An Update And Hiatus

Dear Friends of The Luke Pier Foundation,

Due to the February 2010 death of our son and brother, The Luke Pier Foundation will continue to take a hiatus for several more months. That being said, we wanted to be sure to give you an exciting update on Luke!

Luke is currently recovering from a successful chest surgery in July. Luke and his parents traveled to the Shriners Hospital for Children in Houston, Texas and stayed there for 10 days. The surgeon removed damaged cartilage, realigned Luke's sternum and placed two plates in his chest. Luke was not allowed to fly for six weeks, so the decision was made to rent a vehicle for the long drive home. We made it as comfortable as possible for Luke, and he never complained. To make the trip less traumatic on Luke, we stopped at two hotels to let him rest in a bed. Luke handled this surgery and travel amazingly well – we are so proud of his positive attitude and ambition during such a painful recovery.

At Luke’s latest checkup, the doctor discovered that Luke had broken one of the plates in his chest. The doctor said he has never seen this type of plate break before and that Luke is truly unique. It was decided that Luke will see the surgeon again in March 2011 to discuss removal of the plates. The estimated time for removal is the end of summer 2011.

Luke and we at The Luke Pier Foundation are truly grateful for your prayers during this incredibly sad time for us. Thank you for supporting us during this hiatus. We hope to update you again later this year.

Sincerely,

Extremely Proud Family of

LCPL Noah M. Pier USMC

KIA 02/16/2010

Marjah, Afghanistan

Johns Hopkins Appointment Update

You have probably been wondering about the latest on Luke’s surgery. We finally have an update for you! Luke was seen by Dr. Dietz at Johns Hopkins on June 1, 2010. Dr. Dietz will send his ok for surgery to the Houston Shriners Hospital and stressed that the sooner Luke has this procedure the better it will be for him. Dr. Dietz did not want any more time to pass because of Luke’s age. (Note: The surgery will be more difficult the longer we wait because Luke’s bones are naturally calcifying as he ages.)

Dr. Dietz requested that we have Luke genetically tested for Marfan Syndrome because Luke exhibits so many of the characteristics of the disorder. Dr. Dietz does not want to make an inaccurate decision as to whether or not Luke has a check up every year versus every two years. He said Luke is “growing into his aneurysm.” Dr. Dietz said he has seen this before, but because of Luke’s symptoms his aneurysm could change at any time. Dr. Dietz stressed to us that we should not consider Luke to be out of the woods yet.

We will not find out the genetic testing results for several weeks. In the meantime, Luke is still on the waiting list for the surgery on his sternum at the Houston Shriners Hospital.

I appreciate all of you and the support you have shown to our family and to The Luke Pier Foundation,

Vikki

Shriner's Hospital Evaluation

The following is an update on Luke's appointment at the Houston, Texas Shriner's Hospital for Children:

Luke has pectus excavatum (sunken chest). Many people live with this, never needing surgery. In the past year, Luke’s chest has become increasingly worse and now affects his breathing and causes pain. Dr. Dietz, the doctor that monitors his heart at the Johns Hopkins genetic clinic, referred Luke to a thoracic doctor in order to correct the pectus excavatum.

After being examined at the thoracic doctor’s office we were informed that Luke’s pectus excavatum was severe and he needed corrective surgery. We were sent home to have Luke’s CT scan, pulmonary heart function test performed and to raise the needed funds for the surgery.

We immediately began brainstorming the most effective ways to raise the funds needed for this surgery. In the meantime, I also applied to the Shriners Hospital for Children. We were initially denied help at the Shriners because of Luke’s heart aneurysm. I then reapplied, along with a letter from Luke's doctor at Johns Hopkins stating that Luke’s aneurysm was “slow growing” and that Dr. Dietz was referring Luke for this pectus surgery.

Not every Shriners Hospital performs pectus excavatum surgery so we ended up being accepted at the Houston Shriners Hospital. We met with the surgeon on March 18th, and he informed us that Luke's pectus excavatum was "unique", meaning the Nuss procedure (the less evasive surgery/the one I was fighting for him to have) would not be enough for Luke. The Nuss procedure would place a bar through an incision in both sides of Luke's torso and push the sternum out. He would have had to keep the bar in place for 2 to 4 years. Due to the fact that Luke's sternum is twisted almost 45 degrees, the Nuss procedure would not correct all of the problems.

Instead, the procedure Luke will have performed will open him across the front, going under muscle to realign his ribs and straighten the sternum in the process. The "normal" patient with this type of surgery typically has 3 ribs realigned, but again Luke's case is "unique" and requires the realignment of approximately 5 ribs. Luke will also have approximately 2 plates to hold everything in place. His surgeon expects a successful surgery that will improve Luke's quality of life.

Luke will be scheduled for surgery in a few months and we will be sure to keep you updated on his progress.

Thank you!

Quick Update on Luke

Due to the recent passing of Luke's older brother, LCpl Noah Pier - Marjah, Afghanistan, we have not been able to update you on Luke's progress. Please know that we will be back online soon with some exciting fundraisers and events to share with you. As always, thank you so much for your support - especially during this difficult time.

We do have a quick update to share at this time, though. Luke is being evaluated by the Shriner's Hospital on March 18th. We are uncertain what the future holds because Shriners Hospitals for Children initially denied Luke. We are excited that they have reconsidered due to the slow growth of his aneurysm. March 18th is the first step to begin the evaluation process.

We have a few prayer requests:

1. Please pray that the Shriner's Hospital will agree to perform Luke's Nuss procedure.


2. Please pray for the Pier family as we grieve the loss of Noah, our hero.


3. Please pray that 2010 will be a great year for The Luke Pier Foundation as we continue our mission: "to provide funding for life-saving scientific research focusing on, but not limited to, connective tissue disorders. We are also committed to help provide funding and encouragement to individuals for medical treatment they may not otherwise receive due to limited resources or lack of health insurance."

We will update you as soon as we know more! Thank you for your support!

In His Own Words

Luke wanted to talk about his imminent surgery and tell you what it's like to be in his shoes. We sat down and talked with him earlier this week, & this is what he had to say.

“At first I wanted the surgery for my looks, but now I want it because it feels like I am closing up, like I’m breathing through a tube that’s shrinking. I watch everyone run around and I see how they last longer with their breathing. I have to stop before them and catch up with my breathing. I feel frustrated and less than I can be. I have more energy but I can’t go further, I have limits because I have to catch up with my breathing. I don’t like having limits.”

When asked what his sunken chest feels like, Luke responded, “It hurts! I thought at first that it hurt everyone to run. When people finish running they can take a deep breath. I can’t. It’s like I can’t take enough of a deep breath, but instead I cough it out. Every time I try to take a deep breath, after I’m running, I go to breathe air into my lungs but my lungs are tightening. It blows air out really quickly, and I have to sit down to catch up. Now even when I do little things my breathing feels like my chest is closing in and my lungs are being stopped by my chest.

It’s like my lungs are being pushed, like you put a balloon in a jar and when you blow it up to a certain point you can not blow it up any more until you let the air out and blow again. My chest is the jar and my lungs are the balloon. Sometimes I’m not able to take a deep breath. It feels like I am slowly dying, something slowly is happening and I am getting worse and worse. I know I am not going to die, but that’s what it feels like sometimes.

I can do more, but my chest is holding me back. I feel like I’m less of being myself - that I can go further. I try to make my breathing not noticeable. I try to hide it. I don’t want people to think of me as weak.

I wish people could feel like I do so they would understand. I have so much energy inside of me but my breathing is holding me back. I am never able to go as far as I know I can – my breathing stops me, and I feel like I will bust.”

In his own words.

Support Ehlers-Danlos Syndrome Research

Special thanks to Maya Brown-Zimmerman for allowing us to republish her blog post below. Maya has been volunteering with the National Marfan Foundation since she was 14 years old. Currently she serves as a teen program coordinator for the NMF and local group leader. She also works with the Coalition for Heritable Disorders of the Connective Tissue. Maya was first suspected of having Marfan when she was 8 years old, and that diagnosis was confirmed by genetic testing at age 21, after she was also tested for Loeys-Dietz and vascular Ehlers-Danlos. She loves playing with her toddler son and spending time with her husband, Mark.

Support Ehlers-Danlos Syndrome Research

Today I write on behalf of my friends with Ehlers-Danlos syndrome, a disorder related to Marfan syndrome. There are multiple types of EDS (affecting 1.3 million people worldwide) and NONE have real treatments available to them, let alone cures. One of the most serious of these, vascular-EDS, is particularly close to my heart.

At the end of my freshman year of college, during a routine exam, my geneticist said he was SURE I had vascular-EDS. He was reluctant to give me any details about the illness until I threatened to go home and Google it myself.

He was hesitant because vascular-EDS is a death sentence. With vascular-EDS, aneurysms develop anywhere in the body and organs can spontaneously rupture. There is no way to predict when this will happen, nothing to do to prevent it. The average life-expectancy is in the mid 40s. Children have died from just doing a cannonball into the pool.

However, hope is on the horizon, and that’s where YOU come in. The Ehlers-Danlos Syndrome Network has been named a finalist in Chase bank’s Community Giving Challenge. They are up for a $100,000 prize. What would this money do for the foundation? Well, Dr. Hal Dietz has designed a “mouse model” of Marfan syndrome (basically, mice with Marfan). Our mice have dramatically increased doctors’ knowledge of Marfan syndrome, such that we now have an average life expectancy. $100,000 would be enough money for Dr. Dietz to begin work on a vascular-EDS mouse model.

Go here to vote for the EDSN!!! Then, tell all your friends!

Below, please read what Dr. Dietz has to say:

“Vascular Ehlers-Danlos syndrome (or vascular EDS) is a disorder of the body’s connective tissue – the material between the cells that give the tissues form and strength. In vascular EDS the body lacks sufficient type III collagen, a molecule that contributes to the strength of the skin, intestines, uterus, and most importantly, the blood vessels. People with vascular EDS live with the knowledge that they will die from this condition at an age ranging from childhood to young adulthood. They are also told that there are no effective treatments. There are no medications that are known to strengthen the tissues or delay blood vessel rupture. Attempts at surgical repair are often delayed there is confidence that the patient will die within hours if nothing is tried. This is because the tissues are so weak that they often simply fall apart during surgery – akin to trying to sew together wet tissue paper. Of all the conditions that I care for, I hate this one the most. It not only drastically shortens the length of life, but also robs people of any meaningful sense of hope and quality of life – always anticipating that the shoe will drop at any moment. Indeed, all too often children with vascular EDS lose any sense of ambition and purpose despite truly remarkable talents and potential. To their mind, “Why bother.”

Fortunately, there is now strong reason for hope…It is now our goal and intention to make mouse models of vascular EDS in order to learn more about the condition and to test this and other therapies. If someone had suggested 5 years ago that a pill might be able to treat a connective tissue disorder, I would have considered them crazy. Given recent breakthroughs and sufficient resources for further research, I will be shocked if a revolutionary new treatment for vascular EDS is not in general use within 5 years. I have already begun to share this sense of optimism with children with vascular EDS. Our job is to bring this goal to fruition. Their job is to begin dreaming big.”

Harry (Hal) Dietz, MD
Johns Hopkins University School of Medicine
Institute of Genetic Medicine

From The Beginning

Hello All!

My name is Vikki Pier and I am Luke’s mother. I have decided to try my hand at blogging in order to keep you updated with Luke’s progress, needs, and who knows - this may be therapeutic!

Luke is the 7th of my 10 children. He has always been tall, thin, energetic, tender hearted, mechanically minded and extremely flexible. An orthopedic doctor Luke was once seeing, because of pain in his joints and dislocations, called him “rubber band man”.

In February 2007 I took Luke to a cardiologist because he was complaining of heart pain. The pain was so great at times it would stop him in his tracks. Even with this pain I never dreamed Luke had any problem with his heart. Instead I believed the cardiologist would refer us to a doctor that would correct his sunken chest. During this visit we learned Luke had an enlarged aortic root and a possible connective tissue disorder.

After my initial shock and fear I began researching in order to make sure Luke received the best care possible. I discovered that one of the best alternatives for Luke to have, when surgery was needed, was the valve sparing procedure. This operation is not done at very many hospitals and the few I found would not accept us because of insurance reasons. Johns Hopkins Hospital in Baltimore, MD did welcome us into their genetic clinic and Luke has been seen there since 2007.

Luke’s aneurysm, at this time, is “slow growing”. As of his last visit in June 2009 he has been referred to an orthopedic doctor at Johns Hopkins in order to have surgery on his chest. The doctor said Luke needs this surgery because the progression of his chest deformity has been great and it is now interfering with his breathing. The doctor said it would be best to perform it now because of his age. He would perform the Nuss Procedure costing approximately $70,000. This figure includes the doctor and hospital fee.

Here I go again – I am not in shock and I am not fearful – overwhelmed and desperate is a better description. I am overwhelmed at the prospect of raising $70,000.00 and desperate to do just that. We (The Luke Pier Foundation) must raise this money! Luke does not have a choice; this procedure is not for cosmetic purposes. I contacted the Shriners Hospitals for Children and they have denied Luke because of his aneurysm and there is no insurance to pay for this.

The doctor and hospital at Johns Hopkins will work with us but we must raise the money for Luke’s surgery. Please pray for The Luke Pier Foundation as we brain storm our next fundraiser. Yes, I am overwhelmed, but I will not continue in that state because Luke needs my help. I have chosen to believe that the funds will be raised and Luke will receive this needed surgery.

• Proverbs 3:5 & 6 Trust in the Lord with all your heart; and lean not unto thine own understanding. In all thy ways acknowledge Him, and He shall direct thy paths.
• Jeremiah 32:27 Behold, I am the Lord, the God of all flesh: is there any thing too hard for me?

That should get you caught up on where we are today. I will continue blogging as we navigate through this journey. Feel free to post your questions and I will try to answer them in future posts.

Vikki

A New Approach

We at The Luke Pier Foundation have decided to take a new approach with our blog. Our first "new" post will be later this week, so check back soon! You will hear from us much more often. The focus of the blog will be less about the fundraisers (We'll still talk about those, though! It's why we're here!) and more about the journey.

We'll ask for your feedback along the way, so be ready to ask questions and participate in the conversation.

Thank you, as always, for your support these last three years (can you believe it's been three years already?). And we look forward to sharing the journey with you even more in 2010.

Update on Luke

It has been a busy spring and early summer for all of us at The Luke Pier Foundation. We finished the softball tournament in May and are happy to announce that we raised over $2,000.00 for our cause! Thank you to all of our supporters and teams. And a special thank-you to our sponsors, Community One Bank, Piedmont Natural Gas and Boatsman, Gillmore & Associates!

Luke had another appointment at Johns Hopkins a couple of weeks ago. He received good news about the aortic aneurysm (dilated aortic root) - it is still a good size for his body size and age! They want to continue monitoring him, of course, but he is okay for the time being.

Luke will need a different kind of surgery within the next 12 months, though. He will return to Johns Hopkins to undergo the Nuss procedure. Some people who have connective tissue disorders also develop pectus excavatum (or sunken chest). They want to perform the operation on Luke before he gets much older. Because he is still young (he's 15 now), his bones are still pliable and will adapt to the operation much better than if they were to postpone it. We are thrilled that he will have the opportunity to fix his chest and cannot wait to see the results. We will let everyone know more as the surgery gets closer.

We will be working on the plans for our next fundraiser in the coming weeks. If you have any ideas about fundraisers that you think would be successful and draw a crowd, please leave a comment or send an email to info@thelukepierfoundation.org.

As always, thank you for your support!

People Are Talking!

We are excited about our 3rd Annual Softball tournament tomorrow, & we're even more excited to read that people are talking about us!

SJB Weddings & Events has been a sponsor of The Luke Pier Foundation since our inception, & they're still talking about us after all this time! Click here to read their great post about us!

We're also being talked about on our new Twitter account. If you are on Twitter, feel free to follow us! Our ID is @TLPF, & we post updates about our fundraisers as well as important info on the latest news & research of connective tissue disorders.

Thanks again, SJB Weddings & Events, for your continued support!

Your Chance to Make a Difference

We now offer four options for our softball tournament sponsors! If you are interested in sponsoring our 3rd Annual Softball Tournament, please contact us at info@thelukepierfoundation.org. Thank you!

$1,000 Level - Grand Slam Sponsors

• Logo on www.thelukepierfoundation.org


• Link to your website


• Brief paragraph about your business on www.thelukepierfoundation.org


• Top level logo on volunteer t-shirts


• Top level logo on sponsors banner displayed at tournament

$500 Level - Home Run Sponsors

• Logo on www.thelukepierfoundation.org


• Link to your website


• Mid-level logo on volunteer t-shirts


• Mid-level logo on sponsors banner displayed at tournament

$300 Level - Triple Sponsors

• Link to your website on www.thelukepierfoundation.org


• Lower-level logo on volunteer t-shirts

$100 Level - Base Hit Sponsors

• Your company name on www.thelukepierfoundation.org


• Your company name on volunteer t-shirts

Payment Methods

• PayPal *preferred method (Select the 'Donate Now' button below, or on our website, to sponsor the tournament)


• Check


• Money order


• Payment must be received by April 25, 2009

The Softball Tournament is the Foundation’s largest fundraiser each year and is crucial to our operation. We have set an aggressive goal of raising $35,000.00 in 2009. We need your support to reach this goal. Funds raised this year through the tournament will be used for the following:

• Funding for life-saving scientific research focusing on, but not limited to, connective tissue disorders
• Funding to individuals for medical treatment they may not otherwise receive due to limited resources or a lack of health insurance
• Encouragement to individuals with medical needs

Thank you for your support!

Volunteers Needed

We are looking for volunteers for our 3rd Annual Softball Tournament on May 2, 2009. Volunteers are needed to help us:

• Pass out flyers at local ball fields to advertise tournament
• Make phone calls to potential tournament sponsors
• Tournament set-up & tear-down
• Entrance gate (collect entrance fees & direct teams to the check-in tables)
• Food service during tournament
• Track games & report final scores back to main table
• Other tasks as needed

We will work with your availability! Please contact Katti (katti@thelukepierfoundation.org) to sign up!

It's That Time of Year!

Contact us to sign up your team or sponsor this event!

Luke's Next Appointment

Many of you readers like to follow Luke's progress & hear the latest news on his condition, so we wanted to let you know when his next appointment at Johns Hopkins is scheduled for.

Luke will have another echocardiogram on June 23, 2009, to monitor the aneurysm. Immediately following that appointment, he will have a routine exam at the genetics clinic as well.

Please pray for the doctors' wisdom as well as for Luke's condition.

We also wanted to mention that we have our 3rd annual softball tournament coming up on May 2, 2009! We are really excited about this event and will post more information very soon!

What Is An Aortic Aneurysm Anyway?

So, you have read and heard about Luke & how he was diagnosed with an aortic aneurysm. And you may have even been to one or more of our fundraisers. You may still be wondering, though, "What is an aortic aneurysm anyway?" Well, we're here to help!

As you can imagine, we have done lots of research since Luke's diagnosis, & we have found a great resource that explains what an aortic aneurysm is. As we have stated before, Luke is being treated by Johns Hopkins University Hospital in Baltimore, MD. Their website has so many learning tools to help us understand more about Luke's condition as well as connective tissue disorders, in general.

Here is the definition of an aortic aneurysm, as told by Johns Hopkins*:

"An aortic aneurysm is a weak spot in the wall of the aorta, the primary artery that carries blood from the heart to the head and extremities. There are three common types of aortic aneurysm. Saccular and fusiform aneurysms are balloonlike swellings of the arterial wall that can occur in the portion of the aorta within the chest or just below the kidney in the abdomen. A dissecting aneurysm is a longitudinal, blood-filled split in the lining of the artery, usually occurring in the aortic arch near the heart. As blood is pumped through the aorta, the weak spot in the elastic arterial wall bulges outward.

The risk is that an aneurysm will eventually rupture, with great bleeding internally and complete collapse of circulation. Sudden severe pain, shock, and loss of consciousness usually occur within seconds, and death is imminent in more than 50 percent of cases, even with emergency surgery. Thus, the goal is to detect and treat an aortic aneurysm before it ruptures. Aortic aneurysms generally affect people over 60 and are more common among men."

As evident by the description above, Luke's condition is very rare because he is not over 60 (he was 13 when he was diagnosed!) - yet another reason to donate to The Luke Pier Foundation because so much still needs to be learned about pediatric cases like Luke's!

*Retrieved from http://www.hopkinshospital.org

A Big Thank You!

We had a great time at Holiday From the Heart at Mercedes-Benz of South Charlotte! Approximately 50 people attended, & we were able to get our name out to that many more people in the Charlotte area!

The silent auction table was amazing - so many great businesses & individuals donated to the auction this year, & we are so thankful to them for their participation! Check out our website for more information about the sponsors of this year's event!

We thought you would enjoy seeing a few pictures from the event. If you were not able to attend, you really missed out on a wonderful night of food, fun & spreading the word about The Luke Pier Foundation, aortic aneurysms & connective tissue disorders. Click here to view the full album.

Live cooking demonstration by Blue Restaurant.
The Kimberly Carper Band donated their time to the event & did a wonderful job singing some amazing blues & jazz!
A large view of the dealership, including the great silent auction table right in the center.

Thank you again to all who came & donated their time & money to our great cause. In all we raised approximately $1900 from the silent auction, & Mercedes-Benz of South Charlotte gave us a generous (& unexpected!) donation of $2500. THANK YOU TO EVERYONE!

Holiday From the Heart

*Click on the image to view the high-resolution invitation.

We are still in need of silent auction items for this fundraiser!

Please consider donating* a gift basket from your favorite store or gift card from your favorite restaurant to The Luke Pier Foundation to help make our silent auction a success. We are also accepting cash donations that we will use to purchase items for the silent auction! Please contact us today if you are able to donate* something to this exciting event! *Donations are tax deductible as permitted by law.

Save the Date

To contact us about this event, please send us an email!
*Click on the image to view it in a larger format.

Our Next Event!

Well, fall is officially here, & we here at The Luke Pier Foundation are busy planning our next event. It's hard to believe that this will be our 4th event already!

We have a meeting with the event hosts on Friday, & we hope to be able to give you more details after that planning session. In the meantime, please pray that the event is a success & that we can all pull together to finalize the details!

We have a lot of work ahead of us, & if you are able to volunteer your time & energy to helping us make this event successful, please let us know!

Stay tuned for more details about this exciting event!!!

How Prepared Are You?

We here at The Luke Pier Foundation subscribe to the updates sent by The National Marfan Foundation. Often, the updates are regarding specific drug therapies or research pertaining to the Marfan Syndrome which Luke has not been diagnosed with. This update in particular is important for any of our readers, though.

Connective tissue disorders and the potential aortic aneurysms present themselves in ways other than just the Marfan Syndrome. The following information is very important for those who specifically want to learn more about aortic dissections or have family members who have this condition. The information is important for health care providers, patients and family members alike.

Click on the following links to learn more (information provided by NMF):

1. Emergency Situations Main Page - this page contains a wonderful amount of information, summarized in an easily understandable format
2. Emergency Information Packet - this packet will help guide you through all the steps of emergency preparedness in the event of an aortic dissection. It even includes a printable aortic aneurysm medical alert card that you can give to the emergency room attendant or EMS!
3. Hospital Interview Information - this contains questions to ask your local hospital to ensure that they are equipped to help in the event of an aortic emergency
4. Emergency Diagnosis & Treatment of Aortic Dissection - this is an online booklet that has very helpful Q&A's about how aortic aneurysms and dissections are diagnosed

Considering a donation to The Luke Pier Foundation? Click here to learn more.