#Hope

ea04e4d838d111e38a6422000a1f971a_8Hi Everyone,

Ever wonder what HOPE looks like?  We saw it first hand today.  It looks like hundreds of people in a small community gathered to support a little boy who suffers from MPS II.  It looks like bouncy castles, sugar shacks, candy mountains, dunk tanks, fire trucks, police cars, games rooms, and magicians!  It looks like strangers donating money that some can’t spare to help us find a cure for MPS.  And while HOPE can take on many forms, I was so proud of the form it took today.

photo 1-4We spent the morning and afternoon at Jack’s Family Fun Fair, an event organized by the family of Jack Higginson, the little boy who was diagnosed with MPS II this summer who we’ve had the fortune of getting to know.  Jack’s aunts, Courtney, Sarah, Lee, and Emily, as well as many other family members, worked tirelessly over the past few months to pull this together.  Money raised is going to support Jack’s family as they deal with the high cost of treating this disease, and they will be making a donation to The Isaac Foundation’s MPS II Fund, which is co-ordinated and created by the equally amazing Deb and Ryan Purcell.

We had a fantastic time.  The boys took in all of the activities, dunked Jack’s dad in the Dunk Tank (twice!), and really enjoyed their time with Jack.  The Higginson family all did interviews for local television and did a fantastic job of spreading awareness of this disease and educating the public about how incredibly special our children are.  Everyone who attended seemed to really enjoy themselves.  The Higginson’s should be proud.  They’ve brought us one small step closer to a cure, and I’m so happy we got to be there to see the wonderful work they did.

photo 2-3We’re looking forward to spending more time with Jack, Ben, Kristin and their entire extended family.  We’ve always vowed to find a cure for this terrible disease.  It’s nice to find more partners in our quest along the way; partners who, like us, will never give up the fight for our kids!

Drop over to www.jacksjourney.ca to read about Jack and to follow his fight.

With Love,

A.

#Courage

photo 1Hi All,

It’s been a while since I’ve done an actual blog posting – as usual, things get busy and it falls down on my list of things to do (a list that never seems to end, these days!).  However, I wanted to take a moment to post some photos of the bravest boy I know.

Isaac has given us so much to be proud of throughout his 9 years.  He’s fought MPS courageously, and always with a smile on his face.  2 am MRI’s, countless trips to the hospital, brain scans, heart appointments, neurosurgeon visits – you name it, he’s done it.  Through it all, he never complains.

Today, Isaac’s been showing his new friend Jack around the hospital.  As many of you know, Jack (www.jacksjourney.ca) was diagnosed with MPS II this summer and we’ve had the fortune of being involved with his family, chipping in with whatever small amount of support we can offer.  I’m sitting at my desk shedding tears of pride as these two photos land in my inbox, photos of my son playing “big brother” to Jack.

It’s hard to define true courage – I know Isaac is brave because I’ve witnessed how well he’s dealt with the fight of his life.  But to have the courage to open up and share your experiences with someone else, with an aim of making their fight a bit easier, shows me just how incredibly courageous he is.

Fighting a life or death battle is hard, and it’s heartbreaking as a parent to watch your child deal with the disease.  The work we do is tiring, relentless and, hopefully, making a difference.  Photos like this keep us going, and I’m glad that my son (once again) is giving us the strength to keep at it.

We’re looking forward to our time together with Jack and his family – they are fighters.  And I know we’ll be celebrating together when we find our cure for our kids.

Hope you enjoy the photos.  Share as you see fit.

The photo up top shows Isaac and Jack playing at Marnie’s Lounge at Sick Kid’s Hospital this morning before treatment.  The photo below shows Isaac getting hooked up and ready for treatment.  Jack is watching intently beside him, waiting for his turn to get hooked up and for treatment to begin.  Truly precious and priceless.

With Love from a proud Dad,

A.

photo-11

 

Our favourite clown A. Leboo is coming to the Gala! This is his RSVP to Isaac, but he couldn't find those letters. This stands for "Gonna Go To Your Gala" Our night just got THAT much more exciting!

Shared from our Instagram Feed.
Our favourite clown A. Leboo is coming to the Gala!  This is his RSVP to Isaac, but he couldn't find those letters. This stands for "Gonna Go To Your Gala" Our night just got THAT much more exciting!

J&J – The Evolution of a Lovely Relationship

johnson_and_johnson_noHi All,

I’ve promised myself that I would post new blogs more often that I’ve found time for in the past.  It’s been another crazy year, for sure, but if I’m confident I can find 5 occasional minutes to blog now and then!

Just wanted to post a quick update while it was first and foremost on my mind.  I spoke with Dr. Ray at JnJ this evening and wanted to note how impressed I continue to be with the team at Janssen Pharmaceuticals and, as we’ve always referred to them as, Johnson and Johnson.  Or relationship started off, as you may remember, quite rocky.  The Isaac Foundation, along with our partner organizations, had long lobbied the company to commit to research of a highly promising drug (Elmiron) that the company makes and markets.  After repeated no answers, and constant put-offs, we put our advocacy efforts on behalf of our kids in high gear.  After months of hard work and patience, we finally had the opportunity to present our case to some decision makers within the company.  From that moment forward, things changed, as did our view on the company.

Once the potential of Elmiron was recognized by JnJ, the company acted quickly to repair any damage that was done with our organization but, more importantly, with the MPS community as a whole.  They committed to further study of their product, brought some of the most incredible MPS researchers and physicians together for a collaborative planning and educational session, and took a keen interest in our children.  They put a team together that dedicated themselves to learning about MPS and the struggles families dealing with this devastating disease face, something that I was incredibly impressed with, and continue to be proud of.

What impressed me most was that they didn’t take a serious look at this drug for financial reasons – JnJ stood to lose a lot of money during the entire endeavour.  They chose to look into this product because the data was compelling, and the impact it could have on saving our children was undeniable.  We often took aim at the JnJ Credo Values – values the company promoted and prided themselves on.  Once Dr. Amrit Ray took over the Elmiron/MPS file, that credo was put into action and the company showed me why they put such stock in their credo values.  In short – they undertook this project because it was going to positively impact the lives of our kids, and they felt it was the right thing to do.

Unfortunately, JnJ was prevented from further study of Elmiron due to legal issues relating to patents, along with Mt. Sinai’s deal with another drug company.  However, I’ve been fortunate to continue working with Dr. Ray and have had the opportunity to touch base with him on a regular basis.  He and his team continue to learn about MPS and our children, and I’m incredibly touched at how caring and compassionate he and his team have been.

I spoke with Dr. Ray this evening.  And like every time we chat, I was struck by how empathetic he is as it relates to our kids.  Johnson and Johnson is lucky to have him at the helm, and we at The Isaac Foundation are lucky that our relationship has evolved over time to find us at the place we are today.

Thanks, as always, for the support you provide us.

With Love,

A.

 

J&J – The Evolution of a Lovely Relationship

johnson_and_johnson_noHi All,

I’ve promised myself that I would post new blogs more often that I’ve found time for in the past.  It’s been another crazy year, for sure, but if I’m confident I can find 5 occasional minutes to blog now and then!

Just wanted to post a quick update while it was first and foremost on my mind.  I spoke with Dr. Ray at JnJ this evening and wanted to note how impressed I continue to be with the team at Janssen Pharmaceuticals and, as we’ve always referred to them as, Johnson and Johnson.  Or relationship started off, as you may remember, quite rocky.  The Isaac Foundation, along with our partner organizations, had long lobbied the company to commit to research of a highly promising drug (Elmiron) that the company makes and markets.  After repeated no answers, and constant put-offs, we put our advocacy efforts on behalf of our kids in high gear.  After months of hard work and patience, we finally had the opportunity to present our case to some decision makers within the company.  From that moment forward, things changed, as did our view on the company.

Once the potential of Elmiron was recognized by JnJ, the company acted quickly to repair any damage that was done with our organization but, more importantly, with the MPS community as a whole.  They committed to further study of their product, brought some of the most incredible MPS researchers and physicians together for a collaborative planning and educational session, and took a keen interest in our children.  They put a team together that dedicated themselves to learning about MPS and the struggles families dealing with this devastating disease face, something that I was incredibly impressed with, and continue to be proud of.

What impressed me most was that they didn’t take a serious look at this drug for financial reasons – JnJ stood to lose a lot of money during the entire endeavour.  They chose to look into this product because the data was compelling, and the impact it could have on saving our children was undeniable.  We often took aim at the JnJ Credo Values – values the company promoted and prided themselves on.  Once Dr. Amrit Ray took over the Elmiron/MPS file, that credo was put into action and the company showed me why they put such stock in their credo values.  In short – they undertook this project because it was going to positively impact the lives of our kids, and they felt it was the right thing to do.

Unfortunately, JnJ was prevented from further study of Elmiron due to legal issues relating to patents, along with Mt. Sinai’s deal with another drug company.  However, I’ve been fortunate to continue working with Dr. Ray and have had the opportunity to touch base with him on a regular basis.  He and his team continue to learn about MPS and our children, and I’m incredibly touched at how caring and compassionate he and his team have been.

I spoke with Dr. Ray this evening.  And like every time we chat, I was struck by how empathetic he is as it relates to our kids.  Johnson and Johnson is lucky to have him at the helm, and we at The Isaac Foundation are lucky that our relationship has evolved over time to find us at the place we are today.

Thanks, as always, for the support you provide us.

With Love,

A.

 

Thank You RBC and Arthur Lions Club!

AJR_1089The Isaac Foundation extends a huge thank you to the Arthur Lions Club and RBC for their incredibly generous donation to The Isaac Foundation through our satellite office with the More Family.  All funds donated will go directly to funding research and finding a cure for this rare and devastating disease.

The photo to the left shows Darren More with Jasper, accepting the generous donation from the Club.