her head is spinning
so is mine.
daughter age 12 had a virus in early june, left her with dizziness, nausea (no vomiting), after a few weeks gp ran blood tests all normal...got paed appt - maybe labrynthitis?
followed up referral to ENT - lucked out on cancellation appt with top specialist in audiovestibular issues...ran tests in spinning chair; inconclusive.
back next week for final audiovestibular tests.
referred for MRI.
where now?
some good days; others - she is pale, wan, dizzy ...
Tuesday, 4 September 2012
Wednesday, 18 July 2012
Crashing in Amsterdam
Came across this nice take on Welcome to Holland. -uncommon sense
And it rang true.
Sometimes even in the SN world iulen just stands out as something quite different and so complex.
At the "ballet for special people" show (he has been going for a term) he was the only artiste to get stage fright and run loudly protesting off the stage. It was painful to watch.
His dance support worker was apologetic . He had been fine in rehearsal on the big stage. But he did type "lights scary" so maybe it was that?
The show was lovely. Small kids big kids . A duet with a teacher and a pupil . Wheelchair wheelies.
Uncommon sense also writes about a very disturbing patent lawsuit in USA regarding communication apps.
Iulen's communication app has been developed by the company who created the original software and two years ago a complete package of ultra pc plus software etc cost £2700 . Now they do an iPad package for £1000. They embracing the iPad alongside their more costly high tech eye gaze systems etc.
But the Implications of the huge comms tech companies in US cutting access to much cheaper AAC apps is huge. So many kids now getting relatively low cost easy access to a voice.
I wish maya and her friends god luck in getting their voice heard where it really matters.
irreparable damage
Sunday, 27 May 2012
this and that
lovely sunshine at parliament hill lido with girls on Saturday.
swimming under blue skies...
Sunday day out with aunt visiting sisters and kids in south london.
Ix. very happy visiting his aunts and cousins
so - lots of good stuff.
not much
(not enough?)
cleaning, tidying, sorting, organising - loads long overdue.
(can see the floor tho - everything just gets piled up in the baskets)
but then again,
which is more important on a sunny weekend?
and sleep..could have had more of that
with restless son, hay fever and hot.
but then a full night's sleep without him waking me up at least once is rare.
one day....
Tuesday, 24 April 2012
Holland, Beirut -whatever...
15 years in life with disabled child has settled down somewhat – to a predictable routine and with regular respite life is good. It is a hard slog – something that respite puts into perspective when it is marvellously easy to do this and that with the girls.
He is happy and his frustrations are minor. It is relatively straightforward to cater to his needs and wants. He is demanding like toddler – but get it right and life is smooth. Though “transition to adult services” will be the next big hurdle in terms of decisions and no doubt heartache...
But getting to know two families recently has thrust me back into the early days... remembering and reliving the unknown and the traumatic times. With a child struggling to make sense of their world and parents and professionals struggling to make sense of him. Deep in the valley of a new and scary world...Losing friends. Not fitting into the “norm”.
But gaining new ones - who understood. Gradually finding a way up to the sunny slopes above... the search to make sense of it all.
One family has a five year old with undiagnosed probably genetic disorder. He has come a long way in last two years and gives lovely smiles but when round theirs one day he very neatly reminded me of the times over the years that Ix has smeared poo - the completely oblivious look on his face “so?” and the struggle to clean up. Also the many months Ix had undiagnosed constipation and horrendous overflow – poor boy. We recently went out on a lovely day out to local farm, with Ix at respite and older siblings on the trip there were many helping hands and he seemed to really enjoy the day.
Another family, a work colleague, has a three year old with Williams syndrome, another microdeletion. She is a beautiful little girl, friendly and sweet. But not talking, yet. The unknown of where she will be on the spectrum of her syndrome.... Their search for the right therapy and coming to terms with the fact that this was “not what we signed up for”.
Welcome to Holland indeed but they sure feel like it is Beirut. Though progress recently has seen a glimpse of light thru the fog...we went with S. to a kids rock show. Ix settled with his ipad and later enjoyed the music. S was scared at first and it looked like it could be a disaster...one of those “tried but failed” opportunities...and yet... gradually, she warmed to the rhythm and at the end was dancing on the stage with the other small people. It was lovely to see.
“You are the only person apart from X who knows she has problems..”
I remember that. Colleagues asking : “how’s the baby?” “is he walking yet? Talking yet? “and finding it so hard to say “well no. He isn’t. “
“Coming out” of the disabled closet and saying yes, my son has special needs. Yes he is disabled. And no he isn’t going to get over it like your cousin’s in-laws sister’s best friend’s child who didn’t say word til they were five but now is doing PPE at Oxford.... Shocking a group of parents worried their “neurotypical” child might not get into their first choice of primary school “well it is a different ball game for me anyway, my son will be going to the special school”. “oh, yes. Moving swiftly on...”
And - finding support .
On the internet. People in UK, in America, all over.... with similar undiagnosed children.
I had so naively thought that you only had to worry about Down syndrome! After all, that was what the doctor was worried about when early scans were dubious...
These people became my friends... still are.
Then real life meet ups – people who belonged to the club.
And I turned to books. I have always read.
"What to expect the first year" quickly found its way to the charity shop. My son merited more than a slight reference to the non-typical children in the few pages in one chapter at the back of the book, surely??
Now I turned to the books with the cured-by-diet/special programme/horses/dogs: these I threw out, frustrated. I enjoyed some saccharin chick-lit biographies in a fluffy kind of way but they promised a happy ending which consisted of a cure or a non verbal child talking or other miracle. Somehow I was seeing this was not going to happen...surely the ending did not have to only mean "cured"?
I devoured Greenspan (floor time, makes sense); the out of synch child (sensory issues, makes sense);
I found a cheap copy of The Hypotonic Child which showed Ix to a t.
Special children, challenged parents – the stages of grief; makes sense...
And two biographies which didn’t seek to sugar coat or suggest my child with the right love/care/therapy would change to “normal”:
Growing Up Severely Autistic: They Call Me Gabriel by Kate Rankin told me that life would go on, and I wasn’t alone in having a child with severe and complex needs.
And Jane Gregory’s Bringing up a Challenging Child at Home: When Love is Not Enough too showed the challenges of a complex child without sugar coating. And that if decisions had to made about residential placements – well it could be for the best, for the child...
I was so thrilled to “meet” Jane online recently! http://jgregorysharingsstories.blogspot.co.uk/
Later, with an autism diagnosis I again threw out the “cure” books and leaned towards reality:
George and Sam by Charlotte Moore (the 2007 first edition - but read the 2012 version) and
Joe: The Only Boy in the World by Michael Blastland which explained theory of mind and the logical thinking of a child with autism (when you say to an autistic child look! And he looks at your pointed finger – rather than the object you pointing too –well it makes sense...) better than any text book.
oh and Expecting Adam - love this book
Above all the connections with people – in real life and online who have helped along this journey.
He is happy and his frustrations are minor. It is relatively straightforward to cater to his needs and wants. He is demanding like toddler – but get it right and life is smooth. Though “transition to adult services” will be the next big hurdle in terms of decisions and no doubt heartache...
But getting to know two families recently has thrust me back into the early days... remembering and reliving the unknown and the traumatic times. With a child struggling to make sense of their world and parents and professionals struggling to make sense of him. Deep in the valley of a new and scary world...Losing friends. Not fitting into the “norm”.
But gaining new ones - who understood. Gradually finding a way up to the sunny slopes above... the search to make sense of it all.
One family has a five year old with undiagnosed probably genetic disorder. He has come a long way in last two years and gives lovely smiles but when round theirs one day he very neatly reminded me of the times over the years that Ix has smeared poo - the completely oblivious look on his face “so?” and the struggle to clean up. Also the many months Ix had undiagnosed constipation and horrendous overflow – poor boy. We recently went out on a lovely day out to local farm, with Ix at respite and older siblings on the trip there were many helping hands and he seemed to really enjoy the day.
Another family, a work colleague, has a three year old with Williams syndrome, another microdeletion. She is a beautiful little girl, friendly and sweet. But not talking, yet. The unknown of where she will be on the spectrum of her syndrome.... Their search for the right therapy and coming to terms with the fact that this was “not what we signed up for”.
Welcome to Holland indeed but they sure feel like it is Beirut. Though progress recently has seen a glimpse of light thru the fog...we went with S. to a kids rock show. Ix settled with his ipad and later enjoyed the music. S was scared at first and it looked like it could be a disaster...one of those “tried but failed” opportunities...and yet... gradually, she warmed to the rhythm and at the end was dancing on the stage with the other small people. It was lovely to see.
“You are the only person apart from X who knows she has problems..”
I remember that. Colleagues asking : “how’s the baby?” “is he walking yet? Talking yet? “and finding it so hard to say “well no. He isn’t. “
“Coming out” of the disabled closet and saying yes, my son has special needs. Yes he is disabled. And no he isn’t going to get over it like your cousin’s in-laws sister’s best friend’s child who didn’t say word til they were five but now is doing PPE at Oxford.... Shocking a group of parents worried their “neurotypical” child might not get into their first choice of primary school “well it is a different ball game for me anyway, my son will be going to the special school”. “oh, yes. Moving swiftly on...”
And - finding support .
On the internet. People in UK, in America, all over.... with similar undiagnosed children.
I had so naively thought that you only had to worry about Down syndrome! After all, that was what the doctor was worried about when early scans were dubious...
These people became my friends... still are.
Then real life meet ups – people who belonged to the club.
And I turned to books. I have always read.
"What to expect the first year" quickly found its way to the charity shop. My son merited more than a slight reference to the non-typical children in the few pages in one chapter at the back of the book, surely??
Now I turned to the books with the cured-by-diet/special programme/horses/dogs: these I threw out, frustrated. I enjoyed some saccharin chick-lit biographies in a fluffy kind of way but they promised a happy ending which consisted of a cure or a non verbal child talking or other miracle. Somehow I was seeing this was not going to happen...surely the ending did not have to only mean "cured"?
I devoured Greenspan (floor time, makes sense); the out of synch child (sensory issues, makes sense);
I found a cheap copy of The Hypotonic Child which showed Ix to a t.
Special children, challenged parents – the stages of grief; makes sense...
And two biographies which didn’t seek to sugar coat or suggest my child with the right love/care/therapy would change to “normal”:
Growing Up Severely Autistic: They Call Me Gabriel by Kate Rankin told me that life would go on, and I wasn’t alone in having a child with severe and complex needs.
And Jane Gregory’s Bringing up a Challenging Child at Home: When Love is Not Enough too showed the challenges of a complex child without sugar coating. And that if decisions had to made about residential placements – well it could be for the best, for the child...
I was so thrilled to “meet” Jane online recently! http://jgregorysharingsstories.blogspot.co.uk/
Later, with an autism diagnosis I again threw out the “cure” books and leaned towards reality:
George and Sam by Charlotte Moore (the 2007 first edition - but read the 2012 version) and
Joe: The Only Boy in the World by Michael Blastland which explained theory of mind and the logical thinking of a child with autism (when you say to an autistic child look! And he looks at your pointed finger – rather than the object you pointing too –well it makes sense...) better than any text book.
oh and Expecting Adam - love this book
Above all the connections with people – in real life and online who have helped along this journey.
Friday, 20 April 2012
"I don't care what sex it is, as long as it's happy"
so true.
V in her blog post has said it all
I have also been known to leave people aghast by saying "and what will you do if it isnt healthy? give it back? give it up for adoption?" but in reality this could be what you have to face.... choices.
Ix. is happy. he can have a good life. on his terms. and why not?
Wednesday, 18 April 2012
how time flies
gosh.
time
goes by
kids grow...
five years ago was in an increasingly desperate situation with three small children in small flat living with someone who was self harming, anxious, depressed...building to a creschendo of a massive breakdown...
he moved away but returned to visit at xmas 2007 then refused to leave, life became hell again...
four years ago mid- April just after that year's London marathon - moved with children to safety of a rented flat.
the flat is a haven, with beautiful garden, we have had so many lovely gatherings, barbecues, trampolining, or just pottering....tho sadly not suitable size-wise so still need to sell joint-owned flat where ex is living and put equity towards something. (ex says ""wont sell despite a court order so we shall see...).
not easy reaching a point of stability and learning where to set the boundaries (definitely at the front door), something of a long and arduous journey.
today:
living with a teenage, largely happy bald- headed young person who types more and more stuff on his ipad, loves school and meeting people and is happy spending longer stints at respite. challenging and demanding at times.
leaving more time for me to spend with girls, now 12 (tween/pre-teen moods but still lovely) and nearly 10 (emotional but happy).
working. daily. cut hours to 80 per cent but spread over five days so daily grind of car to school - car to work -work -car to school to pick up from after school - home- evening chores... fab team of carers for son, holiday care for girls throws up costly solutions and tricky in long summer hols..
after many ups and downs and traumas girls see dad a few times per month usually in public places and not on their own - unsupervised contact had to be cut in late 2010 when his depression/anxiety levels were very high and manifested in scary behaviours.....son just wants to see dad (emotional/cognitive level is different to girls) so sometimes goes for dinner.
GP meeting this week (a first!) for some disclosure - "stable" "not low mood". tho the "18 months stable" didn't add up as in June last year eight months ago much trauma and anguish and more scary behavior during court hearing to get a court order to sell joint property (which not yet completed for various ongoing reasons)
however, pushing thru the financial matters (ie flat sale) may well prove a trigger for high levels of anxiety and potential problems...but we shall see.
for now anyway... a certain stability with time to ponder.
time
goes by
kids grow...
five years ago was in an increasingly desperate situation with three small children in small flat living with someone who was self harming, anxious, depressed...building to a creschendo of a massive breakdown...
he moved away but returned to visit at xmas 2007 then refused to leave, life became hell again...
four years ago mid- April just after that year's London marathon - moved with children to safety of a rented flat.
the flat is a haven, with beautiful garden, we have had so many lovely gatherings, barbecues, trampolining, or just pottering....tho sadly not suitable size-wise so still need to sell joint-owned flat where ex is living and put equity towards something. (ex says ""wont sell despite a court order so we shall see...).
not easy reaching a point of stability and learning where to set the boundaries (definitely at the front door), something of a long and arduous journey.
today:
living with a teenage, largely happy bald- headed young person who types more and more stuff on his ipad, loves school and meeting people and is happy spending longer stints at respite. challenging and demanding at times.
leaving more time for me to spend with girls, now 12 (tween/pre-teen moods but still lovely) and nearly 10 (emotional but happy).
working. daily. cut hours to 80 per cent but spread over five days so daily grind of car to school - car to work -work -car to school to pick up from after school - home- evening chores... fab team of carers for son, holiday care for girls throws up costly solutions and tricky in long summer hols..
after many ups and downs and traumas girls see dad a few times per month usually in public places and not on their own - unsupervised contact had to be cut in late 2010 when his depression/anxiety levels were very high and manifested in scary behaviours.....son just wants to see dad (emotional/cognitive level is different to girls) so sometimes goes for dinner.
GP meeting this week (a first!) for some disclosure - "stable" "not low mood". tho the "18 months stable" didn't add up as in June last year eight months ago much trauma and anguish and more scary behavior during court hearing to get a court order to sell joint property (which not yet completed for various ongoing reasons)
however, pushing thru the financial matters (ie flat sale) may well prove a trigger for high levels of anxiety and potential problems...but we shall see.
for now anyway... a certain stability with time to ponder.
Monday, 12 July 2010
summer fun...
ok so the chaotic garden won't make the magazine pages - but it's fun!
birthday for G, bbq, splashing, pool fun, summer walks with Ix...
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