Archive for the ‘Charity’ Category

Forever in shape scv, a santa clarita sports activities and personal fitness education agency, will host a “pumpkin exercise” at its centre pointe vicinity on saturday, october 28, beginning at 9 a.m.

For all time healthy will donate $5 to the american most cancers society for all and sundry who attends.

Members need to carry their very own pumpkins (preferably earlier than carving) for the workout.

Also after visiting “Forever Fit SCV” we recommend you to visit in LA the Quest-room from our partner – TheQuestFactory. What will help you to spend time with great fun. It’s realy good challenge for anybody.

Forever in shape scv is positioned at 26340 diamond place, suite one hundred, santa clarita 91350, in the centre pointe location.

For more records, e mail craig shinkaric at craig@foreverfitscv.com.

In support of augie’s quest, los angeles fitness introduced plans to host its 7th annual in-membership event, action for als, across the company’s over 690 places on saturday, february 25, 2017. Augie’s quest is a nonprofit studies initiative committed to finding a cure for amyotrophic lateral sclerosis (als).

In addition to good fitness, LA is also known for its advanced entertainment industry. A new hobby of young people is quest-room. Our partner TheQuestFactory is the leader of this type of entertainment in LA. Be sure to visit them when the future is in this city.

La health will donate 100% of the proceeds from the occasion to augie’s quest, which immediately finances the als remedy improvement institute (als tdi). als, a debilitating neurodegenerative disorder, is diagnosed in about 6,000 human beings in keeping with 12 months. survival is commonly three to 5 years after diagnosis, and no cure currently exists for the disease.

In march 2005, augie nieto, a prominent chief in the health industry, turned into diagnosed with als, greater normally referred to as lou gehrig’s sickness. Despite the restrictions of the disease, augie maintains to lead an energetic lifestyles and function an activist for others fighting the disease. After his analysis, augie coped together with his infection by means of drawing strength from his circle of relatives, pals and a flood of messages from supporters. realizing that he may want to use his voice to raise attention for others, augie fashioned “augie’s quest” with the sole motive of finding a remedy for als.

“We’re so grateful for the $260,450 that la fitness has raised for als research over the years. that money is making a massive impact within the lab, leading to the identification of at-1501, a promising treatment for als. with the ongoing assist of la fitness and their members, we’re assured we can get this drug into section 2 scientific trials subsequent 12 months,” stated augie nieto, chief proposal officer of augie’s quest. “We recognize all that la health does to growth cognizance and deliver wish to families tormented by this devastating disease.”

“We don’t want any boundaries to face inside the manner of maximizing our companywide fundraising efforts for this worth motive, so we invite members and non-members alike to wait this occasion. We also want to say how proud we’re of our members’ participation and the way grateful we are for his or her generous support,” said invoice horner, senior vice president/leader actual estate officer at los angeles health.

The occasion is open to the public for a minimum donation of $20 in assist of augie’s quest. For details on the event or a way to make a donation, go to unique web page.

About l. a. health

A. fitness is one of the fastest growing fitness center chains inside the u.s. and presently has more than 690 places in 32 states and canada. Its project is to help as many people as feasible gain the advantages of a wholesome way of life by means of creating a national community of fitness golf equipment, providing its participants the widest variety of facilities and the friendliest carrier at an low cost charge.

Approximately augie’s quest

Augie nieto created augie’s quest following his prognosis of als in march 2005. Nieto is co-founder and previous president of life health of chicago, and chairman of octane health. Augie’s quest without delay finances the als remedy improvement institute (als tdi), the sector’s predominant drug discovery middle centered entirely on locating a cure for als. For extra information on augie’s quest and to get concerned, go to unique page.


CRF Grants Support the Quest for a Cure

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The cystinosis studies foundation is the largest issuer of grants for cystinosis studies. whilst we are saying biggest we don’t mean within the united states, we suggest in the global. in fact, final yr the crf provided a total of $2.79 million really worth of research offers in 5 exceptional international locations. this cash funded seventeen clinical research concerning the pathology, remedy, and capacity treatment options for cystinosis.

Please discover the entire press release by using the cystinosis studies foundation below.

Cystinosis is a unprecedented, incurable metabolic disorder that afflicts 500 children and young adults inside the america and about 2,000 humans international. It slowly destroys the organs in the frame (consisting of the kidneys, liver, eyes, muscle tissues and mind) because of a buildup of the amino acid cystine that crystallizes and kills the cells.

The 2016 offers, funded by way of donations from the 2016 natalie’s want gala and golfing tournament and donations from cystinosis own family occasions throughout the yr, are supporting studies inside the united states of america, belgium, france, italy and new zealand. they include:

Nine cell and molecular studies into the pathogenesis of the sickness

2 stem cellular/gene remedy research

Five research into new drug discoveries

1 neurological research take a look at

Crf-funded research has brought about new discoveries approximately the pathogenesis of cystinosis and has helped unlock the mysteries of this uncommon ailment. The muse anticipates that there will be fda approval this year for clinical trials to improve an autologous stem mobile treatment and the development of a nanowafer treatment for corneal cystinosis.

“A number of the research performed by way of crf funded scientists has far-accomplishing implications for other issues.” stated crf founder nancy stack.  “Despite the fact that the cystinosis network is small, knowledge found by using analyzing our disorder has led to advancements inside the discovery of ability treatments for other sicknesses such as huntington’s disorder, parkinson’s disorder and other systemic problems similar to cystinosis.

“Our work inside the vicinity of nanotechnology and corneal cystinosis will undoubtedly assist other corneal sicknesses. the stem cellular paintings performed through stéphanie cherqui, ph.d., (united states) will help treat other lysosomal or even neuro-muscular degenerative disorders. crf research extends some distance past our network; it has the capability to treat thousands and thousands of different folks that be afflicted by different disorders.”

For the reason that 2003, the cystinosis research basis has issued 151 cystinosis studies grants in 12 international locations. amongst other improvements in the take a look at of the disease, crf funded the development of not on time-release cysteamine medicine, accepted in 2013 by the u.s. meals and drug management.

Donations made to crf cross directly to fund cystinosis research.

This year’s research supply awards consist of:


The scripps research institute, la jolla, california

$256,795, to sergio catz, ph.d., “molecular trafficking regulators of dynamic organelles in cystinosis”

$Seventy five,000 to sergio catz, ph.d., and jinzhong zhang, ph.d., “improvement of cell function thru chaperone-mediated autophagy and cell trafficking in cystinosis”

College of california, san diego, california

$A hundred and sixty,589 to ilya gertsman, ph.d., and bruce barshop, m.d., ph.d, “elucidation of altered metabolism and biomarkers in cystinosis the usage of huge-scale metabolomics processes”

$141,082 to stephanie cherqui, ph.d., “improved research software for stem cell research

$Sixty two,895 to doris trauner, m.d.,“sleep disturbance and reminiscence function in nephropathic cystinosis”

Thiogenesis therapeutics, inc., san diego, california

$153,900 to vincent stanton, jr., m.d., and patrice rioux, m.d., ph.d., “pharmacokinetic assessment and optimization of cysteamine precursors”

Harvard medical faculty, Boston, Massachusetts

$225,000 to norbert perrimon, ph.d., and patrick jouandin, ph.d., “profiling metabolic dysfunction because of cystinosis.”

Massachusetts fashionable medical institution, Boston, Massachusetts

$ninety six,129 to florian eichler, m.d., and sherman alexander, m.s.c., “scientific trial readiness for distal myopathy in nephropathic cystinosis (dmnc)”

College of pittsburgh school of drugs, pittsburgh, pennsylvania

$A hundred and fifty five,484 to morgan fedorchak, ph.d., and kanwal nischal, m.d., frco, “development of a topical, controlled release cysteamine eye drop”


De duve institute, Brussels

$209,344, to pierre courtoy, m.d., ph.d., and christopher pierreux, ph.d., “assessment of ctns -/- mice protection by means of oral supplementation with basic amino-acids: focus on kidneys”


Imagine institute, paris, france

$310,000, to corrine antignac, m.d., ph.d., “characterization of mtorc1 signaling in early pathogenesis of cystinosis”

$Ninety one,553 to matias simons, m.d., “lessons from the fruit fly. how cells deal with cystinosin deficiency.”

Paris descartes university, France

$225,000 (a 3-yr supply) to bruno gasnier, ph.d., and yann terres, m.s.c, “mechanism and pathophysiological significances of a genetic interaction of cystinosin”

$Seventy five,000 to bruno gasnier, ph.d., and rossella conti, ph.d., “biophysical observe of cystinosin and pqlc2”


Bambino gesù kids’s health facility, Rome, Italy

$229,660 to francesco emma, m.d., and laura rega, ph.d., “alternative therapies for nephropathic cystinosis”

$One hundred eighty,400 to giusi pencipe, ph.d., and fabrizio de benedetti, m.d., ph.d., “nlrp2 in the pathogenesis of cystinosis.”

New zealand

The college of auckland, new zealand

$One hundred forty five,852 to alan davidson, ph.d., and teresa holm, m.d., ph.d., “kidney organoids: a brand new model to examine cystinosis.”

Approximately the cystinosis studies basis

The cystinosis studies foundation is devoted to locating better remedies to improve the pleasant of lifestyles for people with cystinosis and to ultimately discover a treatment for this devastating ailment. seeing that 2003, it has raised and devoted extra than $35 million to support bench, scientific and translational studies to find better treatments and a treatment for cystinosis. the muse is dedicated to educating the public and clinical network about cystinosis to ensure early analysis and proper treatment.


Q’wemtsin Quest for a Cure

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1 in eight canadian girls will develop breast most cancers in their lifetime. allow’s promise to trade that.

We’re participating on this year’s canadian most cancers society cibc run for the therapy to benefit the breast most cancers motive. we’re jogging in honour of all the amazing girls in our lives, and we want your assist!

Please contribute what you can to our fundraising. each dollar makes a difference and gets us one step closer to making breast cancer beatable. your donation will fund innovative studies to help keep the lives of more girls, and provide help packages to those stricken by this sickness.

Did you realize that just $a hundred ought to fund 2 hours of lifesaving research in a global magnificence laboratory? your contribution lead to the subsequent leap forward!

Together, we are able to exchange the destiny of breast most cancers.

Make donation

For the last twelve months, the Wayfarers have been meeting regularly to brainstorm ways to fundraise and promote the Quest for the Cure to the greater community en route to our goal of $100,000.

We held events (that raised us more than $1000 in a single night), auctions (hundreds of dollars) and are even selling silicone bracelets – which have seen a lot of sales already. But it wasn’t until this project that we had a single campaign that could raise us over $10,000 by itself.

Kemper belongs on the cover of our favourite fantasy novels. This is a preview of the shots we’ll see in the calendar.

The art of pin-up calendars helped soldiers get through World Wars and has recently seen a huge resurgence in popularity, with sites like Suicide Girls becoming a household name in alternate modelling. Fantasy art is no stranger to this style – think of any fantasy novel with a woman on the cover, and chances are good she’s in a chainmail bra and has a whole lot of leg waiting for a sword to bite into it…. just like this one.

When I approached some of my favourite models from Suicide Girls about helping us out, they were eager to do so, offering not only their beauty but also their talent, photography skills, costuming and help spreading the word. I can’t thank them enough for giving us this opportunity to raise some serious cash.

We are crowdfunding the project on IndieGoGo, a fantastic site that not only allows Canadians to participate but also encourages charitable organizations to take part. We need $2000 to get the calendars printed – the cost break-down is all there, and I think it’s entirely reasonable. We’ll be ordering a thousand calendars with this money, and could even order more if demand is that high. Just selling out that first batch will make us more than $10,000. Because this is an international campaign, we are donating all of the proceeds to the Association for International Cancer Research, our least-funded charity so far.

Check out our IndieGoGo campaign and buy a calendar today! There are a lot of great “perks” you can get for helping us out, from buying a calendar (with free shipping for the duration of the campaign) to getting signed prints of the pictures within it, to even getting a hand-written letter from the Wayfarers during our trip this October.

Be a part of the adventure and have some beautiful pictures of beautiful women to prove it.


Twelve Months of Magic

by Dan Clarke

Sword and sorcery meets pin-up in this fantastic calendar featuring some of the most popular alt…

Starting – 0.621 Complete

$1,242 raised


A Training Run for Kids with Cancer

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As the clock ticks closer and closer to 2012, the date we leave for the walk is approaching. This has me looking into what I could do to further motivate myself for training. At work this week, Glen mentioned the Sporting Life 10k Run, so I decided to check out their website and see what it’s all about.

The purpose of this race is to raise money to send children with cancer to summer camps. This aligns quite well with the Wayfarers’ goals in the Quest for the Cure, so that was certainly a positive start. The date of May 13th was far enough away that I didn’t have anything planned yet. (Note: a quick check online led to the discovery that May 13th is Mother’s Day. Mom, I hope you understand why I won’t be able to visit on this weekend. I’ll make sure to call you when I’m done the run!) The date was far enough away that I had time to train, and still well in advance of when I leave for the Quest so it wouldn’t interfere with any last minute planning.

The route is very similar to portions of training walks I’ve been on walked before, so I don’t believe the 10km will feel too long. Also, and thankfully, it’s mostly downhill. Not finishing where I’m starting is less than convenient, and has made my decision to take public transit there and back is better than trying to find parking with my car.

I’ve never done a 10km run in my life, and yet, I had to select my time when registering. The fastest selection was for less than 48 minutes, which I didn’t even want to attempt to get into. I’ll let the faster people leave at 8AM without me there to slow them down. I settled for the third group, with a time of 56 to 59 minutes, with the hopes that I will be able to get myself in good enough shape to run the race in under an hour. I don’t want to admit that it will take me more than an hour and that I will be slower than half the people doing the race. I have a standard to meet now and thus, motivation for training.

With the snow outside now, I’m not even sure where I will be training just yet. The idea of signing up to a gym has come across my mind. I believe seeking professional help to get in top physical shape for the grueling journey of walking approximately 26km a day, every day for four weeks, is certainly a good idea. Having a treadmill to run on and practice doing 10km inside, before taking my run outside in the spring, would also be beneficial to training for this run.


A DCL Donation

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On December 22nd, 2011, DCL International held its annual company Christmas lunch.  Every year, DCL makes at least one charitable donation to an organization where funds are raised until the end of the lunch.  Knowing this, I approached the company president about the idea of the Wayfarers and the Quest for the Cure a couple months before the lunch, and he agreed to help us out.

The deal we struck was that the amount of money I raised from the employees of DCL International by the end of the Christmas party would be matched by the company.  If I raised a 1000$, he said, the company would match that.  Also, if I raised 10$, that’s all DCL would donate.  I was going to have to do a little bit of work to get a large donation from DCL.

However, I was not left to do this all on my own.  I worked with Michelle who was organizing the Christmas party and sent out a mass emails to the employees explaining the cause.  They also received a letter in their pay envelope about the charity at the same time they got their invite to the party explaining the fundraiser.

Employees had two options:  They could donate online ahead of the lunch or to bring cash with them on the lunch, which I would upload to the site as one large donation from DCL employees.  A link the Wayfarer website was given as well as a direct link to our Canadian Cancer Society donations page.

After my initial email and the pay slips went out, I received a couple large donations.  Time went on and not too much more was happening.  The week before the lunch, I sent a reminder email and the donations really started to come in.

Before even going to the Christmas party, a total of 1505$ was raised.  Another 2265$ was raised at the party (including what will be a 1000$ online donation) for a total of 3770$, which will be matched by DCL, bringing the total of money raised by the company and its employees to 7540$!  This also makes DCL International our first contributor to get their names listed under Kings of the Quest for a donation greater than 1000$.

The show of support from my company for the Wayfarers’ Quest for the Cure has been excellent.  I would like to thank my fellow coworkers for donating so much money individually to get the total donation number raised to as high as it reached, and would like to thank DCL International as a company  for agreeing to match the total raised by our employees.


Movember Update IV: The Final Moustache

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So here it is, in all its glory!  My moustache on the last morning of Movember:  The final moustache!

The Final Moustache

As you read this post, I will be moustache free since it’s now December 1st.  This post was actually written on November 29th, while on a plane from Dallas to Toronto.  I was able to check the internet, log in and go over all my work emails and write this blog post, all while flying back home.  Technology has come a long way and always continues to amaze.

So why talk about technology in a blog post about Movember?  Well, the money being donated to prostate cancer research is to help advance technology in the search of a cure for cancer.  It is my honest belief that once any one type cancer is defeated (a cure is found), many other cancers will be conquered as well (if not all).  While being able to go online while flying is pretty neat, more of our money and efforts should be towards our health.  The internet is a neat tool, but it’s useless if we aren’t around to use it.  Events like Movember are great because they bring awareness to such issues.

Will I do this again next year?  Considering I will just have come home from a 500 mile journey through Ireland and Scotland to raise money for cancer research, I think I’m entitled to a year off.  I can’t say I’ll never do it again though.

This month has also taught me that looks matter in the real world quite a bit.  While my friends and people at work didn’t treat me too differently (sure, many more jokes were made about my face), strangers kept their distance a lot more this month. Before growing the moustache, I had grown a beard, and I felt the complete opposite.  I felt strangers were being more friendly towards me, and I returned the favour.

So as Movember comes to a close, I would like to thank everyone who participated and everyone who donated money to a wonderful cause.  Let’s make sure we conquer cancer in our lifetime!


Movember Update III

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We are now more than two thirds of the way through Movember and my ‘stache has reached ‘full grown’ status.  Of course, I will continue to let it grow for the rest of the month and end the month with one more final update.

With the awkward growth face over with, and most of the people I see regularly getting used to the moustache, I often find myself forgetting that it’s even on my face.  That’s why when I get a reaction, it surprises me again.  The shock leaves quickly though as I remember that it’s there.

The most recent of such reactions was at the office, when a couple members of our R&D team were at my  building for a meeting.  I ran into them walking by the boardroom on my way to lunch.  Some laughs happened and I remembered “Oh yeah, the moustache.”

“Do you know what you look like?”

“No,” I responded, thinking of lots of things I’ve heard so far but wondering where this was going.

“A 70s porn star.”

Surprisingly, this wasn’t the first time I had heard that exact comment.  What is it with specifically combining the 70’s as well as porn star with the moustache?  While I have had a few random comments about the 70’s, I haven’t heard porn star without 70’s attached to the comment.  I wasn’t alive back then, so I suppose I’ll never know.

I ran into the same person the next day.  “When’s your movie coming out?” he asked.  Other than men’s health and prostate cancer awareness, at least this moustache is also bringing comedy into my life.

Even though diseases like prostate cancer are very serious and men across the globe are growing moustache to bring awareness to this problem, it is important we find joy in life.  Growing a moustache is a silly way to bring awareness to a real problem.  Follow this link to a Penny Arcade comic that explains just that!


Movember Update II

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After all the laughs I got on the first day of Movember wearing an already full sized moustache, I returned to work clean shaved and everything returned to normal.  I was no longer the company laughing stock.  At least for now.

I didn’t shave for a couple days since it would have been too difficult to try to keep just the moustache.  On November 4thI did my first shave and you can see the results here.

I then hit the road (having taken the day off from work) to go to Syracuse for the weekend to celebrate Dan’s birthday.  The weekend involved seeing a lot of old friends and having some good times getting together.  Dan and I got to join in on some Haranshire fun and attended their coronation feast and made a Wayfarer announcement.  It was a good time and I managed to find the time to continue to shave and took another picture on the 6th.



On Monday morning, I found myself awake at 4:30AM to take a flight to Billings, Montana for work.  I kept on trimming every morning but each one had me up before 6AM and taking a picture was never really on my mind at that time of the day.  While there is never as much time as you want on a work trip to really get to see the places you visit, I did have a couple hour drive to meet our customer and got to see a lot of very beautiful Montana sights, including mountains and deer.  I didn’t actually see too many moustaches out west.  I also saw snow.  The temperature was often below freezing.  Sometimes I really forget how lucky I am that even though I live in Canada; Toronto is a pretty warm place overall!

I didn’t really think about a picture until I was in the airport waiting for my transfer in Denver on the 9th.

While this is being published on the 10th, I wrote this the night of the 9th, and haven’t been to my office since
November 3rd.  In a sense, my plan to get everyone in the office used to my moustache gradually coming in isn’t
going to work with not having to go in for six days.  Still, I believe the moustache I am currently growing will look better than my former eyesore.

I will continue for the month to grow my ‘stache in support of bringing awareness to men’s health issues in support of Movember.  I’ll be checking in again around November 21st to let you know how it’s growing!