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 Latest I can Find

For all those wallies out there, especially Australian and American wallies, who never look therefore never find, updated information, or statistical data about 47XXY/Klinefelter’s syndrome. So next time Hida Viloria wants to make an ass of herself, by repeating unverified crap from her uneducated colleagues, she can come here first and have a decent read of the latest I can find, that a lay person can easily read and understand, the exact reason why NZKA & NZSCS existed, Michael Noble:

Copyright © 2012 N´estor Pacenza et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Clinical Presentation of Klinefelter’s Syndrome: Differences According to Age

The aim of the study was to establish the characteristics of presentation of 94 patients with Kinelfelter’s syndrome (KS) referred to the endocrinologist at different ages. The diagnosis of KS was more frequent in the age group between 11 and 20 years (46.8%).

Most of the patients (83.7%) showed the classic 47,XXY karyotype and 7.1% showed a 47,XXY/46,XY mosaicism. Half of the patients younger than 18 years presented mild neurodevelopmental disorders. The most frequent clinical findings were cryptorchidism in prepubertal patients, and small testes, cryptorchidism, and gynecomastia in pubertal patients.

FSH, LH, AMH, and inhibin B levels were normal in prepubertal patients and became abnormal from midpuberty. Most adults were referred for small testes, infertility, and gynecomastia; 43.6% had sexual dysfunction. Testosterone levels were low in 45%.

Mean stature was above the 50th percentile, and 62.5% had BMI ≥ 25.0 kg/m2. In conclusion, the diagnosis of Klinefelter syndrome seems to be made earlier nowadays probably because pediatricians are more aware that boys and adolescents with neuro-developmental disorders and cryptorchidism are at increased risk.

The increasing use of prenatal diagnosis has also decreased the mean age at diagnosis and allowed to get insight into the evolution of previously undiagnosed cases, which probably represent the mildest forms. In adults average height and weight are slightly higher than those in the normal population. Bone mineral density is mildly affected, more at the spine than at the femoral neck level, in less than half of cases.

Just from a brief reading, skimming through it, I see that the patients with small penis overall was about 16%, contrasting favourably with the Ratcliffe report at 23%. The more patients found and studied the the lower the percentage of those with small penis are discovered. I expect even larger studies to report a similar trend.

It’s best guys that you don’t measure your penis size on the basis of published information. I notice one particular XXY idiot made a video about a site that said effectively we all had a small penis, Milton Diamond’s rubbish. Then reported a couple of years later that same information, as if it applied to him, and was relevant to all of us.

If you don’t understand anything, print this document out from the link provided in the copyright notice, take it your doctors and say these words “What does this mean?” I’ve used this process many times myself and it works a treat!

I can find plenty of information here to complain about, but don’t do that, sift out the good stuff. The first good stuff is, this report exists. Then there’s, you can copy it for free. Then you can repeat confidently – “Ongoing research continues into XXY / Klinefelter’s syndrome to improve our understanding.”

And all those above mentioned wallies can shut the f**k up!

Good day.

Nothing Sophisticated

I’m sure I make better videos than text messages. There’s nothing sophisticated about either of them, I write/speak them all myself, quoting occasionally from an outside source, well maybe more than occasionally?

Who the hell is Michael Noble?

Can you understand that brief sentence, it says I haven’t a clue who Michael Noble is, so if I knew of him from years gone by, I have no recollection of him now. This isn’t very sophisticated, is it! Michael Noble took it upon himself to write a argument against the idea that XXY’s are male, and only male. Of course we both mean XXY boys born with unambiguously male genitalia. Michael wants to assert that he is somehow not really male and cites experiences of his youth as justification for his argument. He quotes extensively from the former NZKA/NZSCS, myself, and Mark Hope. Sexuality, by the way, is not a feature of XXY any more than it is a feature of XY or XX. All people whatever their sex chromosomes can have all manner of expression of sexuality.

Michael Nobles says, only he knows truly for what reason:

“………When writing the paper, I had defended the claim that they (Klinefelter’s syndrome and XXY) were one in the same thing, because of the ‘smoke-screen’ tactics of some online commentators who were exploiting the difference to support their claim that if the physical affects of KS can be masked, then this renders the additional X chromosome as meaningless.”

In Australia (OII Australia)

And

“…………When writing the paper, I had defended the claim that they (Klinefelter’s syndrome and XXY) were one in the same thing, because of the ‘smoke-screen’ tactics of Tucker and such like who were exploiting the difference to support their claim that if the physical affects of KS can be masked, then this renders the additional X chromosome as meaningless.”

Internationally (OII International)

Apparently I have claimed that “if the physical affects of KS can be masked, then this renders the additional X chromosome as meaningless.” and I can tell you I never have made any such a claim. This is pure fantasy. Michael Noble does have a degree in Creative Writing, I wonder if he can discover through his academic contacts, if that can equate to Creative Libel?

This isn’t very sophisticated, or complicated. If I have ever said such a thing, or anybody else for that matter, let him bring his quote forward. Remember to and go and see for yourselves all that he has said, and all that he has quoted, and see from where he got his understanding. I can tell you he invented this information. Michael Noble is a liar.

It is my earnest endeavor to take with me everywhere I go descriptions of the difficulties XXY boys can experience in their lives, and try to get them diagnosed before the onset of puberty, before Klinefelter’s syndrome can develop. That must mean I place great emphasis on the additional X and it is not ‘meaningless’ at all.

I wonder if it is Michael Noble’s position that he does indeed wish to force XXY boys to not be treated, to guarantee Klinefelter’s syndrome does develop? It certainly doesn’t change our sex, that which is determined at birth by way of our physical anatomy. I see the equally ignorant as Michael, Gina Wilson, has written a paper from her unique ilinformed position on XXY too. Is this a case of the willfully blind leading the deliberately ignorant?

Is it Opinion or Official Position OII? from Graeme-xxy on Vimeo.

I think people who are XXY are better suited to answer the question as to what sex they are than Gina Wilson is. We can find plenty of XY males who see themselves as females, live their lives as female, even transition to female, but they are biologically male.

We can’t find so many XXY males who identify as female, or intersex, simply because they don’t identify as anything but male, and I certainly identify as male. Like all other males on the planet I don’t go round saying, day in day out, ‘I identify as male’ as it is self evident that I am male.

The more we find out about human genetics the less some people seem to want to know. I have read reports recently of an XXY phenotypic female who is SRY negative, that is her SRY gene on her Y chromosome does not function. Another report of an XY phenotypic female who is SRY positive, that’s right, her SRY gene is functioning but has no effect.

That I can find 1 report of an XY phenotypic female with an SRY positive gene, does that mean that we can now say all XY males cannot be considered really male anymore? Of course not!

If everybody, including Gina Wilson, walked around naked, there is no way we’d be able to tell if the vast majority were intersex just by looking. Certainly all the XXY males associated with Gina Wilson who identify as intersex, or female, have nothing about their physical characteristics to make such a claim. They are phenotypically male, whether they like it or not. I know this by their own public statements, and the fact that they were not diagnosed at birth! They were declared male like all other males with male genitalia, their chromosomes being unknown.

Sometimes XXY’s are born with malformations of their genitalia, that’s how we know they’re XXY, they have genetic testing done to see what sex they were supposed to be, but had an interference in their development prenatally. The same things happen in XY and XX people too, and hopefully the right decision is made. Considering the known emotional disturbance and personality disorders that are associated with being XXY, I would say leaving such boys in an incomplete state would be seriously hazardous to their mental health and well being.

It seems to me the medical profession is doing nothing to assist this created confusion. Most medical reports link XXY to Klinefelter’s syndrome as if they really were synonymous. They are not. Not all XXY males go on to develop the syndrome Dr Klinefelter described. Even XXY males with normally sized and functioning testes are erroneously described as having Klinefelter’s syndrome, which is the symptoms of the disease Seminiferous Tubule Dysgenesis, brought about by atrophied testes. If your testes are normally sized and functioning ,and you’re XXY, you can’t have Klinefelter’s syndrome. There are many different karyotypes that can lead to the development of Klinefelter’s syndrome, including 46XY and 46XX!

Chromosomes are carriers of genetic information. They have no sex of themselves. It is the combination of the genes that are expressed that bring about our sex, how we are seen and how we see ourselves, in association with our environment, our health, our nourishment and our education.

I suggest people ought to get themselves a better education.

Conversations on Facebook

Michel’le O’Brien
Originally, OII was created because of perceived problems in ISNA, such as it being focused on North America, yet primarily Anglophone, with limited acknowledgement of Hispanic speakers, and no attempt to include Francophones, of whom there are large numbers in Canada as well as Eastern USA. The main opposition was to ISNA’s support of DSD, something I am sure you would support ISNA for (apart from being in a country outside their coverage). It was only when OII became militant in its opposition to the disorder in DSD, six years ago, and ISNA shut up shop, five years ago, that people who had been members of ISNA began to join OII – as it was the only international non-condition-specific organisation in the world. Far from dinosaurs, trail-blazers at that time! As for your suggestion that therapies be denied, that is crap – we support treatment with informed consent, and that the individual has the right to choose what form that treatment should take.

Thanks for your contribution Michelle, and my reply is:

The most fascinating thing of ISNA is the name of it’s newsletter, prior to 2002, “Hermaphrodites with Attitude.” Then Chase and Dreger got involved, two academics who may or may not have DSD’s, or Dreger doesn’t for sure, anyway they steered the ISNA away from Hermaphrodite states to Intersex states, then abandoned ‘intersex’ altogether and initiated it seems against the will of the membership “Disorders of Sex Development” aka DSD’s.

Also in 2002 Dreger wrote an article about why all manner of non ‘intersex’ conditions ought to be included as ‘intersex’ using a theory not of how different diseases come about, but how those with them are treated, inferring everybody with what we now call DSD’s are dissatisfied with our medical care, and from my experience, research, case reports I’ve read, and personal accounts by XXY’s or men with Klinefelter’s syndrome, we’re not.

The problem for us has ALWAYS been getting diagnosed early enough and getting adequate hormone therapy. These are the areas we’re discriminated against as even people with severe mental retardation are not castrated, but we are effectively by the refusal to treat! Quite the opposite to what the ISNA XXY and alike members were reporting.

And an extension was added:

I see I need to qualify that last statement. Men or adult XXY’s always got sufficient hormone therapy, well sufficient to XY average at least. But teenage boys who were found to be XXY and variants were often refused hormone therapy as they had not developed the syndrome, whereas the men were full blown and suffering.

Of course for the XXYY’s being 16 and impotent was no laughing matter, and XXXY’s the same. Their learning and behaviour difficulties were, and still are, being used to deny them hormone therapy. And the adults from ISNA were promoting ideas that they had never experienced as they were not diagnosed as teenagers. They appear to be under some weird impression that their experiences are uniform, which is so far from truth you’d need to be completely naive to believe them.

In reality Michelle, I did not complete male puberty until I was 38 years old for fucks sake! This almost seems typical for XXY males! I didn’t complain when I wasn’t developing as my unaffected peers, and I was delayed anyway, and so long as I could have an erection there didn’t seem any need to make any other changes. I had surgeries willingly to improve my standing in male society, which I do not, of course, regret.

And do not let yourself be led astray, what I had done was and is quite normal for young men with Klinefelter’s syndrome. What your people refer to as ‘normalising’ surgery in the negative, we regard as ‘normalising’ surgery in the positive. We are not the same, and your people who who choose not to be treated for their Klinefelter’s syndrome are making themselves sick. And of course as adults they can choose that course of action. But the changes caused by testosterone therapy are by no means permanent for XXY males, as soon as they stop therapy they regress to a prepubertal state. Information given you by your XXY male members is wrong.

And take out the word ‘intersex’ and we’re blood brothers and sisters Michelle. Yes we all have atypical sex development, I agree. Happy now? 🙂 It’s the real issues that affect each group that is important. We don’t share the same issues, not like the XXY or Klinefelter men who regard themselves as intersex declare. They’re making up stories to fit in, claiming all manner of similarities that aren’t there. By treating us our doctors are doing us a major favour, it’s getting the treatment at the right level that’s the hard part.

But your XXY guys, all diagnosed as adults, are presenting fairy tale events. Claiming they liked their tits, and they were just complying to society, when in fact getting mastectomy if the disease is not severe enough from a doctors viewpoint is almost impossible. Or they like the rounded body shape associated with hypogonadism, but take testosterone that guarantees they won’t have that body shape! Doing a Nicky K D Chaleunphone, arguing in effect both sides of the argument at the same time!

Adults are not forced to take testosterone therapy and my doctors were not prepared to forcibly treat me way back in the late 1970’s either, I had to choose hormone therapy. All the guys who protest about testosterone therapy and take it, saying they were told they couldn’t be “real men” without it, are telling porkies, to fit in!

Michael Noble – Australian Misguided Academic

Michael Noble on OII Australia says:

Even though it’s evident that I possess a blend of male and female chromosomes, the medical and legal professions had proclaimed that it doesn’t matter how many X chromosomes a person may have, if they possess even one Y chromosome, they are legally classified as a male. In recent years, however, this pedantic definition has been challenged, thus enabling XXY to be legitimately recognized, in some sections of the academic world, as an intersex condition.”

Ummm Michael,  Michael Noble, the ‘owner’ of a degree in Communications and Creative Writing, you’re that Michael Noble? Unless you’re completely thick you MUST realise that every XY man on the planet has a “blend of male and female chromosomes” or did sex education pass you by along with puberty?

And of course being that you’re so well educated, (except in sex),  you MUST realise that it was not the Y that gave you your male sex determination, but your physical appearance at birth! Even you admit you were not diagnosed until age 23, therefore for 23 years you were just a run of the mill, ordinary old Australian liar, like plenty of your ignorant countrymen.

We do not put an R in CAN’T we don’t even pronounce an R, you ignorant bastards* just can’t listen!  

Anyway, no matter how many X’s are present only 1 is fully active, and the only parts of the additional X’s that are active are in the PAR, the pseudo-autosomal region of the X.  Oh and every female is the same, they have two X’s and 1 is inactivated, except for the genes in the PAR.  Therefore the more PAR genes  interacting I predict the greater the degree of difficulty experienced by the affected persons.

So the definition of male chromosomally is not “pedantic” but simply “accurate.”  It’s probably your refusal to take the level of hormone associated with your sex, and the hot hot sun you experience in your barren wasteland of a country, that causes you to imagine every X is equally active, even in females!

What is postulated, that may also cause problems for XXY’s is skewed inactivation. It’s just another thing that separates XXY males from our XX female counterparts.  They have random X inactivation, but XXY males such as your totally male self Michael, probably have non random (or skewed) X inactivation.

The more we learn Michael the less impressive your argument becomes, not that it was ever “impressive” I was just being generous!  You’ll get used New Zealanders, we’re like that, generous!

Combined with the PAR genes, and skewed inactivation in XXY males, the reasons for the development of Klinefelter’s syndrome, also known as, “The symptoms of the disease seminiferous tubule dysgenesis”  has probably now been isolated?  It is not that the additional X is female in character Michael, nor that you got yours from your mother – as you claim, (although you’ve never provided evidence of your claim), but rather much more complicated reasons, reasons that are not subject to Folklore genetics!

Michael goes on to say:

“The existence of intersex people has been concealed for many decades, because they threaten the man-made laws of nature, which dictate there are two sexes: male and female. Yet, nature does not manifest in comfortable, finite boxes. Rather it exists as infinite spectra of variation. But to our modern scientific mind this variation threatens to unleash chaos. And what drives science? The desire to control nature.”

Now then Michael, that is complete drivel. The desire of science is not to control nature, but to understand the reasons why things are the way they are, and in the terms of medical science, to alleviate suffering.  If you feel controlled by the medical profession, that may well be your particular psychiatric disease showing through?  Paranoid states & hysterical syndromes are noted features in many men said to have Klinefelter’s syndrome, or as I would say, XXY men.

That pesky little additional X plays a major role in all our lives, and no matter how much you want to pretend I regard it as meaningless, in fact I regard it as the major factor that causes the under educated like yourself, to believe they are mistreated by the medical profession. However Michael, I’m well adjusted, having sought and received proper health care from the very beginning. I took my doctors advice and I do not believe the medical profession has the desires you claim, without any justification.

And again Michael continues with his paranoid ramblings:

“Eventually, the medical profession could no longer pretend that biological sex was confined to the polar binaries of male and female, but rather some infants presented characteristics of both sexes. Yet, instead of simply accepting that anatomical sex could exist as a spectrum of possibilities, the intersex variations were medicalized: thus requiring surgery and/or hormone reassignment therapies in order to ‘cure’ such ‘aberrations’ and ‘disorders’. In other words, the medical profession believed they could play god and determine which sex and gender a child would be reassigned to, and raised as. And they did this, not for the benefit of the ‘afflicted’ individual, but rather to make the medical community, parents, and society in general, feel better.”

I’m certain, completely and totally certain, the medical profession did not set about to make the lives of infants unbearable, nor was there any conspiracy to ruin your life Michael.  Have you actually read this crap you wrote Michael?  Where there are errors in anatomical sex that YOU would see Michael, if you were ever the parent of a child with ambiguity of genitalia, which I expect would be the only way YOU could see, you may well have a different opinion?

You’re not a parent, you’ll never be a parent, you have no concept of parenting and the desire of parents to have their children treated fairly in society.  I can see that some medical procedures as being unnecessary, such as circumcision, but to lump all procedures into that classification by a person such as yourself is somewhat presumptuous.  I believe the medical profession was acting with the best interests of the child in mind,  and for the most part did an excellent job.   Yes they did screw up from time to time, and most of those children had no anatomical differences in sex, until they were butchered, they WERE anatomically NORMAL.

I must remind you that you started your little rampage with the notion that gender plays no role in the determination of one’s supposed intersex status, but here you want to include gender as part of your highly emotively written diatribe.  I wonder how you would feel if you did see the untreated results in an infant that had no interventions, that was born with ambiguity of genitalia?  The indication from opinions delivered by men such as yourself, who were not diagnosed early enough with Klinefelter’s syndrome, suggests the outcomes of no intervention would be disastrous.  It’s a very difficult situation for all involved, and a wee bit of compassion for the parents and individuals concerned would be appreciated.  Blaming and shaming Michael does your argument no good at all.  People are born with disorders Michael,  look around you.

 

*”Bastards” is a term of endearment in Australian common usage lingo.

Pet Hate

Yes I do have a “Pet Hate”  I bet most people have this one too, being deliberately misrepresented by people who ought to know better!  OII Australia Limited, ever heard of OII, (Organisation Intersex International Australia)? In 2008 I seriously investigated the possibility that Klinefelter’s syndrome and XXY were intersex, yes I spent a whole year investigating.  I found the medical description, Klinefelter’s syndrome  is listed under the chapter on “Disorders of Sex Differentiation,” all sorts of other conditions OII would refer to as intersex are described there too, oh and Kallmann syndrome isn’t one of them, it’s described in the chapter on “Disorders of Puberty.”   That seems pretty conclusive I thought, yeah if OII describes a condition as intersex and it’s described in medical literature under chapters to do with sex differentiation, then it must be the same thing!  Of course it must be; right? Maybe not!   Then I went to XXYTALK where I found XXY men referring to themselves as “Men with an intersex condition and identifying as male.”   That seemed pretty clever, I could adopt that I thought, I think I even did describe myself like that for a time, but I had this niggling thought, “Where does the word ‘intersex’ come from?”

It turns out intersex as a word in modern usage derives from the birth of children with ambiguous genitalia.  Only a very few conditions described in the chapter on “Disorders of Sex Differentiation” could have ambiguity of genitalia, and Klinefelter’s syndrome and XXY are not two of them.  Ahaaa, a division of conditions exists!  Those with ambiguity, a small subset,  and those without ambiguity, the vast majority.  And the “vast majority” compared to the worlds entire population is not even a drop in the bucket!  So those with ambiguity of genitalia, those I’ll describe as “True Intersex,”  are a very rare breed indeed.  But XXY is a very common sex chromosome aneuploidy, occurring between 1:500 to 1:1000 live male births.  And “aneuploidy,” by the way, means “not the usual number.”  And Klinefelter’s syndrome is the most common collection of symptoms of disease XXY males can get.  From time to time XXY boys can be born with a small penis, or undescended testes (balls), but XY boys can also have the same  at birth.  Such minor malformations of genitalia are not described as ‘intersex conditions’ as there’s nothing  ambiguous about them.

Then in my travels of discovery I found OII Australia, and an XXY guy called Michael Noble.  Michael is a clever chappy, well he thinks he is at least.  He’s an “ACADEMIC” yes he has a degree in Creative Writing and Communications.  He is very creative in his writing that’s for sure!  Of course being an academic and a creative writer is no reason to assume that person has a clue what he’s talking about, when it comes to matters outside his field of interest!   My field of interest is XXY genetics.   Having wondered what Barr Bodies were, and found them to be the “shadow” of the inactivated X in all people with more than 1 X chromosome, it then became obvious to me that XXY males were effectively XY males with a Barr body, an inactivated additional X, as our sex is assigned us at birth based on our genital presentation, just like everybody else.

Michael Noble says that is asserting the additional X in “meaningless.”  Eh what?  Meaningless?  How does he arrive at that notion?  Ahhhh, he arrives there as he claims I say “…..if the physical affects of Klinefelter’s syndrome can be masked, then this renders the additional X chromosome as meaningless.”  Previous to that Michael claims his understanding that there’s a difference between being XXY and having Klinefelter’s syndrome is derived from “the ‘smoke-screen’ tactics of Tucker and such like…”  and I just happen to be the “Tucker” he’s referring to.

You can see just how creative Michael’s writing really is.  How is educating Michael that there really is a difference between being XXY and having Klinefelter’s syndrome a “smoke-screen tactic?”   Is it because he’s Australian, XXY, or just because he’s Michael?  Actually; regardless of the treatment an XXY man has, whether he prefers the disfigurement of  the symptoms of disease Klinefelter’s syndrome is, or not, plays no role in the effect of the additional X, or to be exactly precise, “the additional active genes on the pseudo-autosomal region of the additional X.”   What is “meaningless” is the rest of the additional X that is inactivated, just like it is inactivated in 46,XX females!

So the whole idea that the additional X brings with it some notion of femininity is just plain ludicrous, folk-lore genetics, pseudo-science, nonsense, XXY University rubbish!  The basis of it is high school genetics in the minds of children masquerading as adults! In short, under educated XXY men, who think they’re intersex.