Chronic prostatitis
Posted , 27 users are following.
chronic prostatitis difficult to live with. Am not thinking stright with this disease any longer. Had a miserable day today. Don't know if I want to live any longer. Does anyone else have these feelings?
0 likes, 57 replies
stuart33428 steven43881
Posted
so tell us, what symptoms do you have? How long have you had them and what medications are you taking???
steven43881 stuart33428
Posted
Hi Stuart, I had a Turp done 61/2 years ago because of my prostatitis. It was horrible. I had 6 bladder stones, 4 kidney stones and a prostate blocking my urine flow. I was retaining about 200 cc of urine in my bladder and my flow rate was only 3.2 cc/ sec. But thats not the reason why I had the Turp done. It was because my prostate was so inflamed that I could hardly walk much less sit. I am so sorry I made that decision. I don't know wether it was the right one or wrong one.
The Prostatitis never went away. That's why I'm wondering if I made the right decision. The dr I am seeing right now just put me on some Cefdinir (omnicef). antibiotic. We' ll see what that does. I don't know if I'm looking at having the prostate removed down the road or not.
jjjj57989 steven43881
Posted
I've been there, not with prostatis exactly but similar. I had a strange kind of arthristis that was eating my spine and all the joints in my body. Riding in a car was excrutiating, lifting a briefcase, turning a door knob, looking to my right or left. I went to pretty much every top hospital in New York City, always asked to be treated by the 'Chief of Rhumetology'. No one offerred any hope. I was 36 and didn't want to spend the next 40 years with it.
I also had serious prostatitis at that time. ?
What symptoms are you sufferring with?
Have you tried every possible cure?
Have you posted about your situation on this forum? The members are very helpful and they have lots of experience to draw on.
Have you sought professional help for your depression?
How old are you?
Do you have people that depend on you?
Leaving aside the long term, Is there anything you could do to have fun tomorrow?
Can you do a kindness for someone else? Spend a couple of hours helping in an animal shelter or a veterans hospital?
steven43881 jjjj57989
Posted
Iv'e had these symptoms for 61/2 years jjjj. I am seeing a urologist now who has me on an antibiotic. In answer two your third question- yes many times trying to find an answer. I'm seeing a psychiatrist right now and I am 65 years old. Had the Turp when I was 59 ?? I don't have anyone who depends on me right now,jjjj. I am alone most of the time because my symptoms bother me so much.
I would love to help other people, but my pain stops me from doing these things.
Thank you for your reply jjjj ????
david19922 steven43881
Posted
Be careful about mention of suicide.If the wrong person hears you, particularly medical professionals, you could be subjected to an involuntary psychiatric examination, which could be of several hours or days in duration.I made that mistake one time after complaining pf depression. After a cursory ninety second exam,an incompetent ER physician decreed I had "suicidal ideation", and it took four hours of waiting before I could convince the Psychiatric Social Worker that I wasn't and was released. Never go to a psychiatric hospital for "voluntary admission". It does not exist.
randy_85492 steven43881
Posted
I sympathise with you.... I, too, have pain, but not near as serious as yours...My pain is caused by a foley catheter inserted into the end of my penis...One thing that helps reduce the pain is a neosporin pain ointment that I apply to insertion area... Also, I take Aleve for 12 hour relief and it helps to reduce the pain too...
You might want to try these...I hope they help!...
If others can make helpful suggestion to help Steven, please do!..
steven43881 randy_85492
Posted
maulmaliq steven43881
Posted
Yes mate, i've got chronic prostatitis for almost 3 years. I am 25 still young, yes. Doctor also shocked that i can get this disease at my young age. Recently I am still consume Clavamox antibiotics everyday, 500 mg 3 times a day. The symptoms decreased significantly but when i stop the medicine, the symptomps will come back. At first felt so depressed, then i can accept it with from support of my family and other people who lived close to me.
Dick2016 maulmaliq
Posted
What are your symptoms before and now? And how have you been dealing with prostatitis for the last 3 years?
Thanks
steven43881 maulmaliq
Posted
jimerskine steven43881
Posted
Steven,
get exercise and do it NOW!
i realize you don't feel like moving much but as someone who has had this affliction for over 10 years the more exercise I get the better I feel.
Bicycling, walking, weight lifting its all good and will make your symptoms SO MUCH MORE BEARABLE!
steven43881 jimerskine
Posted
jimerskine steven43881
Posted
try heat also, heating pad type? If you get even 20 minutes of relief it can seem like days and will get you tremendous emotional relief
Supertractorman steven43881
Posted
nealpros Supertractorman
Posted
Neal
philip1950 Supertractorman
Posted
last year it absolutely ruined my holiday Burning feeling in my penis, pain in my lower abdomen,groin and in my scrotum. Have found relief from ibuprofen (this is a good anti inflamatory) and going out for a walk.
Have suffered from Ed now for ages, think its been caused by long use of meds for other problems. nealpros suggestion of an implant would be great but cost is prohibitive for me and the NHS have given me no help at all.Have tried all the usual stuff like cialis, viagra etc but found then to be useless. Vacum pump works quite well once you get used to using it. have just bought some vitaros and will try that out over the next week and will post on its efectiveness or otherwise.
steven43881 Supertractorman
Posted
steven43881 philip1950
Posted
Prostatis is terrible, isn't it ???
Supertractorman nealpros
Posted
nealpros philip1950
Posted
I am in the US, so I know nothing about the National Health Service, but is there no way to appeal their decision and get some help from them to get a penile implant? It's a well known and accepted procedure here with a 98 % + satisfaction rate among those of us who have them, and their female partners. As far as I know, no research has been done on female partners, but I see no reason it wouldn't be the same.
Neal
Supertractorman nealpros
Posted
Neal, We are very fortunate with the NHS but you do not get much choice and money is limited. It can be very much dependant on your Consultant and if he is into research and bringing sponsorship for trials into the local health authority. I now have a number of good contacts I can speak to, so will try and find out what I can. I am not too bad but can't go near running taps or fountains ! but find dribbles are the worst but it is better than pain.
David
nealpros Supertractorman
Posted
Thanks for the clarification. If you have any questions about the penile implant, I'll be glad to answer them.
Neal
steven43881 Supertractorman
Posted
Supertractorman,
Try pelvic floor physical therapy. It's working a little bit for me. Maybe it will work for you.
Steve