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It is nice to hear that Veeti's treatment has been so succesful.

Congratulations!!!

I simply had to write (as a Finnish mother) because I fear that people here

may have an impression that our Finnish treatment is totally incompetent. My son

is being treated by the same doctor as Veeti was. Yes, my son has had already

two surgeries and has casts at the moment. I may be a lousy mother but I did not

have the ability to travel to the US. and get my son's feet treated without

surgeries. My son's doctor has always been great to us and the same goes with

the other staff members in the hospital..ok, that is maybe not the point, if the

people are nice or not...but to avoid the surgery. Fine, unfortunately my son's

feet are severe and I doubt that only the casting and other " soft methods " would

have corrected his feet. Maybe I am wrong. But there are also other children in

Finland who have had excellent treatment. Just wanted to tell you this there in

the big world that we do have something good here!

Unfortunately Sanna, you cannot do anything for us. But maybe you can spread

the word about the ponseti method and someone else may benefit from that. We

will carry on our lives with the choices we have made without shame. Pity does

not help us!

Anu & Atte

Veeti's second cast,

We saw Dr. Ponseti this morning and got some great news: Veeti's foot

has improved a lot, and it is possible that he needs only one cast

after this one! This means a tenotomy next Monday, and then the last

cast. Dr. P wasn't quite sure yet, but was very hopeful! I was so

amazed when they took the first cast off and saw the foot looking

almost like normal! Even the heel cord which was very stiff had given

up a little!

I'm so truly happy that Veeti is getting the best treatment in the

world, but at the same time I feel bitter because all this could have

been over months ago if there were.. hmmm.. good doctors in Finland,

and I feel sorry for all the other children in Finland who undergo

the four-six-month castings and yet have to undergo one or more

surgeries... What can I do to change it!?

And by the way, Veeti is now 9,5 months old, and a few weeks ago

started standing up. Nevertheless, he has adjusted to casts without

problems, and even tries to stand up with his normal foot. And crawls

faster than mommy can run!:)

Sanna and Veeti (6.5.02, left clubfoot)

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It is nice to hear that Veeti's treatment has been so succesful.

Congratulations!!!

I simply had to write (as a Finnish mother) because I fear that people here

may have an impression that our Finnish treatment is totally incompetent. My son

is being treated by the same doctor as Veeti was. Yes, my son has had already

two surgeries and has casts at the moment. I may be a lousy mother but I did not

have the ability to travel to the US. and get my son's feet treated without

surgeries. My son's doctor has always been great to us and the same goes with

the other staff members in the hospital..ok, that is maybe not the point, if the

people are nice or not...but to avoid the surgery. Fine, unfortunately my son's

feet are severe and I doubt that only the casting and other " soft methods " would

have corrected his feet. Maybe I am wrong. But there are also other children in

Finland who have had excellent treatment. Just wanted to tell you this there in

the big world that we do have something good here!

Unfortunately Sanna, you cannot do anything for us. But maybe you can spread

the word about the ponseti method and someone else may benefit from that. We

will carry on our lives with the choices we have made without shame. Pity does

not help us!

Anu & Atte

Veeti's second cast,

We saw Dr. Ponseti this morning and got some great news: Veeti's foot

has improved a lot, and it is possible that he needs only one cast

after this one! This means a tenotomy next Monday, and then the last

cast. Dr. P wasn't quite sure yet, but was very hopeful! I was so

amazed when they took the first cast off and saw the foot looking

almost like normal! Even the heel cord which was very stiff had given

up a little!

I'm so truly happy that Veeti is getting the best treatment in the

world, but at the same time I feel bitter because all this could have

been over months ago if there were.. hmmm.. good doctors in Finland,

and I feel sorry for all the other children in Finland who undergo

the four-six-month castings and yet have to undergo one or more

surgeries... What can I do to change it!?

And by the way, Veeti is now 9,5 months old, and a few weeks ago

started standing up. Nevertheless, he has adjusted to casts without

problems, and even tries to stand up with his normal foot. And crawls

faster than mommy can run!:)

Sanna and Veeti (6.5.02, left clubfoot)

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It is nice to hear that Veeti's treatment has been so succesful.

Congratulations!!!

I simply had to write (as a Finnish mother) because I fear that people here

may have an impression that our Finnish treatment is totally incompetent. My son

is being treated by the same doctor as Veeti was. Yes, my son has had already

two surgeries and has casts at the moment. I may be a lousy mother but I did not

have the ability to travel to the US. and get my son's feet treated without

surgeries. My son's doctor has always been great to us and the same goes with

the other staff members in the hospital..ok, that is maybe not the point, if the

people are nice or not...but to avoid the surgery. Fine, unfortunately my son's

feet are severe and I doubt that only the casting and other " soft methods " would

have corrected his feet. Maybe I am wrong. But there are also other children in

Finland who have had excellent treatment. Just wanted to tell you this there in

the big world that we do have something good here!

Unfortunately Sanna, you cannot do anything for us. But maybe you can spread

the word about the ponseti method and someone else may benefit from that. We

will carry on our lives with the choices we have made without shame. Pity does

not help us!

Anu & Atte

Veeti's second cast,

We saw Dr. Ponseti this morning and got some great news: Veeti's foot

has improved a lot, and it is possible that he needs only one cast

after this one! This means a tenotomy next Monday, and then the last

cast. Dr. P wasn't quite sure yet, but was very hopeful! I was so

amazed when they took the first cast off and saw the foot looking

almost like normal! Even the heel cord which was very stiff had given

up a little!

I'm so truly happy that Veeti is getting the best treatment in the

world, but at the same time I feel bitter because all this could have

been over months ago if there were.. hmmm.. good doctors in Finland,

and I feel sorry for all the other children in Finland who undergo

the four-six-month castings and yet have to undergo one or more

surgeries... What can I do to change it!?

And by the way, Veeti is now 9,5 months old, and a few weeks ago

started standing up. Nevertheless, he has adjusted to casts without

problems, and even tries to stand up with his normal foot. And crawls

faster than mommy can run!:)

Sanna and Veeti (6.5.02, left clubfoot)

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>I simply had to write (as a Finnish mother)

> because I fear that people here may have an

> impression that our Finnish treatment is

> totally incompetent.

I don't believe anyone has the feeling that Finnish treatment is totally

incompetent. Many, many doctors in the US still use the same treatment

as your son is receiving because it's the " known " and " accepted " way.

>I may be a lousy mother but I did not have the

> ability to travel to the US. and get my son's

> feet treated without surgeries.

Nobody, and i mean nobody, thinks you are a lousy mother for not

travelling to the US or wherever to find the Ponseti method. It's

called life, and we do what we can with the circumstances we have.

Please don't feel like Sanna or ANYONE is looking down on you for your

son's treatment. Each parent tries to do the best they can, and Sanna's

whole point is she wishes everyone had the CHOICE that she had. I don't

think she feels superior to you because she made a big trip to get what

she believes to be the best treatment, she's just ecstatic at the

results (after dreading surgery) and wishes everyone had the same

opportunity.

Joy

http://community.webtv.net/joybelle15/ROSESCLUBFOOTPAGE

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Oh dear, I do not mean that Sanna is looking down on me or anyone else here.

Sometimes it is difficult to express the things one thinks in a foreign

language. I simply wanted to point out that we have also satisfied patients

here. Well, of course as my son is being treated by the same doctor I feel a bit

defensive and of course afraid...what if he has treated my son in a wrong

way...well, life goes on and it is excellent that at least some people do have

the choice. Nevertheless, it is interesting to hear the experiences Sanna and

Veeti have from Ponseti. He seems like an angel on earth :))

peace

anu

Re: Veeti's second cast,

>I simply had to write (as a Finnish mother)

> because I fear that people here may have an

> impression that our Finnish treatment is

> totally incompetent.

I don't believe anyone has the feeling that Finnish treatment is totally

incompetent. Many, many doctors in the US still use the same treatment

as your son is receiving because it's the " known " and " accepted " way.

>I may be a lousy mother but I did not have the

> ability to travel to the US. and get my son's

> feet treated without surgeries.

Nobody, and i mean nobody, thinks you are a lousy mother for not

travelling to the US or wherever to find the Ponseti method. It's

called life, and we do what we can with the circumstances we have.

Please don't feel like Sanna or ANYONE is looking down on you for your

son's treatment. Each parent tries to do the best they can, and Sanna's

whole point is she wishes everyone had the CHOICE that she had. I don't

think she feels superior to you because she made a big trip to get what

she believes to be the best treatment, she's just ecstatic at the

results (after dreading surgery) and wishes everyone had the same

opportunity.

Joy

http://community.webtv.net/joybelle15/ROSESCLUBFOOTPAGE

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Share on other sites

Oh dear, I do not mean that Sanna is looking down on me or anyone else here.

Sometimes it is difficult to express the things one thinks in a foreign

language. I simply wanted to point out that we have also satisfied patients

here. Well, of course as my son is being treated by the same doctor I feel a bit

defensive and of course afraid...what if he has treated my son in a wrong

way...well, life goes on and it is excellent that at least some people do have

the choice. Nevertheless, it is interesting to hear the experiences Sanna and

Veeti have from Ponseti. He seems like an angel on earth :))

peace

anu

Re: Veeti's second cast,

>I simply had to write (as a Finnish mother)

> because I fear that people here may have an

> impression that our Finnish treatment is

> totally incompetent.

I don't believe anyone has the feeling that Finnish treatment is totally

incompetent. Many, many doctors in the US still use the same treatment

as your son is receiving because it's the " known " and " accepted " way.

>I may be a lousy mother but I did not have the

> ability to travel to the US. and get my son's

> feet treated without surgeries.

Nobody, and i mean nobody, thinks you are a lousy mother for not

travelling to the US or wherever to find the Ponseti method. It's

called life, and we do what we can with the circumstances we have.

Please don't feel like Sanna or ANYONE is looking down on you for your

son's treatment. Each parent tries to do the best they can, and Sanna's

whole point is she wishes everyone had the CHOICE that she had. I don't

think she feels superior to you because she made a big trip to get what

she believes to be the best treatment, she's just ecstatic at the

results (after dreading surgery) and wishes everyone had the same

opportunity.

Joy

http://community.webtv.net/joybelle15/ROSESCLUBFOOTPAGE

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Share on other sites

Oh dear, I do not mean that Sanna is looking down on me or anyone else here.

Sometimes it is difficult to express the things one thinks in a foreign

language. I simply wanted to point out that we have also satisfied patients

here. Well, of course as my son is being treated by the same doctor I feel a bit

defensive and of course afraid...what if he has treated my son in a wrong

way...well, life goes on and it is excellent that at least some people do have

the choice. Nevertheless, it is interesting to hear the experiences Sanna and

Veeti have from Ponseti. He seems like an angel on earth :))

peace

anu

Re: Veeti's second cast,

>I simply had to write (as a Finnish mother)

> because I fear that people here may have an

> impression that our Finnish treatment is

> totally incompetent.

I don't believe anyone has the feeling that Finnish treatment is totally

incompetent. Many, many doctors in the US still use the same treatment

as your son is receiving because it's the " known " and " accepted " way.

>I may be a lousy mother but I did not have the

> ability to travel to the US. and get my son's

> feet treated without surgeries.

Nobody, and i mean nobody, thinks you are a lousy mother for not

travelling to the US or wherever to find the Ponseti method. It's

called life, and we do what we can with the circumstances we have.

Please don't feel like Sanna or ANYONE is looking down on you for your

son's treatment. Each parent tries to do the best they can, and Sanna's

whole point is she wishes everyone had the CHOICE that she had. I don't

think she feels superior to you because she made a big trip to get what

she believes to be the best treatment, she's just ecstatic at the

results (after dreading surgery) and wishes everyone had the same

opportunity.

Joy

http://community.webtv.net/joybelle15/ROSESCLUBFOOTPAGE

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I am glad you do not feel Sanna is looking down on you ! It did come

across that way to me. Trust me, these misunderstandings occur even

with people who's first language is English. I just wanted to make sure

that you knew nobody thought you were a lousy mother. You did what you

had to do to correct your son's feet, and that is really what is

important.

As for your doctor, I'm positive he is competent. My daughter Rose saw a

perfectly competent doctor similar to your's. We did find out about Dr.

Ponseti and took her to see him 3 weeks before she was to have surgery.

She ended up responding extremely well to Dr. Ponseti's method and did

not need to see the other doctor again! Dr. Ponseti is an amazing man,

and his method is incredible. It is a shame that not everybody is

presented with the choice, but right now it isn't that way. We all come

from different circumstances, and we make our choices with what we know

and can do.

I think your son is in perfectly capable hands. :)

Joy

http://community.webtv.net/joybelle15/ROSESCLUBFOOTPAGE

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I am glad you do not feel Sanna is looking down on you ! It did come

across that way to me. Trust me, these misunderstandings occur even

with people who's first language is English. I just wanted to make sure

that you knew nobody thought you were a lousy mother. You did what you

had to do to correct your son's feet, and that is really what is

important.

As for your doctor, I'm positive he is competent. My daughter Rose saw a

perfectly competent doctor similar to your's. We did find out about Dr.

Ponseti and took her to see him 3 weeks before she was to have surgery.

She ended up responding extremely well to Dr. Ponseti's method and did

not need to see the other doctor again! Dr. Ponseti is an amazing man,

and his method is incredible. It is a shame that not everybody is

presented with the choice, but right now it isn't that way. We all come

from different circumstances, and we make our choices with what we know

and can do.

I think your son is in perfectly capable hands. :)

Joy

http://community.webtv.net/joybelle15/ROSESCLUBFOOTPAGE

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Sanna,

What great news! I'm so glad to hear things are progressing well. I

know just how you feel.. We experienced much the same thing. It was

remarkable how much improvement there was with just one cast for our

child too.. after months of previous casting that hadn't worked. Best

wishes for continued good luck!

and

>

> We saw Dr. Ponseti this morning and got some great news: Veeti's

foot

> has improved a lot, and it is possible that he needs only one cast

> after this one! This means a tenotomy next Monday, and then the

last

> cast. Dr. P wasn't quite sure yet, but was very hopeful! I was so

> amazed when they took the first cast off and saw the foot looking

> almost like normal! Even the heel cord which was very stiff had

given

> up a little!

>

> I'm so truly happy that Veeti is getting the best treatment in the

> world, but at the same time I feel bitter because all this could

have

> been over months ago if there were.. hmmm.. good doctors in

Finland,

> and I feel sorry for all the other children in Finland who undergo

> the four-six-month castings and yet have to undergo one or more

> surgeries... What can I do to change it!?

>

> And by the way, Veeti is now 9,5 months old, and a few weeks ago

> started standing up. Nevertheless, he has adjusted to casts without

> problems, and even tries to stand up with his normal foot. And

crawls

> faster than mommy can run!:)

>

> Sanna and Veeti (6.5.02, left clubfoot)

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Sanna,

What great news! I'm so glad to hear things are progressing well. I

know just how you feel.. We experienced much the same thing. It was

remarkable how much improvement there was with just one cast for our

child too.. after months of previous casting that hadn't worked. Best

wishes for continued good luck!

and

>

> We saw Dr. Ponseti this morning and got some great news: Veeti's

foot

> has improved a lot, and it is possible that he needs only one cast

> after this one! This means a tenotomy next Monday, and then the

last

> cast. Dr. P wasn't quite sure yet, but was very hopeful! I was so

> amazed when they took the first cast off and saw the foot looking

> almost like normal! Even the heel cord which was very stiff had

given

> up a little!

>

> I'm so truly happy that Veeti is getting the best treatment in the

> world, but at the same time I feel bitter because all this could

have

> been over months ago if there were.. hmmm.. good doctors in

Finland,

> and I feel sorry for all the other children in Finland who undergo

> the four-six-month castings and yet have to undergo one or more

> surgeries... What can I do to change it!?

>

> And by the way, Veeti is now 9,5 months old, and a few weeks ago

> started standing up. Nevertheless, he has adjusted to casts without

> problems, and even tries to stand up with his normal foot. And

crawls

> faster than mommy can run!:)

>

> Sanna and Veeti (6.5.02, left clubfoot)

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Sanna,

What great news! I'm so glad to hear things are progressing well. I

know just how you feel.. We experienced much the same thing. It was

remarkable how much improvement there was with just one cast for our

child too.. after months of previous casting that hadn't worked. Best

wishes for continued good luck!

and

>

> We saw Dr. Ponseti this morning and got some great news: Veeti's

foot

> has improved a lot, and it is possible that he needs only one cast

> after this one! This means a tenotomy next Monday, and then the

last

> cast. Dr. P wasn't quite sure yet, but was very hopeful! I was so

> amazed when they took the first cast off and saw the foot looking

> almost like normal! Even the heel cord which was very stiff had

given

> up a little!

>

> I'm so truly happy that Veeti is getting the best treatment in the

> world, but at the same time I feel bitter because all this could

have

> been over months ago if there were.. hmmm.. good doctors in

Finland,

> and I feel sorry for all the other children in Finland who undergo

> the four-six-month castings and yet have to undergo one or more

> surgeries... What can I do to change it!?

>

> And by the way, Veeti is now 9,5 months old, and a few weeks ago

> started standing up. Nevertheless, he has adjusted to casts without

> problems, and even tries to stand up with his normal foot. And

crawls

> faster than mommy can run!:)

>

> Sanna and Veeti (6.5.02, left clubfoot)

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Anu,

Indeed I don't think everyone in Finland should travel half way

around the world for clubfoot treatment, I mean we should have

Ponseti specialist(s) in Finland too so that there would be an

alternative to surgeries! My previous message wasn't criticism to you

nor to any other Finnish mom/dad who have had their children treated

in Finland.

If you just could have seen what I saw this morning... the magic that

Dr. P had done to my son's foot.. it really makes you want to help

the others in similar situation!!

Joy's message could have been my words exactly.

Sanna & Veeti

> It is nice to hear that Veeti's treatment has been so succesful.

Congratulations!!!

>

> I simply had to write (as a Finnish mother) because I fear that

people here may have an impression that our Finnish treatment is

totally incompetent. My son is being treated by the same doctor as

Veeti was. Yes, my son has had already two surgeries and has casts at

the moment. I may be a lousy mother but I did not have the ability to

travel to the US. and get my son's feet treated without surgeries. My

son's doctor has always been great to us and the same goes with the

other staff members in the hospital..ok, that is maybe not the point,

if the people are nice or not...but to avoid the surgery. Fine,

unfortunately my son's feet are severe and I doubt that only the

casting and other " soft methods " would have corrected his feet. Maybe

I am wrong. But there are also other children in Finland who have had

excellent treatment. Just wanted to tell you this there in the big

world that we do have something good here!

>

> Unfortunately Sanna, you cannot do anything for us. But maybe you

can spread the word about the ponseti method and someone else may

benefit from that. We will carry on our lives with the choices we

have made without shame. Pity does not help us!

>

> Anu & Atte

>

>

> Veeti's second cast,

>

>

>

> We saw Dr. Ponseti this morning and got some great news: Veeti's

foot

> has improved a lot, and it is possible that he needs only one

cast

> after this one! This means a tenotomy next Monday, and then the

last

> cast. Dr. P wasn't quite sure yet, but was very hopeful! I was so

> amazed when they took the first cast off and saw the foot looking

> almost like normal! Even the heel cord which was very stiff had

given

> up a little!

>

> I'm so truly happy that Veeti is getting the best treatment in

the

> world, but at the same time I feel bitter because all this could

have

> been over months ago if there were.. hmmm.. good doctors in

Finland,

> and I feel sorry for all the other children in Finland who

undergo

> the four-six-month castings and yet have to undergo one or more

> surgeries... What can I do to change it!?

>

> And by the way, Veeti is now 9,5 months old, and a few weeks ago

> started standing up. Nevertheless, he has adjusted to casts

without

> problems, and even tries to stand up with his normal foot. And

crawls

> faster than mommy can run!:)

>

> Sanna and Veeti (6.5.02, left clubfoot)

>

>

>

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Anu,

Indeed I don't think everyone in Finland should travel half way

around the world for clubfoot treatment, I mean we should have

Ponseti specialist(s) in Finland too so that there would be an

alternative to surgeries! My previous message wasn't criticism to you

nor to any other Finnish mom/dad who have had their children treated

in Finland.

If you just could have seen what I saw this morning... the magic that

Dr. P had done to my son's foot.. it really makes you want to help

the others in similar situation!!

Joy's message could have been my words exactly.

Sanna & Veeti

> It is nice to hear that Veeti's treatment has been so succesful.

Congratulations!!!

>

> I simply had to write (as a Finnish mother) because I fear that

people here may have an impression that our Finnish treatment is

totally incompetent. My son is being treated by the same doctor as

Veeti was. Yes, my son has had already two surgeries and has casts at

the moment. I may be a lousy mother but I did not have the ability to

travel to the US. and get my son's feet treated without surgeries. My

son's doctor has always been great to us and the same goes with the

other staff members in the hospital..ok, that is maybe not the point,

if the people are nice or not...but to avoid the surgery. Fine,

unfortunately my son's feet are severe and I doubt that only the

casting and other " soft methods " would have corrected his feet. Maybe

I am wrong. But there are also other children in Finland who have had

excellent treatment. Just wanted to tell you this there in the big

world that we do have something good here!

>

> Unfortunately Sanna, you cannot do anything for us. But maybe you

can spread the word about the ponseti method and someone else may

benefit from that. We will carry on our lives with the choices we

have made without shame. Pity does not help us!

>

> Anu & Atte

>

>

> Veeti's second cast,

>

>

>

> We saw Dr. Ponseti this morning and got some great news: Veeti's

foot

> has improved a lot, and it is possible that he needs only one

cast

> after this one! This means a tenotomy next Monday, and then the

last

> cast. Dr. P wasn't quite sure yet, but was very hopeful! I was so

> amazed when they took the first cast off and saw the foot looking

> almost like normal! Even the heel cord which was very stiff had

given

> up a little!

>

> I'm so truly happy that Veeti is getting the best treatment in

the

> world, but at the same time I feel bitter because all this could

have

> been over months ago if there were.. hmmm.. good doctors in

Finland,

> and I feel sorry for all the other children in Finland who

undergo

> the four-six-month castings and yet have to undergo one or more

> surgeries... What can I do to change it!?

>

> And by the way, Veeti is now 9,5 months old, and a few weeks ago

> started standing up. Nevertheless, he has adjusted to casts

without

> problems, and even tries to stand up with his normal foot. And

crawls

> faster than mommy can run!:)

>

> Sanna and Veeti (6.5.02, left clubfoot)

>

>

>

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Anu,

Indeed I don't think everyone in Finland should travel half way

around the world for clubfoot treatment, I mean we should have

Ponseti specialist(s) in Finland too so that there would be an

alternative to surgeries! My previous message wasn't criticism to you

nor to any other Finnish mom/dad who have had their children treated

in Finland.

If you just could have seen what I saw this morning... the magic that

Dr. P had done to my son's foot.. it really makes you want to help

the others in similar situation!!

Joy's message could have been my words exactly.

Sanna & Veeti

> It is nice to hear that Veeti's treatment has been so succesful.

Congratulations!!!

>

> I simply had to write (as a Finnish mother) because I fear that

people here may have an impression that our Finnish treatment is

totally incompetent. My son is being treated by the same doctor as

Veeti was. Yes, my son has had already two surgeries and has casts at

the moment. I may be a lousy mother but I did not have the ability to

travel to the US. and get my son's feet treated without surgeries. My

son's doctor has always been great to us and the same goes with the

other staff members in the hospital..ok, that is maybe not the point,

if the people are nice or not...but to avoid the surgery. Fine,

unfortunately my son's feet are severe and I doubt that only the

casting and other " soft methods " would have corrected his feet. Maybe

I am wrong. But there are also other children in Finland who have had

excellent treatment. Just wanted to tell you this there in the big

world that we do have something good here!

>

> Unfortunately Sanna, you cannot do anything for us. But maybe you

can spread the word about the ponseti method and someone else may

benefit from that. We will carry on our lives with the choices we

have made without shame. Pity does not help us!

>

> Anu & Atte

>

>

> Veeti's second cast,

>

>

>

> We saw Dr. Ponseti this morning and got some great news: Veeti's

foot

> has improved a lot, and it is possible that he needs only one

cast

> after this one! This means a tenotomy next Monday, and then the

last

> cast. Dr. P wasn't quite sure yet, but was very hopeful! I was so

> amazed when they took the first cast off and saw the foot looking

> almost like normal! Even the heel cord which was very stiff had

given

> up a little!

>

> I'm so truly happy that Veeti is getting the best treatment in

the

> world, but at the same time I feel bitter because all this could

have

> been over months ago if there were.. hmmm.. good doctors in

Finland,

> and I feel sorry for all the other children in Finland who

undergo

> the four-six-month castings and yet have to undergo one or more

> surgeries... What can I do to change it!?

>

> And by the way, Veeti is now 9,5 months old, and a few weeks ago

> started standing up. Nevertheless, he has adjusted to casts

without

> problems, and even tries to stand up with his normal foot. And

crawls

> faster than mommy can run!:)

>

> Sanna and Veeti (6.5.02, left clubfoot)

>

>

>

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Horray for Veeti!!!! Sanna I bet you feel such a sense of relief.

Sometimes it really does feel as though Dr. Ponseti is a miracle

worker. I wish you much continued success while in Iowa City.

Here's to an early departure!!!!!!!!!!!!!

Holly :)

Zachary

Unilateral Right c/f

Treated by Dr. Ponseti

>

> We saw Dr. Ponseti this morning and got some great news: Veeti's

foot

> has improved a lot, and it is possible that he needs only one cast

> after this one! This means a tenotomy next Monday, and then the

last

> cast. Dr. P wasn't quite sure yet, but was very hopeful! I was so

> amazed when they took the first cast off and saw the foot looking

> almost like normal! Even the heel cord which was very stiff had

given

> up a little!

>

> I'm so truly happy that Veeti is getting the best treatment in the

> world, but at the same time I feel bitter because all this could

have

> been over months ago if there were.. hmmm.. good doctors in

Finland,

> and I feel sorry for all the other children in Finland who undergo

> the four-six-month castings and yet have to undergo one or more

> surgeries... What can I do to change it!?

>

> And by the way, Veeti is now 9,5 months old, and a few weeks ago

> started standing up. Nevertheless, he has adjusted to casts without

> problems, and even tries to stand up with his normal foot. And

crawls

> faster than mommy can run!:)

>

> Sanna and Veeti (6.5.02, left clubfoot)

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Sanna and Veeti,

Isn't it amazing how fast the feet start to respond, I still remember after

our daughters second cast how almost " normal " her feet looked, it was the

first time her feet ever looked that way and I was beside myself with

happiness!

Congratulations on Veeti's progress so far, I hope all continues well and

you will be able to go home with his shoe brace very soon!

Holly and (bilateral born: 2-11-2000, switched to Ponseti method in

Iowa at 5 months of age. Just recently finished treatment at age 3)

Veeti's second cast,

>

>We saw Dr. Ponseti this morning and got some great news: Veeti's foot

>has improved a lot, and it is possible that he needs only one cast

>after this one! This means a tenotomy next Monday, and then the last

>cast. Dr. P wasn't quite sure yet, but was very hopeful! I was so

>amazed when they took the first cast off and saw the foot looking

>almost like normal! Even the heel cord which was very stiff had given

>up a little!

>

>I'm so truly happy that Veeti is getting the best treatment in the

>world, but at the same time I feel bitter because all this could have

>been over months ago if there were.. hmmm.. good doctors in Finland,

>and I feel sorry for all the other children in Finland who undergo

>the four-six-month castings and yet have to undergo one or more

>surgeries... What can I do to change it!?

>

>And by the way, Veeti is now 9,5 months old, and a few weeks ago

>started standing up. Nevertheless, he has adjusted to casts without

>problems, and even tries to stand up with his normal foot. And crawls

>faster than mommy can run!:)

>

>Sanna and Veeti (6.5.02, left clubfoot)

>

>

>

>

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Sanna and Veeti,

Isn't it amazing how fast the feet start to respond, I still remember after

our daughters second cast how almost " normal " her feet looked, it was the

first time her feet ever looked that way and I was beside myself with

happiness!

Congratulations on Veeti's progress so far, I hope all continues well and

you will be able to go home with his shoe brace very soon!

Holly and (bilateral born: 2-11-2000, switched to Ponseti method in

Iowa at 5 months of age. Just recently finished treatment at age 3)

Veeti's second cast,

>

>We saw Dr. Ponseti this morning and got some great news: Veeti's foot

>has improved a lot, and it is possible that he needs only one cast

>after this one! This means a tenotomy next Monday, and then the last

>cast. Dr. P wasn't quite sure yet, but was very hopeful! I was so

>amazed when they took the first cast off and saw the foot looking

>almost like normal! Even the heel cord which was very stiff had given

>up a little!

>

>I'm so truly happy that Veeti is getting the best treatment in the

>world, but at the same time I feel bitter because all this could have

>been over months ago if there were.. hmmm.. good doctors in Finland,

>and I feel sorry for all the other children in Finland who undergo

>the four-six-month castings and yet have to undergo one or more

>surgeries... What can I do to change it!?

>

>And by the way, Veeti is now 9,5 months old, and a few weeks ago

>started standing up. Nevertheless, he has adjusted to casts without

>problems, and even tries to stand up with his normal foot. And crawls

>faster than mommy can run!:)

>

>Sanna and Veeti (6.5.02, left clubfoot)

>

>

>

>

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Share on other sites

Sanna and Veeti,

Isn't it amazing how fast the feet start to respond, I still remember after

our daughters second cast how almost " normal " her feet looked, it was the

first time her feet ever looked that way and I was beside myself with

happiness!

Congratulations on Veeti's progress so far, I hope all continues well and

you will be able to go home with his shoe brace very soon!

Holly and (bilateral born: 2-11-2000, switched to Ponseti method in

Iowa at 5 months of age. Just recently finished treatment at age 3)

Veeti's second cast,

>

>We saw Dr. Ponseti this morning and got some great news: Veeti's foot

>has improved a lot, and it is possible that he needs only one cast

>after this one! This means a tenotomy next Monday, and then the last

>cast. Dr. P wasn't quite sure yet, but was very hopeful! I was so

>amazed when they took the first cast off and saw the foot looking

>almost like normal! Even the heel cord which was very stiff had given

>up a little!

>

>I'm so truly happy that Veeti is getting the best treatment in the

>world, but at the same time I feel bitter because all this could have

>been over months ago if there were.. hmmm.. good doctors in Finland,

>and I feel sorry for all the other children in Finland who undergo

>the four-six-month castings and yet have to undergo one or more

>surgeries... What can I do to change it!?

>

>And by the way, Veeti is now 9,5 months old, and a few weeks ago

>started standing up. Nevertheless, he has adjusted to casts without

>problems, and even tries to stand up with his normal foot. And crawls

>faster than mommy can run!:)

>

>Sanna and Veeti (6.5.02, left clubfoot)

>

>

>

>

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Sanna,

We are glad that things are going well. We (and many others) had a

similar experience to what you have expressed. When we first went to

Iowa when our son was 6 weeks old and had the first cast put on,

meeting Dr. Ponseti and talking about how it was supposed to work

made us very hopeful. But it was a week later when the cast was

changed and his feet looked almost perfect after one cast that we

were thrilled. Our son also only needed 2 Ponseti method casts and

then the tenotomy cast.

Now you know more of why those of us here are trying to find ways to

let other parents (and doctors) around the world know that the

Ponseti method works. Please keep us informed.

and (3-17-99)

>

> We saw Dr. Ponseti this morning and got some great news: Veeti's

foot

> has improved a lot, and it is possible that he needs only one cast

> after this one! This means a tenotomy next Monday, and then the

last

> cast. Dr. P wasn't quite sure yet, but was very hopeful! I was so

> amazed when they took the first cast off and saw the foot looking

> almost like normal! Even the heel cord which was very stiff had

given

> up a little!

>

> I'm so truly happy that Veeti is getting the best treatment in the

> world, but at the same time I feel bitter because all this could

have

> been over months ago if there were.. hmmm.. good doctors in

Finland,

> and I feel sorry for all the other children in Finland who undergo

> the four-six-month castings and yet have to undergo one or more

> surgeries... What can I do to change it!?

>

> And by the way, Veeti is now 9,5 months old, and a few weeks ago

> started standing up. Nevertheless, he has adjusted to casts without

> problems, and even tries to stand up with his normal foot. And

crawls

> faster than mommy can run!:)

>

> Sanna and Veeti (6.5.02, left clubfoot)

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Sanna,

We are glad that things are going well. We (and many others) had a

similar experience to what you have expressed. When we first went to

Iowa when our son was 6 weeks old and had the first cast put on,

meeting Dr. Ponseti and talking about how it was supposed to work

made us very hopeful. But it was a week later when the cast was

changed and his feet looked almost perfect after one cast that we

were thrilled. Our son also only needed 2 Ponseti method casts and

then the tenotomy cast.

Now you know more of why those of us here are trying to find ways to

let other parents (and doctors) around the world know that the

Ponseti method works. Please keep us informed.

and (3-17-99)

>

> We saw Dr. Ponseti this morning and got some great news: Veeti's

foot

> has improved a lot, and it is possible that he needs only one cast

> after this one! This means a tenotomy next Monday, and then the

last

> cast. Dr. P wasn't quite sure yet, but was very hopeful! I was so

> amazed when they took the first cast off and saw the foot looking

> almost like normal! Even the heel cord which was very stiff had

given

> up a little!

>

> I'm so truly happy that Veeti is getting the best treatment in the

> world, but at the same time I feel bitter because all this could

have

> been over months ago if there were.. hmmm.. good doctors in

Finland,

> and I feel sorry for all the other children in Finland who undergo

> the four-six-month castings and yet have to undergo one or more

> surgeries... What can I do to change it!?

>

> And by the way, Veeti is now 9,5 months old, and a few weeks ago

> started standing up. Nevertheless, he has adjusted to casts without

> problems, and even tries to stand up with his normal foot. And

crawls

> faster than mommy can run!:)

>

> Sanna and Veeti (6.5.02, left clubfoot)

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Anu,

Please be assured that the treatment your child has recieved is most

likely the same " state of the art " as used my most doctors in the US

or other parts of Europe. Until 4 years ago, there were only about

10-15 Ponseti method doctors in the world with most of them being in

Iowa. Dr. Ponseti's method has been largely ignored for 50 years.

It has only been with Dr. Ponseti's book in 1996 and information

being put on the internet about 1999 that it began to be found by

parents. Parents demanding the treatment has been what has helped

make doctors begin to pay attention.

Most of the world's best pediatric orthopedists did not think that

the Ponseti method was a possibility until the past few years and

even know probably most have not yet switched over to it. Our

original pediatric orthopedic doctor was very much against our using

the Ponseti method initially and it took him about 2 1/2 years before

he finally changed over. Now perhaps as much as half of the doctors

who are members of POSNA are trying to implement Ponseti method

techniques into their treatment. But many still are not or else are

modifying it a bit.

That is why we are all trying to help find ways to let parents know

that it exists and works well for almost all children.

and (3-17-99)

> It is nice to hear that Veeti's treatment has been so succesful.

Congratulations!!!

>

> I simply had to write (as a Finnish mother) because I fear that

people here may have an impression that our Finnish treatment is

totally incompetent. My son is being treated by the same doctor as

Veeti was. Yes, my son has had already two surgeries and has casts at

the moment. I may be a lousy mother but I did not have the ability to

travel to the US. and get my son's feet treated without surgeries. My

son's doctor has always been great to us and the same goes with the

other staff members in the hospital..ok, that is maybe not the point,

if the people are nice or not...but to avoid the surgery. Fine,

unfortunately my son's feet are severe and I doubt that only the

casting and other " soft methods " would have corrected his feet. Maybe

I am wrong. But there are also other children in Finland who have had

excellent treatment. Just wanted to tell you this there in the big

world that we do have something good here!

>

> Unfortunately Sanna, you cannot do anything for us. But maybe you

can spread the word about the ponseti method and someone else may

benefit from that. We will carry on our lives with the choices we

have made without shame. Pity does not help us!

>

> Anu & Atte

>

>

> Veeti's second cast,

>

>

>

> We saw Dr. Ponseti this morning and got some great news: Veeti's

foot

> has improved a lot, and it is possible that he needs only one

cast

> after this one! This means a tenotomy next Monday, and then the

last

> cast. Dr. P wasn't quite sure yet, but was very hopeful! I was so

> amazed when they took the first cast off and saw the foot looking

> almost like normal! Even the heel cord which was very stiff had

given

> up a little!

>

> I'm so truly happy that Veeti is getting the best treatment in

the

> world, but at the same time I feel bitter because all this could

have

> been over months ago if there were.. hmmm.. good doctors in

Finland,

> and I feel sorry for all the other children in Finland who

undergo

> the four-six-month castings and yet have to undergo one or more

> surgeries... What can I do to change it!?

>

> And by the way, Veeti is now 9,5 months old, and a few weeks ago

> started standing up. Nevertheless, he has adjusted to casts

without

> problems, and even tries to stand up with his normal foot. And

crawls

> faster than mommy can run!:)

>

> Sanna and Veeti (6.5.02, left clubfoot)

>

>

>

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