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Quote from: yoplait on 09/11/2010 06:39:58monkeyboy : + treatment with testosterone seems to have an constant effect which is not typical for other medical solutions which are less and less effective as the time passes.Each case is different, even those that work with testosterone.
monkeyboy : + treatment with testosterone seems to have an constant effect which is not typical for other medical solutions which are less and less effective as the time passes.
CCconfucius: Yes I am an engineering student although I am concidering changing my major with the bad economy retired engineers are coming back to work flooding the market for engineering jobs and studying advanced math concepts and having your short term memory constantly wiped by pois is enough to make you cry.
Did anyone had a Testosterone treatment that failed? Up to now Demo and Green seem have succes with T-treatment.
As for testosterone treatment. I told my doctor about my symptoms and he said hes never heard of anything like this and I told him people are trying testosterone and beta blockers as a possible remedy. He didn't want anything to do with pescribing testosterone to me he said it makes people feel good but destroys your hair and bones and stuff. He wanted to send me to a neurologist but my health insurance didn't cover it so I couldn't go.
My studies into the possible causes of pois syndrom have led me to the doorstep of neurotransmitters prolactin and dopamine. Dopamine directly affects all the things that we suffer with: motor skills, cogniton, memory, mood...ect Dopamine is counter part to prolactin. If we don't have enough dopamine then you get the symptoms you have with pois. My symptoms take exactly two weeks to completely subside interestly enough it takes exactly two weeks for your body to stop producing prolactin after orgasm. If our bodies are producing to much prolactin which counters dopamine or just not enough dopamine or worse both it could account for the effects of pois. Any thoughts?
POIS used to be around 1-2 weeks long, now it is only a matter of the day I have my orgasm, and the day afterwards. From abstinence and health.
CCconfucius: Yes I am an engineering student although I am concidering changing my major with the bad economy retired engineers are coming back to work flooding the market for engineering jobs and studying advanced math concepts and having your short term memory constantly wiped by pois is enough to make you cry. As for testosterone treatment. I told my doctor about my symptoms and he said hes never heard of anything like this and I told him people are trying testosterone and beta blockers as a possible remedy. He didn't want anything to do with pescribing testosterone to me he said it makes people feel good but destroys your hair and bones and stuff. He wanted to send me to a neurologist but my health insurance didn't cover it so I couldn't go.
Quote from: Vandemolen3 on 09/11/2010 21:17:36Did anyone had a Testosterone treatment that failed? Up to now Demo and Green seem have succes with T-treatment. yeah there was someone who used testosterone injection for non pois reason that said testosterone didnt help their pois.
I don't know if anyone else has also done this or if other people get the same muscle tension headache from pois that I do the feeling like a towel is tightly wraped around the back of your skull but I have found that blowing cool air through your hair such as a fan or a vent or even driving with your window rolled down can greatly reduce the muscle tension in the occypital muscles I believe they are called at the base of the skull. I have also found one thing that seems to drastically reduce pois symptoms almost completely but it would be a rather difficult thing to apply. I have noticed that after doing something really scary for instance I am afraid of heights so when I do things like jumping into the lake from high ledges and rock climbing my symptoms go away so is a blast of adrenaline a fix it for pois? Anything else I have come up wtih to help myself pretty much the same stuff everyone does hi protien food, rigorous excercise, doing things that require a lot of focus or attention like video games or reading.
Today I had an appointment with my urologist. I gave him the POIS-papers. He said there's nothing he can do. The only thing he can do is send me to the men's clinic. This doctor is specialized in sexual disseases of men. So I made an appointment with this doctor for about five weeks. The POIS-papers are in my file, so he can read them.Today I will start with Paxil.
My urologist said he did every research possible. And he said he turned me inside out. And that sometimes I can have the feeling that I have an UTI, but in the urine there's nothing to see. He said it might be something with the pelvic, but there's not much known about that. So his only option was to send me to the men's clinic. So I agreed.Horizon, we must go on with research. We don't know yet if the treatment of dr. Waldinger will be working for all of us. Let's hope so, but we don't have a guarantee. That's why I will go to the men's clinic. And when dr. Waldingers paper is published, and if his described treatment works for me I will stop going to that clinic and to my neurologist. But until then everybody should write to researchers, try things with a GP or other doctor. There's another doctor in the Netherlands who is specialized in inflammation (I posted an article about her earlier). I first try the men's clinic and Paxil. If that doesn't help and about a few weeks if the Waldinger-paper isn't published yet I will write to her. Now I walking on two paths, I will wait for the 3th path, maybe dr. Waldinger or that inflammation doctor.
Certainly not to undermine Dr.Waldinger's research, but, I feel we should also contact Dr. David Resnick...