new to the group

[Guest guest]

Unfortunately, I don't think this is going to stop because I don't

think people will start to die in large enough numbers to make

anyone notice. What happens is that we become ill, but not ill

enough to die. Just ill enough to reduce our lives to a state of

misery and disability. But there is no smoking gun as to WHY we are

ill--at least not in their research.

I view it as taking a similar path as mercury fillings, flouride in

water, chemicals in our food supply, tobacco, and other insidiously

damaging products. There is controversy because there are concerns,

but nothing that points directly to a specific connection. And that

is what the manufacturer's play up in court. With no specific

connection (only theories), nobody pays the piper and the world

keeps turning round. People continue to get sick and everyone just

thinks it is sad, but nobody is at fault.

Tobacco was finally proven to be dangerous....hopefully breast

implants will too. But tobacco is still around, and people still

have the choice to smoke and kill themselves. Dare I say that we

should be prepared for this outcome with breast implants?

What makes me sad is when the children pay a price with their health

through exposure in the womb. It is a tragedy that doesn't have to

be. If implants stay on the market, they should at the very least

make women choose to NOT HAVE CHILDREN, or be DONE HAVING CHILDREN

before being implanted for the sake of their children's health. It

is insane to say that breast implants don't harm anyone, and I do

hope that at least that much truth will be revealed and these people

running around saying that implants have not caused any illness will

look like huge, stupid, ignorant fools and have their licenses to

practice medicine revoked.

We live in a crazy world. I wish I could believe that organizations

are in place to protect us from dangerous evils, but I think the sad

truth is that they've sold their souls to the devil and are in it

for the money, the power, and the prestige over the altruistic

stated goals of their " clubs " . May we learn to be discerning as to

the real motives of people out there. Money definitely rules.

Patty

> I think what adds up is the profit the plastic surgeons and

> manufacturers are making - it certainly doesn't add up from a

common

> sense perspective. The longer I'm a participant of this site, the

> more women I see complaining of the same problems, and it's as

plain

> as the nose on my face that the implants are making us sick.

>

> Sis

[Guest guest]

I talked to Molly the other day. . . She's doing

better. She's working out daily, either in the gym, or

on a treadmill. She's looking into doing some legal

work.

The insurance company agreed to replace their roof

that was severly damaged in the Hurricane.

Rogene

--- Kenda Skaggs <skaggs@...> wrote:

> I have been wondering the same thing. I hope she is

> ok.

>

> Kenda

>

>

> > Honey, where is Molly? I have missed her....love

> you...Lea

> >

>

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~```

> > Re: Re: New to the group

> >

> >

> >> There are a number of journal articles that do

> discuss

> >> implant related problems! . . . Maybe not in

> family

> >> medicine journals, but in rheumotology, plastic

> >> surgery, etc. . . These are seldom studies

> (because

> >> the refuse to study sick women and children), but

> >> observations.

> >>

> >> Rogene

> >>

> >>

> >>

> >> --- Kenda Skaggs <skaggs@...> wrote:

> >>

> >>> It is so odd to me that medical doctors keep

> telling

> >>> patients that nothing

> >>> is coming through in medical journals and the

> >>> patient is the only one they

> >>> have heard of with strange symptoms while my ND

> has

> >>> several implanted

> >>> related patients and does have journals with

> >>> information about implanted

> >>> related disease. Something doesn't add up.

> >>>

> >>> Kenda

> >>>

> >>>

> >>>> Hi Donna,

> >>>> I am really sorry to hear about everything you

> are

> >>> going thru. I am

> >>>> hoping I can offer you some support. First of

> all

> >>> let me tell you

> >>>> that I DR at Mayo. I went to the DR's at Mayo

> >>> with my findings. I

> >>>> will tell you that I was told that they keep

> have

> >>> reoccurring cases

> >>>> of woman coming to get implants out. My family

> DR

> >>> told me that

> >>>> every night he goes home and reads journal's

> >>> (family medicine) and

> >>>> that there is nothing in them about implants.

> He

> >>> has no other

> >>>> patients like me or that has presented with the

> >>> signs and symptoms I

> >>>> am showing. I have been thru several of the

> >>> clinics at Mayo (all in

> >>>> the last few months) to be told that I have

> >>> chronic fatigue,

> >>>> fibromyelgia, Reynolds, etc. But the

> specialists

> >>> I saw couldn't

> >>>> tell me why I have a skin rash/inflamation on

> my

> >>> joints, can't

> >>>> explain my arthritis, nor my MRI and the

> >>> inflamation, and the list

> >>>> goes on. I asked about the possiblity that my

> >>> implants were making

> >>>> me sick -- I was told about all the studies

> that

> >>> have been done. I

> >>>> had a hard time accepting that my implants were

> >>> making me sick and

> >>>> the Mayo DR's didn't help. Having a husband

> that

> >>> works in surgery

> >>>> and knows a lot of the DR's doesn't help

> either.

> >>> But I have

> >>>> researched everything including the studies at

> >>> Mayo. I have talked

> >>>> to people that do research for Mayo -- my

> >>> conclusion my implants are

> >>>> making me sick. My advice is listen to

> yourself

> >>> and your body, read

> >>>> all the information available regarding

> implants,

> >>> and you decide.

> >>>> You find a DR you trust and that will listen to

> >>> you. You have to be

> >>>> your own advocate for your health. Had I not

> been

> >>> an advocate for

> >>>> myself, I would have never found the

> information

> >>> about implants.

> >>>> This group has been a blessing and real

> strength

> >>> for me as I go thru

> >>>> this journey.

> >>>> Hugs, MK

> >>>>

> >>>>

> >>>>>

> >>>>> I think I posted my info on the messages

> instead

> >>> of the post. My

> >>>> name

> >>>>> is Donna and at this time I have Saline

> Implants.

> >>> My first surgery

> >>>>> was in 1997. After the first surgery my

> impants

> >>> would slide under

> >>>> me

> >>>>> arms. The Doc them says we need to go bigger

> by

> >>> the time I was

> >>>> done I

> >>>>> was a DD. I hated them so I continued my

> journey

> >>> to have them

> >>>> fixed.

> >>>>> The 2nd Doc said I would go smaller and that I

> >>> needed silicone and

> >>>> a

> >>>>> lift because I was so stretched out. So I did

> it.

> >>> That last 6

> >>>> months

> >>>>> before i was back getting them removed and

> saline

> >>> back in. A few

> >>>>> years later I was under the knife again going

> >>> smaller and to try

> >>>> to

> >>>>> fix the scars. My journey ended in 2002. I

> still

> >>> have them and for

> >>>>> the last 8 months I have been sick. I have

> gone

> >>> to MAyo and had

> >>>> every

> >>>>> test ran on me for every kind of illness. They

> >>> are all negative.

> >>>> My

> >>>>> symptoms are as follows: headache, numbness in

> >>> fingers and arm,

> >>>> cold

> >>>>> hands and feet, low pulse (38-58) low blood

> >>> pressure 80/60,

> >>>> vomiting,

> >>>>> pain in my right side, all around my scaring

> and

> >>> on the sides of

> >>>> my

> >>>>> breast are tender to touch, stiff in the

> >>> mornings, palpitations,

> >>>>> chest pains and so on. Everytime I ask a

> doctor

> >>> could it be my

> >>>>> implants they ask " Are they saline? " I say yes

> >>> and their respone

> >>>> is

> >>>>> no. I am having a MRI on Feb. 1st I do not

> know

> >>> much about testing

> >>>>> for implants but I am having it. If anyone can

> >>> give my advice I

> >>>> would

> >>>>> be very thankful.

> >>>>>

> >>>>> Donna

> >>>>>

> >>>>

> >>>>

> >>>>

> >>>>

> >>>>

> >>>>

> >>>> Opinions expressed are NOT meant to take the

> place

>

=== message truncated ===

[Guest guest]

Wonderful!!

Tell her hello for me.

Kenda

> I talked to Molly the other day. . . She's doing

> better. She's working out daily, either in the gym, or

> on a treadmill. She's looking into doing some legal

> work.

>

> The insurance company agreed to replace their roof

> that was severly damaged in the Hurricane.

>

> Rogene

>

>

>

> --- Kenda Skaggs <skaggs@...> wrote:

>

>> I have been wondering the same thing. I hope she is

>> ok.

>>

>> Kenda

>>

>>

>>> Honey, where is Molly? I have missed her....love

>> you...Lea

>>>

>>

> ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~```

>>> Re: Re: New to the group

>>>

>>>

>>>> There are a number of journal articles that do

>> discuss

>>>> implant related problems! . . . Maybe not in

>> family

>>>> medicine journals, but in rheumotology, plastic

>>>> surgery, etc. . . These are seldom studies

>> (because

>>>> the refuse to study sick women and children), but

>>>> observations.

>>>>

>>>> Rogene

>>>>

>>>>

>>>>

>>>> --- Kenda Skaggs <skaggs@...> wrote:

>>>>

>>>>> It is so odd to me that medical doctors keep

>> telling

>>>>> patients that nothing

>>>>> is coming through in medical journals and the

>>>>> patient is the only one they

>>>>> have heard of with strange symptoms while my ND

>> has

>>>>> several implanted

>>>>> related patients and does have journals with

>>>>> information about implanted

>>>>> related disease. Something doesn't add up.

>>>>>

>>>>> Kenda

>>>>>

>>>>>

>>>>>> Hi Donna,

>>>>>> I am really sorry to hear about everything you

>> are

>>>>> going thru. I am

>>>>>> hoping I can offer you some support. First of

>> all

>>>>> let me tell you

>>>>>> that I DR at Mayo. I went to the DR's at Mayo

>>>>> with my findings. I

>>>>>> will tell you that I was told that they keep

>> have

>>>>> reoccurring cases

>>>>>> of woman coming to get implants out. My family

>> DR

>>>>> told me that

>>>>>> every night he goes home and reads journal's

>>>>> (family medicine) and

>>>>>> that there is nothing in them about implants.

>> He

>>>>> has no other

>>>>>> patients like me or that has presented with the

>>>>> signs and symptoms I

>>>>>> am showing. I have been thru several of the

>>>>> clinics at Mayo (all in

>>>>>> the last few months) to be told that I have

>>>>> chronic fatigue,

>>>>>> fibromyelgia, Reynolds, etc. But the

>> specialists

>>>>> I saw couldn't

>>>>>> tell me why I have a skin rash/inflamation on

>> my

>>>>> joints, can't

>>>>>> explain my arthritis, nor my MRI and the

>>>>> inflamation, and the list

>>>>>> goes on. I asked about the possiblity that my

>>>>> implants were making

>>>>>> me sick -- I was told about all the studies

>> that

>>>>> have been done. I

>>>>>> had a hard time accepting that my implants were

>>>>> making me sick and

>>>>>> the Mayo DR's didn't help. Having a husband

>> that

>>>>> works in surgery

>>>>>> and knows a lot of the DR's doesn't help

>> either.

>>>>> But I have

>>>>>> researched everything including the studies at

>>>>> Mayo. I have talked

>>>>>> to people that do research for Mayo -- my

>>>>> conclusion my implants are

>>>>>> making me sick. My advice is listen to

>> yourself

>>>>> and your body, read

>>>>>> all the information available regarding

>> implants,

>>>>> and you decide.

>>>>>> You find a DR you trust and that will listen to

>>>>> you. You have to be

>>>>>> your own advocate for your health. Had I not

>> been

>>>>> an advocate for

>>>>>> myself, I would have never found the

>> information

>>>>> about implants.

>>>>>> This group has been a blessing and real

>> strength

>>>>> for me as I go thru

>>>>>> this journey.

>>>>>> Hugs, MK

>>>>>>

>>>>>>

>>>>>>>

>>>>>>> I think I posted my info on the messages

>> instead

>>>>> of the post. My

>>>>>> name

>>>>>>> is Donna and at this time I have Saline

>> Implants.

>>>>> My first surgery

>>>>>>> was in 1997. After the first surgery my

>> impants

>>>>> would slide under

>>>>>> me

>>>>>>> arms. The Doc them says we need to go bigger

>> by

>>>>> the time I was

>>>>>> done I

>>>>>>> was a DD. I hated them so I continued my

>> journey

>>>>> to have them

>>>>>> fixed.

>>>>>>> The 2nd Doc said I would go smaller and that I

>>>>> needed silicone and

>>>>>> a

>>>>>>> lift because I was so stretched out. So I did

>> it.

>>>>> That last 6

>>>>>> months

>>>>>>> before i was back getting them removed and

>> saline

>>>>> back in. A few

>>>>>>> years later I was under the knife again going

>>>>> smaller and to try

>>>>>> to

>>>>>>> fix the scars. My journey ended in 2002. I

>> still

>>>>> have them and for

>>>>>>> the last 8 months I have been sick. I have

>> gone

>>>>> to MAyo and had

>>>>>> every

>>>>>>> test ran on me for every kind of illness. They

>>>>> are all negative.

>>>>>> My

>>>>>>> symptoms are as follows: headache, numbness in

>>>>> fingers and arm,

>>>>>> cold

>>>>>>> hands and feet, low pulse (38-58) low blood

>>>>> pressure 80/60,

>>>>>> vomiting,

>>>>>>> pain in my right side, all around my scaring

>> and

>>>>> on the sides of

>>>>>> my

>>>>>>> breast are tender to touch, stiff in the

>>>>> mornings, palpitations,

>>>>>>> chest pains and so on. Everytime I ask a

>> doctor

>>>>> could it be my

>>>>>>> implants they ask " Are they saline? " I say yes

>>>>> and their respone

>>>>>> is

>>>>>>> no. I am having a MRI on Feb. 1st I do not

>> know

>>>>> much about testing

>>>>>>> for implants but I am having it. If anyone can

>>>>> give my advice I

>>>>>> would

>>>>>>> be very thankful.

>>>>>>>

>>>>>>> Donna

>>>>>>>

>>>>>>

>>>>>>

>>>>>>

>>>>>>

>>>>>>

>>>>>>

>>>>>> Opinions expressed are NOT meant to take the

>> place

>>

> === message truncated ===

>

>

>

> Opinions expressed are NOT meant to take the place of advice given by licensed

> health care professionals. Consult your physician or licensed health care

> professional before commencing any medical treatment.

>

> " Do not let either the medical authorities or the politicians mislead you.

> Find out what the facts are, and make your own decisions about how to live a

> happy life and how to work for a better world. " - Linus ing, two-time

> Nobel Prize Winner (1954, Chemistry; 1963, Peace)

>

> See our photos website! Enter " implants " for access at this link:

> http://.shutterfly.com/action/

>

>

[Guest guest]

Welcome,

I am glad to hear that you are getting help with the tort. The

casting is not so bad, my son has had four. You can look at his

website www.mybandedbaby.typepad.com to see the casting pictures so

you will be more prepared. She may cry a bit, but by the time it is

done(about 15 min) and she is in the bath, she will have forgotten

all about it. You can bring a bottle and a pacifier to help calm her.

A favorite washable toy is good too. You will want to bring any

special bath products you might need, if she has sensitive skin or

anything. They will have everything for you including a bath seat.

Let us know how the consult goes. Don't forget to take advantage of

the files section here, it is full of great info.

CAROLG

>

> Hello. I am sooo relieved that this group exists!! I had no idea

> about plagiocephaly or torticollis before my daughter was born, but

> now it seems it is all I worry about. She was diagnosed with

> torticollis at 10 weeks (I had to point it out to the ped) and has

> been having physical therapy ever since. Now I have a consult with

a

> DOC band prof in the area to see if Aria (my baby) is a candidate.

> I'm pretty sure she will be.

>

> I really think that hospitals and pediatricians need to be more

aware

> of this growing epidemic. We had no idea. My ped still says

Aria's

> head will round out.. but she is 3.5 months now and past the time

when

> heads normally round out on their own.

>

> I'm so glad there is a support group for this. I will post picture

(s)

> of her head so you can tell me how severe you think it is. Thank

you

> in advance!

>

> PS- if she is a candidate and we get the band for her, I DREAD the

> casting.....

>

[Guest guest]

Welcome,

I am glad to hear that you are getting help with the tort. The

casting is not so bad, my son has had four. You can look at his

website www.mybandedbaby.typepad.com to see the casting pictures so

you will be more prepared. She may cry a bit, but by the time it is

done(about 15 min) and she is in the bath, she will have forgotten

all about it. You can bring a bottle and a pacifier to help calm her.

A favorite washable toy is good too. You will want to bring any

special bath products you might need, if she has sensitive skin or

anything. They will have everything for you including a bath seat.

Let us know how the consult goes. Don't forget to take advantage of

the files section here, it is full of great info.

CAROLG

>

> Hello. I am sooo relieved that this group exists!! I had no idea

> about plagiocephaly or torticollis before my daughter was born, but

> now it seems it is all I worry about. She was diagnosed with

> torticollis at 10 weeks (I had to point it out to the ped) and has

> been having physical therapy ever since. Now I have a consult with

a

> DOC band prof in the area to see if Aria (my baby) is a candidate.

> I'm pretty sure she will be.

>

> I really think that hospitals and pediatricians need to be more

aware

> of this growing epidemic. We had no idea. My ped still says

Aria's

> head will round out.. but she is 3.5 months now and past the time

when

> heads normally round out on their own.

>

> I'm so glad there is a support group for this. I will post picture

(s)

> of her head so you can tell me how severe you think it is. Thank

you

> in advance!

>

> PS- if she is a candidate and we get the band for her, I DREAD the

> casting.....

>

[Guest guest]

Hi,

Welcome to the group! I agree hospital and doctors should educate us

about torticollis and plagiocephaly. Hopefully that day will be here soon.

The casting really isn't that bad and it's over pretty quickly. If you

can try and hold off feeding her that way you can give her, her bottle

while she's getting casted. Let us know how you make out.

--- In Plagiocephaly , " cassiesong7 " <song_of_hope@...>

wrote:

>

> Hello. I am sooo relieved that this group exists!! I had no idea

> about plagiocephaly or torticollis before my daughter was born, but

> now it seems it is all I worry about. She was diagnosed with

> torticollis at 10 weeks (I had to point it out to the ped) and has

> been having physical therapy ever since. Now I have a consult with a

> DOC band prof in the area to see if Aria (my baby) is a candidate.

> I'm pretty sure she will be.

>

> I really think that hospitals and pediatricians need to be more aware

> of this growing epidemic. We had no idea. My ped still says Aria's

> head will round out.. but she is 3.5 months now and past the time when

> heads normally round out on their own.

>

> I'm so glad there is a support group for this. I will post picture(s)

> of her head so you can tell me how severe you think it is. Thank you

> in advance!

>

> PS- if she is a candidate and we get the band for her, I DREAD the

> casting.....

>

[Guest guest]

Hi,

Welcome to the group! I agree hospital and doctors should educate us

about torticollis and plagiocephaly. Hopefully that day will be here soon.

The casting really isn't that bad and it's over pretty quickly. If you

can try and hold off feeding her that way you can give her, her bottle

while she's getting casted. Let us know how you make out.

--- In Plagiocephaly , " cassiesong7 " <song_of_hope@...>

wrote:

>

> Hello. I am sooo relieved that this group exists!! I had no idea

> about plagiocephaly or torticollis before my daughter was born, but

> now it seems it is all I worry about. She was diagnosed with

> torticollis at 10 weeks (I had to point it out to the ped) and has

> been having physical therapy ever since. Now I have a consult with a

> DOC band prof in the area to see if Aria (my baby) is a candidate.

> I'm pretty sure she will be.

>

> I really think that hospitals and pediatricians need to be more aware

> of this growing epidemic. We had no idea. My ped still says Aria's

> head will round out.. but she is 3.5 months now and past the time when

> heads normally round out on their own.

>

> I'm so glad there is a support group for this. I will post picture(s)

> of her head so you can tell me how severe you think it is. Thank you

> in advance!

>

> PS- if she is a candidate and we get the band for her, I DREAD the

> casting.....

>

[Guest guest]

Welcome to the group. Repo can work in infants up to 5/6/7 months

old. Babies with tort are notoriously hard to correct with repo (I

had two I know - LOL). Keep us posted. 3 1/2 months is a great age

for correction if a band is needed. They may send you home for more

repo and PT for the tort.

na, DOC Grad X2

Kiersten, DOC Band 1/10/06, Tort

www.thefilyaws.com/plagio/plagio.html

>

> Hello. I am sooo relieved that this group exists!! I had no idea

> about plagiocephaly or torticollis before my daughter was born, but

> now it seems it is all I worry about. She was diagnosed with

> torticollis at 10 weeks (I had to point it out to the ped) and has

> been having physical therapy ever since. Now I have a consult with

a

> DOC band prof in the area to see if Aria (my baby) is a candidate.

> I'm pretty sure she will be.

>

> I really think that hospitals and pediatricians need to be more

aware

> of this growing epidemic. We had no idea. My ped still says

Aria's

> head will round out.. but she is 3.5 months now and past the time

when

> heads normally round out on their own.

>

> I'm so glad there is a support group for this. I will post picture

(s)

> of her head so you can tell me how severe you think it is. Thank

you

> in advance!

>

> PS- if she is a candidate and we get the band for her, I DREAD the

> casting.....

>

[Guest guest]

Welcome to the group. Repo can work in infants up to 5/6/7 months

old. Babies with tort are notoriously hard to correct with repo (I

had two I know - LOL). Keep us posted. 3 1/2 months is a great age

for correction if a band is needed. They may send you home for more

repo and PT for the tort.

na, DOC Grad X2

Kiersten, DOC Band 1/10/06, Tort

www.thefilyaws.com/plagio/plagio.html

>

> Hello. I am sooo relieved that this group exists!! I had no idea

> about plagiocephaly or torticollis before my daughter was born, but

> now it seems it is all I worry about. She was diagnosed with

> torticollis at 10 weeks (I had to point it out to the ped) and has

> been having physical therapy ever since. Now I have a consult with

a

> DOC band prof in the area to see if Aria (my baby) is a candidate.

> I'm pretty sure she will be.

>

> I really think that hospitals and pediatricians need to be more

aware

> of this growing epidemic. We had no idea. My ped still says

Aria's

> head will round out.. but she is 3.5 months now and past the time

when

> heads normally round out on their own.

>

> I'm so glad there is a support group for this. I will post picture

(s)

> of her head so you can tell me how severe you think it is. Thank

you

> in advance!

>

> PS- if she is a candidate and we get the band for her, I DREAD the

> casting.....

>

[Guest guest]

Hi Jess,

Welcome to the group! Wow triplets, you must be one busy mom. :-)

So out of all 3 only one has plagio? Let us know when 's band is

in and how he's adjusting.

--- In Plagiocephaly , " " <boystripletmom@...>

wrote:

>

> Hi my name is Jess. I am new to the group and wanted to say hello. I

> have triplet boys that are going to be one on Wednesday. My son

> just had his casting done at Cranial yesterday. I have been reading

> your posts and find them very helpful. I look forward to chatting with

> you all.

>

[Guest guest]

Hi Jess,

Welcome to the group! Wow triplets, you must be one busy mom. :-)

So out of all 3 only one has plagio? Let us know when 's band is

in and how he's adjusting.

--- In Plagiocephaly , " " <boystripletmom@...>

wrote:

>

> Hi my name is Jess. I am new to the group and wanted to say hello. I

> have triplet boys that are going to be one on Wednesday. My son

> just had his casting done at Cranial yesterday. I have been reading

> your posts and find them very helpful. I look forward to chatting with

> you all.

>

[Guest guest]

Hi JEss,

Welcome to the group. Wow triplets - I bet you get that a lot

Please post some pics of your little guys. Any big birthday plans?

na, DOC Grad X2

Kiersten, DOC Band 1/10/06, tort

www.thefilyaws.com/plagio/plagio.html

--- In Plagiocephaly , " " <boystripletmom@...>

wrote:

>

> Hi my name is Jess. I am new to the group and wanted to say hello.

I

> have triplet boys that are going to be one on Wednesday. My son

> just had his casting done at Cranial yesterday. I have been reading

> your posts and find them very helpful. I look forward to chatting

with

> you all.

>

[Guest guest]

Hi JEss,

Welcome to the group. Wow triplets - I bet you get that a lot

Please post some pics of your little guys. Any big birthday plans?

na, DOC Grad X2

Kiersten, DOC Band 1/10/06, tort

www.thefilyaws.com/plagio/plagio.html

--- In Plagiocephaly , " " <boystripletmom@...>

wrote:

>

> Hi my name is Jess. I am new to the group and wanted to say hello.

I

> have triplet boys that are going to be one on Wednesday. My son

> just had his casting done at Cranial yesterday. I have been reading

> your posts and find them very helpful. I look forward to chatting

with

> you all.

>

[Guest guest]

Welcome to the group. All three with Torticollis? You must have

spent hours upon hours at pt. Do you get any help at home to take

care of them? I have b/g twins. I can't imagine having 3. Were they

premie?

Haylee

Mom to andre doc band grad

--- In Plagiocephaly , " " <boystripletmom@...>

wrote:

>

> Hi my name is Jess. I am new to the group and wanted to say hello.

I

> have triplet boys that are going to be one on Wednesday. My son

> just had his casting done at Cranial yesterday. I have been reading

> your posts and find them very helpful. I look forward to chatting

with

> you all.

>

[Guest guest]

Welcome to the group. All three with Torticollis? You must have

spent hours upon hours at pt. Do you get any help at home to take

care of them? I have b/g twins. I can't imagine having 3. Were they

premie?

Haylee

Mom to andre doc band grad

--- In Plagiocephaly , " " <boystripletmom@...>

wrote:

>

> Hi my name is Jess. I am new to the group and wanted to say hello.

I

> have triplet boys that are going to be one on Wednesday. My son

> just had his casting done at Cranial yesterday. I have been reading

> your posts and find them very helpful. I look forward to chatting

with

> you all.

>

[Guest guest]

My Dear Friend,

How are you? I am also new to the Group. I am a Chinese girl. I hope to

make friend with you.

Best Regards,

Ying

[Guest guest]

My Dear Friend,

How are you? I am also new to the Group. I am a Chinese girl. I hope to

make friend with you.

Best Regards,

Ying

[Guest guest]

Hi , Thanks for the welcome. I have posted some pics. I will post some of getting his casting later on today. : ) <monicash@...> wrote: Hi JEss,Welcome to the group. Wow triplets - I bet you get that a lot Please post some pics of your little guys. Any big birthday plans?na, DOC Grad X2Kiersten, DOC Band 1/10/06, tortwww.thefilyaws.com/plagio/plagio.html>> Hi my name is Jess. I am new to the group and wanted to say hello. I > have triplet boys that are going to be one

on Wednesday. My son > just had his casting done at Cranial yesterday. I have been reading > your posts and find them very helpful. I look forward to chatting with > you all.>Thank you, JessRemember to visit our webpage at:http://www.geocities.com/boystripletmom/

New Messenger with Voice. Call regular phones from your PC and save big.

[Guest guest]

Hi , Thanks for the welcome. I have posted some pics. I will post some of getting his casting later on today. : ) <monicash@...> wrote: Hi JEss,Welcome to the group. Wow triplets - I bet you get that a lot Please post some pics of your little guys. Any big birthday plans?na, DOC Grad X2Kiersten, DOC Band 1/10/06, tortwww.thefilyaws.com/plagio/plagio.html>> Hi my name is Jess. I am new to the group and wanted to say hello. I > have triplet boys that are going to be one

on Wednesday. My son > just had his casting done at Cranial yesterday. I have been reading > your posts and find them very helpful. I look forward to chatting with > you all.>Thank you, JessRemember to visit our webpage at:http://www.geocities.com/boystripletmom/

New Messenger with Voice. Call regular phones from your PC and save big.

[Guest guest]

Welcome, Ying.hzying99 <hzying99@...> wrote: My Dear Friend,How are you? I am also new to the Group. I am a Chinese girl. I hope to make friend with you.Best Regards,YingThank you, JessRemember to visit our webpage at:http://www.geocities.com/boystripletmom/

New Messenger with Voice. Call regular phones from your PC for low, low rates.

[Guest guest]

Welcome, Ying.hzying99 <hzying99@...> wrote: My Dear Friend,How are you? I am also new to the Group. I am a Chinese girl. I hope to make friend with you.Best Regards,YingThank you, JessRemember to visit our webpage at:http://www.geocities.com/boystripletmom/

New Messenger with Voice. Call regular phones from your PC for low, low rates.

[Guest guest]

Hello

Welcome to the group. Glad you found us. You must be very blessed,

and very busy having triplets. That is awsome. Let us know how the

fitting goes, and again welcome. As for the torticollis, work with

them as much as you can. )

Sandy Willow's Mom

torticollis resolved

Cranio Grad (Germany)

www.geocities.com/samipa74/Willow_Lanette.html

www.palmerfamily.armedforcesfamilies.com

--- In Plagiocephaly , " " <boystripletmom@...>

wrote:

>

> Hi my name is Jess. I am new to the group and wanted to say hello.

I

> have triplet boys that are going to be one on Wednesday. My son

> just had his casting done at Cranial yesterday. I have been reading

> your posts and find them very helpful. I look forward to chatting

with

> you all.

>

[Guest guest]

Hello

Welcome to the group. Glad you found us. You must be very blessed,

and very busy having triplets. That is awsome. Let us know how the

fitting goes, and again welcome. As for the torticollis, work with

them as much as you can. )

Sandy Willow's Mom

torticollis resolved

Cranio Grad (Germany)

www.geocities.com/samipa74/Willow_Lanette.html

www.palmerfamily.armedforcesfamilies.com

--- In Plagiocephaly , " " <boystripletmom@...>

wrote:

>

> Hi my name is Jess. I am new to the group and wanted to say hello.

I

> have triplet boys that are going to be one on Wednesday. My son

> just had his casting done at Cranial yesterday. I have been reading

> your posts and find them very helpful. I look forward to chatting

with

> you all.

>

[Guest guest]

Hi Ying,

I didn't even see your post! I just saw Sandy reply to you. Welcome to

the group you'll find a lot of friends here. We're happy to have you

with us. Please tell us a little bit about yourself.

>

> My Dear Friend,

>

> How are you? I am also new to the Group. I am a Chinese girl. I hope to

> make friend with you.

>

>

> Best Regards,

> Ying

>

[Guest guest]

Hi Ying,

I didn't even see your post! I just saw Sandy reply to you. Welcome to

the group you'll find a lot of friends here. We're happy to have you

with us. Please tell us a little bit about yourself.

>

> My Dear Friend,

>

> How are you? I am also new to the Group. I am a Chinese girl. I hope to

> make friend with you.

>

>

> Best Regards,

> Ying

>