Bleeding Love - A Haemophilia Story

$12,450 of $25,000 goal

Raised by 137 people in 17 months
Our son Lachlan had a pretty tough year last year. He was dealing with a still unresolved gastrointestinal bleed and his doctors can't figure out what is causing it. For a normal kid, it probably wouldn't be as big a problem, but Lachie has haemophilia.

Haemophilia is a blood clotting disorder where there is not enough clotting factor VIII (Haemophilia A) or IX (Haemophilia B) in the blood. A clotting factor is a protein in the blood that helps control bleeding.

Haemophilia is not a very well known disorder and funding for research in Australia is very difficult. We want to try and change that. The best way to do this is to raise more awareness of haemophilia and the impact it can have.

This is where you come in. We are making a documentary to raise awareness of haemophilia and other rare bleeding disorders, as well as to tell Lachie's story. We are being very ambitious with this project and want it to be of high enough quality and substance to reach a global audience. We have set a big goal as would like the funds to cover making the documentary, appointments for Lachie and some travel expenses. We would also like to make a donation to the Haemophilia Foundation of Australia.

Lachie has 9% Factor VIII which classifies him as having mild haemophilia A. Mild haemophiliacs should not have the severity of bleeding that Lachie has had. This puts him in a bit of a grey area treatment wise. Doctors are unsure of the best way to treat him and have been unable to find a cause for his bleeding. Spontaneous bleeding does occur in haemophiliacs, but generally only in severe or moderate cases. With Lachie’s factor level he shouldn’t be experiencing spontaneous bleeding, especially at this severity.  We would love to be able to discover the cause of this bleeding, but we are determined to do something to improve his future.

We have begun production on the documentary and were lucky enough to visit some amazing organisations across North America and film some fantastic interviews. We have produced a trailer with some footage from this trip which you can view at the top of this page.

We will now be moving ahead with all the Australian based interviews, speaking with the Haemophilia Foundation of Australia, Lachie's haematologist and some families who are also dealing with life with a bleeding disorder.

Then the long and detailed process of editing the documentary begins. Post production costs are very expensive so at this stage we will be handling all the editing ourselves. Hopefully with enough funds we could have it edited by a production company.

The ultimate goal in making this film is to raise awareness of haemophilia in Australia. Increased awareness should lead to more funding, and more funding should lead to more research.

Hopefully one day there might be a cure for bleeding disorders, but until that time, we want to do our part to get to a point where treatment options are cheaper, more available, and easier to administer. We dream of a future where there is a cure for bleeding disorders, not just for Lachie but for everyone affected.

No donation is too small, and we truly and deeply appreciate any and all support given.

Thank you and lots of love from Lachie, Shannon and Charles (his mum and dad).
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Hi everyone! It's been a while but we are so excited to share the first trailer for Bleeding Love with you all. You can check it out on YouTube by clicking this link:
We hope you all like it, we couldn't have made it without all your generous donations.
We still have a lot of work to do. We have our next round of interviews in the next couple of months and then down to the big job of editing the full documentary.
If you want to keep up to date on everything we are doing please like us over on Facebook:

Thank you all again, we can't do it without you!
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We are home! What an absolutely amazing experience the last three weeks have been. We have spoken to some incredibly passionate and knowledgeable people and have learnt a lot ourselves along the way. We have some fantastic footage ready to put together, but still have a lot of work to do!

We are incredibly grateful to all the people that have helped make this trip possible. Virgin Australia, Alan Johnson at the Ramada Plaza West Hollywood Hotel and Suites, Neil Frick, Dawn Rotellini and Val Bias at the National Hemophilia Foundation, Sonji Wilkes and Katie Verb at Hemophilia Federation of America, Sarah Ford, Vanessa Herrick and Alain Baumann at World Federation of Hemophilia / Federación Mundial de Hemofilia, Helene Bourgaize and David Page at Canadian Hemophilia Society, Michelle Kim at The Hemophilia Foundation of Southern California and Dr Julie Jaffray at Children's Hospital of Los Angeles - everyone was so welcoming and accommodating to two strangers from the other side of the world.

Now comes the hard part of actually making the documentary. Unfortunately it is also the most expensive part, so we are still looking to reach our goal. Keep on sharing and spreading the word!

All of you who have donated or have been been keeping up to date, liking and sharing our posts on Facebook and supporting us on this journey, we couldn't have gotten this far without your support .
P.S. Here's a sneak preview of a couple of our interviews!
Interview preview
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Massive news everyone! We have managed to secure some fantastic interviews and will be heading to the US and Canada very very soon. Check out our Facebook page for the video with all the details.
There is still a fair way to go with fundraising before we are able to finish the project, so keep liking and sharing. Thank you all for your support!
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Big thanks to everyone for spreading the word. It's all of your efforts that are keeping the momentum going! Here's a short video to let you all know how things are progressing.
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$12,450 of $25,000 goal

Raised by 137 people in 17 months
Created April 29, 2017
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Ryan Filippi
5 months ago

Great project. I look forward to seeing the finished product.

Jennie King
12 months ago

Wishing your little family a blessed and healthy future xo

Brett Coates
13 months ago

Shannon, Charles and Lachie, wishing you all, great success with your project. Children should not endure this, so I pray and hope your efforts bring real change to this issue. Much love to you all especially the little man! xx

Deon Powter
13 months ago (Offline Donation)
Becky Carli
13 months ago

Sending heartfelt prayers to Lachie and to his brave parents. Having gone through a very rare blood disorder (Diamond-Blackfan Anemia) with my daughter, I know how difficult and scary life with these rare diseases can be. I send you prayers of strength and hope! Keep smiling that beautiful smile Lachie! :)

13 months ago
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14 months ago (Offline Donation)
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