regarding ETD. I need to know the statistics of ETD so that I can develop a valid research proposal. Health organizations neglect to respond to my questions. It seems that most biological research is involved in diseases such as cancer and heart disease, which is great. But, as I am sure that anyone reading this knows, Eustachian Tube Dysfunction is a debilitating disease that hinders one's ability to live to their fullest potential. As I have recently graduated with a Bachelors degree. I am researching what my next step will be. I am strongly leaning towards statistics and data mining, since that is a much needed position in all research fields.
I am looking for information on the number of people with ETD worldwide and specific to certain regions. A timeline of ETD cases in these regions. Research groups, Academic and Professional, that are researching ETD. Research groups that are investigating ETD from the Neuroscience and/or Ear, Nose, Throat (Head and Neck surgery) perspective. Any other information is helpful as well, especially your own personal accounts of ETD. Please share your history, as much as you care to disclose, so that I can begin to develop an etiology of ETD.
I have read many of the other discussions on ETD and recognize that many of you are suffering and I certainly empathize with you all. I am still trying to decide if my anxiety disorders are the result of ETD, my ETD the result of my anxiety disorders, if they are mutually intertwined, and/or if something else is going on. I very much hope to hear from you so that we may begin to develop a cure for ETD so that we may not be hindered by this ruthless malfunction.
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Having agonised about what to do for over a year now I have finally decided. Nothing. Well, not quite nothing but what is termed ‘watchful waiting’. My PSA has steadily increased over the past two years from 5.4 to 7.4 and in September my GP referred me to a urologist. The urologist, who arrived very late to the surgery, did a quick DRE then said that he would refer me for a biopsy. I wanted to discuss the options, including MRI as I didn’t want to undergo an invasive procedure without proper discussion. Also, I had read that in a test conducted on 223 biopsy-naïve men that biopsy was no better at detecting PCa than MRI. The link to the study is here - [URL....]
We found that mpMRI/MRGB reduces the detection of low-risk PCa and reduces the number of men requiring biopsy while improving the overall rate of detection of intermediate/high-risk PCa.
Unsure how to proceed I asked my GP to refer me to a private urologist with the hope of being able to discuss the alternatives.
In the meantime I did some extensive research and discovered two further studies which concluded that for low grade PCa (PSA<10) the outcome for watchful waiting was no worse in terms of morbidity that invasive treatment and the outcome in terms of quality of life was much better. Both studies were conducted over at least 10 years by reputable agencies. One, conducted by the New England Journal of medicine is here [URL] ... . The other can be found by searching 'PIVOT'. Also, a number of well-known doctors have published articles in favour of doing nothing – Dr Mark Porter in The Times and Dr Sarah Jarvis in this very website, not to mention other articles in The Daily Mail, Telegraph and Independent. I got to thinking that if invasive treatments did not improve my outcome, what was the point of a biopsy?
I finally got to see a private urologist who discussed the options and, although he was marginally in favour of a biopsy, did not object to my proposal. So now I am going to monitor my PSA and I will reassess the situation if/when my PSA goes into double digits. I have since gone on a no-dairy and low red meat diet and my latest PSA (Dec14) was down marginally to 7.2 – still high but moving in the right direction. I appreciate that this course of (in)action is not for everyone and not knowing is frustrating at times, but for me at least, I feel it is the best current option.
I am 56 years of age and my father, who is still very well had an RP for PCa about 15 years ago. All DREs have reported ‘enlarged but benign-feeling’.
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