Monday, 31 December 2012


Went to meet Ryan in Durham yesterday and had a couple of hours with him. He had been sedated that morning and soon fell asleep. However, he woke up and whilst not smiling gave Bob and me the next best thing, a lot of eye to eye contact. He was a bit agitated but Rachel says he settled later and has been generally OK today. Not sure when I will see him again.

Awake to finish.

Asleep to start

Thursday, 27 December 2012

With apologies for the delay (my phone has been playing up and I have only just managed to access my messages).
Rachel says that Ryan has been smiling again and has settled nicely into his new home. Apparently one smile was best for many months. 
New carers, community team  and consultant have all been met and appear to be very supportive.
I hope to see Ryan on Sunday when we, Bob and Becky will meet him at Durham (which is about half way and as far as I can drive without a break at present), where we hope he has saved a smile for us. 
PS. We had a new record viewing last week with 133 hits in one day!
Out shopping at Fenwicks in Newcastle. (I helped design their book department many years ago!) 

Tuesday, 25 December 2012


Ryan has had a good Christmas Day and has even managed to smile. He is still terribly missed by me.

Sunday, 23 December 2012

Rachel said Ryan had about five hours sleep and is reasonably well today.

Saturday, 22 December 2012

Friday, 21 December 2012

Rachel tells me that Ryan has had two Ok(ish) nights followed by two similar days - some good bits and some not so good. At least he is with his Mum who understands his needs better than anyone.

Tuesday, 18 December 2012

A good nights sleep followed by a pretty good day with no sedation needed.  He was visited by the Mayoress of Harrogate this morning, followed by a visit to a small animal sanctuary where Ryan was quite chilled out. He had a relaxing bath when we returned to Martin House and  looked the best I have seen him for a while when I left this evening. Loads of photos for me to post when they are ready.
Tomorrow is his last at Martin House for the foreseeable future and I will miss the many wonderful carers who have looked after him over the last three and a half weeks. It will also be the last time I see him for a while and I hope I can contain my emotions when he finally leaves for Northumberland.

Monday, 17 December 2012

After I left last night Ryan needed another Trachy change and further sedation. He then slept from 1 am to 7 am. Thereafter he has been unsettled again, in spite of two further bowel movements. The only real peace he seems to get at the moment is for a short period of time after sedation.
Father Christmas landed by helicopter today but Ryan was too poorly to see him. He was a bit better later when several Leeds United players called in. I put on his Arsenal shirt and he went to meet them. Hopefully, a photo tomorrow.

A moment of peace in the Sensory Room.
Another peaceful moment post sedation.


Sunday, 16 December 2012

Ryan had a very rough night and had to be sedated twice. A further sedation this afternoon was followed by another bout of  discomfort. However, he did two massive "poos" later this afternoon and was peacefully asleep when I left. Let's hope he has a good night tonight.

Saturday, 15 December 2012

Rachel was with Ryan last night and tells me that he continued to be uncomfortable until he eventually went to sleep quite late. He then slept until 6 am but is starting to get agitated again. I am going in late today and will update again tonight.
LATER. I went in at about 3 pm when Ryan started to get rather agitated and after sedation he managed an hour and a halfs sleep. He was then extremely agitated until a trachy change at about 8 pm quietened him down. He was quite calm when I left at around 10 o'clock.
As you know, all of the carers at Martin House are superb but I must mention particularly how much of a joy it was to be with Joy today. She not only looked after us both but went out of her way to ensure I understood all that was happening in the way of medication etc. Thank you Joy.
Thank you too to the management who let Ryan stay the extra two and a half weeks, whilst a care plan was put in place in Northumberland. The original plan was for just 40 hours per week but he will now receive the 24/7 attention which is now essential.
FRIDAY
After quite a good night Ryan had a horrible day. He had a temperature and was very uncomfortable  At times it was difficult to hold him and his ERT had to be aborted.

Thursday, 13 December 2012

After a pretty bad night Ryan has had a pretty bad day. I am just so thankful he is still in Martin House where we have plenty of carers to help when needed, plus the team of doctors led by the excellent Doctor Mike.
ERT tomorrow and blood tests to see if his defunct Potacath is infected. This could be my last time as helper for his treatment but it is a bonus, as I thought last week would be the last.

Wednesday, 12 December 2012

At last, a good nights sleep and until about 4 pm a good, albeit, sleepy day. He became increasingly agitated after 4 pm and remained so until I had to leave at 5.30. 
A rare good moment with "Princess" Fiona yesterday.


Tuesday, 11 December 2012

If you read yesterdays blog, the same applies to today.

Monday, 10 December 2012

A similar pattern to yesterday. He was quite relaxed and alert when he arrived in Martin House and I had a good hours cuddle with no problems. He was just a bit unsettled when I left at 8.30. 

Sunday, 9 December 2012

Rachel tells me Ryan had a rough night during his first one in Stobswood. Apparently he calmed down a bit as the day progressed. He is back to Martin House on Monday until Friday and then it's "Up North" for good.

Saturday, 8 December 2012

Not a bad night but not much sleep. When I arrived Ryan was a bit agitated and became progressively more so until, in the end, it was difficult to hold him. It turned out that his trachy was quite badly blocked and after a trachy change and some Paracetamol (in case he also had tummy pains) he settled down.I can't imagine the panic a blockage causes. It is not always apparent his discomfort is caused by this and remember, Ryan can't talk so he can't tell us! This was the fourth change this week and it looks as if it could soon be at least a daily event.
He was much better when Rachel came to take him to to his new home. With no proper care package yet in place, it is going to be a 24/7 job for her. He is booked into Martin House again next week. What happens thereafter is something I would rather not contemplate.

Friday, 7 December 2012

Asleep at 1 am and then awake before 6. An emergency trachy change could have been nasty. Two attempts to put the new one in and then, thankfully, success with the third narrow emergency trachy. It must have been traumatic for both Ryan and the three people involved. Ryan had a temperature of over 38 for the second time this week and had spells of agitation mixed with being relatively quiet whilst I was with him. It is lucky he is in Martin House this week, where skilled medical attention is never more than a few minutes away. Not a good day.

Thursday, 6 December 2012

Ryan has had a mixed time over the last two days in Martin House. As usual, he has been very well looked after by his carers and when he has been unwell, the doctors have looked at him promptly and done all they can to make him feel better.
My thanks to all concerned (and to master cook Robin and his team for the amazingly good food).



Tuesday, 4 December 2012

Tuesday
Ryan had a reasonable day in Martin House and I got a huge smile when I visited. Back tomorrow for more of the same!
Monday
My last ERT day started quite badly. It took three attempts to access a vein and the the infusion leaked into Ryan's arm. Luckily a fourth attempt was successful and treatment then proceeded without a hitch.
We then took Ryan to Martin House where he will stay until Saturday while Rachel moves into her new house in Stobswood, some 100 miles away.

Sunday, 2 December 2012

I have not seen Ryan today but Rachel tells me he had a good night and a not too bad day.
ERT tomorrow will be the last I help with and will be a sad time for me. I have attended nearly all of these since they started in 2007.
In the afternoon I will be going with Rachel to book him in to Martin House Hospice, where he will stay until next Saturday when he will leave Harrogate for good. I will of course visit him every day.

Saturday, 1 December 2012

Friday, 30 November 2012

Another day similar to the last few. Awake early, some pain, some agitation and some peaceful moments. I was lucky enough to sit with him for an hour of peace this afternoon - heaven!

The picture on the left is the front of a very large farewell card from Springwater School. We will miss them when Ryan moves up North next week.
The picture under is taken today in my hour of heaven.

Thursday, 29 November 2012

Wednesday, 28 November 2012

Again not much change. Awake at 4 am but not too bad thereafter. I saw him at around 6 pm and had a nice long cuddle but still no smile.

Tuesday, 27 November 2012

No change today, much as yesterday. 
We had a record 95 visits on Monday!

Monday, 26 November 2012

ERT day again and quite a good one for Ryan. Vein accessed first time and not too much agitation.

Sunday, 25 November 2012

Ryan's body clock is out of sync! He has been awake since 2 am. He is not too bad though, a little bit agitated but facially quite relaxed and alert. 

Saturday, 24 November 2012

Ryan eventually got to sleep at 2 am and slept right through until 2 pm today. He was just starting to get agitated again at about 5 pm and the Buccle treatment is being tried again. It is now 7 pm and thank goodness Ryan is now calm. Let's hope he has another good night - at least when he is asleep he is not in pain.

Friday, 23 November 2012

A depressing day as Ryan has been very agitated all day. All sorts of things have been tried, including "Buccle" which often works but to no avail. I wonder if he has an ulcer or if his hernia is troubling him. Whatever it is we need to eliminate these two. It would be good to find out what is causing this extreme discomfort before he leaves for Morpeth where he will be dealing with people who no nothing about him and Rachel has to start from scratch.

Thursday, 22 November 2012

Not a bad night and not a too bad day. Moving up North day is now confirmed as December 4th.

Tuesday, 20 November 2012

A bad night for Ryan. He looked quite well albeit rather fidgety when I saw him this afternoon.

Monday, 19 November 2012

After a reasonable night Ryan's ERT went rather well with no problems. He was a little unsettled at times but that was all. When Rachel returned from her latest trip to Morpeth, she was rewarded by a big smile. Only another couple of weeks or so before Ryan also leaves for Morpeth - for good.

Sunday, 18 November 2012

A better night and day for Ryan. He was just beginning to get agitated when I left and a "trachy" change was being considered. All in all much improved.

Saturday, 17 November 2012

Ryan appears a lot better today. He was a bit agitated when I arrived but nice and calm when I left.
I bought him a CD player and some ear phones and this is a picture of him using them for the first time today. He looks a real cool dude. Click on the photo to view it in a larger format.

Friday, 16 November 2012

FRIDAY
Another very uncomfortable night and day for Ryan. He saw Dr Kate this afternoon and is now on yet another antibiotic. His feed is to be given more slowly and we wait and hope for an improvement tomorrow.

Thursday, 15 November 2012

Not a very happy couple of days with Ryan's food not being properly digested, Rachel, Dr Kate and nurse Jilly have come up with a plan and I hope to see an improvement tomorrow.

Monday, 12 November 2012

Another sleepless night for Ryan but luckily, we were still able to proceed with his ERT. He was a bit drowsy to start with and became a somewhat agitated during the morning. Although he lost what we think was a troublesome tooth, he still appears to be having some discomfort from the others. His tummy is still bloated but he has passed some wind and another messy poo. Mother home this afternoon and is busy arranging her move, 100 miles away, to Morpeth.

Sunday, 11 November 2012

Just back from seeing Ryan. Most upset to see him so disturbed. His tummy is huge and full of wind which we are unable to shift, on top of this it is obvious that his teeth are still troubling him. He managed a bowel clearance just before I left and I was pleased to be able to help by holding him whilst Bob changed the ever wriggling lad. ERT tomorrow and I hope he gets a good nights sleep - he certainly needs it.

Friday, 9 November 2012

Not a bad day but not a particularly good day either. Ryan has lost his smile and we hope it will come back soon.

Thursday, 8 November 2012

Ryan went to Springwater School today and his carer, Justina, helped him make a lovely poppy. He has also had a much needed hair cut and looks really cool. He was not too bad when I called in at 4.30 and I managed a nice long cuddle with him.

Wednesday, 7 November 2012

Ryan had a bad night and was asleep when I went to see him. At least we know he is not in pain when he sleeps.

Tuesday, 6 November 2012

Not able to see Ryan today but Rachel says he is OK and fit enough for three hours at Springwater special school tomorrow.

Monday, 5 November 2012


After a good night, Ryan was rather unsettled for most of his ERT today. After receiving some Diazepam he settled down and looked quite comfortable when I left.

Sunday, 4 November 2012

Yet another unsettled day. ERT tomorrow and fingers crossed for a better day.

Friday, 2 November 2012

Yet another disturbed day for Ryan. I'm told that the treatment to a troublesome tooth should begin to benefit him tomorrow.

Thursday, 1 November 2012

Ryan visited the dentist and a bad tooth was treated. No extractions as that would be dangerous. He is still not smiling.

Wednesday, 31 October 2012

I'm Back!
Ryan has had an unsettled time whilst I have been away. This morning he was looking a bit dozy but was not too agitated - he is on Diazepam. Tomorrow we are taking him to the paediatric dentist in Leeds, when we hope he will be able to sedate Ryan and do some remedial work on his teeth.

Tuesday, 23 October 2012

Another unsettled day.
I am away for one week - in Turkey sorting out the problem with Syria!
If I get any news on Ryan I will try and let you know via the IPad.

Monday, 22 October 2012

After a disturbed nights sleep Ryan was awake for his ERT. Unfortunately, we were unable to access a vein and there will be another attempt later this week. As soon as the nurse had gone, Ryan went to sleep. He was still asleep when I left at lunch time.

Saturday, 20 October 2012

Another disappointing day. I feel that the pain killers are not strong enough and hope alternatives can be found - easier said than done with several being discounted owing to his tummy problems.

Friday, 19 October 2012

It was true good to be true yesterday, for today it was back to an unsettled day for Ryan and strictly no smiles.

Thursday, 18 October 2012

               Remarkable!   Remarkable!  Remarkable!
There is no other word to describe Ryan. Following yesterday's blog and just as I was getting depressed about him, he suddenly rediscovers his smile. Maybe the pain killers are kicking in at last but whatever it is, long may it last.
Ryan, I have said it before and I say it again, you are  one amazingly tough person.
Photo taken late last evening with Bob' phone.

Wednesday, 17 October 2012

Bad news today. Ryan had a long seizure last night and looked washed out when I saw him this morning. He often makes a remarkable recovery and I hope this is the case when I see him tomorrow.

Tuesday, 16 October 2012

MONDAY. Treatment day, which went off without a hitch. Ryan was not too bad but was still having trouble with his teeth. I hope his new prescription will contain better pain killers.

Sunday, 14 October 2012

I bought a Chewy Tubes for Ryan to chew on instead of his hands and he has not let go of it all day. Combined with the pain killing regime, this has ensured a better day for him. It was a pleasure to have a long cuddle without him wriggling about in pain. We will see what tomorrow brings.

Saturday, 13 October 2012

Ryan looks a little bit more with it today. He is receiving some pain killers and that seems to have settled him somewhat.

Friday, 12 October 2012

Off to the Paediatric Dentist today. He was very thorough and confirmed my fear that Ryan is indeed suffering with pain from his teeth. He has new teeth trying to grow and they are pushing his current teeth into his cheeks and causing considerable discomfort. He has told us to keep him on a high level of pain killers and to bring him back on November 23rd. In the meantime he will contact Ryan's doctors to see if he would tolerate an anaesthetic if that becomes necessary.

Thursday, 11 October 2012

No change today, Ryan still looks VERY poorly. Dentist tomorrow to see if there is anything obvious in his mouth which is causing the distress.

Wednesday, 10 October 2012

Ryan is still looking very sad. Apart from the now normal excessive secretions and tummy problems, he now appears to have some sort of teething troubles. He is putting his hands into his mouth almost continuously and when given a teething ring will do the same with it.

Tuesday, 9 October 2012

Ryan looks really poorly and has a sad looking face. Not good.

Monday, 8 October 2012

Ryan's ERT went well this morning. After a good nights sleep he was more alert than yesterday. His main problem today seemed to be a problem with his teeth. It's difficult to be precise when he can't tell us what the problem is.

Sunday, 7 October 2012

Saturday, 6 October 2012

I am rather concerned following my visit this afternoon. Ryan seems to be in  more discomfort than of late and he looks rather sad. His face appears to be bloated and looks a bit like it did last year in Manchester, when he was very poorly.

Friday, 5 October 2012

Ryan is going through a rough time. Most of the problem is with his tummy and it is proving difficult to give him some relief.

Monday, 1 October 2012

Just back from Ryan's ERT which was successful today. He was a bit agitated to start with but settled down and went to sleep. When he woke up he looked a lot more relaxed and even gave me a half smile. He is to receive a catchup treatment on Thursday, to make up for missing last weeks.
                I took this photo on my phone whilst he slept.

Sunday, 30 September 2012

Another good nights sleep but again a subdued Ryan today.

Saturday, 29 September 2012

After a good nights sleep Ryan has been rather subdued today.

Thursday, 27 September 2012

Wednesday, 26 September 2012

If you have the time, please read the following (edited) which sums up so well the way we feel about Ryan, who also can't eat, drink, walk or talk!

Santa Fe, N.M.
MY son, Ronan, looks at me and raises one eyebrow. His eyes are bright and focused. Ronan means “little seal” in Irish and it suits him.
I want to stop here,  my son is 18 months old and will likely die before his third birthday. Ronan was born with Tay-Sachs, a rare genetic disorder. He is slowly regressing into a vegetative state.  He’ll become paralyzed, experience seizures, lose all of his senses before he dies. There is no treatment and no cure.
How do you parent without a net, without a future, knowing that you will lose your child, bit by torturous bit?
Our parenting plans, our lists, the advice I read before Ronan’s birth make little sense now.  No matter what we do for Ronan  he will die. All the decisions that once mattered so much, don’t.
All parents want their children to prosper, to matter. We enroll our children in music class or take them to Mommy and Me swim class because we hope they will manifest some fabulous talent that will set them — and therefore us, the proud parents — apart. Traditional parenting naturally presumes a future where the child outlives the parent and ideally becomes successful, perhaps even achieves something spectacular.
But I have abandoned the future, and with it any visions of Ronan’s scoring a perfect SAT or sprinting across a stage with a Harvard diploma in his hand. We’re not waiting for Ronan to make us proud. We don’t expect future returns on our investment.
 Ronan has given us a terrible freedom from expectations, a magical world where there are no goals, no prizes to win, no outcomes to monitor, discuss, compare.
We are a very permissive household. We do our best for our kid, feed him fresh food, brush his teeth, make sure he’s clean and warm and well rested and ... healthy? Well, no. The only task here is to love, and we tell him we love him, not caring that he doesn’t understand the words. We encourage him to do what he can, though unlike us he is without ego or ambition.
Ronan won’t prosper or succeed in the way we have come to understand this term in our culture; he will never walk or say “Mama,” and I will never be a tiger mom. The mothers and fathers of terminally ill children are something else entirely. Our goals are simple and terrible: to help our children live with minimal discomfort and maximum dignity. We will not launch our children into a bright and promising future, but see them into early graves. We will prepare to lose them and then, impossibly, to live on after that gutting loss.
This requires a new ferocity, a new way of thinking, a new animal. We are dragon parents: fierce and loyal and loving as hell. Our experiences have taught us how to parent for the here and now, for the sake of parenting, for the humanity implicit in the act itself, though this runs counter to traditional wisdom and advice.
Parents who, particularly in this country, are expected to be superhuman, to raise children who outpace all their peers, don’t want to see what we see. The long truth about their children, about themselves: that none of it is forever.
I would walk through a tunnel of fire if it would save my son. I would take my chances on a stripped battlefield with a sling and a rock à la David and Goliath if it would make a difference. But it won’t. I can roar all I want about the unfairness of this ridiculous disease, but the facts remain. What I can do is protect my son from as much pain as possible, and then finally do the hardest thing of all, a thing most parents will thankfully never have to do: I will love him to the end of his life, and then I will let him go.
But today Ronan is alive and his breath smells like sweet rice. I can see my reflection in his greenish-gold eyes. I am a reflection of him and not the other way around, and this is, I believe, as it should be. This is a love story, and like all great love stories, it is a story of loss. Parenting, I’ve come to understand, is about loving my child today. Now. In fact, for any parent, anywhere, that’s all there is.

Emily Rapp is the author of “Poster Child: A Memoir,” and a professor of creative writing at the Santa Fe University of Art and Design

Tuesday, 25 September 2012

A slightly better night and day, with Ryan able to attend Springwater school for three hours.

Monday, 24 September 2012

A rather traumatic morning for Ryan. He had a seizure at 5am and was suffering from asthma like attacks as I arrived for his ERT. He was also very "snotty" from both his trachy and nose. Add to this the fact that we couldn't access a vein plus some tummy pain and you will get the picture. He did eventually fall asleep for an hour before I had to leave.

Saturday, 22 September 2012

Friday, 21 September 2012

Ryan looked good today but is still not giving me a smile.

Thursday, 20 September 2012

I picked Ryan up from Springwater special school today. He looks quite relaxed BUT still refuses to smile!
He is on a new feeding regime in an attempt to reduce the pain from excessive wind. We have also been taught to use a new tummy massage to encourage wind and reduce the need to suction the wind out via his feeding tube. So far, it seems to be working.

Sunday, 16 September 2012

Ryan is back from Alton Towers but is still not smiling, although he looks quite well.
The charity function to raise funds for Ryan was fantastic and it looks like a few thousand Pound's will be coming his way. I will post full details of the event later.

Friday, 14 September 2012

Ryan is still not quite with us. The problem is, we don't know what is wrong and he can't tell us. He is off to the MPS conference at Alton Towers and we hope seeing some of his "Hunter" friends might cheer him up.
I am off to a dinner tonight which follows a charity golf day for Ryan.

Wednesday, 12 September 2012

A quiet day today. Ryan has been to Springwater school but he is not as alert as he used to be. We hope he improves again soon.

Monday, 10 September 2012

The  good news is that Ryan received his ERT today. The not so good news is that he is still under the weather, for what reason we know not!

Sunday, 9 September 2012

Saturday, 8 September 2012

Ryan was asleep when I called at lunchtime. Apparently he had a good morning.

Thursday, 6 September 2012

Just caught Ryan as he was off to the wonderful Springwater school for a couple of hours. He looked quite relaxed and gave me a three quarter smile.
From next week he will be going to Springwater three times a week for three hours each time. I hope he stays fit enough to do this as he always seems happier once he has been there. If staff are available, he will also get an one hour visit on Fridays.
http://www.springwater.n-yorks.sch.uk/

Wednesday, 5 September 2012

After a good night Ryan looked quite relaxed this afternoon and even managed a small smile for me. A change to his feed and antibiotics is being introduced in an attempt to minimise his pain from excessive wind.

Monday, 3 September 2012




Ryan with Bex at rhe Donkey Sanctuary open day.
  
At last! Paula accessed a vein first time and his Enzyme Replacement Therapy continued without any problems. Ryan had a reasonable nights sleep and looked fairly relaxed. I got half a smile to match the half I got last time I saw him.
It looks as if ASGNSS, who fund ERT, are to be disbanded, which leaves the future of Ryan's treatment in the balance. Whilst ERT  is not a cure, it prevents progression of the disease where there is no central nervous system involvement. So, it's letters to our MP, David Cameron and anyone else we think can help.

Saturday, 1 September 2012

It was the donkey sanctuary open day today and that is where we took Ryan. Unfortunately he was not really in the mood for the trip. He had a bad night and he looked worn out today. Let's hope I have better news tomorrow.

Thursday, 30 August 2012

A quiet day for Ryan. He looks quite relaxed but smiles are rare today.

Tuesday, 28 August 2012

A disappointing day! After a good nights sleep we were once again unable to access a vein for Ryan's Enzyme Replacement Therapy. I wonder what affect it will have on him; he has not been very happy since missing the last treatment but this could be a coincidence.

Sunday, 26 August 2012

Sarah, Michelle and I took Ryan out on his power assisted tricycle today so that his legs got some exercise. We had a bit of a scare when he had some breathing problems but with the help of his inhaler and some oxygen, we were able to get him back on track. Still no smiles but he does look quite relaxed albeit still windy and "snotty".

Saturday, 25 August 2012

Not such a good day with Ryan starting it with a seizure. He was OK this afternoon but not in a smiley mood and I can't say I blame him!

Thursday, 23 August 2012

Ryan on the trampoline with Justina today. He loved it.
(Justina did all the bouncing for Ryan)

Wednesday, 22 August 2012

Relaxing with the new puppy.
At the Donkey Sanctuary yesterday.

Tuesday, 21 August 2012

Another day at the donkey sanctuary for Ryan. He was not so smiley this time but still appeared to enjoy it.

Sunday, 19 August 2012

After a good nights sleep, Ryan looked good today. If it were not for an excess of wind and secretions, it would have been perfect.

Friday, 17 August 2012

I thought you might like to see this video Rebecca made. I hope it works on your computer!
After a good nights sleep Ryan has had a very good day. This morning we took him to the donkey sanctuary to ride a donkey. He normally looks quite disinterested but today he really seemed to enjoy it; he even did some trotting!  Then, this afternoon, he did some baking with Rebecca and princess Fiona.


                                                   Getting ready to ride.

Thursday, 16 August 2012

Ryan looked good today. Rebecca was making a short film with him in it. I hope to get it on the blog soon.

Wednesday, 15 August 2012

Ryan looked relaxed when I visited today and gave me the most enormous smile. It made my day.

Sunday, 12 August 2012

SUNDAY. Ryan had a good day today and looked relaxed and happy when we visited this evening.

Saturday, 11 August 2012

Just back from Ryan's. He looked very relaxed. He has been into town today and Princess Fiona has been doing some painting with him. He appears to enjoy putting his hands in the paint to actually painting a picture. A good day.


Top. Ryan greeting Sarah.                     Left. A selection of paintings done with the help of carers Fiona and Michelle

Friday, 10 August 2012

Ryan has had a couple of OK days and was very smiley this afternoon. He has had two seizures since the last entry, which is a bit worrying.

Tuesday, 7 August 2012

Ryan had a good Sunday night but another "snotty" Monday night. No smile today when I saw him but he was suffering with a lot of wind. His antibiotic is being changed and enemas twice a day is what is being trialed in an effort to sort the wind problem out. Physically he is doing really well. He can now sit up straight without help.

Sunday, 5 August 2012

After a good nights sleep, Ryan looked really good, albeit a bit uncomfortable, when I saw him this evening. He is suffering from an inordinate amount of wind and we we need to try and find out why.
Saturday. Ryan is full of wind and very "snotty" today. He woke up at 3am and did not  sleep thereafter!

Thursday, 2 August 2012

Another steady day for Ryan. A fantastic smile when I saw him at lunch time. He was out in his buggy again today and the fresh air seems to be agreeing with him.

Wednesday, 1 August 2012

A good night and a good day so, nothing to report!

Tuesday, 31 July 2012

Ryan had an uneventful ERT session yesterday followed by a tricycle and buggy ride. He had a reasonable night and is looking good today. He did have a quite scary coughing fit but recovered after treatment and was soon smiling again. What a strong and brave lad he is.
Ryan with Becky's new dog - Mia

Sunday, 29 July 2012

Ryan is just back from a "walk" and gave us the longest smile ever. He looks really relaxed and happy. ERT in the morning and let's hope this relaxed, happy mode continues. Becky took a photo and I hope to put on the blog in the next day or two.

Saturday, 28 July 2012

Ryan has broken the 2012 record for the most consecutive good nights sleep! He was taken for a long "walk" in his buggy by Michelle and gave me a nice smile when I called in at about five.

Friday, 27 July 2012

Yet another good night's sleep and Ryan looks really alert today. Super carer/nurse Paula was treading a book to him when we called and his eye contact was great. Paula took him out in his buggy today and bought  a European lottery ticket. She says she is going to elope with Ryan when the ticket wins a million! A good day.

Thursday, 26 July 2012

Ryan has now had three good nights sleep; almost unheard of these last few months. It may be a coincidence but these follow three days when he has been taken out, either in his buggy or on his tricycle. ( He doesn't pedal on his tricycle. His feet are strapped to the pedals so he gets plenty of leg movement which he otherwise doesn't!). Let's hope the better weather continues so he can get out more often.

Monday, 23 July 2012

Although he had a seizure last night, Ryan was quite alert for his ERT today. Nurse Paula managed to access a vein in record time and everything went smoothly. This afternoon his carer, Dave, took him out on his tricycle and then for a stroll in his buggy. A good day.

Sunday, 22 July 2012

                                            Ryan yesterday - as promised!

Saturday, 21 July 2012

A restless night for Ryan (and Bob) has been followed by a good day. Carer Michelle and I took him out on his tricycle this afternoon. We were out for an hour and a quarter and Ryan looked quite relaxed and with it. When we got back he thanked us with the most enormous smile - it made my day. When I can get the photo from my phone to my computer, I will post it on this blog.

Friday, 20 July 2012

I've come back to find Ryan looking quite relaxed albeit with a lot of secretions and wind. Apparently he had a great day at Springwater school yesterday. He appeared to really enjoy the children singing and dancing. What a pity they have now broken up for the summer.
                             Ryan looking very grown up at Springwater school yesterday.

Tuesday, 17 July 2012

Not a bad night and a few smiles this morning. As I write this Ryan is at Springwater School for a two hour session. The fact that he can go is something we would never have imagined a year ago! I am away for two days so the next Blog will be on Friday.

Monday, 16 July 2012

ERT day and almost a repeat of last week. Ryan was awake for the beginning and then slept through the rest of his treatment. Springwater came for an hour to play with him this afternoon and he has been OK since.

Sunday, 15 July 2012

After a good night Ryan had a mixed day. He was lethargic again early on but looked a lot better later this evening. He had loads of wind and needed plenty of suctioning to get rid of it.

Friday, 13 July 2012

Wednesday, 11 July 2012

At last Ryan had a good night's sleep (and half the morning too!). He looked relaxed this afternoon and was being really well looked after by his new super nurse, Paula.

Tuesday, 10 July 2012

Just back from seeing Ryan. He was looking really good and I took this photo of him.

Monday, 9 July 2012

MONDAY. Enzyme Replacement Therapy day and Ryan is awake when I arrive after another restless night (that's for Ryan, not me!). His vein is accessed first time and treatment begins. Ryan then decides to go to sleep and wakes up some three plus hours later, just in time to see the end of his treatment. He does appear to be getting his night and days mixed up.

Sunday, 8 July 2012

Just back from seeing Ryan. Apparently he only slept for one hour last night but you would never have guessed it by looking at him. He was alert and apart from being rather "snotty", was looking good. No carer tonight so I hope he sleeps well for Bob. ERT in the morning.

Saturday, 7 July 2012

Ryan looks really well this evening. Still plenty of secretions and wind but his face was stress free.

Friday, 6 July 2012

Just when you think things are getting bad - I visited Ryan this evening to be greeted by the biggest smile in ages. Apart from non stop secretions, he looked relaxed and very "with it". A good day.

Thursday, 5 July 2012

Ryan had a reasonable night but was asleep when I saw him this morning. He looked stress free though. Yesterday his carers, Paula and Michelle, took him to the library and he has now joined. This means his carers will now be able to read  to him and take away his dependence on TV. A positive move which, allied to Springwater School's involvement, should make life more interesting for him.

Wednesday, 4 July 2012

Ryan is not at his best today as he is suffering from excessive wind and secretions. So, no smile for me this morning!
Afternoon. Just to complete the day, Ryan had a seizure  and Rachel took him to the hospital for a check up. Nothing unexpected yet found.

Monday, 2 July 2012

Ryan had a a disturbed night and was not looking too happy when Rachel went to collect him from Martin House today. The good news is that he is now at home and looking quite relaxed.
He is scheduled to to have two days times two hours a week at Springwater school plus three days times one hour at home. This is excellent news as he seems much happier after these sessions.

Saturday, 30 June 2012

We are now at Martin House and Ryan, whilst not on top form, is quite comfortable and we are all (Becky is here) being very well looked after. There was a bit  of a scare last night when Ryan pulled his Gastro Button out but it was quickly spotted and a new one inserted.

Wednesday, 27 June 2012

I have been away for a few days but keeping up-to-date with Ryan. He has had one or two bad nights with his secretions. Today he went to Manchester for a checkup and the message I get is that he is better than expected!
I will get full details tomorrow. On Friday I am off to Martin House Hospice for a few days with Ryan so that Mum and Dad have a break.

Sunday, 24 June 2012

Just back from seeing Ryan who, after a bad night, was on top form; no doubt helped by the fact that another of his favourite carers (Justina) was back from her holiday in Poland.

Friday, 22 June 2012

Another goodish day with a nice smile when I saw him this afternoon. He "helped" to make a cake today and I am sure the extra attention he is getting is helping him.

Thursday, 21 June 2012

Today Ryan was visited by Rozanne from The Green Hut, where he spent many happy hours as a pre school toddler.

Wednesday, 20 June 2012

A lovely picture of Ryan and Rebecca. I was sitting with him and asked Rebecca to keep an eye on him when I left the room. This is what I found when I came back.

Sunday, 17 June 2012

SATURDAY. After a good night's sleep Ryan proceeded to sleep for most of the day. He woke up at about 3.30 and was nice and relaxed when I visited at about 4.00. This is reflected in the photo I took of him with one of his excellent carers, Princess Fiona.

Friday, 15 June 2012

Although not sleeping at night particularly well, Ryan has been very smiley and appears quite relaxed most of the time. His secretions are still frequent and he also  suffers from excessive wind. The picture below shows him with his Springwater teacher. He seems to have got a new lease of life since she started.
I thought you might also like to see how Rebecca has grown since she started at the Grammer School. Cick on the photos to enlarge them.

Monday, 11 June 2012

Ryan had rather a bad seizure yesterday and was very sleepy whilst having his ERT today. However, he still managed a smile when he woke up.

Friday, 8 June 2012

A good day today. Ryan had some physiotherapy and arrangements were made to try and get him back to Springwater special school, where he used to be so happy. Just for a short time at first and then take one day at a time. WE WOULD NEVER HAVE THOUGHT THIS POSSIBLE A YEAR AGO

Wednesday, 6 June 2012

Ryan was looking good when I arrived for his treatment this morning. Nurse Paula accessed a vein without any trouble and off we went. Towards the end his temperature went up to over 28, as it has on other occasions recently. Paula reduced the speed of the infusion and when I left at the end of his treatment, Ryan was looking and feeling cooler and quite relaxed.

Monday, 4 June 2012

A reasonable night but Ryan was not really with it this morning.

Saturday, 2 June 2012

After a couple of good days, Ryan had a disturbed night and has been sleepy for most of the day. He was awake and alert late this afternoon but smiles were hard to come by. This picture was taken on Thursday and shows Ryan, with his new England coat, looking quite like he used to pre Manchester.

Thursday, 31 May 2012

A good day today with plenty of smiles to send his visitors from Ireland back home feeling happy. Ryan is now receiving an hours "schooling" each day at home. It is provided by those wonderful people from Springwater school, who have kept in constant contact over the many, many months since he last went to school. 
This was Ryan yesterday when his teacher got him ready for the Jubilee celebrations.

Wednesday, 30 May 2012

An exciting day for Ryan with visitors from Ireland and Ware coming to see him. He was not in a smiley mood but he looked relaxed and there was plenty of eye contact. The picture below shows him in 2006 with his beloved Laura and the one above today with her having just qualified as a Doctor. We (and Ryan) are all so proud of her.


Monday, 28 May 2012

A different day today with plenty of smiles. The treatment went well. There was a bit of a problem when his temperature hit 28 but slowing down the ERT flow seemed to help.

Friday, 25 May 2012

After his two not-so-good days, Ryan has had two good nights followed by two good days. This follows a slight change to his medication.

Wednesday, 23 May 2012

Not so good for Ryan over the last two days. Lack of sleep and a lot of diarrhoea. I just popped in to see him at lunch time and Fiona was about to take him out in his wheel chair, this in the hope it would wake him up. I then had a magical moment - I gave him a kiss on the cheek, he slowly opened his eyes, gazed into mine, and gave me a really big smile. He then went back to sleep.

Monday, 21 May 2012

This was Ryan this morning awaiting his Enzyme Replacement Therapy. He was like this for most of the morning. It was particularly unexpected as he had not had a good night. We had trouble getting a receptive vein but once we did everything went well. 

Saturday, 19 May 2012

                              Ryan watching Shrek yesterday.

Friday, 18 May 2012

Another fit this morning but Ryan was looking relaxed at lunchtime when I popped in and even managed half a smile.

Thursday, 17 May 2012

A quiet couple of days. Ryan had a fit yesterday but managed to receive is ERT.

Monday, 14 May 2012

14.00 Hours. Back from my nursing assistant duties where I found a smiley Ryan. Unfortunately, we were unable to access a vein successfully, so he has not had his ERT. Now scheduled for Wednesday.
At our normal Sunday family meal last night, Ryan was so relaxed and full of smiles. He looked as good as he has for a long time. This in spite of having had problems with a bloated tummy.
Every time we tried to take a photograph of him in this relaxed and happy mode. He stopped smiling. So, I regret, no photograph for you to look at.

Friday, 11 May 2012

I'M BACK!
Ryan has had a mixed time whilst I have been away. I'm told that this week has been a smiley one though and I was graced with a few when I went to see him this afternoon. We bought a Ronaldo tee shirt for him on holiday and I will try and get a photo to post next week.

Thursday, 26 April 2012

A good night last night and still rather sleepy during the day.
I am off on holiday for two weeks and am not sure if I will be able to keep this blog up-to-date whilst I am away. So, do not panic if there are no entries!

Tuesday, 24 April 2012

Not a good night but a better day with quite a few very welcome smiles. Ryan continues to amaze us. He is pictured on his birthday with Aunty Sarah and a singing duck!

Monday, 23 April 2012

                                   Rebecca reading from RYAN'S 13th Birthday cards
Where to start! Sunday was Ryan's birthday and the day he became a teenager. He was awake for all but 40minutes on Saturday night and on Sunday morning he finished up in hospital with, what was eventually diagnosed as, a perforated ear drum. So, another course of antibiotics - something which is virtually the norm for him. God knows what pain he was experiencing and how frustrating it must be not to be able to tell people what and where it is.
On his return from hospital he stayed awake for the rest of the day and Rebecca read from the many cards he received. Eventually he went to sleep and had a good nights rest at last. Today he received his ERT treatment. He gave us a smile at the beginning and then slept through the rest of it. He was awake when I left at one  and I hope he has a good rest of the day.

Friday, 20 April 2012

Not a very good day which, after a not too bad night, started with a fit. When I visited at lunch time, Ryan was awake but suffering some discomfort from we know not what.  However, he did manage to give Rachel a little smile.

Wednesday, 18 April 2012

A quiet couple of days for Ryan. No better but no worse.

Monday, 16 April 2012


Ryan had a fit on Friday night and was unable to go for a donkey ride on Saturday. He was OK Saturday night but had little sleep last night. Remarkably, he was alert and gave us some good smiles during his ERT this morning.

This a picture of Ryan on a donkey last November.

Friday, 13 April 2012

Ryan continues to be a bit unsettled and needs additional medication to ensure some sleep at night. He does not look particularly happy at the moment. We are changing his antibiotic medication in the hope that this will help.

Monday, 9 April 2012

Whilst Ryan is not having bouts of extreme pain, he does not appear to be comfortable (most of the time) and smiles are hard to come by.

Friday, 6 April 2012

At last, a really good nights sleep and he didn't wake up until 11.30!

Thursday, 5 April 2012

Not particularly happy but at least Ryan had a good night's sleep.

Wednesday, 4 April 2012

Sunday, 1 April 2012

Two nights with no sleep for Ryan. I don't know how he does it. Not easy for Rachel and Bob who also have no sleep. Ryan is also having a lot of wind and secretions of late and consequently is not looking very happy these days.

Friday, 30 March 2012

Not too bad last night and a quiet time for Ryan today.

Wednesday, 28 March 2012

Ryan is quite subdued today after a rather disturbed night.

Monday, 26 March 2012

A good nights sleep and a big smile when we got him ready for his treatment this morning. A vein was accessed and he then went back to sleep until the treatment was finished.

Sunday, 25 March 2012

It looks as if Ryan may be sickening for something. Not a good nights sleep and no smiles today.

Friday, 23 March 2012

Another good night but average day.
For those of you joining this blog, you can find out about Hunters Disease by accessing this link:
http://mpssociety.co.uk/uploads/Guide-MPS%20II.pdf

Thursday, 22 March 2012

Another good nights sleep has set Ryan up for his second ERT of the week. This is to make up for missing it last week. He is not quite as smiley this week and a bit restless at times. However, he is not showing signs of any significant pain.

Tuesday, 20 March 2012

A good nights sleep again but Ryan is a bit subdued today.

Monday, 19 March 2012

Ryan was still awake when I arrived last evening. However, he had a good nights sleep and was awake but a bit fidgety, when I arrived for his treatment this morning. A vein was located and everything proceeded reasonably well. He fell asleep at about 10.30 and was still asleep when I left.
The Willink team who came to see him last week at Martin House are apparently doing blood tests to see if he is building up anti-bodies to the Enzyme Replacement Therapy.

Sunday, 18 March 2012

Once again Ryan has amazed me. He was awake most of the night and is still awake this morning and smiling! We are going round to see him this evening and I wonder if he will still be awake. Watch this space.

Thursday, 15 March 2012

After a bad night Ryan looked very relaxed when I went to Martin House yesterday. Smiles were few and far between but he looked very "with it" and there was plenty of intense eye contact.
Today Rachel is meeting with Dr Ed (we think) from the Willink at Manchester, who is visiting Ryan at Martin House. It will be interesting to hear what he thinks of his recent progress. Ryan then comes home later this afternoon.

Tuesday, 13 March 2012

Went to see Ryan in Martin House. Got a great big smile there yesterday but none today. However, he had a good nights sleep and I was able to enjoy an hour and a half's cuddle, as we watched Cbeebies together. I will visit again tomorrow and he returns home on Thursday. No ERT this week as there is no one available to cannulate! So, two treatments next week.

Saturday, 10 March 2012

Ryan had a very good nights sleep and had a good day today. He went to the donkey sanctury this morning and out in his buggy this afternoon. A few smiles when I saw him completed a good news day.

It looks as if his diary has at last been closed by BT. Some time ago the British Library Web Archive asked if they could archive it for posterity. They said it would take a long time to get round to it and it looks as if they have now missed the opportunity. A great pity as it covered a large part of Ryan's life.