From the Heart.......

I have a little down time right now. All the babies are sleeping and I felt the need to write. I have just 11 days before I leave for Africa. As you all know I belong to the Regulars and we are a group of altruistic individuals who have signed up with Enzo and his project, 10 mountains 10 years, to draw awareness and raise money to help eradicate Alzheimer's and Parkinson's Disease. With that said.....this is from my heart.......

I have been deeply affected by so many individuals this past year as I have been preparing for Kili. One especially is my dearest and sweetest friend Mary "Cherokee" Rose. She fights the toughest battle I know and still smiles and encourages everyone.My soul sister, the one who pushes me and drives me the hardest. Our dear friend Bill Berndt who lost his battle this past March who will be remembered forever for his kindness and his every chance opportunity to make you laugh. Forever in my heart. Ken Glowienke, a true role model, friend, advocate, loving husband. The day we met Ken it changed my life. I hope you know that. My dearest friend in this fight, Jim Brenner. As I sat the other night at Black Belt Camp and listened to his inspiring speech about making a difference and the ever loving and kind words he spoke about me I want to say you are my reasons I began all of this. I have always said to you for you I climb this mountain and for you I will be the one carrying your spirit with me. That "indomitable" spirit we talk so much of in Tang Soo Do. He epitomizes this in our art. He encourages and inspires everyone he comes in contact with. I was blessed the day we met and for you I continue down any path I can to help you win this battle. Judy, what can I say, I have met another who encourages the heck out of me and has undying faith and confidence that we will win. In10City to the max. I know I could make a long list of people. You all mean the world to me and not a day goes by that I am not thinking of all of you, praying for all of you and pushing the envelope for all of you.

My boys, all of my family, Sandra, Denise, Mark, Ideliza, Kaz, Rob, Mary, Maggie, Sue, Barbara, Charley, Ann, Eileen, Sylvia, Sherry, my teammates. A special thanks to my committee members who have made my fundraiser a reality....Karen, Kathy, Kathryn, Hal, Karen and Glen. Please don't be offended if I didn't mention your name. Know you are all here with me and I will bring you all with me to Africa.

Enzo and Jen.....two of the most important people in my life. Without you my confidence, drive, passion may not have ever reached the heights it is reaching.

There is nothing in life we can not do if we put our minds to it, our sights on it, and our passion and drive into it. "Together is ONE"

Please send out all of your prayers to The Regulars as we head out June 28th to the roof of Africa on our Trail Called Hope IV - Mt. Kilimananjaro.

World Up,
Strong Feather Eileen

http://www.theRegulars.org

Testing Spot - Driving - Spot

Hey, check this out. I'm just testing this little teacking device called SPOT. We'll be using it on our climb of Kilimanjaro, so you can track where we are each day. The waypoints update themselves every 10 minutes, so you can follow us all the way to the top.

Now we really can do this together!

All we have to do now is hope there is enough Satellite reception & communication to find us while we're there. BTW I know this looks a little jagged but that's because while driving, in 10 minutes I've driven quite a distance. On the mountain it will look like a more fluid line given the fact that we're not covering as much distance each 10 minutes.

World up,
Enzo

Testing Spot - Driving - Spot

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In10City - Meeting Judy Good Hensley

In10City - Judy Good Hensley

I had the pleasure of meeting a wonderful woman and spending three days with her and her beautiful family. My son David and I flew to Tennessee to meet Judy Good Hensley. She has Young Onset Parkinson's Disease. She also has the infamous "Da' Coat". When we arrived in the airport she called me and said she was in the observatory deck. My son and I exited our plane and looked up at the deck and low and behold there was Judy waving to us. David at first didn’t see her until I said look for the coat. Oh yeah! When we strolled into the baggage, Judy jumped out literally to greet us and snap our picture. I like this girl. This would be the first of hundreds of pictures the two of us would take. I want to jump ahead here to Sunday night. Judy and I sat for many hours late Sunday sharing, reading each others stories, crying, learning about one another. Being with her for three days I observed this remarkable lady. Moving through her day with Parkinson’s. Never afraid to do anything. Plowing through it all. All the while doting on me and David. She always made us feel at home with her husband and daughter. Planning our days, getting us there. I was exhausted at the end of each day. But the one thing that stands out in my mind is the love she has for everyone and everything. Right down to the tiniest butterfly she tried to capture through the lens of her camera. Her beauty for life pours over into her beautiful daughter Carol, who at only sixteen years old, is well beyond her years. Her husband Bill with his loving support and endless stories that I enjoyed immensely of his faith, his beliefs, his cross country biking. What a wonderful package these three are. They each are the glue that holds each other together.

Judy shared her disease with me. From the day she was diagnosed to the progression, the medications, explaining the medications, the procedures, the adjustments, dyskenisia, tremors. Her faith, her taking care and worrying about her mother. Her darker moments but then her moments of awakening because of the strength she has. How can you not be inspired? She wanted to know about me, my reasons for joining the Regulars, my mom, my boys, karate, my writing. I shared with her the chapter about my mom. She cried. This by far is the chapter in my life that defines me. She learned a lot about me and who I am today based on this. She understood the meaning of my nickname “Strong Feather”.

Intensity: Extreme degree of strength, force, energy, or feeling.
Judy Hensley should be under this word.
In10City: Her “E” name as the newest member of The Regulars.

It fit’s the woman who leads by example, who pushes up mountains of challenges, who never stops believing in herself and most importantly others. She is truly an inspiration on so many levels. To have been given the opportunity to meet her and speak at one of her support meetings is something I will never forget. I met wonderful people who are part of her life on this trip. A special thanks to Mayor Jane Myron and to Peggy Willocks for the kind words they spoke about me at the meeting. For allowing me to speak and to say they are the ones who inspire and I am the one who wants all of there hopes and dreams of finding a cure to come true. It was very a very surreal moment to be the one honored. I applaud everyone who deals with Parkinson’s Disease on an hour by hour basis. Who pushes others to become involved. Who creates foundations, websites for support, teams, fundraisers. I bring home with me a better understanding, a profound drive to support more and to draw more awareness. And of course a new friend, Judy Good Hensley. We stand “Together as ONE”. Oh yeah! I now have “Da Coat” and to the roof of Africa it’s going……..

World Up,
Strong Feather Eileen

Angel & the Devil

Today is Tuesday June 9th. 2009.

My wife is upstairs watching the television, and I’m down stairs in my war room listening to J.S. Bach’s “Siciliano from Violin Sonata 1", and eating a bowl of baked beans and a piece of chicken sausage for dinner. The broccoli burned while we were arguing about our current financial situation, so needless to say dinner was a little sparse tonight. Now the house smells of blackened broccoli. Yummy! Ah the glamorous lifestyle of the un-rich & un-famous suits me doesn’t it? The light coming from behind me is dim. The light bulb doesn’t really cast much light across the room but I’m used to it now. Actually I’m sort of a vamp, and I’m more comfortable typing in a dark room with just the computer screen for light. It keeps me focused on what needs to be done. In the end I suppose it’s good having everything off but the computer, being as it saves us a little money in these positively evil economic times.

Earlier today I called in my Unemployment Insurance Claim. For as much as I completely appreciate a national system which has such a fall back position built into it for it’s people, I’ve never been a fan of being a recipient of it’s benefits. I’d much rather be working. My brother Dan and I are just starting to put an engineering and architecture firm of our own together, but paying jobs are still just beyond the horizon. The ship has it’s sails up, and we’re just trying to catch enough wind to blow us toward the rising sun and better days. As my team mate Bill Glover says, “From adversity, prosperity is born.” I believe it.

I’ve been out of work since December along with so many other Americans. I remember it was just about a week after a little office birthday celebration for me. There were no hard feelings though, in being let go. Drastic measures were needed to keep the firm afloat at a time like this, and we all knew our luck could run out on any given Friday if the economy didn’t improve.

Lucky for my wife and I that at least one person in the family is bringing in a paycheck to help us get by. Economic recessions like this don’t come around very often. In the past, the architecture firms I’ve worked for have been specialized in the design of high-end homes, and the clients which normally make up this demographic could bat their lashes at hard times. You’ve got to admire them though. Their houses are absolutely beautiful, and it’s easy to see why from our perspective, they work really hard for these luxuries. In times of economic uncertainty it seemed as though they had built up an insulation to loss. Every other Joe in the country might be feeling the squeeze imposed by the times, but I always felt as if they were never quite caught up in that grip. One day if would be nice to feel a certain sense of economic security of our own. Our clients had always seemed to steam roll right over the bumps in the road which threw the rest of us for a loop or into a tail spin. Essentially what I mean to say is that in the past, even in bad times, if I was designing high-end homes in a well known and respected architecture firm, then I was always pretty secure in at least maintaining a job, but this recession was different. Everyone top to bottom, rich and poor seemed to have stopped on a dime, then were all forced to jump on it to see who would get it first.

Things are hard now, and I’d have to say that on the inside I feel a bit torn. Questions, feelings, uncertainties, they’re all different bends, and turns on this roller coaster of life.

I’m only human, and I don’t always know the “best” thing to do in times like these. Although, in the spirit of that humanity I do usually have a gut feeling about what is the “right” thing to do from a much larger perspective. My eyes were always better at seeing issues from a global perspective. But more often than not, what I feel is the “right” thing to do clashes dramatically with (just about) all the friends and family looking in at my situation. Although they all have different opinions about my life, their technique in dealing with me seems pretty consistent. They tend to have more of a slash, burn, or break his will until he can’t carry on attitude toward my charity passions. Doing something good is only good if it has no risk involved. Many have no problem in letting me know how selfish I am, and that the longer I persist in my efforts to raise awareness through my 10 Mountains - 10 Years project, the farther I would slide from favor in their eyes.

So be it. Let me slide.

Yes, I know it’s sort of sad. You’d think that the ones closest to me, who could see first hand the devastation of Alzheimer’s and Parkinson’s Disease would be my strongest supporters, but most are not. Maybe they’re too close to me as the subject. Maybe I’m too much like them to make a difference. Maybe they don’t feel they could make an impression on the world, so why would I be able to do it. Maybe they’re honestly trying to save me from myself, or maybe they’re just trying to stop me from do anything they don’t have the confidence in doing themselves? I don’t’ have the answers, I can only guess.

So I reflect on the situation my wife and I are in, and together (though in parallel) we think about how we can cut down on spending so that we can ride this recession out to better days. It could be said that my wife’s philosophy is more in league with my family and friends when it comes to supporting my causes and passions. So in the process of wondering how we could begin cutting expenses, my wheels might be spinning but she’s already at the finish line holding a “Wanted Dead or Alive” poster with a Double-X and a Heart on it.
But in all seriousness, how can I blame her? I’m haven’t had a job or a real income other than unemployment checks for 6 months.

I smell the smoke, and I know the fire is in there somewhere, but my guess is it’s not just the broccoli burning in the kitchen. I know what she’s thinking. The 10 Mountains - 10 Years (A Quest for the Cure) project has got to go. The world can take care of it’s own problems for a while. I should just sit tight, take care of my own, and be content to make a simple small donation to the Alzheimer’s Association and the Michael J. Fox Foundation this year. In everyone’s mind but my own I should be raising the white flag of surrender, handing over my sword and calling it an end to my once great charity epic.

One of the things which I think is so special about our expeditions is the same thing which is making it so hard on us now. All our climbs are run out of our own pockets at our own expense. It’s quite a lesson for us all to know that nothing good in life comes for free, and this is a perfect example of it. When a person wants to join “the Regulars” it’s done with the understanding that they need to pay their own way for everything, and never to expect help or hand outs from anyone to accomplish the goals of the team. We all pay our own way so that 100% of all donations coming in from contributors can go directly to Alzheimer’s and Parkinson’s Disease research. The charities call for our most sincere and altruistic efforts and that’s exactly what they get. Being one of “the Regulars” is a pretty big sacrifice to ask of people during prosperous times, but in a recession it’s a monumental sacrifice, and I extend my gratitude to all my team mates for standing along side me to try their best no matter how hard it gets.

So now imagine this. I know it’s a little Animal House-esque, but the visual helps.
I turn to the left and the devil on one shoulder says, “Just quit it, and think about yourself. Stay home. Relax. Watch TV. Sip some wine. Smell the roses. Go have a beer and grow yourself a nice gut and don’t let these things bother you. You’re not a martyr. Get your head on straight and be serious for a change. You’re no one special. You’re just a regular guy. No one would care about you if you were the one with Alzheimer’s Disease or Parkinson’s Disease.”

I stop to think, maybe this little devil’s right. Maybe no one would give a damn about me if I was the one with Alzheimer’s or Parkinson’s Disease. Maybe someday I am destined to become a shell of what I am now and not a soul would care.

Then I turn to the right and the angel on the other shoulder says: “How could you ever quit this project??? No matter how hard it is, you don’t quit anything...ever! You might be a Simone, but never quitting runs back in your Chadwick bloodline for more than a 1,400 years. Get your game face on you’ve got things to do rough boy.”

“Remember when you were six years old and you wanted to become a musician, then low and behold one day you grew up to hear your own music on the radio? You wanted it and you did it.”

“Remember when you were in kindergarten and loved to collect stones and wanted to become a geologist, and then you went to work for the US Geological Survey. You wanted it and you did it.”

“Remember when you were an elementary school student and you wanted to become an architect? Then, you went on to college and graduated with a degree in architecture. Well, ...it seems to me” the angel whispered, “although your curse may be that all things worthy of pursuit may feel as though they take you a thousand years to accomplish, you have done everything you said you would do...granted you were passionate to do them.”

“Which brings me to my final point”, said this little angel.
“Remember when you were young, and anything is possible? Well I shouldn’t have to remind you that the secret to life is that everything has always been possible. Sometimes people stand in your way, and other times you stand in your own way, but you always get around these obstacles. We both know that you’ll never give up on this 10 mountain epic until you’re done, until you’re dead or until the cures have been found. This is what you were born to do.”

It all brings me back to now. Sitting in a dark room with the smell of burnt broccoli in the air, with no money, no job, and running out of options on how to keep this charity project alive.

Today, tomorrow, this year, the next 7 years. How do I navigate through an ocean of time which stands as still as the Sargasso Sea? I suppose at least part of the answer is in the lessons a climber would learn in the over world.

No one will ever carry you up a mountain.

Those without the will, will never find the way.

Patience is not only a virtue it’s a necessity.

Keep moving and don’t stop.

Never look at the whole mountain, it may overwhelm and turn you to stone.

And lastly, all mountains real or metaphorical, great or small, simple or complex can only be climbed one way. One step at a time.

The lessons learned on the mountains will guide me without a doubt. I need to roll with the punches when they land on me. I need to stay waxed, so that the off color comments of those around me who don’t support my efforts will roll off like water. I need to be focused and true to my cause, and I can never give up.

The financial times are hard and although we may not share the same ideas for what is the right way or best way to get through this, together with my wife I’m sure we’ll find a way.
As for support from most of my family and friends, I can always hope for it. But until that ship comes in I’ll count on motivating myself.

People may ask, will I give up on the 10 Mountains - 10 Years (A Quest for the Cure) project?
It’s no doubt, that the answer to this always in constant battle between my heart and my mind, but the last time I looked the flag of “the Regulars” had a heart on it. There was a time before I was born when my very existence could have been in question, but in my mothers mind, even though I still had not taken my first breath and I had no name to speak of, there was never any doubt that she would “never” give up on me. Why would I give up on her?

So the people may ask again, and again, and again, will I give up on this epic?
I may be broke, and I may be hanging by my last thread, but I’m not done, there is still no cure, and I’m still breathing.

World up,
Enzo

Well now isn't this turning out to be a strange yet cool day on the internet. Here's another quick 2 links for you.

"The Regulars" 10 mountains - 10 Years (A Quest for the Cure) project is also in the brand new Team Fox Magazine right next to Ryan Reynolds. And as it that wasn't enough excitement in one magaxine...our new Team Tom Saborin is quoted in there too from his days as a marathon runner for Team Fox. (You can find Tom right here on my Facebook Friends list). Stop by & say hi to him.

Here's the link to the magazine in PDF format:
http://www.teamfox.org/atf/cf/%7Ba34b4a45-7f40-418e-b2f2-a4fb38e4f769%7D/MJ_FOX_MAG_HI_RES_WEB.PDF

Also, here's a link to the Team Fox video with "the Regs":
http://www.teamfox.org/site/c.nrLXJ0PFKuG/b.4815173/k.9341/Team_Fox_Video.htm


Team Fox is absolutley for anyone and everyone who wants to do whatever they can to raise awareness and funds for Parkinson's Disease research. Contact them and form your own Team Fox Team Event.

World up,
Enzo

Leeza's Place

Hey there everyone,

As you all know this years team is working to help the Alzheimer's Association, Michael J. Fox Foundation (Team Fox), Leeza Gibbon's Memory Foundation & Focus on a Cure to raise awareness to conquer Alzheimer's Disease & Parkinson's Disease.

We're all certainly doing our part to shed light on these diseases, and we're all doing it in different & unique ways.

Leeza's Place has been very kind to become a part of the 10 Mountains - 10 Years story. And Leeza is even going to be filming the introduction to the 10 Mountains 10 Years film. We're all so excited to finally see the first chapter of this epic out in theaters with you all.

Anyway this is just a quick note to say check out Leeza's website and her page for "the Regulars"!

Here's the link:
http://leezasplace.org/climbers.html


World up,
Enzo

Team Fox...Together is ONE

To all my fellow Team Fox members, I have an idea for you.

What a tangled but beautiful web we seem to weave. We never know where we will eventually meet our comrades in arms (so to speak), or who will stick together in this web we call life.

With that being said, I’d like to talk about raising awareness and funds to find a cure for Parkinson’s Disease, but not as individuals. I’d like to talk about looking at ourselves not as islands alone in the world, but as continents of people united by a common cause to conquer Parkinson’s Disease. Together we can do this, but the key word is “Together”.

Team Fox team mates don’t always have to stand alone in their efforts to conquer Parkinson’s Disease. Now, maybe it’s just the way I’ve been brought up having a Sicilian family background which is hugely based on solidarity, but I’ve always felt that there is more strength in numbers than there is in being alone.
As some of you might know, ever since I first started my little effort called “10 Mountains - 10 Years (A Quest for the Cure)” in 2006, our team motto has always been “Together is ONE”.

I honestly believe that through time people have come to understand exactly what my team means when we say “Together is ONE”. They’ve been attracted to the light of comradery and altruistically becoming part of a collective team like Team Fox or part of my team the Regulars. Above and beyond all else, the goal is finding a cure, and if our efforts will be more successful by working together with others in our areas who have common goals, then we should find those people, form our teams, and conquer Parkinson's Disease together.

The idea I’d like to propose to all my fellow Team Fox members:

Look around you, find the other people in your own areas (maybe the same city, same county, or a tri-county area).

Design a big event as a team - which would normally be hard to orchestrate while acting individually.

There’s magic in the effort. There’s strength in the unity of people. There’s energy in exchanging ideas and turning them into reality. I honestly believe you’ll grow, learn, bond and find massive success in working together under our common cause. It’s also a great feeling to know that there is someone out there trying just like you, and it’s even nicer when you’re both trying together.

“Together is ONE”

I’ve been pretty lucky to have great people, real grass roots advocates just like you and I (just like “us”), look into my project and say maybe I can give you a hand with that. I can always use help. I would never consider myself a master at anything but knowing how to see through the eyes of a student. In all truth, my eyes are always wide open to the fantastically kind hearted enlightening people around me. These are my fellow expedition team mates in “the Regulars”, and they are also the fellow Team Fox team mates who freely exchange thoughts and ideas with me. These are the people around me who constantly show me that there are ways to improve on any idea I might have in ways I never considered. They have always shed light on a path which I once thought lead to something good and instead joined me on a journey down a road to something greater.

When I designed my project to span a decade I did so with just that in mind. I knew that if I designed a project as a one day, one shot, one time, one mountain effort I simply wouldn’t have the opportunity to attract like minded people to help with our battle against Parkinson’s Disease. So, the solution for me was to create a bigger, higher, harder, longer project. I would eventually draw the project out to become a decade long instead of a one time effort. Creating an annual event gave me the opportunity to learn from mistakes I would make, and would give me the time to learn and improve upon my effort through each coming year. As it turned out, the year following my first event people remembered my project, and were more willing to help me with it the second year round, and so on through time.

In the case of “the Regulars” and our 10 Mountains - 10 Years (A Quest for the Cure) project, we’ve crossed paths with and attracted other Team Fox members through time. I believe you can do the same with the Team Fox members around you!

Team Fox is all around you.

I met Ken Glowienke (Focus on a Cure) on Myspace then officially met in person at a Team Fox MVP dinner in NY. Knowing how much effort Ken puts into his projects and reading about him on line made the meeting with him at the Team Fox dinner feel like meeting a rock star, because he was already larger than life in my eyes. Even though Ken lives in Illinois, we always supported each other’s efforts in any way we could across the miles via internet. Interestingly, now Ken has become a part of the 10 Mountains - 10 Years story through the feature film documentary by Back Light Productions. Ken very kindly volunteered to have his entire Deep Brain Stimulation surgery filmed as a portion of the movie. This includes his entire process before, during, and after the operation. He like "the Regulars" want to show people that they could and should be proactive about raising awareness for this cause and further they can be proactive in finding better treatments for themselves.

It’s also funny to note that Thomas Sabourin (T-Run) was at the same Team Fox Dinner during which I met Ken Glowienke although we didn’t meet that night. I came across Tom (who lives in Wisconsin) officially on MySpace and saw that he was involved in Team Fox. I could see from photos that he was in great condition and that he had a background in mountaineering also, so I asked him if he would like to join up with the Regulars. Flash forward a year or so to now and he’s getting ready to fly to Africa to climb Mount Kilimanjaro with us. I still haven't met him personally but he got a chance to meet my team mate Eric Buzzetto (Gladiator) at the Team Fox MVP dinner this year, and another team mate named Eileen Colon at the Parkinson’s Unity Walk in Central Park.

Nadyne Perlin who is from New Jersey (we call her Giant) ran in the New York City Marathon for Team Fox in 2007 found “the Regulars” on MySpace. She wrote me to say her dad struggles with Parkinson’s and she wants to continue her efforts with Team Fox by climbing Kilimanjaro with “the Regulars”.

Then I believe there is an outer circle to the advocates and volunteers for Team Fox which we seldom hear about but I see them out there in action all the time. These are the people who quite privately and out of the spotlight do everything possible to help and support those who are officially are Team Fox members. This describes New Jersey’s own Eileen (Strong Feather) Colon. She was a MySpace friend of Ken Glowienke and was extremely moved and inspired by his efforts to conquer Parkinson’s Disease. Through Ken she was introduced to me and we officially met at one of the Parkinson’s Unity Walks in NYC. To make her very dynamic and long story short Eileen has become really well known on both MySpace and Facebook as a person with lots of ideas, support, love and deep compassion for those struggling with Parkinson’s Disease. Eileen has even gone so far as to drive in one long shot epic to the exact middle of the United States (Kansas) from her home in New Jersey (a 26 hour trip each way) just to spend 2 hours visiting her friend Mary who suffers with Parkinsons' Disease. Also, this past May, she also traveled to speak in front of a Parkinson’s Disease caregivers meeting in Tennessee. Eileen is 52 years old, and even in the face of prior medical concerns about her heart she joined "the Regulars" to climb Mount Hood in 2008 and is now back for more with us to climb Mount Kilimanjaro in July 2009. Coincidentally, she has now officially become a Team Fox member.

Then there are the chance meetings which bring people together. Last year on Mount Hood while we were there climbing our third mountain in the series of ten charity mountain climbs. Our team was shattered and demoralized by bad weather on a first attempt on the mountain. In fact they closed the mountains down entirely due to positively evil weather and lightning storms. We had evacuated and gone back to Portland to wait it out, but tucked away high up on Mount Hood was Lori Saviers (from Ohio). She and a friend had found a spot to ride out the weather unnoticed by the park officials and unharmed by the weather. A few days later out of my team of 10 people, 3 went back to try climbing in a second attempt, and 2 made it to the summit of Mount Hood with our team flag, one of which was Troy Parker who personally suffers with Parkinson’s Disease. Troy and my team mate Brett were trying to take photos of themselves on the summit when across the narrow ridge walked Lori Saviers to help them. She grabbed their camera and snapped a few photos then listened to Troy describe how he had Parkinson’s Disease and had become part of “the Regulars” to help raise awareness for this disease. She was so taken by having seen Troy earlier struggling on the slopes below, then finding them on the summit only to hear that Troy climbed all that way with battling with Parkinson’s and was immediately inspired to join “the Regulars” on our next effort. Although Troy is not on the Kilimanjaro 2009 Team Lori Saviers (Premonition) has vowed take the message to the top of Kilimanjaro.

So, in a nut shell I thought it would be nice to let my fellow Team Fox team mates know that we have all been out there doing what we can on our own, but this year look around you and get to know the other Team Fox members living in your areas. Join forces and create big, beautiful, fantastic and inspiring events together. The world is your oyster, the ideas are endless. You don't have to climb mountains in order to take your message to the people, you just need to connect with them. In this army of change our battle is to conquer Parkinson's. Your weapons of choice just may be ideas & inspiration. Aim for the heart and let your arrows fly.

We can do this together. Believe in yourself. Believe in "us" and try.
The success in your results could be larger than life.

World up,
Enzo Simone
www.theRegulars.org
10 Mountains - 10 Years (A Quest for the Cure).


The key Team Fox members in the above (some pages may be out of date):

Vincent Roland Simone (aka Enzo)
http://www.teamfox.org/siteapps/personalpage/ShowPage.aspx?c=nrLXJ0PFKuG&b=4815191&sid=ahJPJ0NGJhJMJXNzGmE

Ken Glowienke
http://www.focusonacure.org/

Thomas Sabourin:
http://www.teamfox.org/siteapps/personalpage/ShowPage.aspx?c=nrLXJ0PFKuG&b=4815191&sid=dtIOL3OPLgJPI8MQLsH

Eileen Colon:
http://www.teamfox.org/siteapps/personalpage/ShowPage.aspx?c=nrLXJ0PFKuG&b=4815191&sid=ivL0LhPYKlKVLeN3LxG

Lori Saviers:
http://www.teamfox.org/siteapps/personalpage/ShowPage.aspx?c=nrLXJ0PFKuG&b=4815191&sid=bfLPJUMxHgKFISOwElG

Nadyne Perlin:
http://www.teamfox.org/siteapps/personalpage/ShowPage.aspx?c=nrLXJ0PFKuG&b=4815191&sid=gsJTJ1NEKcJTK8NJKpG

and
Eric Buzzetto

Here's a link to one of my quick home video music clips, to show you just how big our army of change can be if we all fight for these cures together.

http://www.youtube.com/watch?v=MAzIsMElpnQ