I didn't blog my thoughts on Tuesday because I was too angry. Even now I'm not sure how coherent this will be.
J wasn't x-rayed. We have to wait 2 more weeks. On one level, that might seem reasonable - "our" consultant will be back by then, and the only consultant who was there this week wanted it to be our consultant who dealt with it. You see, "our" consultant (Mr M) put on the form last week that he wanted the x-rays done in cast - but that doesn't make sense. None of the others have been in cast. So we wouldn't have been able to compare like with like. So I rang last week and asked for the x-ray to be without the cast - or to have a justification of why the consultant had put "in cast". I was told by the nurse that they'd sort that out, but arrived to find it hadn't been sorted. No matter what I said/did, there was no changing the decision. It's not just 2 weeks though. I requested the x-ray 2 weeks ago - so I've been waiting 2 weeks already. And the last x-rays were October - so it's actually weeks and weeks.
One other point about the x-ray is that I was told that we might not get the result in 2 weeks time. Even more waiting.
And the nurse (she's a spinal specialist) seems to want to become the go-between between me and the consultant, so she's the one who talks to Mr M rather than me and she can relay the information. I don't want a filtered version of info. If I have questions I want to be able to ask him straight away. I'm really not happy about that turn of events.
So no x-ray this week. I am waiting on tenterhooks to see what state J's back is in. Mr M said he didn't know whether J's scoliosis is progressive. The Oxford consultant thought it is likely that it is, because otherwise it would be showing signs of improvement by now.
If it is getting worse, then we start a whole new ball game. And judging by the track record, there will be endless waiting lists etc as we go into the realms of... whatever!... growth rods? surgery?
My plan was to see what state his back was in and if necessary move heaven and earth to see re treatment in the US.
If the x-rays show the curves have remained static, then I would feel that the wait until 21 March when we have a date to start treatment in Oxford won't be sooooo bad - although that may be cancelled because they are an A&E dept. Still horrendous given that we are losing precious growing time etc. But I can't do anything about the wait and at least the curves wouldn't have got any worse.
To repeat what I've said before: the Mehta type casting should be done before 18 months to get correction. J will be 22 months by then. He's shooting up like a weed- we're losing all this precious precious time/growth.... But if I go down that path in my thoughts, I just end up despairing. This might all mean that J has a lifetime of back problems (and other problems given that it can affect life expectancy, internal organs, fertility etc etc etc). If it had been dealt with when he was very small, he might have had a perfectly straight back by now. How can you not feel angry/despairing when you think about that?????
The other things that made me incandescent were:
1) They didn't think it "relevant" to tell me about J's spina bifida. Even as I write this I can feel waves of outrage and indignation. Relevant??? How can you withhold information like that??? It's not just J who's affected by such a diagnosis! You might recall, I found a note in J's notes in December that the spina bifida had been picked up back in July. I wrote a letter to Mr M to ask about this (as well as other shortcomings with the notes in the file). I still have no response (see point 2))
[It's a side point, but one that also makes me incandescent: I still find it hard to believe that someone I know (who is qualified in a medically-related profession but saw J in a social context not a medical one) thought J had scoliosis at a few weeks old but never said anything. I will never understand that. It's a progressive condition. It can affect life expectancy. And they never said. WHY WHY WHY WHY WHY WHY WHY??????????????!!!!!!!!!!!!!!!!!! If treated at a v young age, it can be fully corrected. Why on earth would you not tell the parent? If you are wrong, then everyone is happy]
2) I still haven't got a response to my letter dated 21 December. The nurse said it may not have been opened yet!!!!! Ok -Mr M's secretary is on sick leave (long-term sick leave as she had an operation). Ok. But he does have a temp working for him. You can't get hold of consultants by phone. Or by email (not the done thing in the medical world apparently). So you have to rely on snail mail. Waiting 4 weeks seemed perfectly reasonable to the nurse I spoke to. They live in a different universe.
It's not fair on J. He deserves prompt, high-quality care.
All I can do is hope that 1) the x-ray shows the curves are still static (or by some miracle have improved???) and 2) that the Oxford casting does something to help resolve them.
I'm sorry J - all the despairing and pushing and everything just doesn't seem to get us very far. I hope that when you read this when you're older that you understand that mummy tried very hard. I sometimes wonder whether these experiences might steer you to a medical career or something else where you can have a positive influence on treatment for scoliosis. But that's just me hoping for a good outcome in some way, rather than any pressure on you!
Thursday, 26 January 2012
Tuesday, 24 January 2012
In the pink again
Initially Patrick only offered J purple, blue and red. J looked perturbed. He knew the one he wanted was missing - and when Patrick returned from the cupboard with the pink packet again, J was very clear in his choice!
Thursday, 12 January 2012
overnight thoughts
Well since I couldn't sleep, I've been googling and emailing overnight and followed up my plans with phonecalls this morning.
Oxford
The booking officer at the John Radcliffe was v patient on the phone this morning. I asked whether she could put a second appointment in just in case the first one on 21 March has to be cancelled through an emergency taking precedence. She doesn't have a rota past March for the consultants, so can't do that yet, but is happy for me to phone her again and put a second one in the diary. She seemed a little wary at first (I don't think it's the usual procedure and I guess would cause problems if everyone did it) but could see the logic. If J is cast on 21 March, then the second date is freed up and that helps others.
She received the faxed form yesterday and it did have "urgent" and "asap" written on it. Shame it wasn't sent start of December. Shame it had the wrong name on it! I have to stop kicking myself for not taking action before now. No good comes of kicking myself! The truth is that Mr N sent a letter to Mr M (copied to me) at the start of December saying that J was on the waiting list for serial casting at Oxford, but he was waiting to hear from me to actually transfer hospitals as I was mulling things over. The wording said he was on the waiting list. So I thought I had time to be sure about things before confirming the transfer. With hindsight I could have confirmed start of December and followed up then so that I knew he actually was on the list. Things would have happened much quicker - and then if I'd been unhappy I could have withdrawn him at any time. But hindsight is wonderful and useless.
We will hear back from Nuffield (Oxford) for the pre-op appointment when they see the entry in the computer system.
United States
Others who have children being treated with Mehta casting in the US said via emails overnight that Shriners (various) and Scottish Rite (Texas) are possible hospitals. There are Europeans being treated there (despite what their websites say about not accepting people from outside the US/Mexico/a few local countries).
My current plan is that I will continue to pursue the US idea until we have evidence with more x-rays about what is actually happening. If J's curves are static still, then the wait till 21 March would be more bearable. If they are getting worse then I would be pulling out all the stops to get treatment ASAP no matter what.
X-rays
I've rung the plaster room at Birmingham to see what's happening (they said yesterday they'd speak to Mr M's secretary). They have been trying to get hold of her, but she's in meetings this morning. She will ring me directly. They were asking to get me a "forced appointment" (ie you don't have an actual appointment, they just fit you in on the day you're there). I wonder how soon that can be.
The whole thing has made me v v v keen to get an x ray asap so that at least we know what's happening inside J's back.
Oxford
The booking officer at the John Radcliffe was v patient on the phone this morning. I asked whether she could put a second appointment in just in case the first one on 21 March has to be cancelled through an emergency taking precedence. She doesn't have a rota past March for the consultants, so can't do that yet, but is happy for me to phone her again and put a second one in the diary. She seemed a little wary at first (I don't think it's the usual procedure and I guess would cause problems if everyone did it) but could see the logic. If J is cast on 21 March, then the second date is freed up and that helps others.
She received the faxed form yesterday and it did have "urgent" and "asap" written on it. Shame it wasn't sent start of December. Shame it had the wrong name on it! I have to stop kicking myself for not taking action before now. No good comes of kicking myself! The truth is that Mr N sent a letter to Mr M (copied to me) at the start of December saying that J was on the waiting list for serial casting at Oxford, but he was waiting to hear from me to actually transfer hospitals as I was mulling things over. The wording said he was on the waiting list. So I thought I had time to be sure about things before confirming the transfer. With hindsight I could have confirmed start of December and followed up then so that I knew he actually was on the list. Things would have happened much quicker - and then if I'd been unhappy I could have withdrawn him at any time. But hindsight is wonderful and useless.
We will hear back from Nuffield (Oxford) for the pre-op appointment when they see the entry in the computer system.
United States
Others who have children being treated with Mehta casting in the US said via emails overnight that Shriners (various) and Scottish Rite (Texas) are possible hospitals. There are Europeans being treated there (despite what their websites say about not accepting people from outside the US/Mexico/a few local countries).
My current plan is that I will continue to pursue the US idea until we have evidence with more x-rays about what is actually happening. If J's curves are static still, then the wait till 21 March would be more bearable. If they are getting worse then I would be pulling out all the stops to get treatment ASAP no matter what.
X-rays
I've rung the plaster room at Birmingham to see what's happening (they said yesterday they'd speak to Mr M's secretary). They have been trying to get hold of her, but she's in meetings this morning. She will ring me directly. They were asking to get me a "forced appointment" (ie you don't have an actual appointment, they just fit you in on the day you're there). I wonder how soon that can be.
The whole thing has made me v v v keen to get an x ray asap so that at least we know what's happening inside J's back.
Wednesday, 11 January 2012
aaaaaaaaaaaaaaaggggggggggggghhhhhhhhhhhh
Not sure how coherent this will be.
Facing the utter madness of the NHS waiting lists. And feeling like screaming.
I contacted Oxford today just to check my letter had been received and to ask about the waiting list. We saw Mr N. on 1st December. J was meant to go on the waiting list as urgent then. His secretary (Ms A) just told me that she only filled out the form last week (6th January). Why????
Apparently Mr N is "on call" at the moment (by which I presume they mean he's doing his private work) and has not yet seen my letter, but it is in his in tray.
His secretary has requested the MRI from Birmingham Children's Hospital she said (goodness knows when and who knows when they'll send it...).
I asked about the waiting list and Mr N's secretary gave me the name and number of the John Radcliffe booking officer (Ms R).
Ms R told me:
1. They have a new computer system and are having problems putting patients on it.
2. The waiting list is 26 weeks, though urgent cases are about 8 weeks.
3. She might be able to slip J in on 21 March (as a provisional date) and took J's details.
4. Cancellations are v v v v v rare so it is most unlikely he'll get an earlier date, though she said she would let me know.
5. There are 5 consultants vying for room in the 2 operating days per week between them (Tues and Wed). There is only room for one child to be operated on on any one day (the ops last for 8 hours, so only one is scheduled).
6. They only do plaster casts on a Wed.
7. If there's an 8 hr child op on a Wed, there won't be any plaster casting that day.
8. They also are an A & E place, so they don't know what's coming in and it can be cancelled.
9. She recommended that I phone Mr N's secretary back and ask her to fax over the booking form so Ms R can see what's written on it.
So I dutifully ring Ms A back. She no longer has the form. She has sent it to Ms W at the Nuffield. She says she'll ring Ms W, but I ask for her number so I can do it myself.
I ring Ms W. She hasn't got the form, but has got his notes. After much rummaging she finds she has got the form. Mr N's secretary used J's middle name as his surname...
(I feel like headbanging the table repeatedly now).
She will fax the form to Ms R at John Radcliffe.
+++++++++++++++++++++++++++++++++++++++++++++++++++++
The bottom line is that we are in limbo at Birmingham and possibly on a waiting list for Oxford. But it's a very long waiting list and although Mr N said he'd put to cast "soon" - does that translate as "urgent" on the booking form??????
The irony is that Mr N's secretary was very clear in my first phone call with her today that it's all in hand and that it's not my role to be phoning/chasing etc.
aaaaaaaaaaaaaaaaaaggggggggggggggggggghhhhhhhhhhhh
Meanwhile we don't know whether the curves are getting worse.
I've just rung Mr M's secretary (J's current consultant) to see whether he can have an x-ray asap, but her phone's on voicemail. So I rang the plaster room and Jo kindly said she'd go over to see Mr M's secretary tomorrow and ring me back. I specifically asked for details about the next x-ray date and asked about my Dec letter as I still haven't heard back about my query regarding spina bifida and J's notes (see earlier blog). Not urgent in the grand scheme of things, but I hope I will hear back at some stage.
WHAT CAN I DO TO SPEED THINGS UP?
Mad ideas come to mind like going to the US for treatment at one of the renowned Mehta casting places (eg a Shriner hospital). But how you get in their system, how much it'd all cost, how we'd manage travel etc etc...
But would it be worth it? At least get that initial cast on J.
We don't even know if 21 March is definite. What if it's cancelled and then we're at the back of the waiting list again????????
These are the things that keep me from sleeping (May was dreadful when we were facing the Birmingham waiting list).
I hope hope hope that there's a way through this. And that the x-rays don't show deterioration in the meantime! Just 5 degrees worse and Mr N was saying about growth rods.
But proper casting could mean the curves get better - never mind fearing deterioration.
Don't know how to finish this blog. So will just end here.
Facing the utter madness of the NHS waiting lists. And feeling like screaming.
I contacted Oxford today just to check my letter had been received and to ask about the waiting list. We saw Mr N. on 1st December. J was meant to go on the waiting list as urgent then. His secretary (Ms A) just told me that she only filled out the form last week (6th January). Why????
Apparently Mr N is "on call" at the moment (by which I presume they mean he's doing his private work) and has not yet seen my letter, but it is in his in tray.
His secretary has requested the MRI from Birmingham Children's Hospital she said (goodness knows when and who knows when they'll send it...).
I asked about the waiting list and Mr N's secretary gave me the name and number of the John Radcliffe booking officer (Ms R).
Ms R told me:
1. They have a new computer system and are having problems putting patients on it.
2. The waiting list is 26 weeks, though urgent cases are about 8 weeks.
3. She might be able to slip J in on 21 March (as a provisional date) and took J's details.
4. Cancellations are v v v v v rare so it is most unlikely he'll get an earlier date, though she said she would let me know.
5. There are 5 consultants vying for room in the 2 operating days per week between them (Tues and Wed). There is only room for one child to be operated on on any one day (the ops last for 8 hours, so only one is scheduled).
6. They only do plaster casts on a Wed.
7. If there's an 8 hr child op on a Wed, there won't be any plaster casting that day.
8. They also are an A & E place, so they don't know what's coming in and it can be cancelled.
9. She recommended that I phone Mr N's secretary back and ask her to fax over the booking form so Ms R can see what's written on it.
So I dutifully ring Ms A back. She no longer has the form. She has sent it to Ms W at the Nuffield. She says she'll ring Ms W, but I ask for her number so I can do it myself.
I ring Ms W. She hasn't got the form, but has got his notes. After much rummaging she finds she has got the form. Mr N's secretary used J's middle name as his surname...
(I feel like headbanging the table repeatedly now).
She will fax the form to Ms R at John Radcliffe.
+++++++++++++++++++++++++++++++++++++++++++++++++++++
The bottom line is that we are in limbo at Birmingham and possibly on a waiting list for Oxford. But it's a very long waiting list and although Mr N said he'd put to cast "soon" - does that translate as "urgent" on the booking form??????
The irony is that Mr N's secretary was very clear in my first phone call with her today that it's all in hand and that it's not my role to be phoning/chasing etc.
aaaaaaaaaaaaaaaaaaggggggggggggggggggghhhhhhhhhhhh
Meanwhile we don't know whether the curves are getting worse.
I've just rung Mr M's secretary (J's current consultant) to see whether he can have an x-ray asap, but her phone's on voicemail. So I rang the plaster room and Jo kindly said she'd go over to see Mr M's secretary tomorrow and ring me back. I specifically asked for details about the next x-ray date and asked about my Dec letter as I still haven't heard back about my query regarding spina bifida and J's notes (see earlier blog). Not urgent in the grand scheme of things, but I hope I will hear back at some stage.
WHAT CAN I DO TO SPEED THINGS UP?
Mad ideas come to mind like going to the US for treatment at one of the renowned Mehta casting places (eg a Shriner hospital). But how you get in their system, how much it'd all cost, how we'd manage travel etc etc...
But would it be worth it? At least get that initial cast on J.
We don't even know if 21 March is definite. What if it's cancelled and then we're at the back of the waiting list again????????
These are the things that keep me from sleeping (May was dreadful when we were facing the Birmingham waiting list).
I hope hope hope that there's a way through this. And that the x-rays don't show deterioration in the meantime! Just 5 degrees worse and Mr N was saying about growth rods.
But proper casting could mean the curves get better - never mind fearing deterioration.
Don't know how to finish this blog. So will just end here.
Tuesday, 10 January 2012
Post casting "wobble"
Every time.
Every single time.
I drop you off at the nursery after we've been to the hospital and am hit by a huge wave of emotion.
I regain my balance later in the day, but it's hard to walk into work straight away.
Why?
You always get upset when I drop you off after casting and walking out when you're so upset is hard hard hard. You don't usually get upset on "normal" work days- we usually have a hug, say goodbye and then you are happy to get involved in what everyone else is doing. I guess it's partly the change in routine - you fell asleep today on the way back and were still quite groggy. Maybe you thought it was a non-nursery day you'd spend with mummy?
It's easier to ignore the impact of scoliosis on our lives day to day. But the hospital days bring it into sharp relief. Today I had to ask about x-rays. You're due your next one in February... but because I've chosen Oxford (that's another blog waiting to be written) and we're on a waiting list for there, we're in limbo at Birmingham. But we need to know whether your curves are getting worse, so we may need to have them at Birmingham anyway.
You were so good at the hospital today - just slight winces when the plasters caught you under your arms. Who wouldn't squirm with that? Lots of singing in the cafe afterwards. Happy, care-free "baaa-baaa-baaing".
(the video clip is from when you were singing in the car - though when you saw I was filming you said "no")
You chose a bright pink cast today - I've been silently daring you to go for that for weeks. Woe betide anyone who says "pink for girls". I think it's a really FUN colour :-)
Now we've had all the colours: red, blue, purple, neon pink...
You chose a fried egg to go with your sausage and mushrooms. Little choices - but big ones in some ways. New things for us.
We were walking down the corridor - you were hand-in-hand with mummy with froggy in your other hand - and a consultant walked past, all smart in his suit. He let out a little cough and you copied him. He turned round, smiling. It made us both smile too.
I don't feel I've had my fill of squishiness this time. I miss my squishy baby so much. Not something I talk about with others much. But it's there. It's a factor in all of this. I asked them to wait with the casting while I held you in just your nappy. Big hug. Big big big squishy hug.
They were all saying how much you've grown. That upsets me. All this precious growth and we're not "using" it with the new casting...
We had a lovely swim on Sunday. You were so happy in the water (each time you're more and more relaxed). You even kicked your legs, copying the other children in the class. You laughed so much when we "whizzed" round and round. It's a shame we won't be able to continue with the swims when you have your Oxford cast - just once every 3 months if we're lucky. But these few times we have managed it recently have been great.
You were so funny in the bath last night. We lined up all your friends (frogs, ducks, hippo, fish) on the side and some were knocked in and some were knocked out of the bath. You wanted to do it again and again. We both laughed at the frogs "weeing" in the potty.
So little one. Back to normal now. You're in the nursery and I'm at work. I hope you have a good day. I'll see you later.
Every single time.
I drop you off at the nursery after we've been to the hospital and am hit by a huge wave of emotion.
I regain my balance later in the day, but it's hard to walk into work straight away.
Why?
You always get upset when I drop you off after casting and walking out when you're so upset is hard hard hard. You don't usually get upset on "normal" work days- we usually have a hug, say goodbye and then you are happy to get involved in what everyone else is doing. I guess it's partly the change in routine - you fell asleep today on the way back and were still quite groggy. Maybe you thought it was a non-nursery day you'd spend with mummy?
It's easier to ignore the impact of scoliosis on our lives day to day. But the hospital days bring it into sharp relief. Today I had to ask about x-rays. You're due your next one in February... but because I've chosen Oxford (that's another blog waiting to be written) and we're on a waiting list for there, we're in limbo at Birmingham. But we need to know whether your curves are getting worse, so we may need to have them at Birmingham anyway.
You were so good at the hospital today - just slight winces when the plasters caught you under your arms. Who wouldn't squirm with that? Lots of singing in the cafe afterwards. Happy, care-free "baaa-baaa-baaing".
(the video clip is from when you were singing in the car - though when you saw I was filming you said "no")
You chose a bright pink cast today - I've been silently daring you to go for that for weeks. Woe betide anyone who says "pink for girls". I think it's a really FUN colour :-)
Now we've had all the colours: red, blue, purple, neon pink...
You chose a fried egg to go with your sausage and mushrooms. Little choices - but big ones in some ways. New things for us.
We were walking down the corridor - you were hand-in-hand with mummy with froggy in your other hand - and a consultant walked past, all smart in his suit. He let out a little cough and you copied him. He turned round, smiling. It made us both smile too.
I don't feel I've had my fill of squishiness this time. I miss my squishy baby so much. Not something I talk about with others much. But it's there. It's a factor in all of this. I asked them to wait with the casting while I held you in just your nappy. Big hug. Big big big squishy hug.
They were all saying how much you've grown. That upsets me. All this precious growth and we're not "using" it with the new casting...
We had a lovely swim on Sunday. You were so happy in the water (each time you're more and more relaxed). You even kicked your legs, copying the other children in the class. You laughed so much when we "whizzed" round and round. It's a shame we won't be able to continue with the swims when you have your Oxford cast - just once every 3 months if we're lucky. But these few times we have managed it recently have been great.
You were so funny in the bath last night. We lined up all your friends (frogs, ducks, hippo, fish) on the side and some were knocked in and some were knocked out of the bath. You wanted to do it again and again. We both laughed at the frogs "weeing" in the potty.
So little one. Back to normal now. You're in the nursery and I'm at work. I hope you have a good day. I'll see you later.
Saturday, 31 December 2011
A is for Owl
J was pressing the button on one of his toys this evening. Again and again it said "a is for apple... crunch"
He was enjoying imitating the crunching sound.
I then asked him what else begins with "a". He looked around and pointed over at the 4 plates with owls painted on them.
He's absolutely correct - "a" is for Owl.
It's our utterly illogical spelling that means it's written with an "o" instead.
How amazing that he could locate something so accurately like that!
Wednesday, 28 December 2011
Peppa Pig episode about casting!
As a reward for opening his mouth ready for teeth cleaning, J gets stickers**. Every 10 stickers, he gets a "treat". His latest treat was the Peppa Pig and Potato City DVD. It is a work of genius - very, very funny for adults and a great cast (eg Brian Blessed as Daddy Pig).
**Just as an aside, I wanted to mention that he has been putting the animal stickers in pairs on the sheet- eg with the two chameleons talking to each other, the two elephants next to each other. Yesterday, the parrot he'd chosen didn't have a "mate", so I suggested he might be friends with the tiger - and J carefully placed them so they were kissing. Ahhhhhh....
Tonight, there was a Peppa Pig episode called "Hospital". I read out the name of the episode to J and immediately he pulled at his cast straps - he instantly knew the link between the word hospital and casting***.
***Another aside (I think it's how my brain is working tonight) - I was talking about alarms ("timer" type alarms) today and J immediately walked to the hallway and showed me the smoke alarm. He's only once seen me test it and tell him it was a smoke alarm and that was a while back. What a memory!!! I am astonished at how much he understands and remembers.
Anyway - we start watching this episode and it turns out that Danny Dog has broken his leg and it's in a CAST. Great piece of reinforcing - he can hear them all saying about how it's helping mend Danny's leg. I talked about it afterwards and how the doctors are helping his back to get better with casts, and in a similar way the doctors in Peppa Pig helped Danny's leg get better with a cast. J pointed to his leg- he understood what had been going on.
I know he's taking it all in - he shows us all the time how he's completely on the ball and following what's going on.
I bet the makers of Peppa Pig didn't have infantile scoliosis in mind when making that episode, but it was good to see something so relevant to J's experiences in one of his favourite programmes.
Correction: More knowledgeable Peppa Pig fans have pointed out to me at least 2 errors in my post above. 1) It is Pedro Pony who breaks his leg
2) Brian Blessed is the voice for Grampy Rabbit
I promise to watch more closely in future!!
Tuesday, 20 December 2011
Unexpected item in J's notes!
As of this morning I now have a copy of all the notes in J's file from the Birmingham Royal Orthopaedic Hospital, plus the x-rays on a disc. They wouldn't let me have a copy of the MRI scan, only the report, as it was taken elsewhere.
I am surprised/shocked by two things:
1. The incompleteness of the file.
Although the initial referral from Mr M's private practice to the NHS hospital says that there will be a full, detailed letter, there is none in the file. The notes from the consultant we saw in July are only a couple of lines long and then it says "tape goes blank here!!".
There's no summary of the issues or findings at all. Just the referral letters and reports about the x-rays and MRI scan! Oh and lots of the "soft cast been changed today" entries.
Is this normal? I know they're very busy, but it doesn't seem right.
2. The line in one of the consultant radiologist's reports on the July x-ray mentioning suspected spina bifida.
"Appearances do suggest the presence of an underlying lumbo sacral spina bifida defect"
What the heck??? Why hasn't this been mentioned before???
Using my calm, rational side, I can only assume that the spinal deformity consultants looked at the x-rays and came to a different conclusion, so decided it would be best not to say anything.
Of course, my not-so-calm side had a field day on Dr Google... but I have to say I can't see any of the symptoms they mention on the web in my son so I don't think it's affecting him if he does have spina bifida. It's true that his "toddler gait" and stumbling/falling over may not be related to his age and could actually be evidence of an underlying problem but he looks like any of the other kids in the nursery to me.
I have composed a letter to Mr M and asked for clarification.
I've read that it's good to have a full copy of all notes and all scans/x-rays and now have most of them. I don't want to be awkward or overly pushy. My aim is to be the best possible advocate for my precious little boy. One big thing I've learnt is that you really do have to be on the ball and pro-active - and I guess being polite and well prepared are key elements too.
Fingers crossed that all is fine...
I am surprised/shocked by two things:
1. The incompleteness of the file.
Although the initial referral from Mr M's private practice to the NHS hospital says that there will be a full, detailed letter, there is none in the file. The notes from the consultant we saw in July are only a couple of lines long and then it says "tape goes blank here!!".
There's no summary of the issues or findings at all. Just the referral letters and reports about the x-rays and MRI scan! Oh and lots of the "soft cast been changed today" entries.
Is this normal? I know they're very busy, but it doesn't seem right.
2. The line in one of the consultant radiologist's reports on the July x-ray mentioning suspected spina bifida.
"Appearances do suggest the presence of an underlying lumbo sacral spina bifida defect"
What the heck??? Why hasn't this been mentioned before???
Using my calm, rational side, I can only assume that the spinal deformity consultants looked at the x-rays and came to a different conclusion, so decided it would be best not to say anything.
Of course, my not-so-calm side had a field day on Dr Google... but I have to say I can't see any of the symptoms they mention on the web in my son so I don't think it's affecting him if he does have spina bifida. It's true that his "toddler gait" and stumbling/falling over may not be related to his age and could actually be evidence of an underlying problem but he looks like any of the other kids in the nursery to me.
I have composed a letter to Mr M and asked for clarification.
I've read that it's good to have a full copy of all notes and all scans/x-rays and now have most of them. I don't want to be awkward or overly pushy. My aim is to be the best possible advocate for my precious little boy. One big thing I've learnt is that you really do have to be on the ball and pro-active - and I guess being polite and well prepared are key elements too.
Fingers crossed that all is fine...
Monday, 5 December 2011
Possible effects of general anaesthetic: neurotoxicity in children?
Mr N mentioned the possible risk of repeated general anaesthesia and neurotoxicity. Below is an article from the British Journal of Anaesthesia that sums up the current research.
If we have the serial casting at Oxford, J will have GA every 3 months from about 22 to 40 months.
The author points out problems with the different studies (eg small numbers in cohorts or changes in anaesthetic practice), but it's still a chilling read as a parent about to subject a child to repeated GA at such a vulnerable age...
Author: L. Sun
(reference: Br. J. Anaesth. (2010) 105(suppl 1): i61-i68 doi:10.1093/bja/aeq302)
Summary
A great deal of concern has recently arisen regarding the safety of anaesthesia in infants and children. There is mounting and convincing preclinical evidence in rodents and non-human primates that anaesthetics in common clinical use are neurotoxic to the developing brain in vitro and cause long-term neurobehavioural abnormalities in vivo. An estimated 6 million children (including 1.5 million infants) undergo surgery and anaesthesia each year in the USA alone, so the clinical relevance of anaesthetic neurotoxicity is an urgent matter of public health. Clinical studies that have been conducted on the long-term neurodevelopmental effects of anaesthetic agents in infants and children are retrospective analyses of existing data. Two large-scale clinical studies are currently underway to further address this issue. The PANDA study is a large-scale, multisite, ambi-directional sibling-matched cohort study in the USA. The aim of this study is to examine the neurodevelopmental effects of exposure to general anaesthesia during inguinal hernia surgery before 36 months of age. Another large-scale study is the GAS study, which will compare the neurodevelopmental outcome between two anaesthetic techniques, general sevoflurane anaesthesia and regional anaesthesia, in infants undergoing inguinal hernia repair. These study results should contribute significant information related to anaesthetic neurotoxicity in children.
Thursday, 1 December 2011
Lots to think about
It's late.
J took forever to get to sleep (2 naps during the ride there and back didn't help).
I'm extremely tired...
But I'm going to post something now just to get it out of my system before I turn in.
I picked J up at the nursery just after his lunch so that he could sleep in the car on the way to Oxford. He only managed an hour's nap (usually 1.5 hours to 2 hours) so was a little grouchy on arrival. The afternoon appointments never seem to work as well as the morning ones.
(photos - they had quite a good selection of toys with dressing up costumes, sticklebrick, dolls house, garage... all sorts)
We were very early (about 75 minutes!) so checked in and went to get a cup of tea - but were called back almost immediately. As J didn't need x-rays they said he could be seen early.
They weighed him and said he's 14 kg!!! On 7 November he weighed 12 kg wearing nappy and clothes but no shoes and no cast. Just 3.5 weeks later he's 2 kg more dressed as above but also with his cast. He has definitely put on weight - which I'm pleased about as he was 12.5 kg in August without a cast and so the half kilo drop between August and November wasn't great. He was well for a good 2 or so weeks before the next cold/cough hit him and that has clearly made a difference :-)
They also tried to measure his height, but he hates that and so it wasn't very accurate (about 84 cm - same as 3.5 weeks ago).
We were called in to see the consultant Mr N. almost immediately.
I had rung Birmingham and Oxford a few days ago to check the x-rays had been sent and received and got a very indignant reply from both ends (we sort that out, it's not something the patients or parents get involved with). But the consultant said he didn't have the x-rays... My heart sank. They hate you interfering in the processes, but we had this before when the x-rays weren't sent on. Mr N said we'd have a chat and then J could have x-rays there. Fortunately a nurse came in with the disk from Birmingham later in the conversation so J didn't need more radiation. I liked it at the end of our chat when Mr N asked me to help make sure the MRI scan and the relevant report get sent over (there wasn't a copy in the notes) - he understood that some chasing can be helpful.
We talked at length about the kind of serial casting they use. He (like Mr M in Birmingham) said that Mehta's results haven't been copied elsewhere** - and they don't call their casting Mehta casting. However, what he described was quite similar to Mehta casting.
**I've been emailing Heather Montoya, the parent who heads up the Infantile Scoliosis Outreach Programme (her daughter is now in her teens), and she said the results have been copied in the US hospitals where they do a lot of the Mehta casting and were trained by Mehta herself.
Heather wrote: "Miss Mehta was the pioneer of early Treatment (ET) and the only surgeon in the UK applying it. When she retired in 2000, the work literally died in the UK. We (ISOP) were fortunate to get her out to the U.S. multiple times after retirement and now countless children are benefitting from her dedication to progressive infantile scoliosis (PIS).
I would mention to any/all docs that J is seen by, the outstanding results children are getting in the U.S. by surgeons that were trained by Mehta and who are following her necessary ET principles. Remind them that ET is not like casting an adolescent. The goals are not the same is neither is the outcome. Remind them that Mehtas ET is harnessing the child's rapid rate of growth to train the young spine to grow straight gently, permenently and 3 dimensionally. Remind them that there is no risk of chest wall deformities if the windows are trimmed properly (widely trimmed mushroom shaped window in front, hole on the concavity side in back to help address rotation).
Please also inform them that ISOP would be willing to help them organize a hands on ET training tutorial with either Dr. Mehta herself or with the multiple pediatric orthopaedic surgeons on our Medical Advisory Board. I would also inform all of them that there are currently 45 paediatric orthopaedic surgeons applying Dr. Mehta's Early Treatment w/ specialized EDF casting here in the U.S. and experiencing the same outstanding results as Min Mehta, MD, FRCS herself... There would not be that amount if this gentle and effective treatment modality wasnt superiorly effective for infants/children with PIS."
Mr N said they have the correct EDF table which holds the head, hands and feet.
They do use windows front and back on the cast to allow for room for the lungs to develop ok.
The unit has just got approval for using magnetic growth rods in a trial. If J's curve progresses by five to ten degrees more then he would recommend using growth rods.
He said they would normally cast every 3 - 4 months (the Mehta technique says every 8 weeks for children below 2, every 12 weeks for children below 3). If it gets too tight they can split (bivalve) the cast he said.
He seemed surprised when I mentioned the timescale above (casting every 8 weeks) but I was able to give the author of the article I read it in (James Sanders is a respected orthopedic surgeon) and that helped me to not look like I'd just made it up!
He mentioned that he'd just come back from a conference in the US where they were talking about a new issue of "neurotoxicity" in younger children who have repeated General Anaesthetic. It is thought it may impinge on cerebral development. However, this is not substantiated. It does serve as a reminder that you want the minimum GA that's effective. On the ISOP message boards there have been discussions lately about how often kids are being cast and when one mother was concerned it was 9-10 weeks for her 16 month old, others said a couple of weeks extra would be ok and minor adjustments can be made if the cast gets tight.
When the x-rays did arrive, he re-measured the angles. Once again, we have new numbers. He said the top angle is 36%, the lower curve is 26% and the RVAD is 13%.
Measuring on the x-rays is not an exact science. The same x-ray was said to be 30-32 degrees at the top by Mr M. There's a 5 * margin of error.
Mrt N said he was hopeful they can control J's scoliosis with serial casting and hold it in a suitable position. He said the aim was not to treat it but control it. That is very different from the Mehta idea of growth as a corrective force. When I said this, he said that the cases where Mehta had success in correcting the curve where when they started casting very early on.
SCREAM!!!!!
It makes me mad when I hear things like that. That's what kept me from sleeping for night after night back in May/June. When you KNOW your child's condition needs action NOW, but you can't access it... it's very painful as a parent.
We had a diagnosis at 9 months, but then waited 3 months to see a non-specialist orthopaedic surgeon who referred us on. We had to go private to avoid a year-long waiting list at that point. We have now had 6 months of soft casting which doesn't seem to do very much at all (Mr N seemed very surprised at the technique - he didn't seem to think it would do anything either... I have never found anywhere at all that does the soft casting technique other than where we go...And J squirming during application can't help when trying to apply pressure!). So to be reminded of something I've known for many months - that time is of the essence in treating infantile scoliosis - is hard.
By the way, Mr N did use the W word. Yes - Waiting list! They do have a waiting list at Oxford. It's not permitted as a word in Birmingham. Mr N has put J on the waiting list - and said that he'll be marked as "soon" (I presume that means it's more urgent) and it'll be about 2 months (but we're not allowed to hold him to that).
I asked about Mr N's experience with the technique. He said he's been at Oxford 3 years and they see v few cases of infantile scoliosis - about 20 per year divided between 4 consultants. So he casts about 5 kids a year. He did some casting when he was in London before Oxford too. Not a huge amount really when you consider the doctors at Shriner's in the US who do so much.
About 50% of the cases he sees go on to growth rods, but we can't read much into that because it depends on how aggressive the scoliosis is (very individual).
All start with serial casting at the Nuffield.
If J's curve gets between 5 - 10 * worse then Mr N would recommend going to growth rods. However, Mr N said that it's really good that J is well balanced (his head is above his pelvis and his shoulders aren't lop-sided) and can walk so well. Looking at him you wouldn't know he had such a serious scoliosis. That means Mr N doesn't want to rush to insert growth rods.
He thought J would probably spend about 18 months in the casts and then go on to a plastic brace.
The problems he listed for children in these casts are: pressure sores, not tolerating the cast, itchiness, and breathing problems. If a child gets lots of breathing problems then they stop the treatment (eg chest infections).
He said it would go over J's shoulders (think American footballer) and down quite low compared with current casts, but the nappy would still be accessible.
I asked what the cast is made of and it sounded similar to Mehta - some plaster of paris and some fiberglass. When I mentioned the special undervests that I've read about (knit-rite ones that contain silver nitrate for anti-bacterial purposes) he looked at me very strangely then said "is that in the US?". It is in the US, but it makes sense to me to have something that will help the skin.Oxford use stockinet, just as we have at the mo.
I tried to ask about the risks of GA. He said they have a specialist paediatric anaesthetist who only does that. I tried to get him to quantify the risk - he looked at me as if I'm mad. You can't. They do spinal surgery all the time and so are used to using GA for kids.
I asked about how long the treatment takes and they are usually cast first thing in the morning and spend the day there - they don't usually need to stay overnight (this ties in with what ISOP parents have told me - it's only if there are complications that people stay overnight. They recommended that I take a couple of days off work for the first one, but after that, J should be able to manage with just one day for the casting and then back into the normal routine the following day).
He showed me pictures of a patient of his with growth rods. They can be lengthened by about 5cm using magnets, so the child simply comes back to clinic every few months rather than being opened up for surgery every time. They can correct the curve to some extent - although it depends on how bad the curve is. Once a curve gets to above 50* then it's beyond what can be corrected. It strikes me that the difference between 36 and 50 is not very big... in the more aggressive cases, kids' curves progress that much v quickly. That's why it's so important to keep monitoring J's curves.
My reaction:
Please bear in mind that it is now v v v late at night.
I think we will go with the more radical technique. I need to sleep on it, but it makes more sense to actually stretch and derotate etc the spine before casting. The other kids on the ISOP website all tolerate the technique and casts brilliantly. J has proved how adaptable he is already. We are late off the blocks (not our fault) but there is a lot going for this technique. I just hope these practitioners are experienced enough to make it a good investment of time and energy...
The practicalities of it all are a bit daunting. No bath/swim etc for 3 months at a time. That's a big change. I'd have to get good at sponge baths (we've been v lax in between casts mainly because 2 weeks isn't that long if you wash hands, feet, face and do thorough nappy changes).
I've been asked about the technique by others - the videos below show how it's done. I haven't actually listened to the sound on these, just watched the videos. Don't know if these are the best videos - it's too late at night to do much searching. If you google youtube and words such as infantile scoliosis and mehta casting, you get others too
clip showing Mehta casting of Haley (note the windows in the cast afterwards too)
news clip featuring Haley
news story incl clip showing the casting of Bryce
http://www.youtube.com/watch?v=rz0E3JfryoM
Just for fun - let me end on a lighter note.
You can buy cuddly toys wearing casts too :-)
J took forever to get to sleep (2 naps during the ride there and back didn't help).
I'm extremely tired...
But I'm going to post something now just to get it out of my system before I turn in.
I picked J up at the nursery just after his lunch so that he could sleep in the car on the way to Oxford. He only managed an hour's nap (usually 1.5 hours to 2 hours) so was a little grouchy on arrival. The afternoon appointments never seem to work as well as the morning ones.
(photos - they had quite a good selection of toys with dressing up costumes, sticklebrick, dolls house, garage... all sorts)
They weighed him and said he's 14 kg!!! On 7 November he weighed 12 kg wearing nappy and clothes but no shoes and no cast. Just 3.5 weeks later he's 2 kg more dressed as above but also with his cast. He has definitely put on weight - which I'm pleased about as he was 12.5 kg in August without a cast and so the half kilo drop between August and November wasn't great. He was well for a good 2 or so weeks before the next cold/cough hit him and that has clearly made a difference :-)
They also tried to measure his height, but he hates that and so it wasn't very accurate (about 84 cm - same as 3.5 weeks ago).
We were called in to see the consultant Mr N. almost immediately.
I had rung Birmingham and Oxford a few days ago to check the x-rays had been sent and received and got a very indignant reply from both ends (we sort that out, it's not something the patients or parents get involved with). But the consultant said he didn't have the x-rays... My heart sank. They hate you interfering in the processes, but we had this before when the x-rays weren't sent on. Mr N said we'd have a chat and then J could have x-rays there. Fortunately a nurse came in with the disk from Birmingham later in the conversation so J didn't need more radiation. I liked it at the end of our chat when Mr N asked me to help make sure the MRI scan and the relevant report get sent over (there wasn't a copy in the notes) - he understood that some chasing can be helpful.
We talked at length about the kind of serial casting they use. He (like Mr M in Birmingham) said that Mehta's results haven't been copied elsewhere** - and they don't call their casting Mehta casting. However, what he described was quite similar to Mehta casting.
**I've been emailing Heather Montoya, the parent who heads up the Infantile Scoliosis Outreach Programme (her daughter is now in her teens), and she said the results have been copied in the US hospitals where they do a lot of the Mehta casting and were trained by Mehta herself.
Heather wrote: "Miss Mehta was the pioneer of early Treatment (ET) and the only surgeon in the UK applying it. When she retired in 2000, the work literally died in the UK. We (ISOP) were fortunate to get her out to the U.S. multiple times after retirement and now countless children are benefitting from her dedication to progressive infantile scoliosis (PIS).
I would mention to any/all docs that J is seen by, the outstanding results children are getting in the U.S. by surgeons that were trained by Mehta and who are following her necessary ET principles. Remind them that ET is not like casting an adolescent. The goals are not the same is neither is the outcome. Remind them that Mehtas ET is harnessing the child's rapid rate of growth to train the young spine to grow straight gently, permenently and 3 dimensionally. Remind them that there is no risk of chest wall deformities if the windows are trimmed properly (widely trimmed mushroom shaped window in front, hole on the concavity side in back to help address rotation).
Please also inform them that ISOP would be willing to help them organize a hands on ET training tutorial with either Dr. Mehta herself or with the multiple pediatric orthopaedic surgeons on our Medical Advisory Board. I would also inform all of them that there are currently 45 paediatric orthopaedic surgeons applying Dr. Mehta's Early Treatment w/ specialized EDF casting here in the U.S. and experiencing the same outstanding results as Min Mehta, MD, FRCS herself... There would not be that amount if this gentle and effective treatment modality wasnt superiorly effective for infants/children with PIS."
Mr N said they have the correct EDF table which holds the head, hands and feet.
They do use windows front and back on the cast to allow for room for the lungs to develop ok.
The unit has just got approval for using magnetic growth rods in a trial. If J's curve progresses by five to ten degrees more then he would recommend using growth rods.
He said they would normally cast every 3 - 4 months (the Mehta technique says every 8 weeks for children below 2, every 12 weeks for children below 3). If it gets too tight they can split (bivalve) the cast he said.
He seemed surprised when I mentioned the timescale above (casting every 8 weeks) but I was able to give the author of the article I read it in (James Sanders is a respected orthopedic surgeon) and that helped me to not look like I'd just made it up!
He mentioned that he'd just come back from a conference in the US where they were talking about a new issue of "neurotoxicity" in younger children who have repeated General Anaesthetic. It is thought it may impinge on cerebral development. However, this is not substantiated. It does serve as a reminder that you want the minimum GA that's effective. On the ISOP message boards there have been discussions lately about how often kids are being cast and when one mother was concerned it was 9-10 weeks for her 16 month old, others said a couple of weeks extra would be ok and minor adjustments can be made if the cast gets tight.
When the x-rays did arrive, he re-measured the angles. Once again, we have new numbers. He said the top angle is 36%, the lower curve is 26% and the RVAD is 13%.
Measuring on the x-rays is not an exact science. The same x-ray was said to be 30-32 degrees at the top by Mr M. There's a 5 * margin of error.
Mrt N said he was hopeful they can control J's scoliosis with serial casting and hold it in a suitable position. He said the aim was not to treat it but control it. That is very different from the Mehta idea of growth as a corrective force. When I said this, he said that the cases where Mehta had success in correcting the curve where when they started casting very early on.
SCREAM!!!!!
It makes me mad when I hear things like that. That's what kept me from sleeping for night after night back in May/June. When you KNOW your child's condition needs action NOW, but you can't access it... it's very painful as a parent.
We had a diagnosis at 9 months, but then waited 3 months to see a non-specialist orthopaedic surgeon who referred us on. We had to go private to avoid a year-long waiting list at that point. We have now had 6 months of soft casting which doesn't seem to do very much at all (Mr N seemed very surprised at the technique - he didn't seem to think it would do anything either... I have never found anywhere at all that does the soft casting technique other than where we go...And J squirming during application can't help when trying to apply pressure!). So to be reminded of something I've known for many months - that time is of the essence in treating infantile scoliosis - is hard.
By the way, Mr N did use the W word. Yes - Waiting list! They do have a waiting list at Oxford. It's not permitted as a word in Birmingham. Mr N has put J on the waiting list - and said that he'll be marked as "soon" (I presume that means it's more urgent) and it'll be about 2 months (but we're not allowed to hold him to that).
I asked about Mr N's experience with the technique. He said he's been at Oxford 3 years and they see v few cases of infantile scoliosis - about 20 per year divided between 4 consultants. So he casts about 5 kids a year. He did some casting when he was in London before Oxford too. Not a huge amount really when you consider the doctors at Shriner's in the US who do so much.
About 50% of the cases he sees go on to growth rods, but we can't read much into that because it depends on how aggressive the scoliosis is (very individual).
All start with serial casting at the Nuffield.
If J's curve gets between 5 - 10 * worse then Mr N would recommend going to growth rods. However, Mr N said that it's really good that J is well balanced (his head is above his pelvis and his shoulders aren't lop-sided) and can walk so well. Looking at him you wouldn't know he had such a serious scoliosis. That means Mr N doesn't want to rush to insert growth rods.
He thought J would probably spend about 18 months in the casts and then go on to a plastic brace.
The problems he listed for children in these casts are: pressure sores, not tolerating the cast, itchiness, and breathing problems. If a child gets lots of breathing problems then they stop the treatment (eg chest infections).
He said it would go over J's shoulders (think American footballer) and down quite low compared with current casts, but the nappy would still be accessible.
I asked what the cast is made of and it sounded similar to Mehta - some plaster of paris and some fiberglass. When I mentioned the special undervests that I've read about (knit-rite ones that contain silver nitrate for anti-bacterial purposes) he looked at me very strangely then said "is that in the US?". It is in the US, but it makes sense to me to have something that will help the skin.Oxford use stockinet, just as we have at the mo.
I tried to ask about the risks of GA. He said they have a specialist paediatric anaesthetist who only does that. I tried to get him to quantify the risk - he looked at me as if I'm mad. You can't. They do spinal surgery all the time and so are used to using GA for kids.
I asked about how long the treatment takes and they are usually cast first thing in the morning and spend the day there - they don't usually need to stay overnight (this ties in with what ISOP parents have told me - it's only if there are complications that people stay overnight. They recommended that I take a couple of days off work for the first one, but after that, J should be able to manage with just one day for the casting and then back into the normal routine the following day).
He showed me pictures of a patient of his with growth rods. They can be lengthened by about 5cm using magnets, so the child simply comes back to clinic every few months rather than being opened up for surgery every time. They can correct the curve to some extent - although it depends on how bad the curve is. Once a curve gets to above 50* then it's beyond what can be corrected. It strikes me that the difference between 36 and 50 is not very big... in the more aggressive cases, kids' curves progress that much v quickly. That's why it's so important to keep monitoring J's curves.
My reaction:
Please bear in mind that it is now v v v late at night.
I think we will go with the more radical technique. I need to sleep on it, but it makes more sense to actually stretch and derotate etc the spine before casting. The other kids on the ISOP website all tolerate the technique and casts brilliantly. J has proved how adaptable he is already. We are late off the blocks (not our fault) but there is a lot going for this technique. I just hope these practitioners are experienced enough to make it a good investment of time and energy...
The practicalities of it all are a bit daunting. No bath/swim etc for 3 months at a time. That's a big change. I'd have to get good at sponge baths (we've been v lax in between casts mainly because 2 weeks isn't that long if you wash hands, feet, face and do thorough nappy changes).
I've been asked about the technique by others - the videos below show how it's done. I haven't actually listened to the sound on these, just watched the videos. Don't know if these are the best videos - it's too late at night to do much searching. If you google youtube and words such as infantile scoliosis and mehta casting, you get others too
clip showing Mehta casting of Haley (note the windows in the cast afterwards too)
news clip featuring Haley
news story incl clip showing the casting of Bryce
http://www.youtube.com/watch?v=rz0E3JfryoM
Just for fun - let me end on a lighter note.
You can buy cuddly toys wearing casts too :-)
Subscribe to:
Posts (Atom)