Today's the day of the bone graft/ gum repair. Feels like a long time coming; since the flurry of activity on this blog in the beginning, life has just become life and cleft stuff doesn't really feature. But I do remember thinking about the nice long break between the palate op and the one Piet Haers is about to start in about an hour from now. That's just under 8 years which has passed in approximately four and a half minutes and here we are back in the same ward of the amazing Lady Evelina hospital waiting for hopefully the last major operation of Jake's cleft journey.
The surgeon will make an inch long incisions into his left hip and borrow a bit to put into the gap he left (on purpose) back in 2009. This will fuse with the rest of the gum and give him a strong foundation for his teeth which are slowly getting straighter and straighter via the brace. I'd imagine that'll come off within the not too distant future.
It's different this time as we're perhaps a little less worried and Jake is more worried; well, he wasn't at all worried last time on account of his being nine months old and had no idea what day it was let alone that he was having major surgery. Less worried is maybe not the right expression and perhaps more experienced is how we feel compared to last time. Jake's main concern is the lack of football for six weeks after the operation and he's been typically cool about the whole thing apart from understable concerns over any pain he'll have. When he wakes up he'll have a morphine button to self medicate through the night and then should be ready to come home tomorrow tea time.
I'll post some photos later.
A blog about our son Jake, born in 2008 with a cleft lip and palate. I started it the day after the cleft was diagnosed and continue to write for people who turn up here every day after getting the same news. A cleft lip and palate is not the end of the world. Start at the first post and then read on...
Monday, 14 November 2016
Thursday, 1 September 2016
Cleft lip photos
Here's a timeline of what to expect from baby to (nearly) 8 years old.
baby
24 hrs post op
3 yrs old
5 yrs old
7 yrs old
nearly 8
baby
24 hrs post op
3 yrs old
5 yrs old
7 yrs old
nearly 8
What to do after you get 'the news'
Hi new visitors. If you're here, it's quite possibly because you just googled 'cleft lip blog'. Just like I did a little over 8 years ago. I didn't get much so I started this blog. In the first 4 or 5 years after starting the blog I had loads of emails from people who went through the same journey of discovery.
Recently I realised it's been a while since I've had any emails. Firstly I checked my settings and then my spam and still nothing. I think it's because it's difficult when you land on a page about me riding a bike in Wales to realise there's a few hundred thousand words earlier in the blog which may be more relevant to your google search!
So, if you've had a recent diagnosis of a cleft or your baby was recently born with one, here's what to do:
1. don't panic (easy for me to say I know, but trust me please)
2. believe me when I say everything is going to be fine (ditto above)
3. visit the post I wrote about receiving the news about a 'cleft lip and palate diagnosis'
4. visit the post I wrote about the 'cleft lip repair operation'
I've also seen that lots of the original photos I found on the internet are now missing from the early blog posts so I will post some more before and after photos again soon which should hopefully reassure you that your babies and children will be absolutely fine.
If you want any advice at all, please drop me an email.
Good luck
James
Recently I realised it's been a while since I've had any emails. Firstly I checked my settings and then my spam and still nothing. I think it's because it's difficult when you land on a page about me riding a bike in Wales to realise there's a few hundred thousand words earlier in the blog which may be more relevant to your google search!
So, if you've had a recent diagnosis of a cleft or your baby was recently born with one, here's what to do:
1. don't panic (easy for me to say I know, but trust me please)
2. believe me when I say everything is going to be fine (ditto above)
3. visit the post I wrote about receiving the news about a 'cleft lip and palate diagnosis'
4. visit the post I wrote about the 'cleft lip repair operation'
I've also seen that lots of the original photos I found on the internet are now missing from the early blog posts so I will post some more before and after photos again soon which should hopefully reassure you that your babies and children will be absolutely fine.
If you want any advice at all, please drop me an email.
Good luck
James
Thursday, 2 June 2016
Wales Velothon
I recently completed the Wales Velothon, an 86 mile cycle
event through the Brecon Beacons. The hills were not fun but I managed it in
just over 7 hours.
At mile 30, it started to rain, biblically, and I wanted my
mum. However I kept telling myself ‘it’s all for the kids, do it for the kids’.
Amazingly it stopped raining after about 20 minutes and everything dried off
before ‘The Tumble’, the first of two notorious climbs. It’s a 4 mile, 8%
gradient zig zag up a picturesque hill. I managed the zig but got off and
pushed half way up the zag; not as hard as cycling but still knackering!
Then it was a mixture of fast downhill, gentle downhill and
doable uphill until, Caerphilly mountain. MOUNTAIN. As I arrived I saw half the
people cycling and half pushing; considering this was the bottom of the mountain
I felt a dismount coming on and ended up pushing all the way up.
As I got to the top, I heard ‘it’s now 12kms downhill to the
finish line’ and felt a wave of euphoria. Imagine my surprise then when at the
bottom of the first descent we turned left and saw yet another bloody hill! So,
not all downhill but knowing it was nearly done and I’d actually manage it
after doubling my previous longest ride just a week before was a great feeling.
Me and my co-rider crossed the finish line with an awkward fistbump slash high
five desperately trying not to crash.
In all we raised £1500 for Great Ormond Street and my work
donated the enclosed £250 for Smile Train. Jake was born with a cleft
lip 8 years ago and the NHS did an amazing job; to think that other kids around
the world don’t get the same support is heart breaking especially when it’s
such a simple issue to fix. Anyway, I’m happy to have done this and also that
someone, somewhere will be the beneficiary.
Knackered on The Tumble |
7:02 - roughly twice as slow as the pros. Gotta start somewhere. |
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