Hey everyone, our good friends over at the Norcal Fighting Alliance are hosting the most bad-ass event in Sonoma County. Teaming up with Cage Combat FC (NorCal), they are exhibiting some truly violent benevolence! On March 3, 2012, which also just happens to be Jon's first birthday, they are going to engage in some straight-up MMA combat craziness and they're including our foundation in the madness! Make sure to buy a ticket to the event at the link below and 20% of your ticket price will be donated to the Jon Michael Martin Foundation!!!
BUY YOUR TICKET HERE!!! http://cagecombat-jmmfoundation.eventbrite.com/ BUY YOUR TICKET HERE!!!
We'll be unveiling some more aspects of the event as it draws closer, but make sure that you reserve your seat today!!! Special thanks to Jessica and Dave Terrell, David Mitchell, Justin Gill and Tom Call for thinking of our little guy.
Monday, January 9, 2012
Tuesday, December 13, 2011
JMM Foundation Fundraiser - Powell's Sweet Shoppe!
Our good friend Elizabeth Rait has put together an amazing fundraiser at Powell's Sweet Shoppe TODAY, 12/14/2011!!! Just go click H E R E for all the details. Make sure you print up a flyer and bring it in to Powell's Sweet Shoppe, 720 Mcclelland Drive in Windsor, and 20% of your purchase will be donated to Jon's foundation!!!
A special thanks to Elizabeth, Hulk Helping Hearts and all the people involved in raising funds for our son's next surgery. If you have any questions, e-mail us at jmmfoundation@gmail.com. Also, if you can't make the event, you can always donate with the button on the top right of this screen!!!
We hope to see you all at Powell's tomorrow. Have a happy holiday season!!
A special thanks to Elizabeth, Hulk Helping Hearts and all the people involved in raising funds for our son's next surgery. If you have any questions, e-mail us at jmmfoundation@gmail.com. Also, if you can't make the event, you can always donate with the button on the top right of this screen!!!
We hope to see you all at Powell's tomorrow. Have a happy holiday season!!
Sunday, October 9, 2011
Hulk Helping Hearts
I just wanted to give a VERY special shout out to this amazing group of people who have started Hulk Helping Hearts: Jessica LaVenter, Joshua Cox, Tye and Bobbie Rivera, and ALL of the Hulksters, their friends and family, and the general Anytime Fitness community. You all give us so much hope and faith in the inherent goodness of humanity, it is a really beautiful thing.
A quick reminder that, if you haven't already, you should go to the Zumbathon and Bake Sale Facebook Event page and learn all about this amazing event that Hulk Helping Hearts is putting on for Jon Michael. If you can't make it, don't fret! You can always donate at the upper right corner of this page. Please specify in the note section of the donation page if you would like us to send you one of the AWESOME Hulk Helping Hearts bracelets that you will see below!!!!! A donation of $5 or more is eligible for a bracelet!!!!!
I really wanted to try and highlight how amazing this support for our son is. These pictures are a small sample of how FRIGGIN' AWESOME this community around us in. We love you all!!!!!
Josh Cox, Tye Rivera and Amanda Valle
Amanda Martin
Brandon Hallengren
Bud Hulk
Cara Tocchini, Repping the Awesome 80's
Carlo Piscitello
Chris Keys
Bracelet close-up
Jeff Martin
From left to right: Bobbi Rivera, Jessica LaVenter, Josh Cox, Kim Yoxall and Tye Rivera
Jon Hallengren
The Stud Muffin himself, Jon Michael Martin
HULK Himself, Joshua Cox
Kids for Hulk Helping Hearts!!!
Mike Mazanec and Holly Hanson
Paul Larsen
Sharon Hallengren
Gill Clan and Sierra and Joey Balkin
Tammy Larsen and Josh Cox
Hulk Girls for Hulk Helping Hearts!
Teygan Mason
Love to you all and have a great Sunday!!!!!
A quick reminder that, if you haven't already, you should go to the Zumbathon and Bake Sale Facebook Event page and learn all about this amazing event that Hulk Helping Hearts is putting on for Jon Michael. If you can't make it, don't fret! You can always donate at the upper right corner of this page. Please specify in the note section of the donation page if you would like us to send you one of the AWESOME Hulk Helping Hearts bracelets that you will see below!!!!! A donation of $5 or more is eligible for a bracelet!!!!!
I really wanted to try and highlight how amazing this support for our son is. These pictures are a small sample of how FRIGGIN' AWESOME this community around us in. We love you all!!!!!
Josh Cox, Tye Rivera and Amanda Valle
Amanda Martin
Brandon Hallengren
Bud Hulk
Cara Tocchini, Repping the Awesome 80's
Carlo Piscitello
Chris Keys
Bracelet close-up
Jeff Martin
From left to right: Bobbi Rivera, Jessica LaVenter, Josh Cox, Kim Yoxall and Tye Rivera
Jon Hallengren
The Stud Muffin himself, Jon Michael Martin
HULK Himself, Joshua Cox
Kids for Hulk Helping Hearts!!!
Mike Mazanec and Holly Hanson
Paul Larsen
Sharon Hallengren
Gill Clan and Sierra and Joey Balkin
Tammy Larsen and Josh Cox
Hulk Girls for Hulk Helping Hearts!
Teygan Mason
Love to you all and have a great Sunday!!!!!
Friday, September 23, 2011
ZUMBATHON AND BAKE SALE!
Hello everyone!!! I just wanted to put out a quick reminder that our wonderful, amazing friends at Anytime Fitness are putting on a Zumbathon and Bake Sale on Sunday, October 16th, from 12:00 to 3:00 pm at Anytime Fitness in Santa Rosa!!! You can RSVP to the event on Facebook at https://www.facebook.com/event.php?eid=209885999073721!!!
Again, so many thanks to Tye and Bobbi Rivera, Jessica Laventer, Joshua Cox and so many others for making this possible and for helping us raise money for our son. We love you all!!! If you have any questions about the event, feel free to e-mail jmmfoundation@gmail.com for information!!!
Again, so many thanks to Tye and Bobbi Rivera, Jessica Laventer, Joshua Cox and so many others for making this possible and for helping us raise money for our son. We love you all!!! If you have any questions about the event, feel free to e-mail jmmfoundation@gmail.com for information!!!
Wednesday, September 14, 2011
Long Overdue
It's amazing how quickly time can pass. I have been derelict in my duties of keeping this blog up to date. That will be rectified immediately.
Jon is doing amazing. Through your prayers, hopes and even your fleeting thoughts, he has been able to buck every norm. They told us he would be in the hospital for 3-4 weeks after surgery...he was out in 6 days after surgery. They told us that he would need his feeding tube indefinitely...he has had it out for over a week now and is eating on his own like a champ. He is an incredible testament to all that is amazing in humanity.
Our amazing family in the Hulk bootcamps at Anytime Fitness in Santa Rosa have come together to create a very special event to help raise money for Jon Michael's next surgery. As I outlined in a previous blog post, our out-of-pocket expenses for this next surgery are going to be (to us) astronomical. I would like to send a special heart-felt thanks to Joshua Cox, Jessiva Laventer and Tye and Bobbie Rivera for helping to organize the first of many events that will be held to help our family make sure that Jon Michael's care will remain unparalleled in excellence and modernity.
The event can be found on Facebook at https://www.facebook.com/event.php?eid=209885999073721. If you are not able to make the event but want to donate, there is always a link up at the top of this blog that goes straight to The Jon Michael Martin Foundation.
Again, thank you to everyone for your love, thoughts and prayers. Our son will one day throw a party for all of you in thanks. Or...at least I will, and I'll let him know why he's paying for it. ;)
Jon is doing amazing. Through your prayers, hopes and even your fleeting thoughts, he has been able to buck every norm. They told us he would be in the hospital for 3-4 weeks after surgery...he was out in 6 days after surgery. They told us that he would need his feeding tube indefinitely...he has had it out for over a week now and is eating on his own like a champ. He is an incredible testament to all that is amazing in humanity.
Our amazing family in the Hulk bootcamps at Anytime Fitness in Santa Rosa have come together to create a very special event to help raise money for Jon Michael's next surgery. As I outlined in a previous blog post, our out-of-pocket expenses for this next surgery are going to be (to us) astronomical. I would like to send a special heart-felt thanks to Joshua Cox, Jessiva Laventer and Tye and Bobbie Rivera for helping to organize the first of many events that will be held to help our family make sure that Jon Michael's care will remain unparalleled in excellence and modernity.
The event can be found on Facebook at https://www.facebook.com/event.php?eid=209885999073721. If you are not able to make the event but want to donate, there is always a link up at the top of this blog that goes straight to The Jon Michael Martin Foundation.
Again, thank you to everyone for your love, thoughts and prayers. Our son will one day throw a party for all of you in thanks. Or...at least I will, and I'll let him know why he's paying for it. ;)
Wednesday, August 3, 2011
Heart Catheter
Guys aren't supposed to cry. We're especially not supposed to lose it. You all know what I'm talking about...that uncontrollable sob that creeps up in the back of your throat like an AA meeting ready to vacate the premises because the coffee guy didn't show up.
We all have a front. I found out today that my front is my indifference. It was an interesting realization.
As I posted on Facebook earlier, the heart catheter procedure was delayed about 2 hours. That gave me ample time to be pissed off at something innocuous instead of admitting that I was incredibly scared about what my son was waiting to go through. It's so interesting how much more aware he is now. It definitely makes all of this a lot harder.
The poor little guy hadn't eaten for 16 hours when we finally were able to get him into his hospital gown and prepare for the surgery. I was hoping that I would get to scrub in and be with him until he was put to sleep, but the anesthesiologist gently made me aware that my being there would take complete focus off their primary objective: Jon Michael. I have a feeling that this wasn't the first time she played to someone's emotions so that her job would run smoothly. Can't say that I blame her.
Amanda and I were able to walk him down to the heart catheter O.R. This procedure was actually done at Stanford Medical which shares multiple entrances with LPCH (Lucille Packard Children's Hospital). When we got to the still swinging doors, we both kissed and hugged him and cried on him and handed him over to the able hands of the heart catheter team.
There really aren't words to describe how hard it is to walk away from your child...especially when you know something he or she doesn't. Like how they're about to get a catheter shoved up a major vein and have various dyes spurt into their heart so that pictures can be taken.
All things considered, everything went really well. We found out that Jon Michael will be a prime candidate for the Glenn Shunt that he is scheduled for on Friday. I have the distinct feeling that I'm taking this a lot harder than he is.

I finally broke down today. I had kept up a pretty good front and been strong for Amanda which, at the end of the day, is any spouse's job. Where one fails, the other must persevere. It's the only way a relationship works. Watching my son writhing on the recovery table, red as a cherry from screaming and having to have morphine shoved in his IV to calm him down...it wasn't the same when he was five weeks old. He was still a person...but he didn't yet have personality. Everything's changed, yet everything's stayed the same.
Life moves in mysterious ways. I guess all we can really do is make sure that we have a life vest when the canoe tips over.
As I type this, I'm sitting next to the little guy at 3West, the third floor of LPCH. Hopefully we will get to take him back to the hotel tomorrow night so we can spend some much needed face time with him before open heart surgery on Friday.
Thank you all again for your prayers and thoughts for Jon Michael. All three of us are blessed to have your support and love. We are still trying to raise some money for the hotel, since we really don't know how long we're going to be here and Ronald McDonald has pretty much ruled out any chance at our staying there any time in the next month, so if you know anyone who might want to donate or you'd like to post this blog on your favorite social media site, we would be very appreciative.
I hope you all have a lovely day tomorrow and we will keep you updated on his surgery schedule.
~Jeff Martin
We all have a front. I found out today that my front is my indifference. It was an interesting realization.
As I posted on Facebook earlier, the heart catheter procedure was delayed about 2 hours. That gave me ample time to be pissed off at something innocuous instead of admitting that I was incredibly scared about what my son was waiting to go through. It's so interesting how much more aware he is now. It definitely makes all of this a lot harder.
The poor little guy hadn't eaten for 16 hours when we finally were able to get him into his hospital gown and prepare for the surgery. I was hoping that I would get to scrub in and be with him until he was put to sleep, but the anesthesiologist gently made me aware that my being there would take complete focus off their primary objective: Jon Michael. I have a feeling that this wasn't the first time she played to someone's emotions so that her job would run smoothly. Can't say that I blame her.Amanda and I were able to walk him down to the heart catheter O.R. This procedure was actually done at Stanford Medical which shares multiple entrances with LPCH (Lucille Packard Children's Hospital). When we got to the still swinging doors, we both kissed and hugged him and cried on him and handed him over to the able hands of the heart catheter team.
There really aren't words to describe how hard it is to walk away from your child...especially when you know something he or she doesn't. Like how they're about to get a catheter shoved up a major vein and have various dyes spurt into their heart so that pictures can be taken.
All things considered, everything went really well. We found out that Jon Michael will be a prime candidate for the Glenn Shunt that he is scheduled for on Friday. I have the distinct feeling that I'm taking this a lot harder than he is.

I finally broke down today. I had kept up a pretty good front and been strong for Amanda which, at the end of the day, is any spouse's job. Where one fails, the other must persevere. It's the only way a relationship works. Watching my son writhing on the recovery table, red as a cherry from screaming and having to have morphine shoved in his IV to calm him down...it wasn't the same when he was five weeks old. He was still a person...but he didn't yet have personality. Everything's changed, yet everything's stayed the same.
Life moves in mysterious ways. I guess all we can really do is make sure that we have a life vest when the canoe tips over.
As I type this, I'm sitting next to the little guy at 3West, the third floor of LPCH. Hopefully we will get to take him back to the hotel tomorrow night so we can spend some much needed face time with him before open heart surgery on Friday.
Thank you all again for your prayers and thoughts for Jon Michael. All three of us are blessed to have your support and love. We are still trying to raise some money for the hotel, since we really don't know how long we're going to be here and Ronald McDonald has pretty much ruled out any chance at our staying there any time in the next month, so if you know anyone who might want to donate or you'd like to post this blog on your favorite social media site, we would be very appreciative.
I hope you all have a lovely day tomorrow and we will keep you updated on his surgery schedule.
~Jeff Martin
Tuesday, August 2, 2011
Pre-op with the Heart Catheter Team
Went down to Lucille Packard Children's Hospital today at 12:30pm for Jon Michael's pre-op with the Heart Catheter Team. He was teething and fussing all night so we knew we were in for a long day. When we were making the turn onto the hospital campus, we both simultaneously let out a sigh...it seemed like a year since we'd made that turn yet seemed like yesterday all at the same time. Either way, it's a heart-breaking turn to make.
Unloading the little guy into the stroller, we enjoyed the warm Palo Alto sunshine on the short walk up to the hospital entrance. Admittance was fairly quick and then we headed over to the Cardiac Intake Unit. He weighed in at 13.2 lbs and is about 25" in height...long? Seems weird to measure someone that can't stand in height. Seems weirder, I suppose, to measure him like a reptile. I still say 25" long.
Next was an echo cardiogram. It took quite a while for the technician to find his shunt which, according to Amanda, happens from time to time. After about a half an hour, Jon Michael was pretty much over listening to Pachabel's 'Canon' and getting his chest pressed on by a gel-coated probe, so he started screaming. Amanda got him to sleep and the technician was able to finish up in peace.Another technician came in and did a quick EKG. After that we got debriefed by one of the members of the Heart Catheter Team. Basically the plan is to bring him in tomorrow at 9:30am. They're going to let me follow him all the way into the operating room in scrubs and stay with him until they put him under. The procedure, barring complications, should be about 4 hours, after which they will discharge him up into another part of the hospital called 3West for overnight recovery. We have been assured that tomorrow afternoon we will find out the results and they will be able to confirm that he is still a good candidate for the Glenn Shunt that he is scheduled for on Friday.
Amanda and I think it's important that you all share this journey with us as much as possible, so I'll post again tomorrow night with pictures and updates. We'd also like to take this time to thank everyone who has donated and made it possible for us to stay here with our son during this difficult time. You are all amazing friends and, as far as I'm concerned, you're all family now.
Please have an amazing evening and a beautiful day tomorrow! Also, feel free to re-post the link to this blog on Facebook, Twitter or whatever sort of social media poison you prefer. We're still trying to raise money on the link to the right, so any re-posts would be much appreciated!!!
Much love,
~Jeff Martin
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