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Hi, .

I'm surprised you didn't hear from me about my little forum. I certainly

meant to invite you. Well, consider yourself invited. I'd sure love to see

somebody actually post there (besides Cam and me!)

But this one is clearly catching on better, so I guess it doesn't matter so

much where we meet as that we meet.

I might as well give a quick update on me. I'm scheduled to see Dr. Rand in

August. I figure I've put it off long enough and I don't want to wait until

I'm in unbearable pain before actually consulting a revision surgeon. I do

think my back is gradually getting worse, and walking is getting harder.

I'm not desperate yet, but maybe with advance planning I won't get that way.

Nothing new in regards to MS. It may be coincidence, but since I've been on

the MS drug Copaxone (over 4 months), I haven't had a single migraine.

Having lots of fun with my new pond, and hoping to get the landscaping

around it done before surgery, if indeed I end up having surgery. I'm

getting record numbers of water lily blooms (yeah, it's probably

over-planted, but who cares?!), and my lotuses are in bloom as well. I've

added more colorful goldfish, and have been training the fish to eat out of

my hands.

If you want, check out some of my favorite pond pics here:

http://photobucket.com/albums/v62/harper97/

I'm glad to see so many friends here, and look forward to forum-ing with you

all.

Sharon

[ ] Hi!!!

> Hi everyone! Cam, I am so happy that you started this. I just finished

> reading all of the posts but because it is my bedtime (yes, don't

> laugh at me!) and I have to work Friday and Saturday, I will not be

> able to post my story until sometime this weekend. I am thrilled to

> see so many old friends and glad we are all together here! Even Sharon

> from NH - how are you girlfriend? I never knew of your forum or I

> would have visited!?! Anyway, didn't want to not take the moment to

> say hello to everyone and let the support and friendship swell!

> from RI

>

>

>

>

> scoliosis vetrans * flatback sufferers * revison candidates

>

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Guest guest

Sharon, Wow!! Your making an appointment with Rand is huge news. I

know that is a big step for you. I am sorry to hear that your back is

giving you more problems but I am glad to hear that the migraines have

stopped. I am also sorry that I did not participate in your forum. I

was concentrating on healing for a bit and honestly I found the

structure of that site a bit difficult to navigate. I must admit that

I am happy that things fell apart on the feisty site and that so many

people have enthusiastically made the move to this group. I hope that

you continue to post here. The pond looks great!

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Guest guest

Hi Sharon - I think your pond flowers are absolutely beautiful. I am

ambivilent upon hearing of your news that you will be seeing Dr.

Rand next month. Part of me is happy that you have finally reached a

point to confront this darn flatback and see where you stand but

another part is unhappy that you feel you have gotten to the point

that many of us have previously reached. I know from experience that

it is something you can only hold off if the pain isn't too bad yet,

but when it gets really bad, you realize that you have no choice but

to face it head-on. Please let us know how you make out - I am so

happy to hear from you as it has been so long since you had posted.

I was a little worried about you! Take care.

> Hi, .

>

> I'm surprised you didn't hear from me about my little forum. I

certainly

> meant to invite you. Well, consider yourself invited. I'd sure

love to see

> somebody actually post there (besides Cam and me!)

>

> But this one is clearly catching on better, so I guess it doesn't

matter so

> much where we meet as that we meet.

>

> I might as well give a quick update on me. I'm scheduled to see

Dr. Rand in

> August. I figure I've put it off long enough and I don't want to

wait until

> I'm in unbearable pain before actually consulting a revision

surgeon. I do

> think my back is gradually getting worse, and walking is getting

harder.

> I'm not desperate yet, but maybe with advance planning I won't get

that way.

>

> Nothing new in regards to MS. It may be coincidence, but since

I've been on

> the MS drug Copaxone (over 4 months), I haven't had a single

migraine.

>

> Having lots of fun with my new pond, and hoping to get the

landscaping

> around it done before surgery, if indeed I end up having surgery.

I'm

> getting record numbers of water lily blooms (yeah, it's probably

> over-planted, but who cares?!), and my lotuses are in bloom as

well. I've

> added more colorful goldfish, and have been training the fish to

eat out of

> my hands.

>

> If you want, check out some of my favorite pond pics here:

>

> http://photobucket.com/albums/v62/harper97/

>

> I'm glad to see so many friends here, and look forward to forum-

ing with you

> all.

>

> Sharon

>

>

>

> [ ] Hi!!!

>

>

> > Hi everyone! Cam, I am so happy that you started this. I just

finished

> > reading all of the posts but because it is my bedtime (yes, don't

> > laugh at me!) and I have to work Friday and Saturday, I will not

be

> > able to post my story until sometime this weekend. I am thrilled

to

> > see so many old friends and glad we are all together here! Even

Sharon

> > from NH - how are you girlfriend? I never knew of your forum or

I

> > would have visited!?! Anyway, didn't want to not take the moment

to

> > say hello to everyone and let the support and friendship swell!

> > from RI

> >

> >

> >

> >

> > scoliosis vetrans * flatback sufferers * revison candidates

> >

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  • 1 year later...

hi Selena! Welcome to the group. My name is . I have a nephew that is 22 months old . He has BPES. Hope you like the group! ---the_artist_219 <the_artist_219@...> wrote: hi im new to this group im 13 and have had 3 surgeries and my name is selena just thought i should introduce myself :D __________________________________________________

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>Hi Selena,

I have a daughter who is 12 and has had a few eye surgeries. She was just

finally diagnosed with BPES. If you would like to contact her please email me

and I will let her know and give you her email address.

From: the_artist_219 <the_artist_219@...>

>Date: 2006/09/14 Thu PM 05:17:38 CDT

>blepharophimosis

>Subject: blepharophimosis hi!!!

>

>hi im new to this group im 13 and have had 3 surgeries and my name is

>selena just thought i should introduce myself :D

>

>

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  • 3 weeks later...

--- In blepharophimosis , <c.jameson@...>

wrote:

>

> >Hi Selena,

>

> I have a daughter who is 12 and has had a few eye surgeries. She

was just finally diagnosed with BPES. If you would like to contact

her please email me and I will let her know and give you her email

address.

>

>

>

>

> From: the_artist_219 <the_artist_219@...>

> >Date: 2006/09/14 Thu PM 05:17:38 CDT

> >blepharophimosis

> >Subject: blepharophimosis hi!!!

>

> >

> >hi im new to this group im 13 and have had 3 surgeries and my

name is

> >selena just thought i should introduce myself :D

> >

> > hi i would like to talk to you. i think that would be so cool. i

have never talk to any one that was my age. hannnah

please write back

>

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  • 6 months later...
Guest guest

no question it is a opening that many woman use when one first meets them in many different venues. russ[one blue one blue/brown] Hi!!!

Well.. im 15 and i have a blue eye, and the other one is green. My

parents didnt noticed when i was baby, because the color is kind of

similar, but now its like changing more, you can see the difference.I

love having heterochromia, its great for getting girls.

BYE!!

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