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Hi ! I wanted to respond to your question about BARD

buttons/tubes. My daughter Sydney had one placed in July last year,

and I don't know if read my other posting today, but it was a surprise

because we thought she was getting a Mic-Key button. The surgeon at

the time told us the BARD is easier for younger children because they

lay flatter against the skin and also you don't have to replace them

out like a Mic-Key. It all sounded great with me...except they didn't

tell me that it couldn't lock in the tubing when she was connected to

the feeding pump. This became our biggest problem with the BARD.

Since you can't lock in your tubing, not only can you not hook your

child up to a backpack during the day (since it'll fall out at mild

twisting)...but at night my daughter rolls around and is pretty active

and it would pop out of her, spilling the contents of her tube and

stomach. I would find her soaked in her sheets the next day,

extremely upset at the loss of calories and time wasted. I finally

discovered that by putting medical tape on her stomach, taping down

the tube on the side of her stomach at night, would indeed fix the

nighttime problem...I still could not do daytime pumpings while she

was awake and upright. I visited Dr. H in December and she said we

absolutely had to get the BARD switched out, it was not doing us any

good. Sydney just had her Mic-Key put in last week and the locking

mechanism on this tube is FANTASTIC. If you have an active child and

you either know or forsee having to have a backpack running during the

daytime... I would suggest not doing the BARD. Ours was nothing but

trouble and ended up breaking a valve in it anyway...so we would have

had to have it replaced sooner or later. Granted, you may not have a

choice in the matter, if the BARD is your only option - but if you do

have the choice - I would go with the Mic-Key. I can't tell you how

frustrated I was with that BARD tube. I wish I HAD taken a picture

of it....I scrapbook and even took pictures during her stay at the

hospital...but never did think to take a picture of her tube! Wish I

had now that you ask about pictures. Sorry I can't offer one to

you. Good luck with everything!

Debbie, mom to Sydney, RSS, 17 months

>

> Does anyone have a picture or any experience with the Bard Button?

This is the only button our Dr uses. Thanks!

>

> Mom to Dasia

> 23mo RSS

>

> __________________________________________________

>

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Thanks for responding Debbie! This presents such a problem for me, after being

on the internet all day (and not getting my house cleaned! ), I know I

definitely want the Mic-Key, I just want this ng tube out so bad that I really

hate to wait for too much longer for this to be rescheduled. I'll email our

genetics/devel ped, maybe he can get us in somewhere quickly. He's at a major

hospital and probably has connections. I had our first one scheduled at a

different hospital. This is making me crazy!

super28chick wrote:

Hi ! I wanted to respond to your question about BARD

buttons/tubes. My daughter Sydney had one placed in July last year,

and I don't know if read my other posting today, but it was a surprise

because we thought she was getting a Mic-Key button. The surgeon at

the time told us the BARD is easier for younger children because they

lay flatter against the skin and also you don't have to replace them

out like a Mic-Key. It all sounded great with me...except they didn't

tell me that it couldn't lock in the tubing when she was connected to

the feeding pump. This became our biggest problem with the BARD.

Since you can't lock in your tubing, not only can you not hook your

child up to a backpack during the day (since it'll fall out at mild

twisting)...but at night my daughter rolls around and is pretty active

and it would pop out of her, spilling the contents of her tube and

stomach. I would find her soaked in her sheets the next day,

extremely upset at the loss of calories and time wasted. I finally

discovered that by putting medical tape on her stomach, taping down

the tube on the side of her stomach at night, would indeed fix the

nighttime problem...I still could not do daytime pumpings while she

was awake and upright. I visited Dr. H in December and she said we

absolutely had to get the BARD switched out, it was not doing us any

good. Sydney just had her Mic-Key put in last week and the locking

mechanism on this tube is FANTASTIC. If you have an active child and

you either know or forsee having to have a backpack running during the

daytime... I would suggest not doing the BARD. Ours was nothing but

trouble and ended up breaking a valve in it anyway...so we would have

had to have it replaced sooner or later. Granted, you may not have a

choice in the matter, if the BARD is your only option - but if you do

have the choice - I would go with the Mic-Key. I can't tell you how

frustrated I was with that BARD tube. I wish I HAD taken a picture

of it....I scrapbook and even took pictures during her stay at the

hospital...but never did think to take a picture of her tube! Wish I

had now that you ask about pictures. Sorry I can't offer one to

you. Good luck with everything!

Debbie, mom to Sydney, RSS, 17 months

>

> Does anyone have a picture or any experience with the Bard Button?

This is the only button our Dr uses. Thanks!

>

> Mom to Dasia

> 23mo RSS

>

> __________________________________________________

>

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,

This may be a stupid question but is the Bard Button made by a company called

Bard International? My sister used to work for them and if information is

needed she still has friends that work there that she can get. I know when

needed a cardiac catheter the cardiologist said something about Bard and

my sister knew what I was talking about and was starting to get me some

information.

B

and Kelli

Malcolm wrote:

Thanks for responding Debbie! This presents such a problem for me, after being

on the internet all day (and not getting my house cleaned! ), I know I

definitely want the Mic-Key, I just want this ng tube out so bad that I really

hate to wait for too much longer for this to be rescheduled. I'll email our

genetics/devel ped, maybe he can get us in somewhere quickly. He's at a major

hospital and probably has connections. I had our first one scheduled at a

different hospital. This is making me crazy!

super28chick wrote:

Hi ! I wanted to respond to your question about BARD

buttons/tubes. My daughter Sydney had one placed in July last year,

and I don't know if read my other posting today, but it was a surprise

because we thought she was getting a Mic-Key button. The surgeon at

the time told us the BARD is easier for younger children because they

lay flatter against the skin and also you don't have to replace them

out like a Mic-Key. It all sounded great with me...except they didn't

tell me that it couldn't lock in the tubing when she was connected to

the feeding pump. This became our biggest problem with the BARD.

Since you can't lock in your tubing, not only can you not hook your

child up to a backpack during the day (since it'll fall out at mild

twisting)...but at night my daughter rolls around and is pretty active

and it would pop out of her, spilling the contents of her tube and

stomach. I would find her soaked in her sheets the next day,

extremely upset at the loss of calories and time wasted. I finally

discovered that by putting medical tape on her stomach, taping down

the tube on the side of her stomach at night, would indeed fix the

nighttime problem...I still could not do daytime pumpings while she

was awake and upright. I visited Dr. H in December and she said we

absolutely had to get the BARD switched out, it was not doing us any

good. Sydney just had her Mic-Key put in last week and the locking

mechanism on this tube is FANTASTIC. If you have an active child and

you either know or forsee having to have a backpack running during the

daytime... I would suggest not doing the BARD. Ours was nothing but

trouble and ended up breaking a valve in it anyway...so we would have

had to have it replaced sooner or later. Granted, you may not have a

choice in the matter, if the BARD is your only option - but if you do

have the choice - I would go with the Mic-Key. I can't tell you how

frustrated I was with that BARD tube. I wish I HAD taken a picture

of it....I scrapbook and even took pictures during her stay at the

hospital...but never did think to take a picture of her tube! Wish I

had now that you ask about pictures. Sorry I can't offer one to

you. Good luck with everything!

Debbie, mom to Sydney, RSS, 17 months

>

> Does anyone have a picture or any experience with the Bard Button?

This is the only button our Dr uses. Thanks!

>

> Mom to Dasia

> 23mo RSS

>

> __________________________________________________

>

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You're so kind . As I was just telling Jodi, this button will not work

for us, I wish it would! Things would be so much easier. Oh well, at least it's

not an emergency, we do have the ng tube, and Dasia's getting what she needs

until we can get the right button, I just wish I had known about all this

already, before wasting this much time, waiting on this appt. I can't

understand why a hospital like Riley's wouldn't have the option of choosing

which button though. Oh well, live and learn.

Mom to Dasia

23mo RSS

Briggs wrote:

,

This may be a stupid question but is the Bard Button made by a company called

Bard International? My sister used to work for them and if information is

needed she still has friends that work there that she can get. I know when

needed a cardiac catheter the cardiologist said something about Bard and

my sister knew what I was talking about and was starting to get me some

information.

B

and Kelli

Malcolm wrote:

Thanks for responding Debbie! This presents such a problem for me, after being

on the internet all day (and not getting my house cleaned! ), I know I

definitely want the Mic-Key, I just want this ng tube out so bad that I really

hate to wait for too much longer for this to be rescheduled. I'll email our

genetics/devel ped, maybe he can get us in somewhere quickly. He's at a major

hospital and probably has connections. I had our first one scheduled at a

different hospital. This is making me crazy!

super28chick wrote:

Hi ! I wanted to respond to your question about BARD

buttons/tubes. My daughter Sydney had one placed in July last year,

and I don't know if read my other posting today, but it was a surprise

because we thought she was getting a Mic-Key button. The surgeon at

the time told us the BARD is easier for younger children because they

lay flatter against the skin and also you don't have to replace them

out like a Mic-Key. It all sounded great with me...except they didn't

tell me that it couldn't lock in the tubing when she was connected to

the feeding pump. This became our biggest problem with the BARD.

Since you can't lock in your tubing, not only can you not hook your

child up to a backpack during the day (since it'll fall out at mild

twisting)...but at night my daughter rolls around and is pretty active

and it would pop out of her, spilling the contents of her tube and

stomach. I would find her soaked in her sheets the next day,

extremely upset at the loss of calories and time wasted. I finally

discovered that by putting medical tape on her stomach, taping down

the tube on the side of her stomach at night, would indeed fix the

nighttime problem...I still could not do daytime pumpings while she

was awake and upright. I visited Dr. H in December and she said we

absolutely had to get the BARD switched out, it was not doing us any

good. Sydney just had her Mic-Key put in last week and the locking

mechanism on this tube is FANTASTIC. If you have an active child and

you either know or forsee having to have a backpack running during the

daytime... I would suggest not doing the BARD. Ours was nothing but

trouble and ended up breaking a valve in it anyway...so we would have

had to have it replaced sooner or later. Granted, you may not have a

choice in the matter, if the BARD is your only option - but if you do

have the choice - I would go with the Mic-Key. I can't tell you how

frustrated I was with that BARD tube. I wish I HAD taken a picture

of it....I scrapbook and even took pictures during her stay at the

hospital...but never did think to take a picture of her tube! Wish I

had now that you ask about pictures. Sorry I can't offer one to

you. Good luck with everything!

Debbie, mom to Sydney, RSS, 17 months

>

> Does anyone have a picture or any experience with the Bard Button?

This is the only button our Dr uses. Thanks!

>

> Mom to Dasia

> 23mo RSS

>

> __________________________________________________

>

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I know what you mean about not wanting to wait! We had to

reschedule our first surgery due to a cold Sydney got (they wouldn't

put her under anethesia with congestion)...so we had to delay it out

a few more weeks and that drove me crazy. Good luck to you - I'm

glad for you that you know what you want and know your options.

Debbie

> >

> > Does anyone have a picture or any experience with the Bard

Button?

> This is the only button our Dr uses. Thanks!

> >

> > Mom to Dasia

> > 23mo RSS

> >

> > __________________________________________________

> >

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Hi ,

had a Bard button for a very short time when he was a baby

maybe 10 or 11 years ago (he is now 12). These may be made

differently now, but if it is the same as the one had, I

wouldn't recommend this type. It is different, because it can only

be replaced by a doctor with a special hook-like instrument. I don't

want to scare you, but the one time had to get this button

changed, he screamed in pain & bled a lot, but I also think the

surgeon who did it had a terrible bedside manner & wasn't too gentle

with him. has a Mic-key button now, as do many of the kids

who have g-tubes. This one you can change yourself, and is easy to

do. It stays in the stomach by inflating a small balloon with water

through a special port. Please don't just take my advice though -

try to get as much information you can on various types of g-tubes

before you make any decisions. Good luck!

Kim C.

On Jan 12, 2006, at 5:22 PM, RSS-Support wrote:

> Does anyone have a picture or any experience with the Bard Button?

> This is the only button our Dr uses. Thanks!

>

> Mom to Dasia

> 23mo RSS

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,

Yikes - I should have read this before I posted my response to your

original question... It sounds like you have thought this out, and

the good thing is that your doctor will use an anesthetic to take the

Bard out. 's doctor did not - hence the reason he screamed in

pain. I think things will go fine for you & Dasia, and I'm sending

good thoughts your way! for the surgery.

Kim C.

On Jan 14, 2006, at 10:04 AM, RSS-Support wrote:

>

> Hi Everyone,

> I just got off the phone with the GI Dr., I've decided to keep

> our appt for Thursday. They can do the MIC-key, but not in a one

> step process like the Bard. So either I could leave surgery with

> the long tube, and go back in 8 weeks getting the MIC-key button,

> or leave surgery with the Bard button, and go back in 8 weeks and

> get the MIC-key. So I suppose I'd rather have the Bard button than

> a long tube for the 8 weeks. That would be nice to get the MIC-key

> right away like did, but oh well, this is better than

> waiting for a rescheduled appt. At least I'll still end up with

> what I want, and I'll have the experience of the Bard. And he said,

> since the Bard button can be painful to take out, he puts the kids

> under light anesthesia first. I'll let you guys know how everythong

> goes!

>

> Mom to Dasia

> 23mo 17lbs 30 1/4in

> Avery 6, Jaden 3

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