LEOSTEAM.BLOGSPOT.COM

Team Leo

Leo is our beautiful boy, diagnosed with a rare cancer called Parameningeal Alveolar Rhabdomyosarcoma on May 7 2008, aged 3 years, 3 months. His treatment was full-on for 6 months with both chemotherapy and radiotherapy. The cancer is inoperable due to the location in and on the brain. The cure rate is 50% so all things crossed that Leo's in the right 50%. This blog is our way of tracking Leo's progress for all our family and friends plus for other parents and families going through the same.

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Team Leo | leosteam.blogspot.com Reviews

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Leo is our beautiful boy, diagnosed with a rare cancer called Parameningeal Alveolar Rhabdomyosarcoma on May 7 2008, aged 3 years, 3 months. His treatment was full-on for 6 months with both chemotherapy and radiotherapy. The cancer is inoperable due to the location in and on the brain. The cure rate is 50% so all things crossed that Leo's in the right 50%. This blog is our way of tracking Leo's progress for all our family and friends plus for other parents and families going through the same.

<META> KEYWORDS

1 team leo

2 long overdue

3 phew

4 phew again

5 no one

6 posted by

7 leos mum

8 no comments

9 eyes update

10 so the neuro

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Team Leo | leosteam.blogspot.com Reviews

https://leosteam.blogspot.com

Leo is our beautiful boy, diagnosed with a rare cancer called Parameningeal Alveolar Rhabdomyosarcoma on May 7 2008, aged 3 years, 3 months. His treatment was full-on for 6 months with both chemotherapy and radiotherapy. The cancer is inoperable due to the location in and on the brain. The cure rate is 50% so all things crossed that Leo's in the right 50%. This blog is our way of tracking Leo's progress for all our family and friends plus for other parents and families going through the same.

INTERNAL PAGES

leosteam.blogspot.com

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Team Leo: 21/03/10 - 28/03/10

http://leosteam.blogspot.com/2010_03_21_archive.html

Thursday, March 25, 2010. Saw the endocrine specialist Tuesday morning and although Leo has grown 3 cms since last June, it's not enough and his bloods as well as the lack of growth show the doctors that his growth has slowed massively. Due to the following reasons, we're likely to start growth hormone injections every night for the rest of his life;. His specialist says that a pot belly is indicative that his thyroid is fine but his growth hormone is stifled. Will ask that question next time we see the ...

2

Team Leo: Just back from Cornwall

http://leosteam.blogspot.com/2010/02/just-back-from-cornwall.html

Monday, February 22, 2010. Just back from Cornwall. Just back from a lovely family break in Cornwall - Leo loved it with all the swimming and playing on the beach at Watergate Bay. He struggled with the sun a lot despite it still being February, but his sunglasses were a constant so no complaining there! Subscribe to: Post Comments (Atom). 1 week post-op, March 2011. 1 week post-op, March 2011. One week post-op, Feb 2011. One week post-op, Feb 2011. Jan 27th 2011 - Leo is 6! Jan 27th 2011 - Leo is 6!

3

Team Leo: Eyes Update

http://leosteam.blogspot.com/2010/12/eyes-update.html

Wednesday, December 01, 2010. Leo has also fallen down the stairs at school and hurt his leg, but shook him up quite a bit. So much so, he doesn't want to go downstairs at home without someone there as he says it's too blurry. We're not sure whether he just wasn't concentrating at school or whether his perception of depth is altered due to the cataracts. Anyway, it was eczema not cancer so phew! Chest x-ray on Monday, Dec 13th with check-up with his oncologist also, followed by three more visits to hospi...

4

Team Leo: 11/04/10 - 18/04/10

http://leosteam.blogspot.com/2010_04_11_archive.html

Sunday, April 11, 2010. To say we've had little to no sleep this last two weeks is an understatement but at least we can move on - although now it's a case of working out what's going on with Leo's eye that it's like this. But it's not cancer so that's a huge, huge relief. We met a new family who have joined our family of those with childhood cancer - a lovely one child family like ours whose son, 7 year old Felix, had his left kidney out 3 weeks ago as he had a Wilms Tumour. Links to this post. Swimming...

5

Team Leo: More Disney Pics and Medical Update

http://leosteam.blogspot.com/2010/06/more-disney-pics-and-medical-update.html

Monday, June 21, 2010. More Disney Pics and Medical Update. Leo's appointment with the neuro. Endocrine people has been brought forward to tomorrow so we await their findings from the Insulin Tolerance Test of two weeks ago. He also endured 3 cannulas. Glucose via the IV to bring his blood sugar up again. Then they check his blood sugar every 5 minutes plus take samples at regular intervals - then finally he was allowed some proper food after the final blood sample. No, nor does it to me some days. Jan 2...

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Team Leo

Monday, March 28, 2011. A long overdue update - lots has been happening. Can't remember when we last 'spoke' but here's the lowdown:. Leo had the cataract in his right eye removed and replaced with an IOL. At the end of February . so far, so good! Implanted lens) does not accommodate. Also This then means he'll need bifocal glasses. So all was going well and the bit PJ. And I dreaded most after finding out the doctors may not be able to put an IOL. Eye drops . forget about it! But lo and behold, why shou...

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