FOP Australia Ltd – Annual General Meeting for Members

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We are pleased to advise that the FOP Australia Ltd AGM for members will be held on Thursday 8th of December 2016 in Brisbane, details are in the attached notice of meeting.

To assist with coordination, if you wish to attend either in person, via phone or Skype (depending on availability) please visit the following site to register https://www.stickytickets.com.au/45988

Please see below for the following documents

Notice of the Annual General Meeting agm-notice_dec-16 fop-australia

Agenda of the 2016 AGM fop-australia_agm-agenda_dec-16

Minutes of the 2015 AGM fop-australia-agm-minutes-2015

Proxy Appointment form fop-australia__agm-proxy-appointment-form_dec-16

A proxy must be registered in advance of the Annual General Meeting no later than 48 hours before the AGM ie 6:30pm Tuesday 6 December 2016, details in the appointment form.

All queries to be directed to the secretary at info@fopaustralia.org

Thank you for supporting FOP Australia.

Brooke Scott

Secretary

 


FOP Australia delivers $34K for research

FOP Australia delivers $34K for research

FOP Australia is making a donation of $34,000 to medical research related to a cure for Fibrodysplasia Ossificans Progressiva (FOP) after a year of successful fundraising which included a launch event in June 2016.

“We want to thank every single person who has helped us raise this amount of money.  All those who generously made a donation, held a fundraiser on our behalf and supported our launch event in any way” said Lara Boniface, Chairperson of FOP Australia’s Board.

Australian and New Zealand based patients and their families and supporters gathered at Rydges Hotel in Brisbane on 4 June to officially launch the patient not-for-profit organisation that was formed mid-2015.

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“It was an amazing night with such a great atmosphere.  Having so many people supporting us and speaking positively about the potential of research towards a cure in the future was very special” said Brooke Scott, an Australian patient.

Oliver Collins and his family have been an integral part of the international FOP community for the past 20 plus years. Oliver spoke at the launch, leaving the audience with a deeper understanding of living with FOP.  He spoke of those practicalities and challenges as a young adult studying at university with a full life ahead of him.  He reminded the audience of the daily support required and the incredible difference a positive attitude makes.

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Thanks to the generosity of more than 200 guests,FOP Australia members, patients, their families and friends, the final donations tallied close to $20,000.

“We are proud to donate all this and more to research because it is one of the reasons we established FOP Australia in the first place” said Lara.

“Our primary goals include contributing to research a cure for FOP, and by donating this money via The International FOP Association (IFOPA) – we can be certain it is used in the best possible ways” she added.

IFOPA is the leading international non-profit organisation supporting medical research, education and communication for those afflicted by the rare genetic condition that is FOP.

FOP Australia received overwhelmingly positive feedback on the launch event as well as a patient gathering that took place in Brisbane from June 2-5.  It was the first chance in recent years for patients and families of FOP in Australia and New Zealand to gather together and discuss recent medical progress, trial results and other related topics.

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“After we returned to Victoria after the event, Tyson was visibly brighter and more positive about life.  I think the chance to meet his ‘FOP family’, hear the support from the community and enjoy a fun party really had a positive effect on him” said Talia Wilson, whose 15 year old son Tyson has FOP.

Since its inception, FOP Australia has been the beneficiary of personal fundraising efforts and donations that have added an additional $14K to our total.  We would like to acknowledge the incredible support of just some of these special people and organisations.  Their efforts, both small and large, have gone a long way to raise awareness and understanding of FOP within Australia.

  • The Collins family for their significant donation
  • Shan Carty, Independent Jamberry Consultant who donated profits from an online Jamberry Nails sale
  • Imogen Taylor and the Sydney medicos who ran the City2Surf
  • Junction Park State School in Brisbane for hosting a gold coin donation ‘free dress day’

Our work does not stop here.  We are an organisation of volunteers who is always looking for ideas and help to achieve our ‘vision’.  You can continue to help us by making a donation at: FOP Australia Give Now page .

If you are not a member, join our organisation for the small fee of $10 annually.  Membership forms are available here.

Our vision and mission is to:

  1. help educate the community, in particular medical professionals, on the symptoms and medical management of FOP
  2. support all patients and families living with FOP in Australia and more widely in the Asia Pacific region
  3. raise funds for medical research both in Australia and overseas through established and world renowned FOP research centres
  4. advocate at community and government level to ensure any future approved treatments be made available to patients in Australia
  5. nurture a community of highly motivated and passionate individuals that will continue to expand our FOP networks around Australia

 

You can stay up to date on our progress and future fund raising plans via our website: FOPAustralia.org

 

 


Medics run to stop FOP

On 14 August, a group of more than 30 doctors and nurses from the Prince of Wales hospital in Sydney will line up with thousands of other eager runners to compete in the annual City 2 Surf event.

What’s special about this group is – they’re running to stop FOP (Fibrodysplasia Ossificans Progressiva) an incredibly rare disease affecting 1 in 2 million people and Imogen Taylor is the driving force behind this team of medics.

“My partner’s sister – one of the best people I know – has FOP. It is appalling to see how dramatically the disease progresses and devastating that currently there is no treatment, let alone a cure. For the past few years, my partner Tom and I have been among those raising money for research into the disease – but mostly centered in the UK where she lives” said Imogen.

Tom went with his family to the International FOP conference in Manchester in May this year. They had the pleasure of meeting Jarvis and his mum Lara from Brisbane and learnt that the charitable organisation FOP Australia was just being established”, she continued.

As Imogen had just arrived in Australia and was working at a hospital in Sydney where a group of doctors were going to run the City2Surf – it seemed like the perfect opportunity to raise awareness about FOP Australia.

There are thirty members in the team- a mix of medical specialists some of whom had not heard of FOP themselves – despite their expertise in the field of medicine.

“FOP is so rare, it is not usual to test for it, or for those in the medical profession to be aware of the symptoms – like turned in toes”, said Imogen.

Imogen has shared information about FOP with members of their running team and have already spread the word about fundraising efforts to our colleagues, friends and relatives.

So why choose FOP over other equally worthy charities out there?

“If we can raise money that will directly support research that could prevent a lot of suffering and, within a few years, we could consign FOP to the history books.”

“Using our networks, the thirty of us can reach out to hundreds of others, telling them about FOP and enlist their support,” said Imogen

While Imogen has never run City2Surf before, she’s amazed at the beauty of the 14km course passing through the CBD to the Eastern beaches.

“The atmosphere will be fantastic. We have some people who are brand new to running and others who are triathletes!” she added.

“Running for a cause like this is extremely rewarding and will motivate us to get over the finish line’” she smiled.

I know everyone thinks ‘I should do that for charity….Well here’s an example of how that has translated in action”.

“Find an event you want to take part in, persuade your friends to do it with you and then raise money for a charity close to your heart – why not FOP Australia!”

To support this amazing team of runners, you can make a donation at: FOP Australia Give Now page

The members of FOP Australia want to extend a heartfelt thanks to Imogen, Tom and the team of runners who contacted us to raise money for FOP.  Their generosity and hard work will help Australian patients and their families living with FOP, and we will donate 100% of the funds raised towards research for a cure.

For information on FOP and our charity FOP Australia visit the  FOP Australia Website

 


FOP Australia Launch

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All tickets to the FOP Australia Launch on Saturday 4th of June 2016 have now sold!

We have been overwhelmed by the response and thank everyone for helping us.

If you have missed out on a ticket, please email us at info@fopaustralia.org to be added to the wait list!

 


FOP Awareness Day – April 23

April the 23rd is celebrated as FOP Awareness Day around the globe.

On this day in 2006 the FOP gene, ACVR1, was discovered by researchers at the University of Pennsylvania School of Medicine.

Discovery of the gene allows research efforts to focus on a treatment and cure. We are extremely grateful to the numerous doctors and scientists who are working towards this goal.

You can directly support FOP Australia by:

Purchasing an Entertainment Book www.entbook.com.au/91408j5

Buy a ticket to our official launch to be held in Junehttps://www.stickytickets.com.au/36347

Sharing our Facebook posts with your network to help us raise awareness of FOP.

We will soon by announcing other ways you can donate to help our cause and we thank you for your ongoing support.


Meet Derek

I was diagnosed at the age of 5 and a half in Melbourne.  After falling while playing chasy at school, I hit the back of my head on a pole where 2 lumps formed at the base of my neck. Nearly every department in the Melbourne Hospital didn’t know what I had, to the point they were making up names to give the disease. Until someone tried the Genetics Department where Dr. Rogers diagnosed me with Fibrodysplasia Ossificans Progressiva (FOP). My name is Derek, friends call me Dez and here are some parts and moments of my life.

This disease certainly is not an easy thing to cope with when you’re a young child without the knowledge of the fear of what will happen when you try things or fail. I still consider myself lucky compared to most others.  I competed in Little Athletics as a child and did things I shouldn’t have, mostly without consequences brought on by FOP.

Until puberty came around most people thought I was faking a disease to get attention at school because it wasn’t really apparent that I was any different than anybody else. Then out of nowhere things changed so rapidly that it shocked my entire school, I had a growth spurt and I am approx 6 foot 3 inches tall. The Doctors recommended I use a kneeling seat rather than a conventional chair, what they didn’t expect was this was to cause my spine to keep leaning forward more and more as I grew older.

I was given a king single waterbed to sleep on to help with comfort since I was twelve. Any other bed since, has been too uncomfortable. After too many falls a mobility scooter was the only option at fifteen years of age.  I wasn’t happy about it but understood none the less and my resilient nature got on with life and adapted as it always does.

At 19 I started a computer business which I ran for 3 years mainly to gain some experience. Due to requiring constant transport it was no longer viable for me to continue, so I closed the business down.

I taught myself scripting and began making websites and graphics in Photoshop to keep myself busy.

I have always refused to let FOP stop me from doing most things that I enjoy, even fishing. I went deep sea fishing and reeled in an 85lb black marlin, I also took family and friends out for another fishing trip and caught my first blue fin tuna. I took the 3 wheeled scooter onto the boat and it was quite a challenge to balance and fish at the same time.

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Photography is another passion of mine that grew the moment I borrowed my sisters cheap little film camera, little did I know that later in life I would buy a camera and be good at capturing moments that caught my eye or my heart. My partner had a love for horses and I wanted to help support that. We bought our first camera and started going to horse shows and events to take photos for an online horse magazine. I’ve always had a love for animals big or small and taking photographs of them was another way to share that love.

We spent three years taking show jumping, cross country and dressage photos before taking the leap and buying our own horse for my partner to ride.  Not just any horse, the one we chose was a horse that nobody really wanted.  A horse that was saved from a slaughterhouse and later bought from a Horse Sanctuary, every owner just used her as a confidence horse before selling her on. So to me this horse never really had a home, until now.  Without realising it I began to mentor my partner with her riding and boosting her confidence, along with that formed a very special bond with a very special horse called Millie.

 

Documenting my partner and Millie’s riding progress with photos and write-ups on a local horse forum we got to share our journey with a large portion of the horse world and give others confidence along the way to continue riding. I was able to teach Millie, give her confidence to try, and show her the love and respect she well deserved. I was told by a few professional riders that the close bond and trust we shared was something many riders strive for, considering I never rode her that it was quite unique.

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We also started a local beginner’s horse riding club together, I took on the jobs of organising riders, the bbq for lunches and photographing riders during their lessons.

Millie was not a young horse when we bought her, unfortunately she died after 5 years from a suspected heart attack while running through the paddock. Her memory lives on in photos of some of the moments we spent together.

Her passing put an end to my photography of horses for over the next 5 years or more. My partner and I also parted ways. I was later to land myself a job in technical administrator role through one of the members of our riding club who suggest I apply for the position at the company she worked for

I began working for a Communications company and handling wireless internet customers, technical support, monitoring the company’s wireless towers and working with a great team of guys. FOP was determined to stop me from working, I fell in the shower fracturing my pubic bone and was involved in a bus accident coming home from work which both affected me but I refused to let that get in the way of a job I needed to do. I had a very busy job helping two companies with all things to do with wireless internet. Unfortunately the entire company was made redundant due to a buy out and we were all no longer needed after 4 years and a lot of hard work.

Currently I’m 44 and although quite restricted now and I no longer work, I still continue with photography when I get the chance.  I did some charity working offering local families photo sessions in the park for a small donation to help raise money for a 3 year old boy with a brain tumour.

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I still live independently with support workers coming and going to do the things I cannot. Mostly these days I am a keen PC gamer who takes life slow but I have learned to take each day as it comes, deal with things when they happen and not to stress too much about the “what ifs”.

Thank you for reading my story.


FOP Australia Launch!

Please join us to celebrate the achievements of the first year of FOP Australia at our official launch.

Where: Fox Hotel, Acadia Room, 71-73 Melbourne Street South Brisbane

When: Saturday 4th June 2016

Time: 7-9pm, official proceedings including drinks and canapes and entertainment. 9-11pm,  Please note after this time, there are no children permitted in the venue and you will need to purchase your own drinks.

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We welcome all of our supporters to attend including family and friends who are not members of FOP Australia, please see the invitation below and forward to anyone you believe would like to support our cause.

We look forward to seeing you there!

For more information please contact us at fopaustralia@gmail.com

Thank you to our sponsor Sticky Tickets.

 


Entertainment book Fundraiser

FOP Australia is selling the Entertainment Book this year to help raise funds and awareness of Fibrodysplasia Ossificans Progressiva.

The Entertainment Book includes discount vouchers for a range of restaurants, cafes, arts, attractions, hotels, shopping and travel. There is a wide variety of vouchers in the book and after only using a few you are likely to have recovered the purchase cost.

Memberships are available for most regions in Australia and New Zealand. You have 2 options when purchasing, a traditional book, or a digital membership which links with your smart phone and is compatible over 2 devices so you can share with a family member.

You can pre-order your book here.

For hard copy Entertainment Books outside of the Brisbane area please contact us to see if we have a representative in your area which will save on shipping costs.

Click here for more information.


Jamberry Facebook Event

To kick off Rare Disease Day, FOP Australia with the help of Shan Carty – Independent Jamberry Consultant held an online fundraiser with Shan generously donating her commissions from the sales of Jamberry products to FOP Australia.

The Facebook event started on Monday 29th of February to coincide with Rare Disease day, and remained open until Sunday 13th of March. Throughout the event Shan run random games with some great prizes.

We are thrilled to say at the end of the event, we raised $902.

Thank you to everyone who supported this event and a big thank you to Shan for her hard work and for making the event fun and enjoyable!

If you still don’t know what Jamberry is, head over to Shan’s Facebook page to find out more she is more than happy to answer your questions, and if you are based in Melbourne contact her about a Jamberry Party


Rare Disease Day celebrations

One of the objectives of FOP Australia is to educate the community about FOP.

Rare Disease Day was held on February 29th, on this day Lara and her son Jarvis who has FOP visited Junction Park State School in Queensland wearing yellow to support the day.

Lara gave a talk about FOP and helped the school to learn about the most common clue to FOP which is malformed big toes.

Thank you to Junction Park State School for your support, we raised $443 on this day which will help us with our patient event in June.