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Jo - so sorry for Bayly - he had just started to respond well with the MTX

injection and to have this happen. I always say that Mother's intuition is

always right. My Ken always thinks I am over reacting - but 99% of the time I

am right. I stopped getting upset with him though - I think it is just his

way of coping with Hunter's illness. I hope Bayly gets to feeling better soon

- and I hope your week get's better, too. Sandi Ken Hunter (7 Systemic)

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Seems our really rotten run of luck continues.

After a mysterious accident Tuesday afternoon (I was at work and

can't get a full story) my beautiful brave little Bayly boy has ended

up with a broken arm!

A Greenstick fracture just below the head of the Radius, so not a big

break, and doesn't need manipulation, but a Back Slab cast, and more

physio.

Poor little fella has been telling me it's so sore, and it is

obviously swollen (to me, not Grant apparently), and it's taken me 24

hours to get him into a doctor and X-Ray. Had to pull some strings

with the Chief of Paediatrics at the hospital. I suspected a

fracture, but Grant kept telling me there was NO fracture, and 'Bayly

was just putting it on'. Now here's my vent- Nasty flashbacks to the

onset of Bay's arthritis, as that's what Grant said then, but I kept

saying something was wrong with him. Mother's Intuition wins again.

Sadly.

I told Grant that Bayly is so brave, and doesn't complain about pain

he lives with every day. So why would he 'put it on " ???

Why do I feel like a single parent, going through this?

Jo

Bayly, 4, Extended Oligo

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Jo,

Sorry to hear about Bayly's arm. I hope it heals quickly.

(Aundrea 11 systemic jra)-

-- In , " Jo & Grant " <joking70@...> wrote:

>

> Seems our really rotten run of luck continues.

>

> After a mysterious accident Tuesday afternoon (I was at work and

> can't get a full story) my beautiful brave little Bayly boy has

ended

> up with a broken arm!

>

> A Greenstick fracture just below the head of the Radius, so not a

big

> break, and doesn't need manipulation, but a Back Slab cast, and

more

> physio.

>

> Poor little fella has been telling me it's so sore, and it is

> obviously swollen (to me, not Grant apparently), and it's taken me

24

> hours to get him into a doctor and X-Ray. Had to pull some strings

> with the Chief of Paediatrics at the hospital. I suspected a

> fracture, but Grant kept telling me there was NO fracture,

and 'Bayly

> was just putting it on'. Now here's my vent- Nasty flashbacks to

the

> onset of Bay's arthritis, as that's what Grant said then, but I

kept

> saying something was wrong with him. Mother's Intuition wins

again.

> Sadly.

>

> I told Grant that Bayly is so brave, and doesn't complain about

pain

> he lives with every day. So why would he 'put it on " ???

>

> Why do I feel like a single parent, going through this?

>

> Jo

> Bayly, 4, Extended Oligo

>

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Jo, can totally relate to the whole cast thing..bummer. Hope he heals quickly.

I'm sure it won't slow him down too much. Sending happy thoughs & hugs your

way!!

Jo & Grant <joking70@...> wrote: Seems our really rotten run of

luck continues.

After a mysterious accident Tuesday afternoon (I was at work and

can't get a full story) my beautiful brave little Bayly boy has ended

up with a broken arm!

A Greenstick fracture just below the head of the Radius, so not a big

break, and doesn't need manipulation, but a Back Slab cast, and more

physio.

Poor little fella has been telling me it's so sore, and it is

obviously swollen (to me, not Grant apparently), and it's taken me 24

hours to get him into a doctor and X-Ray. Had to pull some strings

with the Chief of Paediatrics at the hospital. I suspected a

fracture, but Grant kept telling me there was NO fracture, and 'Bayly

was just putting it on'. Now here's my vent- Nasty flashbacks to the

onset of Bay's arthritis, as that's what Grant said then, but I kept

saying something was wrong with him. Mother's Intuition wins again.

Sadly.

I told Grant that Bayly is so brave, and doesn't complain about pain

he lives with every day. So why would he 'put it on " ???

Why do I feel like a single parent, going through this?

Jo

Bayly, 4, Extended Oligo

Beth Yohnk

Happy Thoughts..Be Well

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-Jo,

I'm still playing catch up, I was sorry to read that Bayly has

broken his arm, poor little tyke. Hows he doing now with the cast?.

Is he coping ok.

How are the MTX shots going, are you getting use to it now. Its sad

really how routine it all becomes. Sticking needles into our kids

should never feel routine :o( it sucks....

hugs Helen and (9,systemic)

-- In , " Jo & Grant " <joking70@...> wrote:

>

> Seems our really rotten run of luck continues.

>

> After a mysterious accident Tuesday afternoon (I was at work and

> can't get a full story) my beautiful brave little Bayly boy has

ended

> up with a broken arm!

>

> A Greenstick fracture just below the head of the Radius, so not a

big

> break, and doesn't need manipulation, but a Back Slab cast, and

more

> physio.

>

> Poor little fella has been telling me it's so sore, and it is

> obviously swollen (to me, not Grant apparently), and it's taken me

24

> hours to get him into a doctor and X-Ray. Had to pull some strings

> with the Chief of Paediatrics at the hospital. I suspected a

> fracture, but Grant kept telling me there was NO fracture,

and 'Bayly

> was just putting it on'. Now here's my vent- Nasty flashbacks to

the

> onset of Bay's arthritis, as that's what Grant said then, but I

kept

> saying something was wrong with him. Mother's Intuition wins

again.

> Sadly.

>

> I told Grant that Bayly is so brave, and doesn't complain about

pain

> he lives with every day. So why would he 'put it on " ???

>

> Why do I feel like a single parent, going through this?

>

> Jo

> Bayly, 4, Extended Oligo

>

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  • 1 year later...
Guest guest

Big hugs! I hope that this is a brief flare or something that can be gotten under control once his doctors return. They always seem to be out of town when you need them!! That'sa good he has PT especialy with using a wheelchair because of course their's the problem of muscle contractions from not using the legs while at the same time trying not to aggrivate it. Such a paradox.

This diasease is terrible and it's hard because so many people don't understand it. Anyways, I hope things improve real soon.

Issadora

On Wed, Apr 16, 2008 at 2:04 AM, Jo & Grant <joking70@...> wrote:

Well what a day we've had. Still having, in fact (except for Grant whohas finally crashed out and trying to get some sleep before his midnightstart again).We suspect there is jaw involvement, as Bayly hasn't been able to open

his mouth fully for about two weeks, has terrible trouble chewinganything, and is talking in the funny little voice he uses when he hasarthritis pain in his neck. He's also complained of ear pain. There even

appears to be a slight swelling around the TMJ, right and left.On top of that, for the past few days on and off, Bay's been unable towalk first thing in the morning, and at night. The last 2 days, he has

barely been able to walk at all. We've narrowed the pain down to hisleft hip- a previously unaffected joint. The final give away thatsomething was really wrong, was him asking for pain medication! HeHATES the stuff, yet has even tolerated a full dose without it giving

much relief.So with our Paed Rheumy out of the country for the last couple of weeks,and Bay's paediatrician here off on medical leave himself, I managed to get Bayly into his physio and GP for urgent appointments today.

In short, a number of the physios at JHH Children's Hospital, and twoOTs, are pretty sure it's arthritis in his hip. To the point where theyrecommended a wheelchair! See, with my current back pain, I can't even

carry him great distances, and really shouldn't be lifting him. And thelooks you get when you push a child his size in a stroller! Some mightrecall that rude bloke at Westfield one day who told us Bayly was too

big to be getting pushed around in a pram (expletive deleted here forthat jerk)!Now, Bayly thinks it's a grand adventure, and we're trying desperatelyto help him think that. But I have been in or near tears for the entire

day. Grant even broke down (but don't tell him I told you). But Bay haspicked up the skill of getting himself around quite well- hey, what's afew more dents in the walls anyhow? :-)Since we've already had a pre-Enbrel discussion with the Paed Rheumy, it

may be where we're headed.We are just now back from the family doctor who has diagnosed JIA inBayly's left hip, and at least one side of the jaw. So it's off for anultrasound tomorrow, more blood tests, and probably increase the Pred at

the very least.That's 4 more joints since the car accident in November...Can I say again, I hate this bloody disease?!JoBayly, 5, extended oligo (looks like up to 12 joints, and counting!!!)

-- " Life- Like the flutter of wings... feel your hollow wings rushing... " (AFI- Silver and Cold).

my Flight in life is a metamorphosis of growth and this flutter of wings is within me awaiting to find a space to find it's flow...

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Jo,

So sorry to hear that you are having such a rough time of it and even more sorry that Bayly is in the pain and so immobile. I hope that things turn around for your quickly. It is good to know that Grant can break down with this with you. It just shows that you have his support as you go through this. I would love for Jaye's father to show sympathy and really let her know he sympathyzes with her. Instead all we get is him grumbling because I pay the medical bills rather then reducing his child support so that he could have more fun. I hope you have a better day.

Veri & Jaye 14 poly

bad news for Bayly

Well what a day we've had. Still having, in fact (except for Grant who

has finally crashed out and trying to get some sleep before his midnight

start again).

We suspect there is jaw involvement, as Bayly hasn't been able to open

his mouth fully for about two weeks, has terrible trouble chewing

anything, and is talking in the funny little voice he uses when he has

arthritis pain in his neck. He's also complained of ear pain. There even

appears to be a slight swelling around the TMJ, right and left.

On top of that, for the past few days on and off, Bay's been unable to

walk first thing in the morning, and at night. The last 2 days, he has

barely been able to walk at all. We've narrowed the pain down to his

left hip- a previously unaffected joint. The final give away that

something was really wrong, was him asking for pain medication! He

HATES the stuff, yet has even tolerated a full dose without it giving

much relief.

So with our Paed Rheumy out of the country for the last couple of weeks,

and Bay's paediatrician here off on medical leave himself, I managed to

get Bayly into his physio and GP for urgent appointments today.

In short, a number of the physios at JHH Children's Hospital, and two

OTs, are pretty sure it's arthritis in his hip. To the point where they

recommended a wheelchair! See, with my current back pain, I can't even

carry him great distances, and really shouldn't be lifting him. And the

looks you get when you push a child his size in a stroller! Some might

recall that rude bloke at Westfield one day who told us Bayly was too

big to be getting pushed around in a pram (expletive deleted here for

that jerk)!

Now, Bayly thinks it's a grand adventure, and we're trying desperately

to help him think that. But I have been in or near tears for the entire

day. Grant even broke down (but don't tell him I told you). But Bay has

picked up the skill of getting himself around quite well- hey, what's a

few more dents in the walls anyhow? :-)

Since we've already had a pre-Enbrel discussion with the Paed Rheumy, it

may be where we're headed.

We are just now back from the family doctor who has diagnosed JIA in

Bayly's left hip, and at least one side of the jaw. So it's off for an

ultrasound tomorrow, more blood tests, and probably increase the Pred at

the very least.

That's 4 more joints since the car accident in November...

Can I say again, I hate this bloody disease?!

Jo

Bayly, 5, extended oligo (looks like up to 12 joints, and counting!!!)

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This disease is horribly sad and so unfair. I'm crying for Bayly,

crying for you, it just tears my heart out that he has gone through

all of this at the tender age of 5. I just don't understand and hope

and pray that in our lifetime we will have a cure....

I am still holding onto hope for Bayly. Isabelle showed signs of hip

involvement about a year ago but then it just as mysteriously

vanished. It spread to both ankles and the other knee though at the

time and that's when we started MTX. It's a very out of control

feeling to sit by and see your child's disease progress so rapidly

for no apparent reason. It's vicious that way.

Many prayers, Hadley (Isabelle 4 yrs. JIA)

>

>

> Well what a day we've had. Still having, in fact (except for Grant

who

> has finally crashed out and trying to get some sleep before his

midnight

> start again).

>

> We suspect there is jaw involvement, as Bayly hasn't been able to

open

> his mouth fully for about two weeks, has terrible trouble chewing

> anything, and is talking in the funny little voice he uses when he

has

> arthritis pain in his neck. He's also complained of ear pain. There

even

> appears to be a slight swelling around the TMJ, right and left.

>

> On top of that, for the past few days on and off, Bay's been unable

to

> walk first thing in the morning, and at night. The last 2 days, he

has

> barely been able to walk at all. We've narrowed the pain down to his

> left hip- a previously unaffected joint. The final give away that

> something was really wrong, was him asking for pain medication! He

> HATES the stuff, yet has even tolerated a full dose without it

giving

> much relief.

>

> So with our Paed Rheumy out of the country for the last couple of

weeks,

> and Bay's paediatrician here off on medical leave himself, I

managed to

> get Bayly into his physio and GP for urgent appointments today.

>

> In short, a number of the physios at JHH Children's Hospital, and

two

> OTs, are pretty sure it's arthritis in his hip. To the point where

they

> recommended a wheelchair! See, with my current back pain, I can't

even

> carry him great distances, and really shouldn't be lifting him. And

the

> looks you get when you push a child his size in a stroller! Some

might

> recall that rude bloke at Westfield one day who told us Bayly was

too

> big to be getting pushed around in a pram (expletive deleted here

for

> that jerk)!

>

> Now, Bayly thinks it's a grand adventure, and we're trying

desperately

> to help him think that. But I have been in or near tears for the

entire

> day. Grant even broke down (but don't tell him I told you). But Bay

has

> picked up the skill of getting himself around quite well- hey,

what's a

> few more dents in the walls anyhow? :-)

>

> Since we've already had a pre-Enbrel discussion with the Paed

Rheumy, it

> may be where we're headed.

>

> We are just now back from the family doctor who has diagnosed JIA in

> Bayly's left hip, and at least one side of the jaw. So it's off

for an

> ultrasound tomorrow, more blood tests, and probably increase the

Pred at

> the very least.

>

> That's 4 more joints since the car accident in November...

>

> Can I say again, I hate this bloody disease?!

>

> Jo

>

> Bayly, 5, extended oligo (looks like up to 12 joints, and

counting!!!)

>

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