2010

Home Hydrocephalus First Year 1999 2000
2001 2002 2003 2004 2005
2006 2007 2008     2009  2010
2011 2012
Special Mothers Useful Links Problems Contact Us  
You can click on any picture to view the full size photo.   If you then click on that photo again you may see it even larger.
Use your browsers "Back" button to return to the page.

 

This year Ryan has come on in leaps and bounds.  In January Ryan joined a "special" football club.   There do not seem to be any set number of children on either side and they are all of very varied ability/disability.   Jan-01.jpg (1307001 bytes)   I have the utmost respect for the people who run  it.   Trying to organize children into a football team must be hard enough but with children the like our Ryan the task must be even harder and must require a fantastic amount of patience.    Frequently you see a child just sit or lay down on the pitch in the middle of a game.   Someone checks them and they either get up and carry on playing or go and sit on the sidelines with an adult.  The children enjoy it

 In March we went on holiday to Lanzarote, it was the first time Ryan had flown.   Rebecca sat with her mum and dad and Ryan sat with us - he said he should do that because "you won't have a child and that's not fair, so I'll sit with you".

He got a bit bored in the airport (but then don't we all) and held on tight when we went through the various checks.   He did not like the metal scanning and got quite worried when his grandpa had to hand over his bottle of water - "what can we drink now".   

We did not have any idea how he would be on take off or flying.   As it was he sat there looking out of the window and when we started to move he asked "will we go any faster than this ?".   I said yes we would  "well he better be careful then" was his only comment on the speed.   He felt the bump as we took off and looked out of the window,   "we're not going any higher are we ? "   I said yes we would so that we could fly safely.   He looked out of the window again and saw the houses looking so tiny   "Oh my Lord, that's not right, that's too high.   I'm not looking out there again Granny".

He then played with his Nintendo DS until the food arrived.

Landing was fine, he held my hand and took it all in his stride.

The holiday was wonderful Debbie & I were in the pool every day with the children and everyone loved the Jacuzzi.   

I hope it did Ryan some good, I know it eased my arthritis.       

Ryan and his dad on Timanfaya      2010-03-11-032.JPG (4251380 bytes)        lz-002.JPG (4427083 bytes)

just a selection of shots of Ryan taken on holiday  lz-00018.JPG (677826 bytes)            lz-006.JPG (1309852 bytes)     

 

The summer at home passed quietly, we did the normal things that families do in the summer holidays, visiting the Maritime Museum at Falmouth                                        2010_0612MuseumMaritime0010.JPG (854672 bytes)                               2010_0612MuseumMaritime0018.JPG (1324449 bytes)

 and play parks  2010_0416Crealy-0011.JPG (856058 bytes)  and of course the beach.   

In August we took Ryan up to Bristol for the International Balloon Fiesta.  Rebecca followed two days later with their mum.            ball fest 001.JPG (4028446 bytes)                                       ball fest 084.JPG (1126059 bytes)

 

Its now September and On Wednesday 18th Ryan was rushed to the Neuro Unit at Frenchay Hospital in Bristol (2 - 3 hours away) His shunt was not working.   We all worried, he had the op and came home again.   Its amazing, brain surgery then home !   We were all very happy and relieved to have him back safe and sound.   Then the following Wednesday (22nd September) it happened again.   This time his ventricles were even larger than the previous week, he went downhill very quickly.   The neuro surgeons performed an emergency operation and he is recovering even better than before.   We are of course watching him very carefully, but he appears to be fine again now.

The rest of the year passed quietly.