Elite Warrior Project

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Elite Warrior Project The Elite Warrior Project podcast is sponsored by the Paralyzed Veterans of America (PVA) to cover e

Rollerblading with  to get her some exercise and tire her out 🐾 When actuality I’m the one that gets tired and needs a n...
20/10/2022

Rollerblading with to get her some exercise and tire her out 🐾 When actuality I’m the one that gets tired and needs a nap 💤🤣

26/08/2022

I love this! For anyone that knows me, I cannot do spicy food 🤣 .20.19 is the complete opposite and puts spice and sauce on EVERYTHING 🌶

Happy Easter 🐰💐
17/04/2022

Happy Easter 🐰💐

30/03/2022

🎙Elite Warrior Project Podcast🎙

💼 Paralyzed Veterans of America’s Director of Veterans Career Program - Charles McCaffrey

🚨Tune in Monday April 4th to learn about the PVA’s Veterans Career Program.

So proud and excited to be part of this committee and the amazing things ahead!💙🧡❤️
22/03/2022

So proud and excited to be part of this committee and the amazing things ahead!💙🧡❤️

Super excited about our upcoming episode March 7th with Associate Director of Medical Services, Juliet Pierce.Topic: Dys...
03/03/2022

Super excited about our upcoming episode March 7th with Associate Director of Medical Services, Juliet Pierce.

Topic: Dysphagia and Swallowing Challenges in MS

Meet our guest: Juliet has been a multidisciplinary Registered Nurse for 30 years with expertise that includes ER/trauma, ICU, OR, and neurology. In 2013, she began a collaboration with Paralyzed Veterans of America (PVA) on behalf of Veterans with neuromuscular disease. In April 2021, she joined PVA as an Associate Director of Medical Services. Growing up the daughter of a Marine instilled in her a lifelong desire to support our Veterans.

MS is often called an invisible disease. Why?Because there are people with MS who struggle with some symptoms that are n...
02/03/2022

MS is often called an invisible disease.

Why?

Because there are people with MS who struggle with some symptoms that are not outwardly visible.

Every day that I wake up, I never know what I’m going to get or how I’m going to feel. Although I am highly functional with my MS there is a constant struggle each and every day with symptoms that I can’t always explain and others can’t see.

People often assume that because they can’t physically see anything wrong with you that you are good.

This makes it challenging sometimes to explain to others how or why we can feel so bad or be in so much pain.

🧡 MS Awareness 🧡

March is Multiple Sclerosis Awareness Month 🧡🧡 March 7th - Elite Warrior Project Podcast New Episode - Dysphagia and swa...
01/03/2022

March is Multiple Sclerosis Awareness Month 🧡

🧡 March 7th - Elite Warrior Project Podcast New Episode - Dysphagia and swallowing challenges in MS with PVA’s Associate Director of Medical Services, Juliet Pierce.

🧡 March 10th - Veterans MS Support Group

🧡 March 15th - Ask an MS Expert: Veterans program, “Adapting to a New Identity with MS”

❤️🤍💙 Paralyzed Veterans of America’s service officers specialize in MS, ALS, and Spinal Cord injuries.

MS Walk West Palm 2022 🧡This year with the move we were a little unprepared for the walk and were unable to raise money ...
27/02/2022

MS Walk West Palm 2022 🧡

This year with the move we were a little unprepared for the walk and were unable to raise money or make shirts to sell and we almost missed it because we had no idea it was today until last night.

We did it 🧡

Very excited about this upcoming webinar! The National MS Society, the VA MS Center of Excellence and the PVA are joinin...
19/02/2022

Very excited about this upcoming webinar! The National MS Society, the VA MS Center of Excellence and the PVA are joining forces for MS Awareness month.

Drove through to see the Christmas lights tonight with my favorite girls 💞
14/12/2021

Drove through to see the Christmas lights tonight with my favorite girls 💞

What a difference a year makes ☺️I love this sweet bundle of joy and all the adventures we have had exploring and introd...
05/12/2021

What a difference a year makes ☺️

I love this sweet bundle of joy and all the adventures we have had exploring and introducing her into this great big world💕

Skye was absolutely exhausted from playing with her 4 German Shepherd cousins for 5 days ❤️ This picture makes my heart ...
02/12/2021

Skye was absolutely exhausted from playing with her 4 German Shepherd cousins for 5 days ❤️ This picture makes my heart explode 💓

First snow…❄️🥶❄️
27/11/2021

First snow…❄️🥶❄️

Road trip North for Thanksgiving 🗺It’s been 6 years since I have been home for Thanksgiving and this is the first time ....
24/11/2021

Road trip North for Thanksgiving 🗺

It’s been 6 years since I have been home for Thanksgiving and this is the first time .20.19 and I will have thanksgiving with my family since we have been together.

Home infusion today (Ocrevus)…only a minor hiccup with trying to get the IV in. For some reason my veins hear infusion a...
19/11/2021

Home infusion today (Ocrevus)…only a minor hiccup with trying to get the IV in. For some reason my veins hear infusion and decide to disappear 💉🩸

Good thing .20.19 was home to help bring me back from the twilight zone 🌌

Skye was so good and so sweet 💕

I am so thankful for this little family of mine. They bring me so much joy and happiness ❤️ p.s. a little sneak peek at ...
16/11/2021

I am so thankful for this little family of mine. They bring me so much joy and happiness ❤️ p.s. a little sneak peek at our Christmas card!

📸:

For some reason I always have to share my snacks with someone…busted 🤣
13/11/2021

For some reason I always have to share my snacks with someone…busted 🤣

Love knows no bounds…🤍 It was a long sleepless night with two trips to the ER Vet for Miss Skye 💔 She is still pretty ou...
08/11/2021

Love knows no bounds…🤍

It was a long sleepless night with two trips to the ER Vet for Miss Skye 💔
She is still pretty out of it from the sedation but slowly starting to eat soft food and drink water 💞

It’s that time of year folks…sweater weather 🥰 We went to get coffee ☕️❄️❤️ then let Skye run around the park for a bit🌲...
06/11/2021

It’s that time of year folks…sweater weather 🥰 We went to get coffee ☕️❄️❤️ then let Skye run around the park for a bit🌲🍂🌳🍃

Last Friday was a day that brought up a lot of thoughts, emotions and self-reflection as I hit my 3 year mark of militar...
03/11/2021

Last Friday was a day that brought up a lot of thoughts, emotions and self-reflection as I hit my 3 year mark of military separation.

Looking back on my time in the service I learned a lot about myself, I challenged myself, I had setbacks, and I had great achievements, but for the first time in my life I knew exactly who I was and what I was meant to do.

As many of you already know I was medically retired when I was diagnosed with MS in 2017 and I was forced to make a pivot in my life and my career.

That first year after being separated was a turning point in my life. I had some really low moments during that time and I had to decide if this transition was going to “refine me” or “define me”…and the decision rested solely on me.

So I used the lessons I learned during my time in the service and charted a new path for my life and my career.

✔️I learned that I can do hard things.
✔️I learned the value of discipline and hard work.
✔️I learned that success comes from challenging ourselves and stepping outside the boundaries of our comfort zone.
✔️I learned how to manage stress and take care of myself because I can’t show up for my team if I am not ready.
✔️I learned the power of teamwork, support and encouragement of others - you are only as strong as your weakest member
✔️I learned the power of persistence because things don’t always go according to plan and we need to be able to make adjustments and pivot.
✔️I learned that having a mission, being part of something bigger than myself provides a great sense of pride and self-confidence.

I am grateful for where I am today!

Trying to do some neck stretches and of course the whole team has to come and help 🐾🐾🐾
01/11/2021

Trying to do some neck stretches and of course the whole team has to come and help 🐾🐾🐾

Go green 💚Go white 🤍🏈🏈🏈🏈Michigan State won 👏🏼 Thanks for being the best wife and supporting me and cheering on my time ....
30/10/2021

Go green 💚
Go white 🤍
🏈🏈🏈🏈

Michigan State won 👏🏼 Thanks for being the best wife and supporting me and cheering on my time .20.19 ❤️

So grateful for all the love and support that this podcast is receiving 🧡🧡 We have over 500 downloads in just a few shor...
28/10/2021

So grateful for all the love and support that this podcast is receiving 🧡🧡

We have over 500 downloads in just a few short months and I cannot wait to watch it grow as we continue to add expert guests, resources and programs!

The MS community is full of so many amazing people and supporters 🧡

That’s one proud pup 🐾 and two very happy dog parents ☺️Skye graduated her two week board and train with  🎉🎉🎉
26/10/2021

That’s one proud pup 🐾 and two very happy dog parents ☺️

Skye graduated her two week board and train with

🎉🎉🎉

Yesterday was our first real test with Skye. We took her to Surf City to try out Wings & Spirit Co. then to pet supplies...
24/10/2021

Yesterday was our first real test with Skye. We took her to Surf City to try out Wings & Spirit Co. then to pet supplies plus and we rewarded her with some play time at the dog park!

I love having our adventures and being able to include Skye 💞

Is it too early for Christmas? 🤣🤣🤣 Skye got her first Christmas toy and she’s so happy 🎄
23/10/2021

Is it too early for Christmas? 🤣🤣🤣

Skye got her first Christmas toy and she’s so happy 🎄

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Our Story

In 2017 my life changed forever. I was diagnosed with MS and found out that my military career would be cut short. Before my diagnosis I had heard of MS, but I knew nothing about it. The only image that popped into my head repeatedly was being in a wheelchair. I was completely ignorant and uneducated about autoimmune diseases like MS. One thing I knew for sure is that my life would never be the same again. I was going to have to make some lifestyle changes and get used to a new normal. We spent the next several months talking with a neurologist and researching MS. Like me, I feel that there are a lot of people who are unaware of autoimmune diseases and the effects that they have.

A simplistic explanation of an autoimmune disease is that the body’s immune system attacks healthy cells causing a variety of symptoms and disabilities. Having an autoimmune disease is not just a one and done episode, rather it is a life altering disease that presents daily challenges one must overcome.

At Elite Warrior Project we know and understand the daily uncertainties and struggles, whether you have an autoimmune disease or you are a caregiver of someone with an autoimmune disease. If there is one thing we have learned throughout this battle with MS it is that we CANNOT do it alone.

Elite Warrior Project has set out to raise awareness and build a community of fighters and supporters. Through education, love, and support we can spread awareness and fight for a cure!