Archive for the ‘Quest’ Category


Quest for the Cure: A Survivor’s Story

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The college of hawai’i cancer center hosted its annual quest for the cure event in october, countrywide breast cancer recognition month, with first-account memories by breast most cancers survivors and updates from hawai’i-primarily based researchers who’re attempting to find treatment options, and enhance cancer treatments for people in our island kingdom.

Over 1,000 ladies in hawai’i discover each yr that they’ve breast cancer. Katie Manuma bravely describes her prognosis, how she broke the information to her own family, and the way she struggled via remedy and survived.

Our video is with the aid of amanda shell, uh med now journalist.

Last month Katie was in LA. She recommends everybody a good place for weekeng trip – TheQuestFactory.  It’s really a good place for fun and good mood for long period of time. What’s good for your health.

Within the time that it takes me to put in writing this weblog, a scant hour, every other 30 women can be identified with breast most cancers. every yr, it is envisioned that more than 246,660 girls in the united states can be diagnosed with breast cancer and that more than forty,000 will die. The chances are sobering, about one in 8 girls inside the u.s., will expand invasive breast most cancers over the path of her lifetime. within the bay area, the percentages may be a ways more alarming, up to twenty percentage higher than the countrywide common.

As we input october, breast most cancers attention month, i can think of no better time to introduce a brand new subject matter to our interconnected planet. Up to now, we’ve been that specialize in how mellanox answers effect research in earth and planetary sciences. We would now like to feature scientific and health troubles to the mix, taking our adventure into the area of scientific research, fitness and advancements in each that enhance the human situation, all with the assist of mellanox answers.

Basic, the scientific discipline maintains to make strides, progressing in diagnosing, treating and the ultimate quest to remedy most cancers which remains the second one leading cause of demise within the u.s. for starters, girls are beating breast cancer and becoming a member of the ranks of the 2.eight million breast most cancers survivors in the u.s. in addition, breast most cancers occurrence quotes in the u.s. had been decreasing in view that 2000, after growing for the preceding two a long time. they dropped by using 7 percentage from 2002 to 2003 on my own.

Immunotherapy is one speedy developing vicinity of most cancers studies that is helping to improve survival rates. it includes developing cures that use a affected person’s personal immune device to fight and kill most cancers. The her2 protein is overexpressed in nearly 25 percentage of all breast most cancers tumors and is related to an aggressive for of the sickness and poor analysis. researchers have proven that immune cells are much less capable of apprehend and goal cancer cells that specific her2 as breast cancer progresses right into a more superior and invasive stage. This indicates that strategies that may re-stimulate the immune machine to apprehend and goal her2 early throughout cancer improvement may be effective remedy alternatives.

What all this boils right down to is that researchers around the sector are difficult at paintings on vaccines for both secondary and number one prevention. all of this takes massive amounts of computational energy, a place in which mellanox excels. In reality, all varieties of medical breakthroughs are viable. A collection of researchers at the middle for genome architecture at baylor university of medicine used mellanox to help acquire the 1.2 billion letter genome of the west nile virus. this has enabled scientists to provide you with better approaches to fight the deadly ailment. in step with olga dudchenko, publish-doctoral fellow at baylor, “taking gain of ibm power8 and mellanox infiniband join, we’re now able to exchange the manner we bring together a genome.”

This represents a recreation changer for researchers tackling the cancers and different diseases of the arena. stanford, a associate of mellanox using our infiniband solutions, maintains to make strides within the use immunotherapy for curing cancer. every other mellanox accomplice, nvidia, has teamed with the country wide most cancers institute, the u.s. department of energy (doe) and numerous national laboratories on an initiative to boost up cancer studies with their strength supercomputer based totally on the dgx-1 layout, known as “saturn-v”. The initiative most cancers moonshot goals to supply a decade of advances in cancer prevention, analysis and treatment in only five years. The research efforts include a focus on constructing an synthetic intelligence framework called candle (most cancers dispensed learning environment), so that it will offer a not unusual discovery platform that brings the energy of ai to the combat towards cancer. Backside line, mellanox promises the high performance interconnect for the “saturn-v” system.

Dell and tgen are tackling pediatric cancer head on. formerly, an individual affected person’s rna evaluation took seven days. along with tgen and dell, we had the modest goal to attempt and decrease that to five days knowing that with youngsters mainly, even an afternoon could suggest the difference between life and death. Mellanox’s infiniband decreased the rna-sequence information evaluation time for patients to simplest one hour! from seven excruciating days to simply one hour. This accomplishment is at the heart of how mellanox era is going to assist crush pediatric cancer.

An alarming 38.five percentage of human beings will should fight a few form of cancer in their lifetime. meaning cancer touches each person both immediately or through a close member of the family. It also method that it’s miles a priority for the clinical field in standard as they collectively power relentlessly in the direction of a therapy.

Some years ago, i was at a charity occasion for hers breast most cancers basis that turned into honoring dr. mark pegram, the first director of the breast most cancers oncology software at stanford ladies’s most cancers middle. He is likewise the co-director of stanford’s molecular therapeutics application. i desired to recognise – i think all of us need to understand – when will there be a therapy for breast most cancers? He told me, and i’m able to by no means forget about this, that the aim changed into to create a treatment, a vaccine in order to save you breast most cancers. Consider, our children and our grandchild in no way understanding the worry of having most cancers or the horrors of fighting for their lives the manner so a lot of us have. Imagine that we’re the ultimate generation to fear the massive c.

So, with this desire and goal in thoughts, please comply with alongside as we discover the lifesaving studies and advancements inside the discipline of clinical and fitness.

Medical doctors and advocates for spinal twine remedy studies say multiplied taxpayer greenbacks to help cure the uncommon however devastating injuries should store clinical charges on a large scale.

“The activities of daily residing, the in a position take them without any consideration,” stated dr. Eric ruby, founding father of massachusetts walks again, the neighborhood chapter of quest for the treatment, a country wide employer for research, political activism and fundraising for spinal cord damage patients. “Once you’re disabled, all of a surprising your world is turned the other way up,” ruby said.

Spinal cord harm (sci), even though uncommon, can be devastating. Whilst the spinal wire is broken, it cuts off communication between the mind and the rest of the body. The fees of treatment and equipment to address the incapacity over a lifetime can grow into the millions of greenbacks for character sufferers.

Injuries sustained from vehicle injuries, sports, bad falls or acts of violence leave 17,000 humans a yr with headaches like lack of sensation, lack of reflexes and paralysis. in step with ruby, 400 massachusetts residents receive a spinal twine damage every yr and almost 1.3 million people currently live with the condition.

Tim brown, who broke his neck in a snowboarding coincidence five years ago, said that it’s critical to “recognize human beings with spinal twine accidents as individuals.”

“It’s a circumstance that really considerably influences people’s lives,” he said, “just because it’s maybe a smaller subset of the populace in comparison with other matters along with most cancers or coronary heart ailment, it’s vital that we still get collectively … and get the phrase obtainable.”

At a country house occasion wednesday, ruby called for multiplied funding for spinal wire research and scientific trials, specially in massachusetts’ bustling medical region. Ruby mentioned that investment for a cure isn’t always an “fee” for taxpayers, but an “funding.”

Ruby said massachusetts has a “high concentration of hospitals, scientists and sufferers” in boston and the capacity for clinical studies may want to “significantly reduce the amount of health care bucks spent by using residents.”

The kingdom’s spinal twine research fund has issued three primary presents from the fund, in line with ruby. one of the $250,000 presents went to researchers on the harvard stem cellular institute to map out how the mind and spinal wire speak. Others have long gone to investigate tasks at brigham and ladies’s health center and kid’s health center.

“The federal authorities sincerely needs to take into account that if we ever cured diabetes, we can shop healthcare billions, if we treatment spinal wire damage, we’d save healthcare billions,” ruby said.

In step with the countrywide spinal cord injury statistical middle, a spinal twine harm can fee a median of extra than $1 million for tetraplegic sufferers, for the first year. Every subsequent 12 months after expenses a median $185,000. This only debts for healthcare and dwelling expenses and no longer for misplaced wages or lost blessings.

Taunton state sen. marc pacheco hosted the event to replace the advocates and supporters on studies improvements, new legislation, and funding for spinal cord research.

Pamela daly said spinal twine damage sufferers are a minority within the clinical community. “It’s like any minority,” she said, “we don’t have a massive lobbying group, there aren’t loads of us … [but] we want funding like every body else.”

The advocates did score a victory last november, whilst the legislature placed into law steady investment for the state’s spinal cord studies fund, named after the past due brockton nation sen. thomas kennedy. kennedy changed into paralyzed at 19 after a horrific fall, and become one in all few quadriplegics to preserve political office. The fund heavily relies on driver’s license suspension expenses, but after adjustments inside the manner the prices were passed down, the cash dried up. the new law restored tons of the investment for studies. Pacheco’s office stated the fund’s current stability for financial 2016 is $forty eight,seven hundred, up from $23,600 in fiscal 2015.

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.


Quest for a Cure 2017

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The 8th annual quest for a therapy walkathon will be held sunday, september 24, 2017 at vfw park in royal oak, michigan. This event is organized with the aid of 9 metro detroit-place households on behalf of their kids with rett syndrome: the cardinalis (giavanna), the casses (ashton), the macdonalds (annie), the petersons (jillian), the pettys (hailey), the rokickis (olivia), the scappaticcis (isabella), the weinrauchs (emily), and the zerials (mia).

Even as we actually inspire anyone to attend the walkathon – it’s always a top notch day for the entire family with correct meals, true amusing, and notable raffle prizes – we are hoping even people who cannot make it’s going to recall creating a donation in help of our occasion! For more records at the event and the way to participate, click on right here to go to the internet site.


Words from the Road: Glasgow

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When an adventuring party in Dungeons and Dragons needs to cross a river or a part of the ocean like we did on Sunday morning, they go down to the docks and hire a boat.

In modern UK it’s not quite that easy – much better to talk to P&O Ferry, who does all the crossings between Larne, Ireland, and Troon, Scotland.

We woke bright and early on Sunday morning, scarfing down a quick meal before heading to the harbour before 6:30am. There were a dozen or so other foot-passengers waiting for the boat as well when I checked in and was told the bad news: Larne to Troon had been cancelled due to high winds and rough seas. The good news was that they would be giving us a ferry to Cairnryan and then sending us by bus up to Troon port. Even though my stomach was starting to bother me, the ferry’s foggy portholes and comfortable seating made for an interesting little trip.

If it weren’t for the delay of more than an hour and a half it wouldn’t have bothered me; we saw some of Scotland’s beautiful Ayrshire countryside from the bus, including some great castle ruins and a whole lot of cows.

By the time we got to Troon, rain was coming down. It was 11:00 already, so we decided on an early lunch. Our waitress Natalie was kind enough to find us some alternate directions to Glasgow. Which is when things started going really wrong.

Unable to find a proper street map of Troon, we asked a local who – after telling us she didn’t understand why our directions would point us a certain way, we should go this way, instead! – pointed us down a road… which is where I have to tangent onto two things: road signs and spoken directions.

Road signs in the UK are absolutely ridiculous. Roughly as ridiculous as purple unicorns, in fact: they’re not what you’d expect, and that’s because they’re just not there. They don’t exist, no matter how much you may wish they did. When they’re there they aren’t somewhere that is necessarily visible to the naked eye; you have to search at each street corner, and hope and pray that someone thought “this street should be marked somehow!”

And when you finally think you might be lost, asking someone for directions may not be as helpful as you would like because, well, directions in the UK revolve around landmarks you’re not familiar with. “Just go a wee bit down the street here and you’ll pass a wee church and a big church; turn at the big church – not the wee church, mind, the big one – and take the second left after… no, maybe the third, aye, the third.” And before you think I’m exaggerating, yes, those are exact directions I got from someone yesterday afternoon.

We got almost 50 minutes down the road, having run into some Canadians from Orangeville who were having remarkably similar problems (but with access to a car, so perhaps less annoying), before getting back on track with the help of, without a word of a lie, a young man with bagpipes wearing a kilt.

So we walked back, much more careful about streets and landmarks. We turned right immediately after the library, and then left again when we came to the end of the street (according to the map, at least; the driveway for the building started right there too, so it was a bit misleading). Then we were on the right road and started walking along the shore, a beautiful site that was marred only by our frustration with the wrong turn so early on. One or two more helpful citizens later and we’d cemented the fact that we knew where we were going.

Part of our Google directions took us on a bike path, right through a wilderness reserve that was absolutely beautiful and reminded me so strongly of Ontario that it felt like home. We stopped a few times along the reserve, both to rest and to drink it all in. Trees and streams everywhere, not a building in sight; only the asphalt of the trail showing me that there were humans about at all.

Apparently there are biking trails that could have taken us all the way up to Glasgow, only occasionally by highway. It’s something to think of if I’m ever silly enough to do something like this again.

Part of the problem with directions is Google, which uses one street name when the street has four, only two of which are on any given sign. A fine gentleman on the bike path with his two sons gave us the best news we’d heard all day: we were on the right track and, in fact, on the road that would lead us all the way to Glasgow. “Just keep following the signs up ahead,” he told us. “As long as the roundabout exit says Glasgow, just take it. You’ll get there.”

So we did. We walked another two hours or so after meeting him, and the sun was sliding beneath the trees on the horizon when we thought we should make camp. The highway shoulders were much smaller than we had anticipated, forcing us between walking on the road – we weren’t ever honked at, and I can only imagine it’s because we looked so funny rather than because we weren’t frustrating some people – or walking through wet grass. We alternated depending on how heavy traffic was, but eventually came to a flat ground that we pushed through to find a camping site.

We came into a small forested area near a subdivision of Irvine, where we poked a bit at the ground, hoping to find something without so many roots. Eventually Drew decided to set off on his own, sans heavy pack, to search something out. We both took off our packs and he left me to watch them in the dying light of the sun.

As soon as my pack came off I was swept with a wave of nausea, something I’d felt twinging that morning but hadn’t actually succumbed to. Cramps in my stomach redoubled, and I had to sit down with the pain. Standing up made me light-headed. Something was definitely wrong, and only the adrenaline of being on the trip and the exhaustion of the pack had kept it down.

When Drew returned I let him know, and we hurried to set up camp on the stretch of beautifully flat grass he had found nearby. The tent went up easily, and we pushed everything inside as carefully as we were able. I was asleep twenty minutes later, around 8pm. Drew had cracked a glowstick – one of our nods to D&D’s “adventuring pack,” where you can buy an item called a sunrod that operates on a similar principle – and was reading to pass the early evening by.

I woke again throughout the night with cramps and waves of nausea, thankfully never having to run outside. The rain came down heavily at one point, and I am happy to say that our tent worked in every way but one (it’s too short; the feet of our sleeping bags got wet). We finally woke ourselves at almost 10am, and I knew as soon as I woke up that there was no way I could walk today.

We packed slowly, Drew having spoken to a gentleman named Richard who was out walking his dog and told us that the train station in nearby Irvine could get us to Glasgow.  Before we finished, Richard had returned with an offer to drive us to the station itself.

Let me say this now: the kindness of people we have met, from Marleen in Belfast to Richard in Irvine, has been unsurpassed by anyone I’ve ever met before. Going so far above and beyond their call to help out strangers… we could not have come even this far in our adventure without Marleen, and I’d be significantly more miserable right now if not for Richard.

I’m fairly certain it’s food poisoning. I’m even more certain that I won’t be up to walking tomorrow morning either, given how hard it is for me to even walk up the stairs, much less do it with some light-as-feathers bags that I have with valuables that I don’t want to leave in the hostel luggage room.

Drew and I are looking at alternatives for the next few days to ensure that we are still walking the full distance, to make up for the distance lost today and the distance we will surely be losing tomorrow and maybe even the next day. The advantage to us staying here overnight is that we’ll be able to ‘blog about those changes fairly soon – you won’t have to wait ’til the 8th of October for our next check-in, but unless this illness gets worse overnight instead of better, we are still very solidly finishing this trip, even if part of it has to be done by train and made up for by walking in the city.

We’re a little discouraged by all the early setbacks, but we’re not giving up. We’ve still got plenty of time to reschedule, remap, and finish up the full 500 mile walk by the end of the month. Thanks for all your support and well wishes!


Words from the Road: Larne

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This post is being posted on October 1st, but was written on September 29th from Larne, Northern Ireland, and that’s why it is dated as such. Check out our “Journal” page to get all the latest updates!

Belfast was an amazingly beautiful city, full of great sights, wonderful people, and exactly the weather they describe in travel books. I’m not kidding, folks, and I’m not being paid by the insidious travel industry* to say this, but Belfast’s weather – indeed, the whole of Northern Ireland, as I’m told – is absolutely unpredictable. Rain will turn to too-hot sun in a matter of minutes. A cool morning will turn hot at 9am and cold by 10, only to rain and be sunny again before lunch.

We started off late Saturday morning, getting a bit of extra sleep with the help of our friends David and Kim, two SCA players from just outside Belfast who were unbelievably generous to us. Their children, Andrew and Zach, helped them serve breakfast (a traditional Ulster Fry, which, let me tell you, was exactly what one needs before going on the road – full of energy and everything’s fried, so if you die, you die happy) while teaching us about the Skylanders. I’ll tell you sometime. Really.

At 9am we arrived at Belfast Castle, a modern castle offering a beautiful view of the city. We didn’t leave the castle ‘til 10; re-packing our bags and getting everything on took what could generously be described as a ridiculous amount of time. Throughout it all, David and Kim waited. Kim took a picture of us pretending to be horses:

Ridiculous, right? Just wait.

About five minutes after the fine folks who had been so patient with us drove away, my leg armour shifted and started pinching and bruising in entirely unpleasant ways. Two minutes of shifting around later and I knew there was no way I could wear them: I would have to take the offer to ship them to us in Edinburgh that our other Belfast friend Marleen, who had shown us around the city Friday afternoon, had given. I took the legs off, readjusted and, with a hearty groan, we were off. Again.

It didn’t take long for the schizophrenic weather to catch up wth us, and we alternated between shivering and sweating like crazy. Less than an hour later and my gorget slipped when I adjusted my pack, cutting off my air supply.

I’m a large man, almost six feet and with a hundred pounds on most guys. I have a great deal of upper body strength and I’m not used to being unable to physically do something that involves brute force. Which is why, when I tried to re-adjust my gorget so that I could breathe, it freaked me out a bit when I found myself unable.

Drew, thankfully, noticed and came quickly. He helped unstrap the gorget and we removed the pack as smoothly as possible… which wasn’t really very smoothly. It was very clear very soon that the pauldrons that I love so dearly would have to go.

Leaving bracers, and chainmail that is the heaviest thing – pack included – that I had with me. The 30 pounds of steel, combined with the extra-thick gambeson beneath it that allowed me to walk in chainmail with a backpack digging into my shoulders without hating life, was causing serious issues with heat regulation that I had hoped would remedy itself in the cooler climes of the United Kingdom. They did not, and so I have come to eat my hat.

Or Paul’s hat, as it were.

No, we’re not giving up. But I am leaving my armour to be shipped to me in Edinburgh. All of it but the (pleasantly visible) bracers are already safely back in Belfast, ready to go. An expensive mistake, but less than if I had tried to continue and, as Paul prophecied, left my armour “piece by piece, scattered throughout the trip.**”

With Marleen’s help we had a very nice lunch, and then – very sore and after a terrifying rolled-ankle incident caused by the armour I’d hung from my pack – got a drive to Larne, where we will start afresh in the morning with a ferry ride across to Scotland. It means that our entire mileage, other than the ferry trip itself, will come from Scottish walking; we’ll be adding some during our stay in Edinburgh, and including some of the wandering we were otherwise intending to do in Ireland. We will still be travelling 500 miles, from Larne Harbour instead of Belfast Castle, but because of the injury (still sore, but entirely walkable, don’t worry – I’ve been exercising it carefully!) and some other problems (like my backpack breaking ten minutes after the trip began) requiring a visit to a store nowhere near our route, we decided that this was worth doing to make sure that we made it the rest of the way.

Don’t worry, folks: we’re still alive, and we’re ready and rarin’ to go. I am more excited than ever to start our trip properly tomorrow, and very ready to step off that ferry in Scotland and do a 25-kilometre hike with a much lighter load on my back.

Next ‘blog will be on Monday evening from Glasgow. See you all then!

(Don’t forget to follow us on Facebook and Twitter, both being updated this month!)


Heavy Armour, Hard To Carry?

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My armour is probably the most visible thing we’ve worn to date on our public training walks. It has gotten a few comments from people, from ex-SCA players to people who wanted to know if we were making a movie; some people have wanted to touch it or even try it on. (Sadly, I have to turn down the ones who want to try it on – I would have to take off my pack, and I’m always worried that once I take it off I’ll never convince myself to put it back on…)

In a recent article on the Science NOW website, some researchers at the University of Leeds did tests on a person’s energy output when walking in 30-50kg of plate armour and found that it expended “more than twice” the energy that just walking did.

The linked article explains that a lot of that comes from leg armour, of which I won’t be wearing much – greaves, sabatons and cuisses are just things I do not own and likely won’t by the time we leave (though if you’re looking to get rid of some…). My chainmail and other armour is mostly arm and torso protection; while the arms are far enough away from my centre of gravity to cause a bit more wear, the fact that I can swing them close (or even fold them, if it comes down to it) will mitigate that.

The armour is heavy, and it certainly takes a toll – I was more tired after my last training walk than the one before it, despite more training in between them, because of the armour being worn. I also just received more armour that I’ll be wearing – some plate for my arms and shoulders – which adds probably 15-20 pounds by themselves. I’ll be doing a full weigh-in on my entire kit very soon so that everything’s accurate by the end of it all, mostly for my own interest.

In addition to all the gear we’ll be carrying – tent, food, cooking ware and health supplies – this armour will be a great strain across my back that I can’t share with the rest of my party. As I play D&D – fairly regularly again, starting just a couple months ago – every time our characters stop for the night I imagine how it’s going to feel to take off the armour…

… and I realize that they don’t, if they want to stay protected during that first watch.



The Final Roster

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Since the inception of the Quest for the Cure, we have seen a number of roster changes, for reasons ranging from personal to professional to health-related. It has been a long road – no pun intended – and when we bought our tickets last week, we had our final roster in mind.

On September 27th, Dan and Drew will be boarding a flight to Belfast.

This final roster change – bringing us to just two Wayfarers making the trip – does mean a few things will be changing. First and foremost, we won’t be able to hold watches; doing so while also trying to sleep enough for our physical activity levels is just impractical.

We will also be carrying the gear ourselves, but that might not make much of a change – we’ll have less gear to carry, simply because we have fewer people in tents, fewer people eating food, so on and so forth. We’ll still have to carry all of our cooking gear between the two of us, but we can be more selective about what we bring even for that.

To answer a few questions we’ve gotten, though:

Yes, our goal is still $100,000. We are not lowering our fundraising goal, and with your help – everyone reading this – I am confident that we can still reach it.

No, there is no chance that we will cancel the trip. No chance at all. We are committed – and not only because those plane tickets are non-refundable!

We leave Toronto on September 27th, and return on October 28th. We’ll be walking for about 24 of the days in between there, taking a few days off here and there to recuperate and rest our legs. A more detailed itinerary will be posted closer to our flight, I promise – we want anyone in the area to come out and say hello!

What was once akin to the Fellowship has come down to just a pair of guys making their way, but that didn’t stop Frodo and Sam and it won’t stop us.


Betting Against the Wayfarers

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“The trip is impossible.”

We have been hearing this since the beginning. Between family members and friends, I don’t think we had a better than 50% faith rate – and, to be fair, most of them thought it was a crackpot idea of mine that would fade into obscurity and become a matter of “hm, that would have been neat, eh?”

I’m sure they are all still shocked that I even bought the plane ticket, much less intend to step into the highway between Belfast and Larne three weeks from tomorrow.

When I told a friend this, they said I should tell people to put their money where their mouth is – and this is what we’re doing now?

Think we’re going to fail? Here’s your chance to tell us while also supporting charity.

We’re starting a betting pool. Minimum donation of $10, and you choose a day: anything from September 28th (our first day of walking) to October 27th (the day before our flight). This is the last day you think we’ll be walking, not the day you think we’ll wake up and say “no more!” – just to be absolutely clear.

There is no maximum contribution. Want to bet $50? Bet $50. Want to bet $100? Fantastic!

When we win If we win, 100% of the money goes to the Association for International Cancer Research at the end of October. The Wayfarers themselves will not be taking any of the money, obviously.

If we do not finish the trip, whoever chooses the last day that we will walk will get 50% of the pot. This 50% will be split between as many people as choose it; if you’re the only one to choose October 4th, you get the whole amount. If you and three others do, you each get a quarter. The other 50% of the pot will be going to AICR. Everyone wins!

If you’re interested, contact Paul (paul@wayfarerquest.com) any time before midnight on September 28th – you have three weeks to get in on this. If you seriously think that we’re going to fail in our Quest, put your money where your mouth is and contribute to charity while buying yourself a chance to win a bit of money on top of your bragging rights.

Some things to help your bets:

We are travelling roughly 27km (or 17mi) a day. We have some lighter days, but only one harder day – the first day, Belfast to Larne, which is 34km.

We stay in beds ten times by the current schedule:

Larne, evening of September 29th
Glasgow, evening of October 1st
Fort William, evening of October 8th
Inverness, evening of October 12th
Perth, evening of October 20th
Stirling, evening of October 22nd
Edinburgh, evenings of October 25th, 26th and 27th

Obviously, injuries or just finding the walk too hard could slow those down – I don’t think they will, but keep that in mind. That’s why we’re accepting bids even on October 26th and 27th – days that we should be done. You want to bet against us that hard? Go for it.

I would wish you luck, but that would be betting against us, and I don’t do that sort of thing!