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I live in Vista, San Diego County. She was originally diagnosed by Dr. Haas

at UCSD. I am thinking of taking her back to him. She does do pt, ot,

speech, and vision therapy. I see the most benefit from the speech therapy

because now she is a real chatter box. PT and OT kinda have written her off.

She can sit alone unassisted for a short period of time indian style. She

is so hyper tonic, though, she scissors her legs when held in a standing

position. Does anyone have any experience with Dr. Haas at UCSD?

Thank you

Carey.

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Carey

I live in Iowa, so I'm not much help about San Diego physicians. But I did

attend Mitochondrial Medicine conference in San Diego, I believe 2 yrs ago.

Dr Haas was the organizer of that conference. He appeared to be quite caring

and knowledgeable.

Good luck.

Janelle McGuire

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  • 1 month later...
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Kim-Were you sitting next to Lyssa at the NWH pre-op meeting last Tuesday?

If so HELLO! I still can't match names to faces very well. Best of luck on

your upcoming surgery! I love your last name. It's so positive! Wishing

you tons of good fortune next Monday!

:o),

Steph in Rockport

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Thank you so much Crystal!! I can't wait to be on the other side. I'm

starting to get excited and nervous at the same time!!

(((hugs)))

Nance

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I can hear your excitement :)

Hugs

Lyssa

Re: (unknown)

Thank you so much Crystal!! I can't wait to be on the other side. I'm

starting to get excited and nervous at the same time!!

(((hugs)))

Nance

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  • 3 weeks later...
Guest guest

Thank you! He's my Knight in Shining Armor! :)

(unknown)

Dawn,

Congratulations!!! Even though we've never met, I'm sure that you deserve

the very best. Must be your light shining. God Bless.

Crystal

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Reserve your name now at http://www.email.com

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Old school buds here:

http://click./1/5536/3/_/675032/_/961161174/

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On Fri, 16 Jun 2000 10:04:27 -0400, OSSG-NewEnglandegroups wrote:

> Thank you! He's my Knight in Shining Armor! :)

> dawn,

congratulations on your engagement. may you be blessed with a long

healthy and loving marriage.

maura

> (unknown)

>

>

> Dawn,

>

> Congratulations!!! Even though we've never met, I'm sure that you deserve

> the very best. Must be your light shining. God Bless.

>

> Crystal

>

> -----------------------------------------------

> FREE! The World's Best Email Address @email.com

> Reserve your name now at http://www.email.com

>

>

>

> ------------------------------------------------------------------------

> Old school buds here:

> http://click./1/5536/3/_/675032/_/961161174/

> ------------------------------------------------------------------------

>

>

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  • 1 year later...

Good Evening or Good Morning (for some of you..)

I just want to say thank GOD for those hormones... right? I mean, I can think of no one who really likes them. My husband, for one, he thinks I am going to loose it. Since I cannot justify wanting to cry all the time, he (of course, like all males) wants to "fix" it. Since my emotions are NOT fixable at this time, I need something to keep me level headed. I don't think I can really handle the "what is wrong?" speech every night.

My husband, a good man, does not seem to understand how personally I am taking my diagnosis... All he says, "don't worry, it'll all work out..." but, right now, that really is not good enough. Ever since I have been diagnosed with AS he has not wanted to touch me... I am not sure if he thinks he'll contract it or what, but it is really depressing. So from the fact that I want to cry anyways, I feel lonely from my own husband.

Since, my son is not his biologically, I feel real strongly that I need to get pregnant with his child. He just says, "we'll adopt..." That is fine and all but it is those little comments he makes,which really do sink in pretty deeply. Don't get me wrong, we love in every way, we think that he is truely a blessing to both of us. If the time comes, and we need to make the decision to adopt, than that will be that. I miss being pregnant...

Needless to say, I am not really doing that well tonight. Sorry, but I think only you people can really understand.

Bethany

>From: thepostmans@... >Reply-To: Ashermans >To: Ashermans >Subject: (unknown) >Date: Sun, 12 Aug 2001 22:33:17 -0000 > >Hi Bethany, >My name is Glenda and I was diagnosed with Ashermans in May of this >year. I have a 7 year old daughter and a 4 and a half year old son. >I also had a stillborn daughter almost 2 years ago and a D & C after >which caused the ashermans. I have not been treated yet but am >waiting to see a specialist. I know the fear of hearing the >diagnosis and also the fear when you find out it is not a quick fix. >But there is hope. I know you will find it here. I wanted to >welcome you. If you have questions, just ask and you will get a >response. There is a lot of support here and such wisdom. Take time >and read the posts and you'll soon get a handle on everything. Sorry >to hear of your tragedy...behind every person here is a story of >pain. Blessings to you. >Glenda > Get your FREE download of MSN Explorer at http://explorer.msn.com

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  • 1 month later...

Cherilyn, I too, am a new member and your letter sounds exactly like how I

feel most days. Somewhere between agonizing torture and small glimpses of

hope, we all wait every freaking day. I know it can be overwhelming. I

have learned so much in the 2 weeks I have been logging on to this group.

People know so much, they are good listeners and they have good advice. I

saw where you already received some nice nots from people, asking lots of

good questions. I just wanted you to that there are people out here who

feel exactly as you do. We just have to keep the faith. Carol S

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  • 3 weeks later...

Yeppers, ....Fern is 100% right. I have a good

friend with FMS, she simply cannot work. Her

depression was so severe, she started an on-line

depression support group which has been her " work. "

Perhaps it's just that your therapist only views work

as one narrow definition....so maybe your therapist

needs to go to an in-service about this and be given a

chance to rethink her attitude!

Lynn

--- Starflower wrote:

> ,

>

> How dare your therapist compare you to anyone else.

> Everyone is different

> whether they are well or have an illness. It is

> absurd to compare because

> we all react differently. Besides, I have never

> heard of one fibro patient

> that could keep working full-time on an indefinite

> basis. Most of them

> either play out and have to go to part-time or quit

> altogether or they push

> themselves to the point that they hurt so bad that

> they are no good to

> anyone including their employer or family. What is

> the point of pushing

> yourself to the point of severe pain? Is there some

> award we are supposed

> to win when we disregard our bodies way of telling

> us to slow down? I

> really get angry when someone who has NO clue what

> we go through tells us

> that we don't hurt bad enough for it to change our

> lives. Even small

> amounts of chronic pain will change your life. No

> one can have pain day in

> and day out with no relief in sight and be able to

> function at the level

> they did before.

>

> Gentle hugs,

> Fern

>

>

>

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,

How dare your therapist compare you to anyone else. Everyone is different

whether they are well or have an illness. It is absurd to compare because

we all react differently. Besides, I have never heard of one fibro patient

that could keep working full-time on an indefinite basis. Most of them

either play out and have to go to part-time or quit altogether or they push

themselves to the point that they hurt so bad that they are no good to

anyone including their employer or family. What is the point of pushing

yourself to the point of severe pain? Is there some award we are supposed

to win when we disregard our bodies way of telling us to slow down? I

really get angry when someone who has NO clue what we go through tells us

that we don't hurt bad enough for it to change our lives. Even small

amounts of chronic pain will change your life. No one can have pain day in

and day out with no relief in sight and be able to function at the level

they did before.

Gentle hugs,

Fern

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  • 5 years later...

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