Larry Page posts about his voice
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This is almost the exact same thing members of the band Def Leppard said about their drummer when he lost his arm in a tour bus accident. They said the limitation caused him to become a better drummer.
Def Leppard subsequently became one of the most successful hard rock bands in history when their first album post-accident, "Hysteria," sold 20M copies. Several of the beats on that album became legendary, including the beat to "Pour Some Sugar On Me" [1]
I wonder how we could teach ourselves these lessons (without injury, of course).
John Bonham, Dave Lombardo, Bill Ward, Peart, even Dave Grohl is better than Rick Allen.
Many people have stronger voices than Page, but the point still stands that it's how you approach your adversity that counts.
Ah well, HN giveth and HN taketh away...
I won't recap, but read up on the terrible burn injury on his playing hand and how he developed a new playing style of his own to compensate.
He's regarded as one of the fastest, cleanest guitarists ever. Here's an example: http://www.youtube.com/watch?v=LoIJ4W7kXiQ
One of my favorite bars has a lot of cool rock memorabilia including an ink print of Jerry's truncated hand. It's fun to compare the size with your own.
SPOILER ALERT: His hands were huge!!
I am a big fan of The Dead.
There's a wide-ranging and productive history of people expanding their creative capacity through self-imposed constraints.
http://www.amazon.com/Creativity-Constraints-The-Psychology-...
Curiously, I went to fill out the survey linked from Larry's post, and after I indicated that I don't have vocal cord paralysis, the survey was over for me. Somehow, I'm surprised they weren't interested in collecting denominator / negative information from those without the condition.
They're not collecting information from people without the condition.
This is simply their way of getting rid of people who shouldn't be filling in the survey.
I think it's actually a reasonable UI decision. They could have done it one of two ways:
1. Have the page say, "Fill in the survey ONLY IF you have the condition".
2. Anyone can fill in the survey. But the first question determines whether you are a candidate or not.
They chose #2.
I'm surprised by the business decision. My feeling is that there is often value in collecting information on people without the condition (negative data), should those people somehow feel compelled to participate.
No doubt he'll open his wallet and for research that will help others that still haven't had the vocal cord issue.
http://www.voicehealth.org/research.php
However, the survey does not give you the option to select for other conditions say, RRP.
http://www.voicehealth.org/research.php#rrp
One would think that they would try to capitalize on the publicity of Larry's post to try to gather as much data as possible for various conditions and not just vocal cord paralysis.
It appears they have to follow strict medical checkups after the operation and thus have to leave work to attend these appointments. As such, many are denied jobs or are conveniently fired from their positions. And even though the law protects them from some of this discrimination it's hard and expensive to prove the discrimination.
Same thing happened to me.. I was told by my doctor that it was like winning the lottery twice
I was not amused
It really sucks that so much of those things will probably never be treated properly because there is no incentive to do so. That's why initiatives like this are so great.
</sarcasm>
It was either naïve, ignorant, or a bit of both.
I don't know a source that I would say is the definitive and best source of information to learn more about Regenerative Medicine, that's why I encourage you to do your own research. I don't want to convince anyone, just give you hope. =)
* Hope you get better dude!
Larry Page did sponsor research in the field of his disease, but I don't know why he didn't consider Regenerative Medicine or something else promising. Maybe he didn't know about it, or it's less promising than I think.Rare diseases are generally not huge money makers for big pharma. That is why there isn't as much money being devoted to them to find a cure. The fact that Larry Page is donating is a great reason to capture some of that long tail for whatever reason.
While perhaps not blockbuster, orphan drugs for rare diseases can turn quite a profit for pharmaceuticals.
http://www.forbes.com/sites/johnlamattina/2012/05/02/how-com...
http://online.wsj.com/article/SB1000142412788732392610457827...
Genzyme was built on rare disease drugs.
Of course it's his money and his choice, and there's nothing bad or wrong about funding something that's important to him, but it does seem a little... shallow, I suppose.
Behind many non-profits and causes there was a similar personal catalyst. People trying to get rid of the three strikes law or drunk driving were many times similarly motivated into action by a personal tragedy.
Maybe he just had the chance to learn a lot more about this particular disease and so it's more natural for him to invest there. It sure would feel more natural to me to contribute to research on a disease that I have experienced first-hand than to some other random one, even if the random one is more "important." No selfishness there. I would just identify better with the victims and have a more real urge to help them.
Give the man a break. It's good that it's not life threatening at this point as there are certainly much worse CEOs in the world.
I can be selfish too.
I think it's selfish/egotistical for someone who wants to donate a TON of money to medical research to choose a disease that he/she happens to have instead of sitting back, doing some research, and supporting research that will help the most people. That's just my opinion. I can see the other side of the coin too. Hell, maybe the amount of money we're talking about here is peanuts compared to the amount of money Larry already donates to other more widespread medical causes, maybe Larry just failed to mention that in his writeup. I suppose one shouldn't jump to conclusions.
Bottom line is that it's none of your business.
Why is his financial allocation a problem? Nobody was complaining when he wasn't donating to VHI at all. I'm sure it pales in comparison to what the public donates to sports teams and the movie industry.
Just getting a rich guys attention and having him throw some money research's way is a crap-ton better than another jet-helicopter or mega-yacht.
I find this rather awkward. Here we have someone with a ton of money giving a tiny fraction of it away in a very public manner to a cause that seeks to remedy one of his own personal afflictions. He comes off looking like a good guy, and in the process generates excellent PR for his company and social network. What is the downside? It's as if there isn't one. I don't know why, but it gives me the squeamy jibbly icks. Same vibe as when he gave away flu shots at Target.
I guess I have the following questions. Why do the rich need to be our saviors? Do we really need to justify extreme wealth disparity with extreme condescension? Can't we just shuffle some defense money to healthcare and make democratic decisions about how to allocate healthcare funds? Or, god forbid, raise taxes on the wealthy?
Is the answer really, sorry, no, that's how it has to work in "free market" capitalism?
Choosing to donate to a cause that affects him personally is no different than when people create charities or foundations or donate money to fund research for diseases that affect their immediate family members - which happens quite often.
And anyway, it's not necessarily the spending itself, but the way that he announces it that makes me feel uneasy.
And then, the rare conditions are starved of funding because everyone votes to throw more money at cancer/something well publicised because they spend a lot of money in marketing.
How does that help the rare sufferers, if their vote is never enough, and their voice drowned out by the megaphones?
I wouldn't be surprised if quite a lot of funding for rare (and not photogenic) stuff came from 'selfish' wealthy individuals with a vested interest.
Larry is indeed very lucky.
One of my good friends was diagnosed with Hashimoto's thyroiditis after ten years of misdiagnosed and ignored symptoms. (It's a very rare disease, and many of the early signs - weight gain, mood swings, fatigue, etc. - can easily be mistaken for typical adolescence).
In Larry's case, it seems they caught the disease and began treatment before it completely destroyed the thyroid, which is a real danger - if the disease isn't diagnosed by this point, treatment becomes much more difficult, and patients develop heart problems.
Unfortunately, my friend has not been so lucky, and has been suffering with the complications for several years now.
Thyroid problems are routinely misdiagnosed as non-existent, not only for adolescents. Hypothyroidism in particular may be routinely under-diagnosed due to unspecific symptoms and far too stringent thresholds on thyroid levels.
I've read that site several times. Frankly, while I'm sure a lot of patients don't do well enough on levothyroxine or need more intensive tests than the TSH, I'm very skeptical of people who develop fanatical, rigid opinions about how to treat hypothyroidism without extremely careful and rigorous study, largely because I'm very skeptical about people who develop fanatical, rigid opinions about anything without extremely careful and rigorous study.
Hashimoto's is not a rare disease. It is one of the most common forms of hypothyroidism and one of the most common autoimmune disorders. The diagnostic metric for it is also well-known--check TSH levels and, in some cases, the free T4 as well. I'm sorry to hear about your friend, but his experience is not entirely typical.
Mine has been detected at age 24 (I'm a male) after a palpation by the company works doctor who found the thyroid slighlty abnormal. Confirmed by echography and blood tests. There are genetic predispositions though, my mother suffers from the same thing.
Some doctors/researchers believe that hypothyroid (typically caused by Hashi's) is not rare in young people at all (or adults!), but merely underdiagnosed. Alleged symptoms of youth hypothyroidism include constant and recurring ear/nose/throat and upper respiratory infections, severe allergies, fatigue, sensitivity to cold, slow healing, etc.
I was recently diagnosed with low thyroid (not specifically hashi's but, again, probably) and had 100% of those symptoms (and many others) for my entire life. I nearly died as a child from asthma and have had constant sinus and lung issues since.
Since I've been on a very low dose of thyroid medication, the "allergy shiners" that I've had since I was 2 years old have disappeared… in a week.
[1] http://blogs.wsj.com/digits/2013/05/14/google-ceo-larry-page...
Seriously though, I hope Larry Page will recover. It was sad to see Roger Ebert lose a bit of his zest when he could no longer speak and I wouldn't want any more people to be forever silent.
I also wonder what happened to selfless, anonymous donations. His affliction doesn't seem (medically or statistically) like something that would require rallying people to the cause, raising awareness, etc. There are conditions that matter, that affect millions (incl. children), that don't let people live normal lives (not kitesurfing - very basic everyday stuff).
The Target flu shot promo didn't seem genuine, neither does this.
I wonder how it will be perceived. Will stock traders buy or sell GOOG differently now that they found about it (or found out that the public found out) about this issue.
Did he have to get the approval of the PR or board of directors before disclosing it.
Not sure why you think humming/playing kazoo should be a good exercise for someone who has damage in the vocal cords. E.g. the common medical advice for someone who with a hoarse throat (due to a cold etc) is to let it rest, i.e., refrain from speaking. But I'd be happy to see studies proving that wrong.