Nicky K D Chaleunphone is an IDIOT

Nicky K D Chaleunphone likes to make all manner of unfounded comments about me and what my sex is, then from time to time the little wanker manages to say something true, I am not intersex, like him I am male.

Nicky is male because he has male genitalia. I have seen pictures of his genitals, he kindly made them available, so I can say for certain he is a man. He’s not a very nice man, he’s not a very smart man, he’s not a very good looking man either, unless your eyes behold more than mine?

Nicky the Bigot

Now remember this blog is supposed to be about Kallmann syndrome, which Nicky K D Chaleunphone is supposed to have. Kallmann syndrome affects both males and females so one must ask how on earth can it be an intersex condition? Like CAH also affects both males and females, so how can that be intersex too?

Anyway, the intersex grouping of people, well it’s their business, if they want to include or exclude anybody, for any reason, it’s not really a concern of mine as I’m not intersex. The reason Nicky K D Chaleunphone hates all Transsexual people is because he is Asian. I was surprised to discover that Asian’s generally regard Transsexual people as not real men and not real women. Even though Nicky K D Chaleunphone wasn’t raised in Asia, only born in Asia, his parents were. They took with them to America their culture of hatred and raised him to hate. This is why Nicky never has a nice thing to say about anybody.

Transsexual Empire

I’ve recently obtained a copy of Transsexual Empire by Janice Raymond and you can get your updated copy from here too:

Trans Empire

Janice Raymond’s book is essentially about how men are invading into women’s space by artificially reconstructing themselves to be female looking. Janice Raymond also asserts the same of female to male transsexuals, females invading into men’s space, but with less emphasis.

The below video is used to be titled “From 45X/46XY True Hermaphrodite with CAH to Intersex Fraudster”

Rudy Alaniz has been on YouTube for years asserting ‘she’ is a True Hermaphrodite, has Congenital Adrenal Virilising Hyperplasia, and has 45X/46XY mosaicism, and that ‘she’ is in the process of transitioning male to female. I’ve already proven ‘her’ True Hermaphrodite and 45X/46XY claims to be absolute lies. However ‘her’ claims to be in transition and to have CAH I’ve not yet proven to be false, but I think the likelihood of them being true is so close to zero they might as well be zero.

Rudy Alaniz aka Mishakailana as ‘she’ is known as on YouTube has been in transition ever since I first started on YouTube in 2008, which has to be the longest transition I have ever heard of, for a male to female transsexual. It has been so long and so little change has occurred I’m more inclined to believe these days that ‘she’ is in fact a Female Impersonator.

It appears to me that ‘radical feminists’ and persons with Disorders of Sex Development have a great deal in common when it comes to healthy males invading into spaces set aside for them. Of course persons with Disorders of Sex Development can be either male or female and can be, or not, feminists. My criticism of is of persons who pretend to be Transsexual using a medical diagnosis to justify their claims, which are in fact medically impossible.

The latest false claimant of a Disorder of Sex Development to justify transitioning to female is Chloe Prince, who pretended to be diagnosed with Klinefelter’s syndrome, and still pretends to be diagnosed with Klinefelter’s syndrome. However, Transsexualism is a bona fide psychiatric illness characterised by no other disorder of a sexual, or gender identity, being present.

The diagnosis is not made if the individual has a concurrent physical intersex condition (e.g., androgen insensitivity syndrome or congenital adrenal hyperplasia) (Criteria C). In proposed changes to DSM 5 the statement is “B. The individual does not have an intersex or sexual development condition”

Therefore their claim of a medical diagnosis automatically cancels their Transsexual claim. If these people really do have the Disorders of Sex Development they claim, they would never get any Medical Insurance, or other medical surgical assistance, to transition, as they don’t qualify. If they have accessed Insurance to pay for their transition surgery, this is strong indication that they do not have a Disorder of Sex Development.

Originally I intended to debunk Janice Raymond’s book as I thought it heavily relied on information from disgraced psychologist Dr John Money, when determining at which point gender identity is established. As it happens she has as much support for his theories as many other people, not much at all.

Transsexual male to constructed female, are not female. They did not live the life of a female, with the prejudice Janice Raymond describes. They were in fact the privileged male, and then decided that they wanted what they perceive as the best of both worlds.

They tend to be males who have had their family, I’ve observed. They’re heterosexual, when the’re male attracted to females. They are reconstructed males to look like females, that makes perfect sense to me.

The motivation for their reconstruction is what Janice Raymond seeks to explain. I can’t, I can’t understand why any normal fertile man wants to emasculate himself, when he can just as easily dress up as a female, and pretend like Mishakailana, Nicky K D Chaleunphone, and Gavan Coleman.

None of these people have lived a life as a female would, and cannot possibly claim to be female as a result, yet they all do. They are all anatomical males with a Y chromosome and at least 1 X. They are also very good friends, suggesting a certain ‘copy cat’ mentality.

I can’t understand females who say they feel male, yet don’t understand why biological males they grew up with reject their transition. All the males ever knew the person as was female, how can they be expected to accept the person as male, simply because s/he says so? And why, if she feels so male, does she not understand her biological male counterparts?

Wanting to be male or female is not the same as living male or female. I tend to agree with Janice Raymond.

The Post That Didn’t Make It

Since some here want to accuse me of all manner of impropriety with children, specifically boys, I will now show everyone why that is so. This won’t be above your pay scale, this is really simple.
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This is one such message I received, and I think the ‘person’ who gave the me the ‘you’re banned’ message must have let it though so Amy here could leave his/her not quite intelligent comment, the caliber of which you can get used to if you regularly take part in “Debate This”

amy da bitch

So now you know why XXY boys rarely get diagnosed before adulthood, this is the type of fear non erotic sex information receives from ignorant people.
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Boys usually have testicles in their scrotum at birth. Testicles grow throughout childhood and at puberty they massively increase in size, as the diagram below shows.

Testicles grow in puberty as they produce more and more testosterone, which is caused by increasing levels of a hormone called Leutenising Hormone, which is made in the Pituitary gland in the brain.

Some boys’ testes don’t grow and puberty does not begin and they can have a disease called Kallmann syndrome. If your boy gets to 14 and has not started puberty, take him to a doctor and insist on LH and FSH hormone level checks. Girls can have Kallmann syndrome too. The most obvious sign for all people with the most common form of Kallmann syndrome is anosmia, no sense of smell.

Like most other boys XXY boys start puberty sometime about age 11. Their testes do grow in response to LH from their brain, however soon after puberty’s onset their testicles atrophy, they shrink, severely, back to childhood size or less. This is caused by a disease called seminiferous tubule dysgenesis.

Whether you think your sons and daughters are progressing through puberty properly or not, I think it is important to have all teenage boys and girls examined by a doctor to make certain everything is progressing as it should.

A teenage boy with atrophied testes will not notice, nor will anyone else, as this is about sex, and sex is frowned upon by society at large. In fact I read just recently how a 16 year old teenage boy died of testicular cancer because he was taught to be ashamed of his body, in my opinion.

Is there any mature person here who wishes to have an adult discussion about any of the topics I have raised?

orchidometer

Not Uncommon

I just wrote a post to somewhere, to a group of people, but I think it’s worth posting here too:

cropped-ktype.jpg

I think what most people fail to consider in their determinations on how things happen and why is the most basic start point. We all need to remember we are dealing with a life long disease.

How did you feel when you first found out?

Can you remember?

I can remember being different, always, in everything. The diagnosis for me was just another nail in the coffin.

Do you recall going to doctors saying ‘there’s something wrong, there’s something wrong, there’s something wrong, and hearing back ‘it’s nothing you’re ok, it’s nothing you’re ok, it’s nothing you’re ok?’

Maybe you can recall instances of when you should have been diagnosed and weren’t? Maybe that happened many times?

Do you remember the frustration of being told nothing sensible?

Do you remember being treated like an imbecile? This information is far too devastating, serious, complicated, for a mere patient to understand! You must be kept in the dark, you might even imagine the disease is much more serious than it is, if you’re told anything.

What does all this cause, all this stuff that goes on around your diagnosis?

What about when you remember those times, what emotions do you feel?

Have you known a close relative who has died, or a close friend? How did you feel when you discovered your loss? What is that called?

That’s called ‘GRIEF’ isn’t it, I’m sure it is. The grief of the loss is very powerful, your mood might even change, you might very sad, cry, maybe even be inconsolable for a time. And as time passes that grief fades and life continues.

But when you’re diagnosed with a life long disease, your grief remains. You remember all those difficult times associated with your diagnosis, and you feel it again, and again, and again. Regardless of how much you know, and I know, the grief remains.

If only it can be forgotten about, just do whatever you need to do and never consider it. That would be easy if it were possible to never need therapy. But by the end of the regime you’re on, you remember it all over again. And your mood might change, it might be so regular that you don’t even know why anymore, this is life the way you know it. My life is the only one I’ve had, other people must be the same as me, they must be re-experiencing that initial diagnosis and the emotions surrounding it, over and over again.

I can be going about my work and thought just pops into my mind of a long lost relative, and I feel the grief of that loss, just for a moment, then it passes. But this disease is a constant, and I remember the emotions associated with it regularly, and I feel the grief again. My mood might change, just for a moment, maybe a bit longer, and life goes on.

When I don’t have my therapy properly I experience another grief. It’s called tiredness. Yeah I get very tired when I don’t maintain my dose. When I was taking Panteston Capsules I mapped my dosage very carefully for a month, taking careful notes of when I took my medication. Over a month I’d miss a third of all doses. I was tired a lot, and I was very moody, and irritable, and tired. And all the guys I hung around with at work, they had much more energy than me, and I couldn’t keep up. They’d encourage me to go to gym, and weight lift, but it’s just too hard to explain, constantly why I’m not that get up and go-ish.

All these things add to grief, that elusive emotion that sweeps in like a mist as if there was no cause, but there is, and I need to recognise it. I think you do too.

Graeme,
XXY4LIFE

Is No Body Shameful?

Of course there are ‘shameful’ bodies!

Anybody who insists their chromosomes dictate their sex is deluded. Do you know people with XY sex chromosomes can have female everything external, and do you know that people with XX sex chromosomes can have male everything external?

Actually the XX male persons are said to have Klinefelter’s syndrome as they have seminiferous tubule dysgenesis, and to have that disease they must have testes of course! So they’re obviously male, always were.

So where am I going…..? I get really pissed off with some of these intersex types, like most of them are so fucking lucky, they got diagnosed at birth! Then they bitch and moan about the medical care they received as if it were a bad thing!

Do you know there’s a theory out there in ‘research land’ (that’s a mythical world where people in white coats a hang out and read reams of paper literature) that says that XXY males suffer greatly from insufficient testosterone during puberty, that they’d be better off if they had no puberty at all, like males with Kallmann syndrome, effectively!

True, males with Kallmann syndrome don’t suffer they types of difficulty XXY males suffer, and it is theorised this is because males with Kallmann syndrome their testes fail to produce testosterone, thus saving their brain from psychiatric illness. XXY males on the other hand experience puberty normally, then their testosterone level markedly drops off, sometime after the onset of puberty. Nobody knows exactly when and nobody seems interested in finding out exactly when! They’re males after all, who gives a shit about males sexual & mental health?

Of course there are always exceptions to the rule.

Remember also, psychiatric illness has NOTHING to do with learning ability.

But these intersex types, their only problems are man made! Yeah they discover they’d been lied to all their lives, (that’s something for transsexual people to remember, when you lie about a matter your entire life the people you lie to get hurt!) And intersex types, they feel betrayed, depressed, anxious, angry, that can lead to psychological problems. But they’re so lucky that they had doctors who gave a shit about them, who made sure they had a NORMAL puberty, the very thing all XXY guys don’t have!

Transsexual people usually have a NORMAL puberty too! Be it the wrong sex but hey, normal all the same.

Now you’ve got to read the fine print in “The Interface Project” on YouTube, these intersex types have an introduction video, and what the people say is compelling, but the text in the video is off putting.

I know for a fact they all believe XXY guys are intersex, not that it’s any of their business of course! They wholeheartedly believe all XXY guys have Klinefelter’s syndrome, these intersex types are really good at spouting medical dogma, when it doesn’t apply to them! They want to force XXY boys to develop psychiatric disorders, because they’re receiving information from crackpots who lie about even how they a were diagnosed, about their medical care, the structure of their internal organs, anything to fit into the intersex group they will lie about.

So why do some of the XXY guys want to fit into a group they don’t belong in? Could it be that they’re all homosexual and the support groups of the 1990’s didn’t cater for them, and they had nowhere else to go? Of course, I think it’s pretty well proven sex chromosome numbers do not dictate sexuality, but these homosexual XXY guys really want it to be true for them! If XXY causes homosexuality then all XXY males MUST be homosexual, and we know for a fact that’s not true!

Should an XY female have her internal, non sperm making, testes removed, and if they are removed is that sterilisation? I do know of AIS, 46XY females who were not diagnosed until adulthood, and none have ever elected to keep their non sperm producing, testosterone producing gonads. They’re not being sterilised, they’re being assisted. So I don’t think AIS females diagnosed at birth, or in childhood are being sterilised either, they’re being assisted. They’re given what most XXY guys don’t have a NORMAL life! Now if Eden Atwood wants to have the effects of her testes back, all she need do is have testosterone supplementation, if she wants?

So getting back to XXY boys, should they be forced to have testosterone therapy? I don’t think they are forced to. It’s only the crackpot XXY guys who pretend they’re intersex who claim they are! Oh no I do know of 1 XXY man who was forced to have testosterone therapy when he was a teen by his parents, and as soon as he hit 18 he stopped the therapy, at grave risk to his health! That is exactly what doctors want to avoid, which is exactly why they INSIST it’s the XXY boy HIMSELF who decides if he wants hormone therapy. Of course stupid parents will do stupid things regardless of the best advice!

Of XXY boys in puberty this is what I have NEVER found, they don’t want erections, they don’t want sex, they don’t want to masturbate, they don’t want to ejaculate. When they realise they need testosterone to do all those things, they agree to hormone therapy. It’s only these pretend intersex crackpot XXY adults who want to claim their hormone therapy was a disaster. One famous XXY idiot maintains he was better off being sexually incapable, and wished he’d never started testosterone therapy, but only did so because he was not informed of all the consequences of that therapy. So who as an adult needs to be informed as to the effects of testosterone when as an adult he sought out therapy? Oh he also claims he might die if he stops the therapy he was ‘forced’ to take, which is utter nonsense!

Who the hell’s he trying to kid here? This sort of crap might be really well received by the intersex types, the true intersexers I mean, but it just doesn’t wash with normal bodied people. Normally testosterone is produced by the testes in males at about 50-70mgs per day, when the men are resting. Many men seem to think they wake after resting with an erection as they need to piss, but it’s pure co-incidence. Just ask yourself men, during the day, and you’re awake when you need to pee do you have an erection? Well I’m a man and I don’t, but I do have morning erections, because the testosterone I have is not being used for all the other things it’s needed for and goes straight to my penis, just the same as any other man, when he’s resting.

So what happens if they don’t produce that 50-70mgs per day? Do you really think they still wake up erect? Do they have sexually explicit dreams? Do they think about sex at all? So if an XXY man doesn’t want these terribly manly things what does he have to do? Cut his balls off! Not on your life he doesn’t, all he has to do is stop having the testosterone therapy. Making that personal choice might be quite difficult for some XXY men, when it all goes wrong who can they blame but themselves?

Now if these intersex types want to influence the medical profession to not treat them with hormones, of course they can feel free, they’re adults after all and it’s their health that’s at stake, nobody can be hurt but them. But for them to advocate that NOBODY with a DSD should be treated with hormones because of their not necessarily true accounts, is just plain nonsense. How can they possibly expect to have any influence in the health care of persons not related to them, not even in their circle of friends, based on their dubious accounts?

XXY boys deserve to be diagnosed early, before the onset of puberty, and ought to have the right to go through puberty just like any other males on the planet, and not be forced to develop possible psychiatric illness just because these intersex types have not got a clue what they’re talking about. If they want my continued support they’re going to have to tone down the text in their video. They’re going to have to accept that XXY boys forced to develop Klinefelter’s syndrome will not have a good opinion of their own most ugly body, as it’s counter intuitive for healthy males to look like that! Even their crackpot XXY colleagues don’t have that fat ugly body, BECAUSE they have testosterone therapy!

In my opinion.

XXY Boys should not be referred to as having Klinefelter’s syndrome

For parents out there, your children are children, this fact seems to be lost on many parents, thinking of a related matter I read a couple of days ago. I read of a mother who described her sons penis as a ‘doodle.’ I think children can get their minds and tongue around ‘penis’ more easily than ‘doodle.’ Maybe the mother does’t refer to her sons penis as a ‘doodle’ to him, maybe she was just nervous about mentioning the correct word where she was? People confident to talk about sex have no problem referring to sex organs of both sexes by their correct name, wherever they are.

Children are learning, and I know you all know that, and their first teachers are their parents, I know you all know that too. So if your son is prenatally diagnosed XXY and you decide to keep him, not kill him, I think it would be an excellent idea to learn up on genetics. Not just go along with whatever the prevailing attitude is. Actually think about it, with an analytical, mature, mind.

Go to my previous post if you want links, you can find out all you need to know there when it comes to what Klinefelter’s syndrome is, and how it got it’s name.

Bearing in mind that Klinefelter’s syndrome is the SYMPTOMS of a DISEASE, not a DISEASE in itself. So when are you parents likely to notice your XXY son is developing the beginnings of Klinefelter’s syndrome?

According to common knowledge Klinefelter’s syndrome is seen in very young boys, even babies, and there is nothing the parent can do about it. There’s a nice defeatist attitude, saves having to think about what you’re doing and and why. You’re just observers of your sons predictable life, as you’ve read about other XXY boys who appear the same. That they have 44 unique autosomes and 3 unique sex chromosomes means absolutely nothing to you. Like when you walk down the street and see other men and women you think to yourselves how all just like YOU they are!

The additional X is mostly inactivated. It’s mostly inactivated in everybody with more than 1 X chromosome, that’s all you XX mothers out there too. You can’t resign from the study of genetics just because you’re a mother. So if we look at XXX females, what SYMPTOMS of DISEASE are they named after? It must have slipped my mind, I am XXY after all and I do have a poor short term memory. Maybe I can blame that extra X? Or Klinefelter’s syndrome – the symptoms of a disease? Or my parents for me having a poor short term memory?

Getting back to XXX females, it turns out they do have noticeable educational difficulty, fancy that! They seem to have growth issues too, being slightly taller than average females, in childhood. At puberty they’re fertile, they don’t have interference in their cells preventing the development of complete puberty, and interference of their ovaries to release eggs. They don’t develop soon after the onset of puberty hypergonadtropic hypogonadism or hypogonadtropic hypogonadism. They don’t have any kind of hypogonadism. I think it’s proven, the additional X can have an effect on education and growth regardless of the sex of the person with the additional X.

So those growth issues you parents see in your XXY sons before puberty have nothing to do with Klinefelter’s syndrome, and everything to do with the fact that there is an additional X, but not in every XXY boy. In fact if you decided you could find all XXY boys by karyotyping all tall boys, you’d miss most XXY boys. Most boys who are taller than average have normal sex chromosomes. But by karyotyping ALL boys you’d find ALL XXY and XYY boys, and ALL XX boys, and ALL XXXY boys, and ALL XXXXY boys, and every other variation there is.

So why is it then that some XXY boys are more affected than others? That might have something to do with their parents? For some reason every time I chat with parents of XXY boys they all seem to assume they’re the ‘bees knees’ of parents. How can that be when they have usually never trained to be parents before they were parents? Like most parents who discover they have a child who’s different, they have to learn how to care for that child. I don’t read how the parents of these XXY boys took themselves off to parenting classes after the diagnosis. They always seem to want to be involved in genetic counselling for themselves, and be involved with support groups to compare notes with other parents, and console themselves that they’ve done nothing wrong, and never could.

Curiously Dr Johannes Nielsen (deceased) in Denmark found that of all the XXY boys who did poorly in school, who had behaviour and educational difficulty, and ‘brushes with the law’, all came from poor parenting homes. Other XXY boys who experienced educational difficulty, and emotional disturbance, were assisted by sensible parents, and their children did not end up ‘before the courts’ as they say. Parents do have a lot to do with the way in which their XXY boys learn and communicate, and their progression to adulthood.

Did I mention the 44 unique autosomes and 3 unique sex chromosomes? Oh yes I did. They all came from their parents, the genetic providers. Are the genetic providers related to all the other genetic providers of all the other XXY boys on the planet? Are all XXY males the offspring of the same family of incestuous genetic providers? I would find that somewhat hard to believe, (makes great science fiction though.) So we all have different autosomes and sex chromosomes that come from different parents, so the possibility of other genetic conditions existing in an XXY boy, that are undiscovered, is just as good as anybody else having an undiscovered genetic anomaly, or maybe even better, since they all do have an additional X chromosome. Genetics is the only area where parents can be freed from responsibility, since XXY is a random event, that cannot be predicted.

The way in which genes work is that they are said to ‘express’ like the expression of a opinion. That expression has an effect somewhere else. So since all our genes are not exactly the same as any other person on the planet, it is conceivable that genes expressing to cause good memory, do not have the intended expression and the signal is interrupted by failing genes, or non existent genes. Just because we have the same shape and number of autosomes and chromosomes does not mean the same genes on that additional X are expressing in all of us, to the same degree. It could be that the most severely affected XXY boys have more genes that escape inactivation on the additional X than most XXY boys?

One way to further settle the matter is to look at a population of persons who have no sex hormone in childhood, do they have poor short term memory? Actually no, not as a group. Maybe there are individuals with Kallmann syndrome with poor short term memory, but it is not a feature of their syndrome, that they are born with, they are hypogonadal in the womb and at birth.

It seems the only time these people have difficulty is when they fail to enter puberty properly. The initial changes of puberty do start, they just fail to continue as they have hypogonadtropic hypogonadism, where the gonadtropins are not produced to tell their gonads to start working.

So if hypogonadism is the cause of all the difficulty in XXY boys before puberty’s onset, why is hypogonadism not the cause of difficulty in childhood for Kallmann syndrome people?

Well I’m convinced:

“Nobody was ever born with Klinefelter’s syndrome. XXY pre pubertal boys cannot have Klinefelter’s syndrome. Klinefelter’s syndrome is the post onset of puberty symptoms of disease XXY men and, XXY teenage boys can develop.”

XXY boys should not be referred to as having Klinefelter’s syndrome.

Why we XXY’s with/without Klinefelter’s syndrome aren’t Intersex

  • Klinefelter’s syndrome is the symptoms of disease and according to Organisation Intersex International ‘Intersex is not about pathology or disease’ therefore Klinefelter’s syndrome can’t possibly be ‘intersex.’

    “INTERSEX is not a medical condition or a disorder or a disability or a pathology or a condition of any sort.”

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