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nice to have you here mike...so many people in wisconsin! we really should

get together...you guys (you and lauren and I know there are more out there I

can't think of names right now) are really close. I'm only a short distance

away.

anyone else near madison wisconsin...I work at UW-Madison and the short

version of this is that I was able to convince another research group to include

SMA in their brain study. (beck was in the study until she passed away)

Their research does not directly help sma, but it will hopefully make living

with sma easier in the near future. They need more volunteers to participate

in

the study. if you want more information just email me privately.

(_tstefonek@..._ (mailto:tstefonek@...) ) They compensate monetarily.

(not a

lot, but enough I think to cover any costs to you) the study involves using

a computer with your thoughts only...it's really cool. my husband (john) is

also in the study and can probably answer questions you might have related

to what it's like.

tj

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Whats up mike!! My name`s Tammia. *WELCOME!!*

- Greetings and Salutations

'Sup everybody! The name's Mike, I'm new to this group. I've

kind of been lurking around and reading, just trying to get a feel for

what I was getting myself into, and I've decided an introduction was

in order. It seems you all are great people, and I look forward to

getting to know you all better.

As I said my name is Mike, and I'm a fellow SMA guy. I have type II,

and was diagnosed about 21 years ago somewhere around 6 months of age.

My older sister, , is 24, that's three years older than me for

those not so good at math, and was diagnosed with SMA II at about age

1. I also have a younger brother, , 20, who doesn't have any

clinical disabilities, although he's does have a severe case of

laziness. My parents, Jim and , are wonderful people, who have

sacrificed a ton to raise three children, two with severe

disabilities, although they would never look at it that way.

Talking about my family reminds of something. I want to give a quick,

but sincere, thank you to all of you parents/friends of people with

SMA out there. Those of us affected by this disease depend on you so

much, and although we don't necessarily always show it, we appreciate

it and love you more than you could ever know! Sorry for that mushy

interlude, I just wanted to make sure everyone knows that.

Now that you all know about my family, I can tell you all a little bit

about the rest of my life. Currently I attend the University of

Wisconsin - Whitewater, and am in my fourth year pursuing a B.S. in

Management Computer Systems (basically computer programming). I'm

living on my own in an apartment, that is without any ABs (able-bodies

if you don't understand my lingo) and have been doing so for almost a

year now. I have two roommates, both have different forms of MD sd

well. One has SMA II, of whom you all should know as she also just

recently joined this group. You should know her as O or

sweetleo03. The other is Matt, who has Duchenne.

I've written entirely too much about myself, so I'm going to stop

before you all think I'm full of it. (to : no comments!) If

you want to know anything else about me though feel free to ask. I'd

be happy to share experiences about anything.

Thanks for reading, and I look forward to speaking with all of you more!

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Whats up mike!! My name`s Tammia. *WELCOME!!*

- Greetings and Salutations

'Sup everybody! The name's Mike, I'm new to this group. I've

kind of been lurking around and reading, just trying to get a feel for

what I was getting myself into, and I've decided an introduction was

in order. It seems you all are great people, and I look forward to

getting to know you all better.

As I said my name is Mike, and I'm a fellow SMA guy. I have type II,

and was diagnosed about 21 years ago somewhere around 6 months of age.

My older sister, , is 24, that's three years older than me for

those not so good at math, and was diagnosed with SMA II at about age

1. I also have a younger brother, , 20, who doesn't have any

clinical disabilities, although he's does have a severe case of

laziness. My parents, Jim and , are wonderful people, who have

sacrificed a ton to raise three children, two with severe

disabilities, although they would never look at it that way.

Talking about my family reminds of something. I want to give a quick,

but sincere, thank you to all of you parents/friends of people with

SMA out there. Those of us affected by this disease depend on you so

much, and although we don't necessarily always show it, we appreciate

it and love you more than you could ever know! Sorry for that mushy

interlude, I just wanted to make sure everyone knows that.

Now that you all know about my family, I can tell you all a little bit

about the rest of my life. Currently I attend the University of

Wisconsin - Whitewater, and am in my fourth year pursuing a B.S. in

Management Computer Systems (basically computer programming). I'm

living on my own in an apartment, that is without any ABs (able-bodies

if you don't understand my lingo) and have been doing so for almost a

year now. I have two roommates, both have different forms of MD sd

well. One has SMA II, of whom you all should know as she also just

recently joined this group. You should know her as O or

sweetleo03. The other is Matt, who has Duchenne.

I've written entirely too much about myself, so I'm going to stop

before you all think I'm full of it. (to : no comments!) If

you want to know anything else about me though feel free to ask. I'd

be happy to share experiences about anything.

Thanks for reading, and I look forward to speaking with all of you more!

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Hello Mike! My name is and I have SMA Type I. I am married and we are

expecting our first child.

Welcome!

Milinovich

Greetings and Salutations

'Sup everybody! The name's Mike, I'm new to this group. I've

kind of been lurking around and reading, just trying to get a feel for

what I was getting myself into, and I've decided an introduction was

in order. It seems you all are great people, and I look forward to

getting to know you all better.

As I said my name is Mike, and I'm a fellow SMA guy. I have type II,

and was diagnosed about 21 years ago somewhere around 6 months of age.

My older sister, , is 24, that's three years older than me for

those not so good at math, and was diagnosed with SMA II at about age

1. I also have a younger brother, , 20, who doesn't have any

clinical disabilities, although he's does have a severe case of

laziness. My parents, Jim and , are wonderful people, who have

sacrificed a ton to raise three children, two with severe

disabilities, although they would never look at it that way.

Talking about my family reminds of something. I want to give a quick,

but sincere, thank you to all of you parents/friends of people with

SMA out there. Those of us affected by this disease depend on you so

much, and although we don't necessarily always show it, we appreciate

it and love you more than you could ever know! Sorry for that mushy

interlude, I just wanted to make sure everyone knows that.

Now that you all know about my family, I can tell you all a little bit

about the rest of my life. Currently I attend the University of

Wisconsin - Whitewater, and am in my fourth year pursuing a B.S. in

Management Computer Systems (basically computer programming) . I'm

living on my own in an apartment, that is without any ABs (able-bodies

if you don't understand my lingo) and have been doing so for almost a

year now. I have two roommates, both have different forms of MD sd

well. One has SMA II, of whom you all should know as she also just

recently joined this group. You should know her as O or

sweetleo03. The other is Matt, who has Duchenne.

I've written entirely too much about myself, so I'm going to stop

before you all think I'm full of it. (to : no comments!) If

you want to know anything else about me though feel free to ask. I'd

be happy to share experiences about anything.

Thanks for reading, and I look forward to speaking with all of you more!

__________________________________________________

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Hi Mike, Welcome to the group.

Lori

pronto_r2 wrote:

>

> 'Sup everybody! The name's Mike, I'm new to this group. I've

> kind of been lurking around and reading, just trying to get a feel for

> what I was getting myself into, and I've decided an introduction was

> in order. It seems you all are great people, and I look forward to

> getting to know you all better.

>

> As I said my name is Mike, and I'm a fellow SMA guy. I have type II,

> and was diagnosed about 21 years ago somewhere around 6 months of age.

> My older sister, , is 24, that's three years older than me for

> those not so good at math, and was diagnosed with SMA II at about age

> 1. I also have a younger brother, , 20, who doesn't have any

> clinical disabilities, although he's does have a severe case of

> laziness. My parents, Jim and , are wonderful people, who have

> sacrificed a ton to raise three children, two with severe

> disabilities, although they would never look at it that way.

>

> Talking about my family reminds of something. I want to give a quick,

> but sincere, thank you to all of you parents/friends of people with

> SMA out there. Those of us affected by this disease depend on you so

> much, and although we don't necessarily always show it, we appreciate

> it and love you more than you could ever know! Sorry for that mushy

> interlude, I just wanted to make sure everyone knows that.

>

> Now that you all know about my family, I can tell you all a little bit

> about the rest of my life. Currently I attend the University of

> Wisconsin - Whitewater, and am in my fourth year pursuing a B.S. in

> Management Computer Systems (basically computer programming). I'm

> living on my own in an apartment, that is without any ABs (able-bodies

> if you don't understand my lingo) and have been doing so for almost a

> year now. I have two roommates, both have different forms of MD sd

> well. One has SMA II, of whom you all should know as she also just

> recently joined this group. You should know her as O or

> sweetleo03. The other is Matt, who has Duchenne.

>

> I've written entirely too much about myself, so I'm going to stop

> before you all think I'm full of it. (to : no comments!) If

> you want to know anything else about me though feel free to ask. I'd

> be happy to share experiences about anything.

>

> Thanks for reading, and I look forward to speaking with all of you more!

>

>

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> Talking about my family reminds of something. I want to give a quick,

> but sincere, thank you to all of you parents/friends of people with

> SMA out there. Those of us affected by this disease depend on you so

> much, and although we don't necessarily always show it, we appreciate

> it and love you more than you could ever know! Sorry for that mushy

> interlude, I just wanted to make sure everyone knows that.

Amen to that!

Welcome, Mike and !

Jenn

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Welcome to the group! My name is Camilla, 35, SMS II from Germany.

Have a nice day!

Camilla

>

> 'Sup everybody! The name's Mike, I'm new to this group.

I've

> kind of been lurking around and reading, just trying to get a feel

for

> what I was getting myself into, and I've decided an introduction

was

> in order. It seems you all are great people, and I look forward to

> getting to know you all better.

>

> As I said my name is Mike, and I'm a fellow SMA guy. I have type

II,

> and was diagnosed about 21 years ago somewhere around 6 months of

age.

> My older sister, , is 24, that's three years older than me

for

> those not so good at math, and was diagnosed with SMA II at about

age

> 1. I also have a younger brother, , 20, who doesn't have any

> clinical disabilities, although he's does have a severe case of

> laziness. My parents, Jim and , are wonderful people, who

have

> sacrificed a ton to raise three children, two with severe

> disabilities, although they would never look at it that way.

>

> Talking about my family reminds of something. I want to give a

quick,

> but sincere, thank you to all of you parents/friends of people with

> SMA out there. Those of us affected by this disease depend on you

so

> much, and although we don't necessarily always show it, we

appreciate

> it and love you more than you could ever know! Sorry for that

mushy

> interlude, I just wanted to make sure everyone knows that.

>

> Now that you all know about my family, I can tell you all a little

bit

> about the rest of my life. Currently I attend the University of

> Wisconsin - Whitewater, and am in my fourth year pursuing a B.S. in

> Management Computer Systems (basically computer programming). I'm

> living on my own in an apartment, that is without any ABs (able-

bodies

> if you don't understand my lingo) and have been doing so for

almost a

> year now. I have two roommates, both have different forms of MD sd

> well. One has SMA II, of whom you all should know as she also just

> recently joined this group. You should know her as O or

> sweetleo03. The other is Matt, who has Duchenne.

>

> I've written entirely too much about myself, so I'm going to stop

> before you all think I'm full of it. (to : no comments!) If

> you want to know anything else about me though feel free to ask.

I'd

> be happy to share experiences about anything.

>

> Thanks for reading, and I look forward to speaking with all of you

more!

>

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  • 2 years later...
Guest guest

Greetings and Salutations! Hello All!

I've been gone for a bit, and glad to be back! During that time I have missed this group! Majitha, how are you? Curtis in Hawaii, how are you?

I took a class on grounding and shielding 1 week ago today. I can post some of the info if any of you out there is interested in it.

Namaste'!

Love, Light, & Blessings,

, Reiki Practioner, Traditional Usui Ryoho

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