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From what I have seen any man or women can do this taking TRT.

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Phil

> From: gin2c <no_reply >

> Subject: Re: new to the group

>

> Date: Tuesday, March 1, 2011, 8:00 AM

> Not all XXY are the

> same.   I use T injections & I raised my

> T from 120 to 700.

>

>

>

> >

> > Yes in deed that is true, I'm sure many XXY are the

> same as the rest of the XY

> > male population, in gender expression but I personally

> tip to the side of XX.

> > Plus I did have ovary tissue in me and my type of

> cancer was ovarian cancer.

> > Plus I was asked to be in a study or the treatment of

> Ovarian cancer in women. I

> > was told at the Mayo clinic that most men that have

> this type of cancer can be

> > cured but for some reason treatments are not

> successful in women. I was at stage

> > 3B or4 at the time. The chemotherapy really messed up

> my body, nervous system,

> > bones and some minor organ damage. Screws in my bones

> from fractures pulled lose

> > and came though the skin. My remaining testis shutdown

> for over a year, as well

> > as some liver and kidney damage, that has subsequently

> returned to near normal.

> > (I have had my share of fractures and last year I

> drove my motorcycle to Alaska

> > with a broken arm. )

> > To be honest about my heart issues, I was on Vytorin

> for hi cholesterol for five

> > years and I just as started waking up after by-pass

> surgery a doctor asked why I

> > was taking Vytorin, all that drug does is plug blood

> vessels. Why did they give

> > the stuff in the first place. Now I'm on Lipitor and

> they want my LDL at 70 or

> > less.

> >

> > Of course my LHndFSH levels are high as to be

> expected.

> > Unfortunately I take a bunch of medications,

> Oxcarbazepin, cymbalta,

> > metopolol,lipitor,

> glumetza,losartan,glipizide,naproxen,

> > niacin,omepazole,glipizide, aspinin, ect.ect.

> ectttttt.

> >

> > As far as (allergies) to testosterone, I think I

> touched on this in my last

> > letter. Someone who has PAIS or AIS (Partial Androgen

> Insensitivity Syndrome)

> > Cannot use the testosterone that is being produced or

> taken into the body. The

> > theory is the extra X mimics a woman and doesn't

> completely absorb the available

> > testosterone. I think a better answer is the X

> effectively  blocks

> > some receptor sites in men. My description may be off

> a little bit but you get

> > the idea I hope. Then there are men who are

> (completely AIS) and cannot asbsorb

> > any of their testosterone from the testes and are born

> as women that have testes

> > still in the abdomen. A few of these people have given

> birth to children.

> >

> > Now you wonder why I'm confused. LOL

> >

> > H/D

> >

> >

> >

> >

> >

> >

> >

> >

> >

> > ________________________________

> > From: " uu1845@... " <uu1845@...>

> >

> > Sent: Mon, February 28, 2011 4:07:35 PM

> > Subject: RE: new to the group

> >

> >   

> > Being XXY doesn't define Hannah. This is what I Was

> referring. Only you can help

> > us better understand who you are and what issues you

> are facing. Be well this

> > evening.

> >

> > RE: new to the group

> >

> > I appreciate you sharing but please dnt make it seem

> like no one here can

> > understand but folks like yourself. Its really your

> job if you take it on, to

> > educate people on who you are. The human element isn't

> perfect, and it can

> > confuse, scare, or even make someone feel inferior or

> trapped into being one way

> > while feeling another. You can continue to feel its

> " your kind against the

> > world " or you can educate the ones th

> >

> > [The entire original message is not included]

> >

> >

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>

> I am new to the group but not to Candida.  I have been taking supplements to

control the yeast since 2003.  Please add me to the group list so I may actively

be involved with the topics.

+++Hi . Welcome! It's good to know your name.

You are already added to the group, but before posting questions you need to do

the required reading, which was emailed to you when you joined this group, as

follows:

How to Successfully Overcome Candida:

http://www.healingnaturallybybee.com/articles/intro2.php

Curing Candida, How to Get Started:

http://www.healingnaturallybybee.com/articles/intro1.php

For encouragement and inspiration see these 200 wonderful Success Stories by

members of this group:

http://www.healingnaturallybybee.com/success/index.php

The best in health, Bee

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Hello all! My name is and I am a mom of 4 children ages 9, 7, 4, and 18

months. Our 7 year old was diagnosed by an IEP team with having aspergers two

weeks ago. Things are still a little raw emotionally for us. Not only did we

discover this news about our son, but two days later moved and had to switch

schools. He is surprising us with how well he is adjusting to this new

environment (he HATES change) and we believe it's from all the individualized

attention he is now receiving at school. However, he's still not engaging with

other children and plays alone at recess.

I have two questions. One, do we tell him what is going on specifically? Do we

use the term aspergers? On one hand, we don't want to seem ashamed of it (we

aren't and don't want him to be) and want to use the AS language nonchalantly

and on the other hand we don't want him to feel labeled. Any advice?

My next question is are there things we can be doing at home to help him? He is

very high functioning and discovering he has AS has actually come as a shock to

us. We always knew he was a bit different than our other kids, but we just

passed it off as him being quirky and funny. He really does have an excellent

sense of humor. What are some good resources? We are just starting out and want

all the help and information we can get. We are heartbroken at the diagnosis

but are relieved, in a way, to know what is going on and that there are things

we can be doing to help him learn to cope and succeed.

Thank you so much for your help and advice!

in California

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I admit, I am a bit concerned about your son being diagnosed in an IEP

meeting. Asperger's is a medical/psychologicl issue, and most school

folks are NOT qualified to diagnose it! Yes, they can certainly observe

that your kid has a problem, but they are generally NOT qualified to

give a MEDICAL diagnosis! Yes they can ABSOLUTELY point out that there

is a problem, but they generally are NOT qualified to diagnose! Sorry,

that kinda hit one of my hot buttons.

Ok, setting all that aside, and assuming you get your son evaluated and

diagnosed by medical/psychological folks, where do you go from here? I

would say it depends on your kid. Fortunately for us, Isaac loves

science, and for him, knowing what his diagnosis is is a good thing.

I do think it's important to use a " team " approach when dealing with

Asperger's. This means parent(s), teachers, school psychologist, doctor,

etc. For Isaac, it has been very important to include him in ALL

decisions. This means that any decisions aren't imposed on him by

external forces, but rather that HE participates in them. That doesn't

mean that he is the final word, because he is still a kid, and WE are

the ones responsible for his well-being, but he is also heard, and there

are indeed times when his suggestions change what the end result is.

Good luck!

Eleanor, San , CA

Aspie son Isaac, 10.5 years old

On 03/22/2011 15:38 , brennie26 wrote:

> Hello all! My name is and I am a mom of 4 children ages 9, 7, 4,

> and 18 months. Our 7 year old was diagnosed by an IEP team with having

> aspergers two weeks ago. Things are still a little raw emotionally for

> us. Not only did we discover this news about our son, but two days later

> moved and had to switch schools. He is surprising us with how well he is

> adjusting to this new environment (he HATES change) and we believe it's

> from all the individualized attention he is now receiving at school.

> However, he's still not engaging with other children and plays alone at

> recess.

>

> I have two questions. One, do we tell him what is going on specifically?

> Do we use the term aspergers? On one hand, we don't want to seem ashamed

> of it (we aren't and don't want him to be) and want to use the AS

> language nonchalantly and on the other hand we don't want him to feel

> labeled. Any advice?

>

> My next question is are there things we can be doing at home to help

> him? He is very high functioning and discovering he has AS has actually

> come as a shock to us. We always knew he was a bit different than our

> other kids, but we just passed it off as him being quirky and funny. He

> really does have an excellent sense of humor. What are some good

> resources? We are just starting out and want all the help and

> information we can get. We are heartbroken at the diagnosis but are

> relieved, in a way, to know what is going on and that there are things

> we can be doing to help him learn to cope and succeed.

>

> Thank you so much for your help and advice!

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