WHAT IS THE FELLOWSHIP OF THE RINGLETS?


In January 2015, following a routine check by my vigilant GP, I was diagnosed with invasive breast cancer.

As a Brit living in Sydney, Australia since 2008, I realised over the following days just how many of my friends and family were scattered across the globe and different timezones.

The Fellowship of the Ringlets was originally just a tremendous pun and the title of a closed Facebook group I created to keep those distant friends and family in the loop and worry-free.

But over 12 months, my little group somehow grew from 80 to 800+ and became a veritable band of brothers, a support team like no other and a true Fellowship in every sense of the word.

Their love, laughter and rallying cries have been the greatest tonic a little ringlet'd cancer-face like me could have wished for.

The following letters, musings, incoherent ramblings and occasional bouts of bad language are for them all.

Welcome to the Fellowship of the Ringlets.

VC x

Monday, 29 February 2016

*RELAY FOR LIFE - HELP NEEDED!

Dear Fellowship,

Now I was going to start this post with 'When have I ever asked you guys for ANYTHING????' and then I remembered that the last post I wrote was in fact to ask you for hard cash. Hmm. 
To be fair, that cash was for a very deserving little boy and both his parents and I were properly overwhelmed and hugely grateful at the sheer generosity of total strangers. Much of that generosity came from this here totally fabulous Fellowship so I must say thank you to each and every one of you that donated - so far over 6500 pounds has been raised which is completely amazing!
So on the subject of such staggering generosity of spirit, time and cash, let me simply mention that this Saturday, I will be partaking in the annual Cancer Council Relay for Life event in Sydney. This is my fundraising plea and there are a few reasons you should sponsor me: 

1. I have known about this for 3 weeks but forgot to set up a fundraising page ‪#‎cognitivefatigue‬ and now I am panicking about being the worst cancer-surviving fundraiser ever. 

2. I have, somewhat terrifyingly, been asked to speak at this event in front of hundreds of people as a cancer survivor. This is terrifying both for me ("do not swear, do not swear") but also for those innocent folk who are currently unaware of my enormous capacity for chat. My speech needs to be 3-5 mins. LOL. I think we all know how that will work out. Anyway, it will be quite awkward if the speaker who rambled on for 20 mins at the Candlelight Ceremony before no doubt falling off the stage in the darkness is then exposed as a fundraiser without funds. 

3. There is some walking involved. Lots of walking. Apparently through the night. Which should be interesting. Luckily, it gets dark at night and therefore I plan to dress all in black like a cancer-surviving ninja so no one will notice my repeated unauthorised pit stops. If you sponsor me, I promise to stop less and potentially even moan less about my bad foot.

It would be tremendous if I could reach my little goal of $500 to help other little cancery faces just like mine, so if you can help me get there then that would be just fabulous.
Lastly, special thankyou to Cheryl Ayres for inviting me to join her Relay team and for also bravely putting her own reputation on the line and suggesting me as a fellow speaker. I fear she may live to regret at least one of those decisions...

http://fundraising.cancer.org.au/site/TR/RelayforLife/CCNSW?px=1473807&pg=personal&fr_id=3410

Love, 
VC x

Friday, 12 February 2016

*THE FELLOWSHIP GETS PUBLISHED! (KIND OF)

Dear Fellowship, 
Best Valentine's surprise ever - 'Tales from the Fellowship of the Ringlets' is now in print!! 
It's something of a limited edition right now - limited in fact to one copy, so that makes it literally one of a kind! Priceless, in fact! I may have to get contents insurance on the flat! 




Massive shout-out and enormous thanks across the seas to my little Welsh pal Nicola Daniel for spending her days and precious time secretly doing this when she should have been tending to the needs of her perfect new daughter, Cassie Valentine! 
Seeing it all written up like this is fairly overwhelming, not least because I've realised how much I MISS that GODDAMN wig *sob* but also because I've been dithering about over the last few weeks, wondering whether to write FotR up properly or just leave my cat litter'd memories languishing in the bowels of t'interweb for people to eventually stumble across. I am going to read it by the pool this weekend in the Hunter Valley and see if I get bored. If not, then we may just return to this publishing quest...standby for my Amazon rating of my own inane ramblings! 
Whatever happens, this is frankly one the most sensational, thoughtful and fabulous gifts ever. If the internet ever collapses (which it eventually will do, probably under the weight of the Fellowship posts), I now have a proper book to remind me of the cancery madness of 2015. 
Love you, Davey-Daniel, you Welsh legend. You have made my year (all 6 weeks of it)!! 

Have great weekends, all... 

Love,

VC x

Friday, 15 January 2016

*A MAMMOGRAM, AN ULTRASOUND, A HAPPY VC

Dear Fellowship, 

Let me be very clear - there is generally no excuse for posting a smug-faced picture of oneself wafting about on a boat at an age when one should really know better. No one likes a show-off, even a ex-cancery-faced one. 


But today is an important day and so the normal rules do not apply. And to be fair, I do love a boat-related photo. Today was my 12 month mammogram and ultrasound, the first actual scan I've had since treatment started that has officially confirmed the ongoing absence of Lumpy, Lymphy and their merry gang of thieves. 
I didn't realise quite how anxious I was about these scans till I started properly hyperventilating like a freak this morning and almost threw up into a bin outside Darlinghurst XRay. All class. 
I haven't wanted to previously and still don't want to shout 'woohoo, cancer-free!' from the rooftops because that kind of chat makes the fate-tempter in me a bit nervous but I'm not sure Dr Dave was quite ready for the bear hug I sprang upon him when he nonchalantly told me everything was fine an hour ago.
So yes, everything is fine. Phew. Dr Dave is happy. My boobs are delighted and loving their own work. And I have stopped holding my breath and no longer want to throw up into a bin. Which is good. And this photo is the best one I can find right now that accurately portrays my current happy face and relieved mind. 
So the first of hopefully many annual scans is done and I'm officially a massive ex-cancer-faced show-off with two working arms and a ginger tan, wafting about on any boat that'll take me at an age when I should know better. 
And I'm ok with that. :)
Love,
VC x
P.s I also feel like an actor who keeps coming out from the wings for another encore. Will totally understand if you've all now left the Fellowship, pushed off home and there's just a bloke in overalls sweeping up at the back...

Saturday, 2 January 2016

*ONE YEAR ON - SOME THOUGHTS..

Dear Fellowship,

So here it is. Skidding in at the eleventh hour. The 2 Jan anniversary post. The one I've personally been looking forward to the most. The one where it's exactly a year since GP Jacqui slid her chair over to mine at 9.04am and uttered the immortal 'it's not good news, I'm afraid' words. The one where I finally get to quietly celebrate stepping over the 2015 finish line into the relative calm of 2016. The one where I get to look back on the last 12 months with wide eyes, aching limbs, a dubious haircut and think ' what the beejaysus just happened?'
I wrote an article for Mamamia back in May about 6 lessons I'd learnt since being diagnosed with breast cancer. It was the abridged version - even at the time, I secretly had way more than 6 lessons under my belt but time, audience interest level, word count and a deadline dictated that I reined it in slightly. 
I've been thinking about the content of this particular anniversary post for a while and after much deliberation and procrastination, I'm going to attempt to articulate and share some of the most valuable lessons I've been taught over the last 12 months. Maybe one day, they'll help someone else to navigate these cancery waters...

1. Friends and family are everything. 
They say friends are like walls. Sometimes you lean on them and sometimes it's just enough to know they're there. And if friends are like walls, then family is the cement that holds everything together. So build your walls well, lean on them enough to leave an indent and you'll find your Fellowship.

2. It's good to talk. 
A friend of mine, shortly after I'd been diagnosed, told me that if he ever got cancer, he would disappear into his flat and not tell a soul. I kind of understood this in a 'man retreats into man cave' type way but it can be a lonely old trip, this cancery shizzle, so why make it lonelier? There's safety in numbers and I've found that the more open I've been, the more open people have become. Or maybe they're just smiling sweetly at me and thinking 'where has all her decent non-cancer chat gone?' Believe me, I wish I knew...

3. Never judge those who seem to disappear for a while.
 But never forget those who turn up every day and help pull you through the storm when you can't see your hand in front of your own face. They're your tea-makers, your temperature-takers, your bad day maraca-shakers, they're your best people so keep them close and occasionally smother their stoic little faces with kisses.

4. It's not all about me. 
What??? Madness. But being the friend or family of a cancer patient is the hardest gig in the world. Even harder than working in a media agency. True story. I know this because I've been the friend, I've been the family and now I've completed the cancer trifecta and done a stint as the patient so I'm officially qualified to comment on this subject with authority.

5. Write it down. 
My friend Becca, another beautiful cancer-kicking mentor of mine, told me on Day 2 to keep a diary. You don't have to publish it anywhere, she said, but I guarantee you'll forget stuff so just get it out and get it down. 51 posts and 12 months later and here we are. And thanks to Bec's sage advice, I will never forget how I trapped my dead arm in a bin chute, threw 4 day old cat litter all over myself or shot up hormones in a bridal ensuite. Good times..

6. It's good to wallow sometimes. 
Cry yourself a river. Lose your temper. Kick a plant pot. Send inflammatory and irrational texts to people you love and who (hopefully) love you back. Slither down a wall in dramatic fashion like a 1980's Joan Collins character, sobbing hysterically. You are not Gandhi. Or Oprah. Nor should you attempt to be. And to be fair, even Gandhi probably had days when he angrily threw a flip flop at a passing cat. What's important though is that once you're done, pull yourself together and go for a latte / walk / green juice / lie-down / delete as appropriate.

7. Make plans. 
Dream big. Imagine the future. Chuck some mad ideas around. But don't beat yourself up if that entirely reasonable idea you had about renovating a rundown chateau in France with one arm and a dog falls by the wayside for a while..

8. Work the short hair. 
It's a goddamn badge of honour. As I approach the Slim Shady phase of my hair re-growth, every day starts with a sigh of bouff-related exasperation. But every exasperated sigh is then followed by a quick reminder that it wasn't too long ago that I thought I would be forever condemned to managing a Benjamin Button style combover. Be grateful that you are not Benjamin Button and work the crop like a pro.

9. Look on the bright side. 
And then the dark side. And then the bright side again. Try to remember that there is always someone worse off than you who's probably moaning less than you are. But sometimes at 2am in the dark when you can't sleep and you think your hair is never going to come back or that your hand will always be numb, there will probably be no one worse off than you. IN. THE. WORLD. And that's ok. At least till morning, when it's time to man up again.

10. Gossip is good.
I don't like my overflowing jug of secrets to be empty. No one with cancer just wants to talk about cancer and we hate it when people don't want to bother us with their dramas because they're supposedly not as important as the whole cancer thing. We of course reserve the right to raise an occasional 'is that it?' eyebrow at your 1st world problem but that is our prerogative as the cancer patient. Suck it up and make me some more tea, princess.

11. You have more strength than you think. 
Mentally. Physically. All of it. But not because you choose to put on a cape every day and become some sort of superhero cancer-fighting warrior legend. There is no 'shall I wear my 'brave' face or my 'weak as a kitten' face today?' type-choice for any of us caught in this cancery web. You turn up, get your head down, get on with it, hopefully make it through the day in one piece, with limbs intact and repeat. The human spirit is a resilient and impressive beast. Test it and see for yourselves.

12. It's ok to ask for help. 
It's also ok to just ignore everyone for a while and submerge yourself in 19 back-to-back episodes of Suits. And sometimes it's ok to just howl at the moon and eat Pickled Onion Monster Munch till your mouth goes numb and your teeth fall out.

13. Try not to overplay the cancer card. 
Do as I say here, not as I do. I am the shameless and unapologetic mistress of the overplayed card and the cancer-related hashtag. ‪#‎cancerface‬ ‪#‎chemoface‬ ‪#‎radiohead‬ ‪#‎chemobrain‬ ‪#‎cancerfatigue‬

14. Prepare for your new life 
Your new life as a raging hypochondriac. Or, as I prefer to call it, a super-vigilant, boob-checking cancer survivor. It's a fine line.

So there we have it. A year in the life. The maddest sabbatical I'll ever take is finally at an end. Phew.

All that's left to do is to thank you all for being such tremendous walls and cement to this ringlet'd fool this year. The Fellowship is one of the greatest things I've ever accidentally done, so thank you again for coming to the proverbial party and for staying to clear up afterwards. You're all welcome back anytime.

Happy belated New Year from Ko Samui! :)

Love,
VC x
P.s it's still 2 Jan somewhere in the world, right? :)


Sunset from our balcony at Kamalaya, Koh Samui. Average. :)


Friday, 25 December 2015

*A 24 HR FLIGHT & A CHRISTMAS SURPRISE!

Dear Fellowship, 
5 years ago, I travelled home from Sydney secretly to surprise my mum and family on Christmas Day. Apart from the bit where Mum shut the door in my face upon seeing me stood there in the snow shouting "Surpriiiiiiiiise!!!' at her in a Santa hat, it worked like a dream. 
So when I returned to Sydney in mid-November just before my niece Matilda was born, I was already considering whether potentially repeating the great Connerty Christmas surprise of 2010 in 2015 was the best idea I'd ever had or in fact absolute lunacy. Turns out it was probably a bit of both...
And so yesterday, after a month of very uncharacteristic VC secrecy and 24 hours after leaving Sydney, I arrived in Henley wearing a jazzy elf hat (I like to mix up my festive headwear choices) and successfully scared the living daylights out of my poor unsuspecting sisters and mum. 
My bro got the same treatment on his eventual arrival this afternoon, the reason for this delayed Yuletide greeting - I don't know how Cilla Black managed 'Surprise, Surprise!' for all those years - it's exhausting! 
Jetlagged auntie, milk-coma'd niece

Probably more scared than my sisters was my brother-in-law Martin who I'd dragged into my Focker-style circle of trust only a day earlier and who I'm pretty sure barely spoke to my sister following my phone call, so fearful was he of letting the Christmas cat out of the bag. Thanks for being the Ben Stiller to my Robert de Niro, Mart.
So today I'll be enjoying all the chaotic trimmings of a UK Connerty Christmas in leafy Henley and it feels like the right place to be, especially this year. 
A year ago, I was in Jervis Bay awaiting the results of my Christmas Eve biopsy, opening presents in the sun, watching sunrises on the beach and being altogether blissfully unaware of the cancery storm racing towards me. 
This year, my latest Christmas accessory is my 3 week old niece, I've drunk way more water than wine and jetlag is the only reason I'll be seeing sunrise this week. What a difference a year makes indeed! 

Niece carnage
3 cousins, 1 squashed auntie
So all that remains is to send a very merry Christmas to all of you and yours from me and mine. I hope you're having the most delightful of times with the people you love the most. Because really, that's what Christmas is all about, innit? 
I know. I'm a bit like a ginger Oprah nowadays. Call it my Christmas gift to you all...
Love, 
VC x
Happy Christmas!

Monday, 7 December 2015

*AEROBATICS OVER SYDNEY & A NEW NIECE!!

Dear Fellowship, 

Meet Fishy. David Fish has a lot to answer for. He hired me, probably very much against his better judgement, as a Strategist for a big Aussie radio network when I first arrived in Sydney back in 2008. What he really wanted was someone to do copious amount of research, put together beautiful presentations and help sell some tremendous radio-based media solutions to some cynical agency types. What he got was me. Let’s just say I interview well.
Fishy & me pre-flight!
Working with Fish for 2 years was probably one of the greatest gigs I ever scored. I had no idea what a strategist really did (still don't, to be fair) nor did I possess the remotest inclination to do any actual strategising - instead I spent most of my days scornfully correcting my sales team’s grammar and spelling mistakes or rolling my eyes and sighing heavily every time someone started a presentation with ‘digital is the future’…
But regardless of my being the least strategic so-called strategist in the southern hemisphere, Fishy let me stay and a firm friendship, mostly based on me bending his ear for hours on end and him waiting patiently for me to finish, was born. 
In 2014, Fish was diagnosed with Hodgkins lymphoma. In true Fishy fashion, he tackled the whole cancery tale with his legendary sense of calm and unwittingly set me the best example of how to face a cancer diagnosis head-on. 
He finished his treatment plan this year just days after I started mine and is now happily all-clear - I like to think of us as a cancer-fighting relay team, him coming round the bend and passing the cancery baton over to my outstretched hand to power it down the home straight. It’s like the Olympics - just more legal drugs, way less lycra and thankfully, zero running. 
While I learnt how to hand-tie floral bouquets during my months off work, Fishy decided to learn how to fly aerobatics with a view to one day taking part in those mad-arse Red Bull stunt flying competitions. And whilst I was proudly showing off some flowers in a vase this year, he was busy perfecting the art of stalling a plane in mid-air. 
When I returned to Sydney a few weeks ago, Fishy offered to take me up in his little flying machine and demonstrate his new-found stunt flying skills.Never being one to turn down a free scenic flight over Sydney with a fellow cancer survivor, I of course said yes and so yesterday, we flew up the coast, over the Harbour and Opera House and up to Palm Beach where 4,000 feet up, we executed a loop, a roll, a wing over and a stall turn in a tiny 2-seater plane! Gulp. 
Thanks to Fish for the most epic, scenic and brilliantly stomach-churning experience yesterday. The twin sensation of utter exhilaration combined with buttock-clenching terror is hard to beat. I am very glad we managed to re-start the stalled engine as we plummeted towards the ocean or this would have been an awkward ‘what Vix did next’ tear-stained blog that someone would have had to write on my behalf…
Meanwhile here are a few comedy pics and video evidence for you - the genius and tragedy of my new haircut is that there are no upside-down ringlets spinning about for you all to enjoy...shame.

Narrabeen

View over the stunning Harbour from the cockpit!

And roll!

Gaaaah. 

ohmigodohmigodohmigod



In breaking (waters) news, I’ve also just been told that my super-organised sister has gone into labour, just hours into her due date! So in the next few exciting hours, I shall be battling for that 'favourite auntie who sends us nothing but stuffed koalas but she lives in Oz so let’s keep in with her because when we’re 16, we’ll need a foreign bolthole' status once more and we shall have another gorgeous member to add to the clan!! 
Good luck to my beautiful sis Liz Connerty (and my brother-in-law Martin Christie, who is breaking all sorts of speed limits on the roads of Oxfordshire as we speak) and get ready to be introduced very soon to the latest recipient of my much in-demand, baby-whispering cuddles! Wahay!

Love, 
VCx

*update : I have a little niece and Molly has a little sister!! Welcome to Matilda Christie - apparently a touch of red hair as well - an Aussie name AND a ginge, I have this fave aunt shizzle in the bag! (Sorry Magz Connerty)

Monday, 23 November 2015

* BACK IN SYDNEY & THE BOUFF'S FIRST TRIM!

Dear Fellowship, 

So welcome to National Hypochondriac Day. Where I mostly wander around Sydney complaining to anyone (who’s paid to listen to me) about my various ailments.


Back in Sydney. Hideous view. 


As far as I know there isn’t actually a day in the calendar dedicated to imaginary aches and pains but if there was one, it would be today and if there was an award involved, then I would almost certainly win some sort of Grand Wizardy Whingeing Pom Lifetime Achievement type accolade.

My long-suffering GP Jacqui, after a 3 month respite from listening to my arm, foot, hair and boob-related woes, reluctantly booked a whole hour in her diary with me this morning to ostensibly sign some forms and write some referrals. 48 minutes later, I suspected that behind the sympathetic head tilt, she was mentally banging her head against her desk whilst I regaled her with yet more symptoms to have a crack at.

The good news is that the nerve pain in my foot that has had me muttering about neuropathy and gulping down old man levels of nerve drugs since July isn’t actually anything to do with chemo, cancer or neuropathy.

The bad news is that it’s probably something called ‘Morton’s Neuroma’ which is basically a delightful-sounding thickening of nerve tissue and is commonly found in women who wear heels a lot. Anyone who’s ever seen my Imelda Marcos-size shoe collection will not be remotely surprised by this new twist in the tale.

The good news is that it can be treated by either injecting steroids into it (gulp) or via surgery to remove it (gulp), resulting in a few days on crutches.

The bad news is that the last time I had to use crutches for more than 10 minutes back in 2004, I accidentally flung a whole pint of Lucozade onto a brand new cream carpet, resulting in our whole flat having to be re-carpeted. The lesson is never balance a pint of Lucozade on a book whilst moving from one room to another on crutches. Seems obvious, I know...

Anyway, I digress. X-Ray and ultrasound locked in for later this week but it’s looking like there is at least a better outcome for the old right foot than ‘it’s just down to the chemo, innit?’ explanation I’ve been offering up for months. Well done to Cath Walters for listening to me whinge for half an hour about it last week before getting on Google and texting me ten minutes later “I reckon the pain in your toe could be a Morton’s Neuroma…”. She’s so smug right now.

 Meanwhile, I now have good old Morton to add to Lumpy, Lymphy and Limpy - together, they sound like the ugliest Scandinavian boy band ever.

Next up and a trip to Sunburn Sue. I’ve said it before and I’ll say it again. I bloody love Sue. We had a nice chat about my holidays, how much we both love the Scottish Highlands, isn’t Skye amazing and wasn’t the Harry Potter train over the Viaduct fun etc - if I hadn’t been sat there chatting away with top off and boobs out, it would have been a bit like going to the hairdressers. As it was, she’s very happy with everything and reassured me that yes, I am now definitely, most assuredly 'well' and no, I did not need to take up precious space in her room anymore. Then she booted me out. Sad face. I miss Sue already.

Then I popped upstairs to see Dr Dave to book in my annual mammogram for January, which as a breast cancer survivor, I am now entitled to. Sadly, Dave wasn’t in - probably off saving women everywhere like the legend he is - so I had a chat with his PA, Kate.

“When do you want to do it?" she said “You choose.”
“Next week?”
“Nope”
“December?”
“December’s terrible. Don’t say December.”
“Ok then, how about mid-Jan?”
“Locked in. Want an ultrasound with that? You might as well.”

I’m not even joking. It was like being at a McDonalds Drive-Thru for boobs. Which I know would be a dream come true in many ways for several of you lads.

Then I spent 5 minutes explaining to Kate and her colleague on reception exactly how a mammogram worked while they both pulled faces only 22 year olds can pull when confronted with the words ‘boobs’, ’squashed’ and ‘like an ice cold sandwich press’.

I’ve been back nearly a fortnight and am starting to settle back in after ten tremendously recuperative and gorgeous weeks back in the Motherland. The ridiculous 30+ degree temperatures are certainly helping with this re-adjustment back into Sydney life but if it makes my English pals feel better, I did cry for pretty much the whole day when I landed. Cried driving to a massage, cried during the massage (not recommended), cried unpacking my bag, cried on my friend and her baby. Literally, all day. Then I took a sleeping pill, had 12 hours solid sleep, the sun came out and I felt much better. I still miss you all very much though. :)


In other exciting news, the Bouff has had its first official haircut! Yes! The Return of the Ringlets is all systems go! Both my mum and my sister both remarked in the UK how much like Dad’s hair it looked which, though I loved my Dad and his hair very much, is not exactly the look that I was quite aiming for. Another friend who shall remain nameless suggested it looked a bit like a wet tennis ball. He is still apologising, 2 weeks later. So the first thing I did post-crying massage was push off and see my hairdresser Roger.

“Too soon?” I said, anxiously as he strode towards me in the salon. “Never too soon!” he replied, whipping out his tiny nail scissors. Had a lovely time, a little ‘fro trimmage and Rog pretended there was a long-term strategy in place for Bouff-growth and maintenance which made me happy.


Before - wet tennis ball...

After - tennis ball. hmm. 

 I have to say as an aside that wrestling with the new Bouff has become my least favourite pastime. How much wax is too much wax? Why, o why does it insist on curling out at the sides like Count Duckula’s tail? I mostly just look like I’m auditioning for a role in Bugsy Malone. As a lad. And now they’re telling me I’ve got to go easy on the heels. Man alive. No online dating for me for a while...

But for now, sensible shoes and hair wax aside, we shall simply press on with getting back to normal. Whatever the devil that might be. :)

Love,
VC x