TeamCamden

TeamCamden Camden is a 6 year old boy who loves his 2 brothers, sister, mom, dad and all his family very much. Army.

He is a typical boy that loves playing video games. He is outgoing, talkative and very sweet! Camden's parents are both veterans and his father is still actively serving in the U.S. They are very proud to be a military family! Camden first experienced pain in his legs that was later followed by overall muscle weakness. He began having problems climbing stairs, rising from the floor, keeping up with his siblings, running, jumping, sitting up, lifting his head and became extremely fatigued. We quicly realized something was very wrong. After one trip to his pediatrician we learned his ck was 25,000 along a few other abnormal tests. He was then sent to a neurologist and geneticist in San Antonio and was diagnosed with Duchenne Muscular Dystrophy. This was devastating to our family. From there we asked to be referred to another neurologist in Dallas where Camden was then checked by a pulmonolgist and cardiology. He was discovered to have an abnormal EKG, sinus tachycardia and restrictive lung disease. He also immediately began physical therapy, put in leg braces, given a wheelchair for his quick progression and sent home with a cough assist to help with his lungs. Other the next few months Camden went through extensive testing, a muscle biopsy, echocardiogram, EMG, tons of genetic tests, numerous muscle exams and labs. He began to progress at such a fast rate, losing tons of weight and muscle around his chest arms and legs. He was now using the wheelchair constantly and was unable to do much. After numerous tests continued to come back negative for a certain type of dystrophy, we took Camden to a Reumatologist in Austin for a second opinion. He was almost convinced that Camden indeed had an unknown, extremely progession MD but was questioning the fact that he also presented with a few autoimmune disease like symptoms such a Raynaud's Phenomenon and rash with sun exposure. He sent off Camden's case and tests to Dr. Rider in DC and she had camden do a myositis antibody panel with two different labs. A few months later his labs came back positive twice for anti-srp polymyositis and we were quickly flown to DC to see Dr. Rider and her team and begin treatments. Camden has a very tough case that has involved his heart and lungs and caused a huge amount of muscle damage, however he is on very aggressive treatments that include high dose daily steroids, IVIG infusions, chemotherapy injections, daily immunosupressants, nexium and vitamins. He continues to wear leg braces and do twice a week physical therapy sessions. All the medications have caused stomach issues along with loss of bone density and an overlapping autoimmune thyroid disease. There is currently no cure and is life threatening condition. This page is for those who want to follow this little boy and his family's incredible and courageous journey. "Never let the fear of striking out get in the way."- Babe Ruth

MAILING ADDRESS:

Matthew Camden McAlpine
218 Lottie Lane
Harker Heights, Tx 76548

DONATIONS:

Donations for Camden's Person Medical Fund and Bucket List can be sent via paypal to teamcamden@outlook.com. If you would like to send a donation via postal service, please make checks payable to Matthew Camden McAlpine. Cure JM Foundation to help families and research for a CURE! http://www.curejm.org/donate/index.php

Congrats to the Texas Rangers on winning the World Seriws!  We will never forget what you did for our Cam!
02/11/2023

Congrats to the Texas Rangers on winning the World Seriws! We will never forget what you did for our Cam!

Like all little boys, Camden already has big dreams. He wants to be a baseball player for the Texas Rangers when he grows up. With all th...

We haven’t used Cam’s page in a while due to his privacy.  However, Cam was recently given a service dog!  Him and I cre...
20/07/2021

We haven’t used Cam’s page in a while due to his privacy. However, Cam was recently given a service dog! Him and I created an Instagram page for his boy, Buddy! He has just as much control of it as I do. This is something Cam is very passionate about. The Walter Reed Facility Dogs played a huge role in his love for them for him. To finally get his own is amazing! Here is a little blip of what we shared on Cam’s new “Buddy”. We’d love for you all to follow Buddy and Cam on IG. Let’s make social media positive again!😉🥰😍😘🐶. Follow Buddy and Cam

“Meet Buddy! Buddy will be Cam’s very own service dog!!!

This beautiful Aussie was gifted to Camden by a sweet angel, Maddy Jo, who is the breeder and trainer at Legendary Canines, LLC. Maddy picked this boy out of her litter for Cam after hearing what he liked, a black tri with white on his head and two different colored eyes! Cam he told me he always loved dogs with two different colored eyes and that they were different, like him. Well, she certainly delivered on his dream dog!

Buddy is beautiful and him and Cam are living it up during this important bonding time. He will be in training for a while with us and then go back to Maddy for official training. He will be trained based on Cam’s specific needs and be able to go to anywhere with Cam, especially all medical. I’ve never seen our boy so excited about something! It comes at such a crucial time in his life and there couldn’t have been a better blessing for him. Mental health is so important in these chronic diseases and I truly feel Buddy is going to be such a wonderful component with his companionship for Camden.

Maddy and another amazing angel, Melanie Scott, made this happen for Cam. Melanie shared Cam’s story with Maddy and together they dreamed of this plan for Cam to have a trained service dog. Maddy told me she felt in her heart she needed to gift Cam the right dog and Melanie wanted to provide the means for his service training with her. Maddy, who has a chronically ill sibling, understood a lot of our journey and shared with us how therapeutic dogs have helped her, her sister and her family. When she reached out with this plan her and Melanie had I come up with I was just in shock and simply just awe. Melanie has always loved and supported our son and then she brought Maddy in our lives too! This year, the move and Cam’s health have been a struggle and our boy needed something so badly.

While we were in DC for Cam’s hospital evaluation we talked a lot of having a service dog and what that would look like and mean for Camden. He literally lit up at the possibility of it. He watched many soldiers at the hospitals with their dogs and several in the airports. He couldn’t believe he could have one to be with him for everything too! Once he found out he would be getting one he started counting down the days til we could drive to Fate, TX and pick him up! These two ladies made a way for so much more joy in this journey. We are so grateful and I’m so thankful to have them both in my life.

Buddy loves Cam and he is such a good boy! Maddy sure knows what she is doing because we have had him for 5 days now and he has yet to have a single accident! He has learned quickly that Cam is his person and we are eager to help do our part in his early training.

One thing we hadn’t thought of that Maddy said she will have him do is be trained to go get Mom or Dad when Camden commands him to when he needs help or there is an emergency. Love that!!!❤️❤️❤️

We can’t wait to share as these two grow and work together. This is the beginning of a beautiful friendship for sure. Cam is one very lucky and loved boy.”

08/09/2020

To Ty, Jax and Fia💗

DEAR SPECIAL NEEDS SIBLING,
I know you don’t have a diagnosis next to your name or an extensive medical history. You’re used to being known as so and so’s brother/sister. You wonder sometimes if anyone even remembers your name. Your sibling is called special by the world, and unintentionally seems to attract all the attention in your family. There are so many times when you feel forgotten, but I want you to know something. You are not forgotten, and you are far from typical. You are incredible. I know it’s hard watching your brother or sister struggle. Your name may not be on the chart, but your life has been changed by their diagnosis. I know it doesn’t seem fair, and it’s not. It’s not fair for you or them. It’s hard, and it hurts way more than it should.

I know your life doesn’t look like your friends’ lives. You’ve had to sacrifice so much, even if you don’t understand what that word really means yet. You’ve missed out on sports teams, birthday parties, sleep overs, and fancy holidays. Waiting rooms are the norm, and you can rattle off medical terminology like your ABC’s.

You’ve had to grow up too fast. You’ve listened to doctors and therapist tell your parents all the things your sibling isn’t going to do. You’ve heard all the side effects and possible complications. You’re scared more than you’re willing to admit. You’ve watched as your mum and dad fought back tears and tried to smile. They told you nothing was wrong, but you knew different.

And it broke your heart, but you pretended like it didn’t. You put on a brave face, and you tried to make your mom smile. You’ve taken on more responsibility than you even should, and you feel like it’s your job to keep everybody smiling and laughing even when you’re sad and scared inside.

I wish I had a way to make it all better for you, but I don’t. I can’t wave a magic wand and make your brother or sister all better. I can’t give you back all the time you’ve sat waiting at doctor’s offices and therapy centers. I can’t make the difficult parts of your childhood better, but I can tell you this. Your suffering is not wasted. You are going to be the most amazing adult. I am convinced that the next generation of great world changers are going to be from special needs families because in the middle of all the hard and all the heartache, you’ve learned what really matters in this life. You’ve learned so many things that so many adults can’t grasp. You’ve learned things that a textbook could never teach you. You have seen real life. You’ve stood in the middle of a raging storm with no umbrella, and instead of running to hide, you’ve waited for the rainbow never doubting that it will come.

You’ve learned the value of hard work. You’ve learned to never give up. You’ve helped out in therapy sessions. You’ve been your sibling’s biggest cheerleader. You’ve encouraged them more than anyone else, and you have learned to celebrate every little milestone.

You are going to change the world because you look at the world and see each person as equal. You don’t see physical or mental ability as a gauge of a person’s worth. You understand that every life is worth fighting for even if it looks different from what the world considers normal. You know what it means to treat someone with true dignity and respect, and you consider it an honor to serve others. You don’t think of yourself as better than anyone, and you know that a smile is the best form of payment.

God hasn’t placed you in your family by accident. He is grooming you to be more than you can ever imagine. You are being refined in the fire. Special needs siblings, take heart. You are not forgotten. You are a world changer, and I can’t wait to see all the good you will do.

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Walk Strong Across America for CureJM!!!Thank you to those who walked with us this morning and those who walked "in spir...
04/07/2020

Walk Strong Across America for CureJM!!!

Thank you to those who walked with us this morning and those who walked "in spirit" with us in support of Camden! We love you all so much!

Link in the comments to donate to CureJM for Team Camden!

Happy Birthday to one of the most amazing ladies with a heart of gold!  You and your dogs have changed our entire family...
04/07/2020

Happy Birthday to one of the most amazing ladies with a heart of gold! You and your dogs have changed our entire family! We have never felt so loved and supported! Your love for Cam has kept us grounded at Walter Reed.

Amy, we hope you had the best day ever! We love you!

On Saturday we will be walking to help raise money and awareness for the CureJM Foundation. For the last 7 years Camden ...
30/06/2020

On Saturday we will be walking to help raise money and awareness for the CureJM Foundation. For the last 7 years Camden has been battling this disease. This foundation is run by family members of JM patients. All of the money raised will go towards finding better treatment and a cure. As of right now, there is no cure for JM. Please consider helping us in our efforts. Thank you to those who have already contributed!

Join or Donate to the Team for the 2020 Walk Strong Across America - Maryland fundraising event

I'll never forget this happening in Texas to Camden!  I wish more people saw all the good there still is in the world wi...
24/06/2020

I'll never forget this happening in Texas to Camden! I wish more people saw all the good there still is in the world with our amazing first responders! Worth the read and the share!

These two firemen were driving down our street tonight while I was sitting out front watching the kids play. Camden was taking his brother's YFlickr and riding it down the rode and then walking it back up. I had turned my head to listen to Ty ask me to watch him do something and when I turned back around to check on Camden I saw the passenger fire fighter jump out of their truck and head out to Camden. He stood like this talking to him for about 10 whole minutes, placed a sticker on him and then jumped back in. When they passed our house they waved and turned the lights on for a sec for the kids to see. A minute or so later when Camden got back to our driveway he had a huge smile on his face and was proudly showing me his sticker the firemen gave him. I asked him what they were talking about. He told me he was asking him how he was, how his summer was going and invited him to come down to the fire station this week to see the fire trucks and what all they do. He was so proud and couldn't wait to run inside and tell his Daddy about his special visitor. These sweet, simple acts of kindness go a long way. These men had no idea they were talking to a child daily fighting a disease who had just come back from a long trip to San Antonio after more tests and more blah news. They made his day and they certainly made mine. I sat there in awe of their kindness. I can never get over how good God is and how he is constantly SHOWING my family just how much he loves us and my son. Despite it all, life is good and I continue to believe that so are people.

Due to Covid, our CureJM walks could not take place this year anywhere.  Our kids depend on our families to raise these ...
23/06/2020

Due to Covid, our CureJM walks could not take place this year anywhere. Our kids depend on our families to raise these funds to help fund the research for treatments and a cure! On July 4th we will be having a virtual walk across AMERICA for CUREJM! Please consider joining us virtually and/or donating in honor of Team Camden! We have always been so blessed with so many amazing supporters! Now we need YOU more than ever!

Join or Donate to the Team for the 2020 Walk Strong Across America - Maryland fundraising event

Who is our fav?!?!?!?!  How can you even ask that?!?!  They are ALL such AMAZING dogs! BUT...if we must, Dillion, Luke a...
21/06/2020

Who is our fav?!?!?!?! How can you even ask that?!?!

They are ALL such AMAZING dogs!

BUT...if we must, Dillion, Luke and Sully! Luke is Cam's boy! So full of life and ready to make anyone's day! They've been together since he was a puppy! Dillion has always stolen my heart with his soulful eyes and sweet disposition. A kiss from him melts me. Cam was Dillion's first patient. Sully is so gentle, lovable and such a special dog!!! Being able to love on him has been an honor.

However, we have met and loved on them all numerous times and they are just wonderful animals. Ellie Mae makes me laugh the most and so much like our own Calamity Jane!!! Can I just have them all?!?!?!?!

☀️WRNMMC Facility Dogs prepare for Summer kickoff!! 🏖Who's your favorite? (we won't tell the others 🤫)

07/06/2020

I hope all are doing well and hanging in there. Life has been very rough in these unprecedented times. I haven't updated in a while. Honestly, our hearts are all hurting. Life goes on for our sick kids though. Cam's labs disease wise are holding stable on meds but weight is dropping steadily despite continuous tube feeds. We are trying to stay away from going in but it looks like his rheumatologist wants us in. It really stinks constantly fighting unknowns. Why is my child still wasting? We had the opportunity to meet a mom of a similar child who is now 20 and continually fed still. I'm grateful but heartbroken to know this is the life, they get it, but it sucks. Why can't we figure this all out?! Why can't one thing go easy?!

It has been a hard week for Cam, however he got a nice surprise today.  A sweet supporter sent goodies in the mail today...
21/05/2020

It has been a hard week for Cam, however he got a nice surprise today. A sweet supporter sent goodies in the mail today and then the Mac Pac and Cam all got to facetime with our fav three Team Camden boys! Sully, Luke and Dillion popped in to say hello and check on their boy since we can't see them right now! We got kisses through the screen!😘

Thank you Amy and Daniel for thinking of our boy and family this week!🥰

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