I realize how lucky i am (having read many posts on this forum), that i have got through the system and am due surgery in 2 days! I know the nhs does not have a great record on this site, but from what i have experienced thus far (still awaiting the actual surgery!) they are definitely worth a try. From seeing my gp, i had to wait 1 month to see a plastic surgeon, then a further 2 months for this surgery, no psychologists and no hearing panel. My experience with the NHS up till this point has been great. I aim to go into more detail as to how I got to where I got to after the op, hopefully if its a success.
But it gets even better, I know the nhs has come in for criticism for providing just general surgeons not qualified plastic ones and that they often do lipo only. It was a fully qualified plastic surgeon i saw (Mr Malata) who does 50+ gynecomastia corrections a year and he said straight away that lipo only would not be good enough, that glandular excision is a must as well, the guy has even written a book on why lipo only is not enough! Anyway I am having the op at Addenbrookes Cambridge, i guess i was very lucky with the post code lottery.
Obviously like everyone else my anxiety levels are 10/10, excitement 10/10 and nervousness 10/10! to be quite honest if was told a punch in the face five times over would get me the same result i would take it, at least I know what to expect. I also dislike needles, i bricked a simple blood test 3 times in a row 2 years ago, but the IV etc is probably the least of my worries! Is anyone able to describe the pain (hard i know)? and the worst bits of the op?
Finally this will be that start but most important step in dealing with several socially embarrassing conditions i developed due to side effects of an anti convulsant several years ago. Like everyone else i had never heard of the condition until a few months ago (I am 22), before which i just thought i was a freak! But after going through the tests, the docs said the condition had been induced by something to the liver, i was unaware of any medications i might of been on that would have induced this. But i pull up the medical records, find out i was diagnosed as an epileptic which maybe explains why i get severely lightheaded 40 times a day and that i had been on the resulting medication 4 years. There is one further complication, another side effect of this, is that i have a very low white blood cell count , which is what is used to heal parts of the body i think! so i am worried about how well my recovery is going to go! Furthermore I also developed hyperhydrosis (extreme and constant sweating) as a result of this and will get electric treatment for it as soon as i am able to after the surgery! but i am worried i am going to sweat like hell in one of those compression garments. Of the two gynecomastia definitely hits me the hardest, but they do act like a double negative, i have to change shirts five times a day due to hyperhydrosis, yet gyno stops me from doing this just anywhere and because i get nervous about people seeing my gyno and having to always wear hoddies, even in the summer it obviously makes the hyperhydrosis even worse so i have to change more shirts. Actually i think there is quite a bit of common ground between serious hyperhydrosis sufferers and gyno sufferers, maybe they should talk it over! sorry for the rambling!
I will provide a full update when the surgery is done! and if anyone could answer my pain questions that would be great!