Pippa Rea

Pippa's Journey with a Brain Tumour

Fearless

Not only did our Make A Wish Trip allow Pippa to snorkel with the fish on the Great Barrier Reef, we were also able to visit the Cairns Zoo, ride the train and Sky Rail to Karrunda to visit the butterflies, do more snorkelling on Green Island and catch up with some old friends and make some new ones.  In addition, the trip  also highlighted to us our fears………..

Patrick, for example, is incredibly fearful of butterflies landing on him;  James, is not that great with riding above the tree tops in a sky rail capsule; and my fear of snakes came as no surprise at all!  (I’m sure all three of us are not alone in our fears either!!)

Pippa on the other hand, fears nothing.  We tried our hardest, but could not come up with anything she is scared of!

A week in Palm Cove, a few days in Melbourne and some time at home.  We have spent the past two weeks with no hospital appointments, doctors or drugs.  Now we start on the next 12 months.   Needless to say Pippa is not fearful of anything ahead of her (except perhaps of no longer having Jessie from Peter Mac doing her blood tests).  Our trip to Melbourne this afternoon was spent singing Taylor Swift songs at the top of our voices, a bit of Taylor Swift education for me in case I didn’t know a few facts, and a brief discussion about killing tumours with chemotherapy drugs that may or may not be pleasant to take.  All in her stride!

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A Magical Reef Wish

The anticipation leading up to today was indeed high.  Even though Pippa has had a wonderful time over the past 3 days on our Palm Cove holiday, she was terribly excited about today, “Her Wish Day”.  And she was not in the least bit disappointed.  The weather was absolutely perfect –  30 degrees and crystal clear turquoise water of glass.

The Quicksilver Outer Reef staff were expecting her and they treated her as the VIP she deserved to be.  The underwater observatory and a ride on the semi submersible where we saw turtles and a reef shark prepared her well for her snorkeling experience.

At first it was difficult.  Combining the breathing with the deep water and the vast ocean to eventually overcome natural trepidation took a little perseverance but Pippa was determined.  Quicksilver and Make-A-Wish had organised a marine biology snorkeling tour which was amazing.  In my previous life I have been to the reef many times but to snorkel alongside my children with a marine biologist explaining the different corals and fish was truly special.  Our guide would dive down and point out special fish and corals to look at and do it all whilst wearing a Go Pro for us so we could bring home our own memories.

Pippa swam and swam.  She saw everything and did not miss one piece of coral she snorkelled above or pretty fish that swam past her.  As the horn sounded to come aboard she was still swimming.  As everyone else was climbing our of the water Pippa was darting in, around and under the platform.  Eventually, the last person in the ocean the Quicksilver staff member who was getting great enjoyment watching her bob around tapped her and said, “Pippa, you’ve got to come aboard now or you’ll be left behind.”  To which she replied, “That’s OK, I’m busy following a fish anyway!”

Thank You Make A Wish and Quicksilver.

In the semi-submersible

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Suited up – sun protection, stinger protection, sea lice protection and looking oh-so-fine!

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Pippa snorkelling

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What do 3 children do after a long and tiring day snorkelling on the Great Barrier Reef?…………..

Pippa; have a shower, write some postcards and fall fast asleep

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James & Patrick; fold each other up in the rollaway bed!  And yes, it did close all the way!

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Three Wishes

On Tuesday Pippa was granted a wish from Make-A Wish Australia.  The local branch delivered the wish to her and although she didn’t have a lot to say at the time, she woke up Wednesday morning and hasn’t stopped talking about it since.

http://www.standard.net.au/story/1783432/pippa-flies-to-the-sunshine-after-great-barrier-reef-wish-granted/

Tomorrow morning we fly to Cairns for a week staying in Palm Cove so Pippa can live her wish and snorkel with the fish on the Great Barrier Reef.

Our whirlwind life continues.  A crazy mix of highs, lows and lots of in betweens.  It will be wonderful to be in some hot weather, enjoying the beach and some amazing adventures.  We will create some more wonderful memories and I’m sure that snorkelling on the reef will be an experience Pippa will always remember.

I am currently the laughing stock of my family as my wish is to just lie on the beach for the entire week and be rotated every now and then;  my children’s wish for me is that my memory returns!

Thank You Make-A-Wish.  Pippa’s smile will be permanently on her face for the next 7 days.  Whether or not the other two wishes come true remains to be seen………

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Entering the Last Week of Radiation

This is now the 7th week we have walked through the doors at Peter Mac for Radiation. I think I speak for both Pippa and I when I say it has not been as frightening nor as bad an experience as either of us had anticipated. Pippa’s amazing ability to handle anything she faces with a positive and happy attitude combined with the doctors’ careful planning have meant that aside from being uncomfortable from the weight gain due to the steroids and some tiredness, she has charged through. And I do mean charged – quite often the radiotherapists do not keep us as she runs down the tunnel to the treatment room!

What better way to mark our final week than including James and Patrick for one last visit? They joined in on the French lesson where they played a game of French Bingo and James realised that his sister probably knows more French than him and poor Patrick was doing his hardest to try and pronounce the numbers. We went for a wander through Captain Cook’s Cottage and the Conservatory in the Fitzroy Gardens. Pippa decided that the house was small and she thought it would be hard to live in.

The highlight of the visit was being the first to listen to Pippa’s very own recording. She has written her own words to Mylie Cyrus’ Party in the USA named Party in Peter Mac Today. Immensely proud of both her attitude and her music, the smiles on their faces beamed with pride and the applause was loud 🙂

The next time we see James and Patrick Pippa will be finished with radiation forever. Fingers crossed that while she’s been coping so brilliantly on the outside the treatment has started to kill that rotten lump on the inside.

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A Catch Up Post

This post is particularly for my children – I have been told off tonight for not posting anything for a while!  The truth is, I have been exhausted and I couldn’t be bothered turning the computer on.  In fact, so exhausted that yesterday I had to say no to going to Pink!  Oooh, it even hurts to think it, but Pippa was so tired and I was barely able to comprehend my own thoughts (sometimes that would be a good thing at the moment).  I simply would not have done the tickets justice and I am very glad for who went instead of me – I hope you all enjoyed the show.

So, for my darling boys who are at home, and for my Pippa who wants to share a couple of this week’s fun things, here’s what we’ve been up to…………..

On the weekend we said goodbye to our beloved Chelsea (Pippa had such a fun time at the party) who is going off to follow her rowing dream in the US and come back a bigger champion than what she already is.  We had such a fun but relaxing weekend without the long drives – it was great; our second home.   Pippa also had another game of glow in the dark mini golf with Phoebe (photos are pointless).

On Monday we watched St Joey’s win the school footy Grand Final and visited a friend in hospital.

Other than that a relatively quiet week –  a dinner out and some board games.  Today the staff at Peter Mac started to make a short movie for Pippa as a keepsake.  She and Elly are writing their own background song (changing the words to Mylie Cyrus’ Party in the USA) for it and clothes were chosen and hair styled especially for the occasion.

This evening Pippa and I went to see the movie “Now you See Me” at Gold Class, Jam Factory.  Great fun movie and I hope that our own magic can be created in time.  She loved the Gold Class experience and we think we might treat the boys next time they come down.  We have had a little giggle tonight as on reflection I have realised that perhaps the staff may have been a little overwhelmed by an above mentioned celebrity who I now realise is being “guarded” by her minder in the background as I unknowingly snapped a photo of Pippa for our own purpose to create our memories.  Mistakes happen, we ended up being taken to the (very) wrong movie in the wake of someone else’s entourage.  All was fixed in time for us not to miss the correct movie and I must commend the Gold Class Jam Factory for their above excellent handling of the situation.  As far as I’m concerned it has just created another story to tell on our journey.

We have also continued to enjoy the cafes and lovely surrounds we have nearby and are very grateful for the accommodation we were able to obtain.  It turns out that by not having hospital accommodation available to us at the start we are much better off being in a “non hospital” location.

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Therapies & New Experiences

I have been on a very steep learning curve and I by no means profess to be able to keep pace completely with what is going on in our lives.  What I know is that medically, our options are what they are and Pippa’s doctors are treating her individually at the highest level of knowledge and research possible.  The other thing I know for sure is that this treatment is concentrated inside her brain – inside the very inside of the part that controls the central nervous and cognitive systems of our body.

Apart from supporting Pippa and being the most positive influence I can on our family, I truly believe that this time and in the next few years ahead it is vitally important that I help stimulate as many parts of her brain that I possibly can.

Currently our week includes music therapies from two different therapists, yoga, reiki and French lessons.  In addition, Pippa uses many items from her suitcase full of goodies and also plays a variety of games and board games that require strategy, concentration and memory.  Each of these activities is not only fun and enjoyable for her, but also imperative to keep her brain active, and her cognitive development aroused.  For all of us parents who “lose it” over the time our children spend on iPads, some of those games are also important for hand/eye speed reactions.  Who would have thought I would ever say that???!!!!

We plan to continue with these experiences when we return home and will  also combine them with our next phase of treatment.

As is always the case with whatever Pippa tries, she takes to it like a duck to water and is so good at everything:

Music; singing, percussion, lyrics – she rocks it all!

Reiki;  she completely relaxes and opens her mind.

Yoga;  loves it and her balance and capabilities are amazing.

French; ………well, we both try to learn……..one of us is doing tres tres bien (very very well), the other of us is a bit more comme ci come ca (so so).  In fact, to put it bluntly, one of us spends most of the lesson trying to keep up – and I’m being well and truly left behind!

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