Wednesday, 19 September 2012

Radiotherapy gets underway (and all the rest...)

WHAT a month.  Both very good and some very bad.  I honestly don't know where to start - can you imagine trying to go back and write a diary account of your life for this past month?  Where you were, what you did, how you felt... I don't know whether to split it up into separate posts or just do a huge "brain dump" in this one.  Please don't switch off on me, just go and make a cup of tea and have a packet of chocolate digestives to hand before you sit down to read this one...

First and foremost, the most important thing of all - Oscar.  He has been well, REALLY well, during this break in treatment.  He is full of fun, pestering his little sister Izzie, and just BEGINNING to act like any other child his age would/should.  We are trying to build him up again since all that nasty chemo which really took its toll on him.  His favourite foods right now are pure butter, carrot and parsnip mash, porridge and honey, and of course a full fry.  At least McDonalds cheeseburger Happy Meal is no longer a daily request!

11mths old and several hair cuts already!
His finger nails have all fallen off, but are almost completely regrown, and there are hints of hair regrowth!  Most people assume little kids Oscar's age wouldn't be too worried about their hair, but he really misses his.  If we draw pictures with him we MUST draw his spiky hair, when he is getting bathed I have to "wash" his hair, and when Izzie is getting hers dried after their bath I have to dry Oscar's too.  He asks me to do all this, go through all the motions, but will then say things like "I need a new head, this one is no good".  When he first lost his hair he wouldn't look at himself in the mirror, and seemed embarrassed by his appearance.  It is the one thing that has constantly bothered him about all this - he asks almost everyday: "Mummy is my hair coming back yet?"  Of course now everyone knows our little man as he is, everyone new in Oscar's life is shocked by the fact he used to have a mop of thick red hair!  I just CAN'T WAIT to buy gel for him, and run my fingers through it again, and take him to the hairdressers.  Those will be great milestones, because I know it means so much to Oscar.  Come on hair follicles - DO YOUR JOB!

Our fundraising campaign is going AMAZINGLY well - we've said it many times already, and will many times more I'm sure, but the kindness of strangers is unbelievable.  It's surprising the new people who come into your life at times of need, and who quickly become very important and special friends.  Each and every single person who has organised or attended an event, bought a wristband or made a donation, is helping to give us hope of a future for Oscar - that kind of thanks can never be expressed.  But THANK YOU, from the bottom of our hearts.

Oscar has an amazing effect on people - "Oscar is such a friendly and engaging four-year-old.  He's such an inspiration and of such good character" (said Lord Mayor of Belfast, Gavin Robinson).  Others have commented on how "mature" his conversation skills are, how funny he is, and what a sweet nature he has.  He has now 12,500 followers on Twitter - people feel like they know him as we post regular details of his progress (and his antics!), and we feel as though we have a huge army of supporters all helping us get through this awful nightmare.  Some days I even think "Oscar has to get through this, there is no way anything bad can happen him with all these people aware of his story and right behind him", but unfortunately there are no guarantees on this journey, we just have a lot of people sharing our highs and lows and it really really makes a difference.  The positive energy we get from Twitter helps us to get through, and stay positive for Oscar.  But we also like it when, if things are bad, there are people right beside us cursing this world and venting their frustration about what Oscar, and indeed our wee family, has to go through.  So all in all, THANK YOU #TeamOscar, you are doing a great job!

So - we're back to treatment now, radiotherapy started on Monday, and all is well so far.  His liver is the target for this phase of treatment, as that's where the stubborn neuroblastoma still remains.  To think he has come this far - cancer from the top of his skull right through his whole body down to his right ankle - and now just 2 small areas still detected on his liver!  10 months of extremely tough treatment, and our little champ is still winning this battle.  Radiotherapy is expected to make him feel a bit sick, and very tired, but that is is nothing compared to the hell he has endured already.  We just want to keep him comfortable, rested, and well fed, and hopefully nothing too bad will come of this.  Nutrition is a concern apparently, as he may go off his food due to the nausea, but today and yesterday he woke up after anaesthetic and asked for a fry!

His radiotherapy treatment sessions only last minutes, but it is vital he remains totally still so the beams hit the target precisely, and so he is having a general anaesthetic every morning to allow this.  He's enjoying all the fun of being in a different hospital, and the attention he gets from all his new nurses!  He looks forward to seeing "the sleepy doctor" (anaesthetist).  As his body is still tiny, movements caused by breathing, and the "route" the beam takes through his body to reach his liver mean that his lung, bowel, and right kidney are also getting exposure to the radiation.  These are healthy areas of tissue which will now get damaged, there are numerous side effects both immediate and long term for that, including possible future cancers, but we were simply told we don't have a choice.  Everything that can be done needs to be done right now.  The other effect of radiotherapy is that his skin (where the radiation hits) may become very red - like severe sunburn - so we have to put loads of cream on to try to prevent this.  I often think, that in 20 years from now, we'll look back at the best treatments we had available for cancer sufferers, and be disgusted by how crude they were and the damage they caused in the quest for a cure.

I've just realised I've been waffling on, and haven't even got around to talking about what we've been up to!  Oscar had a busy week last week, but it's getting late and I know I won't do it justice if I start trying to talk about it now.  6.30am starts for radiotherapy, research into complex treatment options for Oscar, pushing the Appeal forward as much as we can, running around after 2 (squabbling) toddlers, all the pressures of our situation, "normal" concerns like remembering to submit child tax credit forms on time, grocery shopping, laundry and cleaning - I could bore you to tears moaning about the stresses we are under but I'll stop there! Both me and Stephen are physically, mentally and emotionally exhaused.  20 hour days have been taking their toll, but adrenaline is driving us on, and nothing is going to stop us on our mission to get Oscar well again.  So I'll shut up for now and try to get some sleep - everything else can wait until tomorrow!

Sunday, 19 August 2012

#TeamOscar busy busy busy!

I was going to write "why do I never learn, always leaving these updates so far apart that it is difficult to cover what has happened", but the truth is we simply don't have time to cover all that needs done right now.  Which is fantastic, the interest in and support for Oscar's Appeal is absolutely amazing, but we are struggling to keep up.

Stephen is still in full time work, his phone NEVER stops ringing about the appeal, he is running around from A-B-C-A, attending most bucket collections across Belfast, and me and the kids really need him.  I'm doing similar - chasing new leads for the appeal, following up emails and tweets, taking Oscar in and out of hospital for check-ups and blood/platelet transfusions every couple of days, and trying to be a good mum to 2 demanding toddlers.  We have a great team of family and friends who are supporting and helping us with a lot of the tasks, but I don't think anyone really understands how much work is behind the scenes of such an activity.  We have been averaging 4 hours sleep per night, but decided on Friday that it must stop.

We are giving our ALL to this appeal, of course we are, look at what is at stake for us, but taking a step back we know that we need to get back in control.  The harsh reality is that for all we know, these months could be very precious times for us with Oscar and Izzie, and we can't ever look back and wish we had done things differently.  We have been so scared of missing out on an opportunity to fundraise for Oscar's treatment, that we have actually been putting those things ahead of simply spending quality time with him.  It will be so difficult to strike a balance, both these things are vitally important, but we do need to make some changes.

Oscar has been doing AMAZINGLY - he is eating and enjoying food like we would never have imagined a couple of weeks ago.  He is constantly complaining that he is hungry, that the tiger (who roars in his tummy when he is hungry) is back, and asks "what are we going to eat?" every 30mins.  His mobility is still very poor - he can't walk properly, and needs to be in his buggy to get around.  Very weird to think that if he wasn't still (just about!) small enough to fit in his buggy, he would be in a wheelchair.  Izzie is in charge most of the time - she is much stronger, can run faster, and always has the better of him when they fight.  Sometimes she exploits this, and when she is really annoyed with him she tries to pull his feeding tube out of his nose, but at other times she is so gentle and loving - as if she knows he needs her to be careful with him.  We can't leave them alone for 1 minute or all hell breaks loose - I have to put both of them in the bath to even have a shower (in the same room), so EVERYTHING is a lot of work and very tough going right now.

But the main thing is always that Oscar's treatment is continuing and still going in the right direction - we can't ask for anymore than that right now.  We had a radiotherapy consultation last week, and so Oscar is to begin radiotherapy in September which will last around 3 weeks.  This involves general anaesthetic and treatment every day (Mon-Fri), but hopefully no overnight stays.  Sounds like a lot of hard work, but we are used to that with the aggressive treatment plan we are on.  After radiotherapy will come immunotherapy which is what we are fundraising flat-out for, so at least we have a little more time now to reach our target.  There are also lots of side effects of radiotherapy, including it causing future cancers, but as the doctor said - we have no choice.  We get him through this cancer and pick up the pieces afterwards.  The medical professionals and ourselves are all in agreement that we need to throw EVERYTHING we can at this neuroblastoma - it is notoriously difficult to get rid of and Oscar's chances are poor, so nothing can be overlooked.  When I write that it seems normal, but after the end of a long day there are often a lot of tears when we think about the reality of what we are facing.  In truth, the only way we get through it is to not think about it, and that annoying cliche "take one day at a time" becomes so true for us...

To end on a positive note - August has been an amazing month of fundraising for us so far!  We REALLY have seen the good in people in our hour of need.  So many people, groups, businesses willing to help us in any way they can.  We just can't start thanking people publicly as there are so many, and there is no way we want to leave anyone out.  In my next post I'll update you on all our events, with plenty of pics!

Wednesday, 1 August 2012

Fundraising Events in August

Oscar is getting better and stronger by the day, despite us finding out yesterday he has a bacterial infection in his gut!  Poor little man, we were devasted to hear of another setback, but he truly is a warrior - he is in such high spirits you would never imagine what is going on with him. He is one amazing little boy.  This means Oscar has to remain in isolation for much longer, to protect other children and adults around him.  Such a pity - he is such a sociable little boy, it's so unfair that he has to be kept away from people!  However, the only thing keeping us from going home right now is the fact that he can't/won't eat, so all our energies are going into making food fun and appealing again.  So far we're getting nowhere...

There are lots of #TeamOscar fundraising events confirmed for August, so PLEASE have a look to see if there are any near you or that appeal to you.  What a great way to spend a day/night out, having fun and knowing that you will be helping wee Oscar!  If your event isn't listed below, please let us know teamoscar@hotmail.co.uk

MONDAY 30th JULY - FRIDAY 3rd AUG
  • Spamount - Ivan Sproule memorial tournament, Spamount Playing Fields, Co. Tyrone
FRIDAY 3rd AUG
  • Omagh - all day Street Collection by Omagh Council representatives
  • Glengormley - St Endas half hurling, half gaelic football match kick off 6.30pm.  Refreshments served in the lounge after, then a disco! :-)

SUNDAY 5th AUG
  • Belfast - Feile Festival Opening Carnival Parade - our stall will be located in Falls Park selling #TeamOscar and Neuroblastoma Alliance UK wristbands and promoting Oscar's fundraising campaign.

FRIDAY 10th AUG
  • Belfast - A Night at the Races - King's Head, organised by Fujitsu.  Doors 7.30pm.  Tickets £5 at the bar.

SATURDAY 11th AUG
  • Belfast - Comedy Hypnosis show - Ligoniel Working Men's Club

SUNDAY 12th AUG
  • Belfast - Feile Festival Finale - our stall will be located in Falls Park again selling #TeamOscar and Neuroblastoma Alliance UK wristbands
  • Killeter - 5k walk and cyle run
  • Belfast - Cool FM Cash for Kids "Goliath Bungee Jump!" (300ft) - 20 VOLUNTEERS REQUIRED!  Contact teamoscar@hotmail.co.uk
FRIDAY 17th AUG
SATURDAY 18th AUG
  • Enniskillen - Street Collection confirmed.  VOLUNTEERS NEEDED PLEASE!  Contact @davinamcm or teamoscar@hotmail.co.uk
  • Belfast - Disco and raffle in Davitt's Bar (Michael Davitts GAC) 8-LATE, organised by Shana

FRIDAY 24th AUG
  • Castlederg - Dance/fundraising night in Charlie's Bar.  Music by White Lightening, tickets on sale soon!
  • Belfast - ASDA Shore Road bag-packing event
SATURDAY 25th AUG
  • Greenisland - "The Oscar's" tablequiz for Oscar - Greenisland Sports Club.  Contact @pm842 for quiz and ballot tickets
  • Belfast - ASDA Ballyclare bag-packing event

SUNDAY 26th AUG
  • Peatlands Park, Lough Neagh - Terex team of 20 will cycle 86 miles around Lough Neagh.  Show them your support!

FRIDAY 31st AUG
  • Belfast - Charity Football Match: Doctors v Porters (Belfast HT), QUB pitches.  VOLUNTEERS REQUIRED contact teamoscar@hotmail.com if you fit the bill!
Remember you can contact #TeamOscar directly by emailing teamoscar@hotmail.co.uk.  Let us know if you would like to volunteer to help with any of our events, or if you are planning to hold one of your own.  There are plenty more events in the pipeline, watch this space!

Thanks to everyone who has been involved in organising an event so far.  We know the mammoth task it is to get these things off the ground, and we appreciate every effort being made for our wee Oscar!