hi i'm Judiana

[Judiana]

Hi,

i'm Judiana, and diagnosed 2 months ago with Genderdysphoric, and feeling transgender....

i'm 32 and since 2009 i'm able to feel the way Judiana wants, sadly there's no room for expression outdoors so i'n an inside girl who sometimes goes to a place where i can charge my battery's and feel the way i want...

i'm from outside the UK so apologies for maybe my bad englisch writing

i'm also diagnosed Cranio frontal nasal dysplasia, a rare facial disorder, and the upmost strange thing is, i'm 1 of the 2 males in my country and it is a disorder that is foremost diagnosed by 99.99% of the womens... so thats a real strange thing... i'm hoping to get some info about that more in the future...

i'm hoping to have a nice stay here and learn a lot by reading, and maybe helping a bit in my short way of life since 2009 when i discovered my feminine side....

thanks a lot !

Judiana

[Jamie D]

Greetings, Judiana.  That is a lovely name.

I am glad that you joined us.  You English is fine - no worries.

To help you navigate the site ...


Please be sure to review:

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Welcome   

[Judiana]

Hi Jamie,

thanks for your kind words!

is there a closed section on the forum to place photo's and so on?

thanks !

[Jamie D]

By "closed" do you mean a private area that can not be viewed by the public?

[Judiana]

hi Jamie, yes i'm sorry for the confusement, yes thats what i mean...

i've noticed the blog section, can i safely post some pictures ? not to spam or scare the bleep out of everyone?

[Jamie D]

Sorry about the delay in the reply.  There is a section of the website that is only open to subscribers, and is not seen by the public, or even most members.  In my personal blog, I have an area reserved for Androgyne members, to post pictures or whatever, but one needs 50 posts first to get access.

So for now, your options are somewhat limited.  By the way, my wife is a teacher and one of her students has craniofrontonasal dysplasia.  The child has had several operations.

[Judiana]

Sorry about the delay in the reply.  There is a section of the website that is only open to subscribers, and is not seen by the public, or even most members.  In my personal blog, I have an area reserved for Androgyne members, to post pictures or whatever, but one needs 50 posts first to get access.

So for now, your options are somewhat limited.  By the way, my wife is a teacher and one of her students has craniofrontonasal dysplasia.  The child has had several operations.

no problem Jamie, could you tell me how i can get this option? you may explain it via an PM if you wish...
i dont want to have my very personal story public only for "lurkers"
apologies for my opinion by the way and no offence for the members who sincerely mean the good things by reading my stuff maybe and so on....

thanks

[Judiana]

By the way, my wife is a teacher and one of her students has craniofrontonasal dysplasia.  The child has had several operations.

looks like a small world with CFND... maybe you can guess how hard it is to live with this condition and how much i cant express myself feminine... 

[Ms. OBrien CVT]

Hi Judiana,

Welcome to our little family. Over 7506. That would be one heck of a family reunion.

Feel free to post your successes/failures, Hopes/dreams.  Ask questions and seek answers. Give and receive advice.

But remember we are family here, your family now. And it is always nice to have another sister.


Janet  )O(

[Judiana]

Hi Judiana,

Welcome to our little family. Over 7506. That would be one heck of a family reunion.

Feel free to post your successes/failures, Hopes/dreams.  Ask questions and seek answers. Give and receive advice.

But remember we are family here, your family now. And it is always nice to have another sister.

Janet  )O(

Hi, Miss Obrien CVT,

thanks so much for your kind words !

nice to know that i'm part of the sisters, as soon i can tell more about me in a safe way on the forum i shall talk a bit more about me...