Ron, U are an idiot! I have a good friend with cancer, but as another has said there are many other issues that need research as well. And you might be surprised to find out they have been working on cancer for quite a while now! If you are so damn smart I would think you already have cancer cured yourself.
Maybe if you suffered from this disease or knew someone who did, you wouldn't write things so stupid. Why don't you do something creative like look up this disease on the internet instead of trying to be a "smart ass"!!!!!!!!!!!!!!
When I read this article I was afraid that some people would interpret it saying that Lou Gehrig's disease does not exist, but then I assured myself people wouldn't be so heartless and stupid.
Thanks, Ron, for ruining my (tentative) faith in humanity. My father died of ALS and it was every bit as tortuous for him and our family as dying of cancer, which HIS father died of. Perhaps more so, because there is no known behavioral cause for ALS, and no treatments either--and there are for cancer.
Hey Ron - My mother died from ALS, it was not a pretty sight! You can't control you body at all, you can't walk, you can't talk, you can't swallow food or water, you have to be fed using a tube placed into your stomack, but the good news is that you mind is still there as good as ever. You can honestly see your self die!!! So, Ron, you are a complete and total idiot! It would be completely reasonable for someone like me that had lived throught this problem like I did with my mother to actually hope that you or one of your closest family member would come down with this disease just so we could see how your slow mind might change!!!!
"Ron, you are a complete and total idiot! It would be completely reasonable for someone like me that had lived throught this problem like I did with my mother to actually hope that you or one of your closest family member would come down with this disease just so we could see how your slow mind might change!!!!"
The remarks made by you are insane. Flippant, and no knowledge of Neurological Diseases. How about Parkinson's Disease, Multiple Sclerosis, Lou Gehrig's Disease, and other severe Neurological/ possibly inherited genetic diseases. Not all are afflicted with them by genetic makeup.
You one day, may get one of these. It is highly likely--most are genetic. I've know people with all these terrible, crippling diseases. They have died, some are still alive. There is no dignity to any of these diseases.
It is torturous to watch someone who is fully healthy one day, just crumble slowly or fast in front of your eyes.
You are one insensitive, immature, little wimp, who shows everyone on this board how really stupid you are.
Please read rons comment carefully he said it was a waste after 71 years to try to figure out why a sports figure died when the money and time could be spent curing a disease. He did not say ALS wasn't a bad disease he said why do they waste time trying to figure out why a guy died 71 years ago. So lighten up.
They are all bad diseases and there will be no cure for most in my lifetime so all you can do is pray you are afflicted by none of them.
I don't know why you would defend Ron's later remarks to others. They are rude, and insensitive. "Treat others with kindness, and it will come back to you".
While there are folks known as "cancer suvivors" there are no "ALS survisors." There are theories on the cause of ALS and one not mentioned publicly as a commonality to those who served in the military is the vaccines. I lost my 80-year old dad last year to ALS only 8 months after diagnosis. In the military yes, but not combat. One theory is due to the multitide of vaccinations & boosterss given our service folk, many contained a preservative that's derived from Mercury. A huge percentage of today's ALS patients are Gulf War vets. It's not a disease--it's a confirmed death sentence. MDA shares funding of research for this other diseases. On a final note, it is unfortunate tdon'that for most of us--including me-don't pay much attention to such diseases until it hits someone we know.
This disease, ALS, is just not reserved for men who have served in the Military (vaccines). We just had a woman friend die of ALS very quickly. It was astonishing how fast it ran it's course. Am sure you know it happens to both genders. Thanks.
bklynj, it may be that you and the ever-popular Ron, misread the article. Although the title of the article would lead one to that conclusion, the underlying point of the study and the article was not really that "Lou Gehrig may not really have had ALS". The study itself did not even mention Lou Gehrig as the article points out. The point of the study is that many of those diagnosed with ALS may not actually have it and may benifit from a different treatment than that which would normally be used for ALS. That certainly is valid research. The article does talk about the irony that Lou Gehrig may not have had the disease that bears his name but, again, it really isn't the case that the scientists in the study blew money on answering that particular question.
This could explain why so many football players are diagnosed with ALS. I thought maybe it was something in the grass, fertilizer or something from all the time spent eating dirt. I knew a football player, a genuine genius, Academic all American, very hard driving who was diagnosed with the disease. He paid me once to babysit a track meet for him, one of the things he had to do I guess to earn his scholarship. I can still remember seeing my high school track coach down on the field laughing when I was supposed to announce "Class M and S Hurdlers please report" and the M bounced back to me from the speaker system when I was about to say "S" and said "Class M&M" instead.
ludvig I think your first thought is more on target than the brain trauma . The fertilizer should be investigated and studied more than the brain trauma. The fertilizer is all kinds of potassium fertilizers used for lawn care. People with ALS should check there past for any contact with this fertilizer in my opinion.
amazing it has been known for centuries that an injury to the brain or spinal cord can cause nerve damage an slow death. i fail to see anything new from this article? He did have lou gehrigs disease it was named for him. If he had als is another question. His brain was injured the nerves were damaged he died. My head was damaged,my brain was damaged, my neck an nerves were damaged, i am slowly dying. I am waiting for the cure? How do they reverse the nerve damage? the physicians ignored the broken skull with brain matter protruding, ignored the subluxated neck bones compressing the esophagus causing a restrictive airway. I wonder how many organ failures are caused from neglected nerve damage? Cristopher reeves could have used some help. From what i have read preventing the injury is the only thing available. once you have the injury forget getting medical help. with five minutes allocated to you from the doctors you will run out of breath prior to saying what you are experiencing. If i had not put on my hard hat i would have been instantly dead. Instead i have suffered for decades.maybe amino acids can repair some nerve damage?
Scientists have been looking at the fertilizers for at least 30 years. As a biologist and anatomy and physiology instructor that they may be on to something with the brain trauma. We are learning that it is extremely devistating to the nervous system especially with repeated trauma.
"Lou Gehrig may not have had Lou Gehrig's disease"
wow
The medical information behind this revelation is explained quite well even a layman like me nods in agreement.
Which brings me to the other puzzlement tickling my brain. Was Lou Gehrig's disease ever really Lou Gehrig's?
The disease that used to be formally known as Lou Gehrig's disease. Never really was Lou Gehrig's disease.
But something else. A disease that needs a new name. Lou Gehrig didn't bring this disease into this world upon his birth, or spawn it in during his life. Just like a cold or flu isn't your's or mine it just is.
So funny that the Times is just reporting this. About 10 years ago, my physician told me he learned this in med school. My father suffered from this horrible disease 25 years ago and virtually no progress has been made since. I truly believe if they can crack this case, it will lead to so many other discoveries. I think Gehrig will always with it be associated no matter what.
My father died in the mid 70's of what was diagnosed as ALS but now I have to wonder. He was in an automobile accident in which he received a serious whip lash and his neck did not get better. Then came the other symptoms. He also servered in Europe for the duration of WW11. Interesting that they don't autopsy people who die from ALS. The have never found a genetic marker either.
My sister was diagnosed with ALS about nine months after a really serious fall. I have learned that returning servicemen have twice the incidence of ALS as the general population - Congress now considers it a combat-related illness - so this trauma connection makes perfect sense. Perhaps, now that stem cell research is a viable option, we can make progress on this. Thanks for the info!
My father died of ALS 20 years ago. He had been diagnosed 8 months before he died. It's a horrible disease; not being able to move, swallow, or blink his eyelids. And although ALS doesn't create pain, all the results of the ALS did-bedsores, hunger, thirst, dry eyes, emotional and mental. He was claustrophobic and said it was like being in a casket with your eyes open. Panic most of the time.
Was the diagnosis wrong? I don't know. But that is why they call it "practicing medicine", no one, even doctors, can be 100% correct all the time. Did the doctor and health staff do everything they could to make my father as comfortable as he could be? Yes. Do Ihope that a cure will be found? Every minute of every day as I think of my three sons and their future.
It may no longer be ALS but it still seems to be 'Lou Gehrig's Disease.' And it should serve as a heads-up warning to parents whose children start contact sports at such an early age today--and that includes soccer which so many people think is benign compared to football.
Being a nurse and watching people die from this disease, I cannot fathom a doctor making this type of mistake. It is a disease that follows a fairly common progression. With that said, no matter what it was, let the poor man rest in peace. A great man passed away tragically. Let's leave it at that.
If we left everything at that, the practice of medicine would still be at the Stone Age level. Research into causes, manifestations and progression of diseases all contribute to the knowledge needed to find treatments and hopefully ways of preventing many of the devastating diseases man is vulnerable to.
My Mom was diagnosed with ALS over 50 years ago (after many many misdiagnoses since it was rare). I was 12 yrs old when she passed. It was seriously debilitating and terrible for her. Cindy - no one else in our family has come down with this disease and among our family we have 40+ year old children - no symptoms on any of us. My Mom was diagnosed at about 42 - passed away at 46-47 years old. Hope this helps allay some fears for you and your family Cindy2223407.
I was diagnosed 7 years ago, and I tell people everyday that I am "pass the expiration date" so don't make me mad!!!! Since the average life span is 3-5 years, but in some cases it is 30 or more years. I hope they are able to find some relief for everyone that suffers with this awful disease, as well as the family members who must suffer along.
Oh Abby, I am so sorry for your diagnosis, and hope you pass many more expiration dates!!! Be well and I know how much you and your family are suffering from this terrible disease. I am glad to see your comments about making you mad tho. I honestly feel that people who have this attitude, make it work for them.
Thanks, I go back to the Mayo Clinic tomorrow, and once again will be told that I am "past my expiration date' (lol) I have twin daughters that are seniors in high school this year. I just hope I am able to see them both graduate in June, and enroll in college. Ron is just an immature joke, that needs to take his energy and go something positive with it instead of trying to make people mad. I can at least say that today is a good day, and I hope nothing or no one changes my attitude today!!!!!!
My dad was diagnosed with ALS in 1975 and died mercifully within 14 months. He had been a career shipbuilder who performed heavy physical labor on a daily basis. Watching him waste away, not being able to lift a spoon, swallow, or speak was the most horrific thing that I have ever witnessed. But his mind was alert until the end. To all of you " a** hole posters" making those asinine remarks, I sincerely hope that neither you, nor any friend or family member, is ever diagnosed with ALS.
My sister-in-law died of ALS a couple of years ago, maybe a couple of years after a head injury.
My husband's grandmother's maiden name was Gerig (different spelling, but probably same ancestor), and that family was from the same area of France where ALS was first identified.
Should I be concerned about a possible genetic connection?
at your next physical ask the doctor to do a blood test. check for alpha 1 deficiency this lack of an important enzyme can cause nerve damage an paralysis if left untreated for decades. easy fix add protease enzyme to your body. they sell it in powder an capsules. If you have a lot of constipation beware that is a symptom. using a microwave to cook your food kills the enzyme natural in the food that is needed to properly metabolize the food. Russia banned microwave because it is very bad for the health. the united states should ban microwave ovens also. in my opinion it is the number 1 cause of cancer. it stops the food from providing nurishment to the body.
My father suffered for 3 years with ALS before he died. He wasn't in any physical pain but he was in mental torment. His body was reduced to that of a helpless baby while leaving his brain sharp as a tack. I wish ALS had also affected his brain so he wouldn't have been aware of just how bad his physical condition was. I also watched my mother die of cancer. Given the choice, I would rather suffer an extended, painful cancer death than suffer one day with ALS. I cannot believe the stupidity of some these posters. FORGIVE THEM LORD, FOR THEY NO NOT WHAT THEY ARE TALKING ABOUT.
PS. About 6 years before he was diagnosed with ALS he was in a bad car accident and had a severe head injury.
My grandmother had something like this disease. She gradually became paralyzed. She was a very active, rambunctious and energetic person before the disease. I am glad that she did not linger excessively.
I may someday get the disease, whatever it is, because I sustained a severe head concussion as a child. Knowing that you have something like this is a good recommendation for Dr. Kevorkians actions. I think people should have the right to voluntarily end their lives if they are not comfortable with what is left of their lives. Regardless of the inconvenience and loss of income for medical parasites and life insurance companies.
I agree with you. we have mercy to put dogs,cats an other animals to sleep. why so unmerciful to people? let the sick person decide when an how. as for me i have been paying for life insurance to leave something to my spouse so i will linger on till policy term ends or i do.
well,excuse me! There was no advance tests in 1939 and the medical field was just getting started.But as for ALS...two of my classmates died from it and it does exist.And the sight of it isnt pretty.She was in a closed coffin,so was he.They wasted away to nothing.To come out about this 60 years later shows that the American people want something else to talk about and I am getting tired of hearing about that oil spill and Tiger Woods.The world is changing and we must be aware of other events in the Middle East.It is very dangerous over there now and so far no reporter has had the guts to say so....who is next? Michael Jackson? Please let me read more stories that are important and stop worrying what happened 60 years ago especially when you were not there.
you missed the ENTIRE point of the story. Contact sports, military injuries, etc cause trauma that may lead to a disease that mimics ALS. Lou Gehrig was one of the first people to bring the disease to the publics attention. Now his fame may help bring the attention necessary to research not only ALS, but also this trauma based neurological disorder. It didn't happen 50 yrs ago, it happens everyday to a person and their family....I can't imagine how devastating it must be to a family....if you didn't like this story, go to another blog and comment there!
I totally agree deb, in this story they are basically saying that his death could have been caused by a trauma that mimics A.L.S. Lou Gehrig is the one that the disease was named, they are just letting the public know that his death could have been caused by something other then A.L.S. My grandmother died from A.L.S in 1971, it is very rare for women to get this disease. The more research for A.L.S and trauma neurological disorders or any disease should be researched, the medical field and technology has come so far since then, granted there hasn't been a cure found for A.L.S but the difference between the two diagnoses can be determined with more research.
yeah well first thing you have to do is figure out what it is that you're trying to cure. Much like cancer, HIV, etc., that's not a trivial question. The article is basically hinting that they may not know what ALS really is. When one is trying to find a cure, knowing the cause is a big plus. Maybe they'll rename the S to syndrome rather than sclerosis.
It is an unfortunate condition. Whether Lou had the disease or not means little or nothing at this time. I am sure in some way he is thankful that his memory lives on and that he might have contributed to advancing the research via the use of his name.........The "Iron Man" of Baseball still lives on to this day.......
Glad you finally got that out of the way,Now maybe you can work on curing cancer.
Ron, U are an idiot! I have a good friend with cancer, but as another has said there are many other issues that need research as well. And you might be surprised to find out they have been working on cancer for quite a while now! If you are so damn smart I would think you already have cancer cured yourself.
The most surprising part of that statement is that you have a good friend.
Maybe if you suffered from this disease or knew someone who did, you wouldn't write things so stupid. Why don't you do something creative like look up this disease on the internet instead of trying to be a "smart ass"!!!!!!!!!!!!!!
Please read my response to you!
When I read this article I was afraid that some people would interpret it saying that Lou Gehrig's disease does not exist, but then I assured myself people wouldn't be so heartless and stupid.
Thanks, Ron, for ruining my (tentative) faith in humanity. My father died of ALS and it was every bit as tortuous for him and our family as dying of cancer, which HIS father died of. Perhaps more so, because there is no known behavioral cause for ALS, and no treatments either--and there are for cancer.
Hey Ron - My mother died from ALS, it was not a pretty sight! You can't control you body at all, you can't walk, you can't talk, you can't swallow food or water, you have to be fed using a tube placed into your stomack, but the good news is that you mind is still there as good as ever. You can honestly see your self die!!! So, Ron, you are a complete and total idiot! It would be completely reasonable for someone like me that had lived throught this problem like I did with my mother to actually hope that you or one of your closest family member would come down with this disease just so we could see how your slow mind might change!!!!
You people are complete lunatics, I never said Lou Gehrig's disease was not a bad disease.
You make stuff up in your mind and then you buy into it,What a joke.
No Ron, you just forgot to turn your A$$ off before you turned your mouth on!!!!
"Ron, you are a complete and total idiot! It would be completely reasonable for someone like me that had lived throught this problem like I did with my mother to actually hope that you or one of your closest family member would come down with this disease just so we could see how your slow mind might change!!!!"
Sorry about your mom.
good luck with your life.
Ron:
The remarks made by you are insane. Flippant, and no knowledge of Neurological Diseases. How about Parkinson's Disease, Multiple Sclerosis, Lou Gehrig's Disease, and other severe Neurological/ possibly inherited genetic diseases. Not all are afflicted with them by genetic makeup.
You one day, may get one of these. It is highly likely--most are genetic. I've know people with all these terrible, crippling diseases. They have died, some are still alive. There is no dignity to any of these diseases.
It is torturous to watch someone who is fully healthy one day, just crumble slowly or fast in front of your eyes.
You are one insensitive, immature, little wimp, who shows everyone on this board how really stupid you are.
sosaddened and OnTheRoad-1943197, 1 isn't a great comment. It's a bit of a derail and you apparently read it as trolling.
So don't respond to it. If you're going to, don't break the first rule on the site:
Tyler:
Anger comes easily when reading insensitive and noneducated remarks. Mine also, bottom paragraph. Sometimes, ire is an instant response. My apologies.
Please read rons comment carefully he said it was a waste after 71 years to try to figure out why a sports figure died when the money and time could be spent curing a disease. He did not say ALS wasn't a bad disease he said why do they waste time trying to figure out why a guy died 71 years ago. So lighten up.
They are all bad diseases and there will be no cure for most in my lifetime so all you can do is pray you are afflicted by none of them.
bklynj:
I don't know why you would defend Ron's later remarks to others. They are rude, and insensitive. "Treat others with kindness, and it will come back to you".
Ron
Your taking an unjustified hit here.
Myself and Bklynj understood what you were trying to say.
Coot19:
The second comment is what upped the ire from Ron. It was needless and cruel. #1.2.
Hawaii2
Agreed! I missed it.
While there are folks known as "cancer suvivors" there are no "ALS survisors." There are theories on the cause of ALS and one not mentioned publicly as a commonality to those who served in the military is the vaccines. I lost my 80-year old dad last year to ALS only 8 months after diagnosis. In the military yes, but not combat. One theory is due to the multitide of vaccinations & boosterss given our service folk, many contained a preservative that's derived from Mercury. A huge percentage of today's ALS patients are Gulf War vets. It's not a disease--it's a confirmed death sentence. MDA shares funding of research for this other diseases. On a final note, it is unfortunate tdon'that for most of us--including me-don't pay much attention to such diseases until it hits someone we know.
Lacy:
This disease, ALS, is just not reserved for men who have served in the Military (vaccines). We just had a woman friend die of ALS very quickly. It was astonishing how fast it ran it's course. Am sure you know it happens to both genders. Thanks.
bklynj, it may be that you and the ever-popular Ron, misread the article. Although the title of the article would lead one to that conclusion, the underlying point of the study and the article was not really that "Lou Gehrig may not really have had ALS". The study itself did not even mention Lou Gehrig as the article points out. The point of the study is that many of those diagnosed with ALS may not actually have it and may benifit from a different treatment than that which would normally be used for ALS. That certainly is valid research. The article does talk about the irony that Lou Gehrig may not have had the disease that bears his name but, again, it really isn't the case that the scientists in the study blew money on answering that particular question.
This could explain why so many football players are diagnosed with ALS. I thought maybe it was something in the grass, fertilizer or something from all the time spent eating dirt. I knew a football player, a genuine genius, Academic all American, very hard driving who was diagnosed with the disease. He paid me once to babysit a track meet for him, one of the things he had to do I guess to earn his scholarship. I can still remember seeing my high school track coach down on the field laughing when I was supposed to announce "Class M and S Hurdlers please report" and the M bounced back to me from the speaker system when I was about to say "S" and said "Class M&M" instead.
ludvig I think your first thought is more on target than the brain trauma . The fertilizer should be investigated and studied more than the brain trauma. The fertilizer is all kinds of potassium fertilizers used for lawn care. People with ALS should check there past for any contact with this fertilizer in my opinion.
amazing it has been known for centuries that an injury to the brain or spinal cord can cause nerve damage an slow death. i fail to see anything new from this article? He did have lou gehrigs disease it was named for him. If he had als is another question. His brain was injured the nerves were damaged he died. My head was damaged,my brain was damaged, my neck an nerves were damaged, i am slowly dying. I am waiting for the cure? How do they reverse the nerve damage? the physicians ignored the broken skull with brain matter protruding, ignored the subluxated neck bones compressing the esophagus causing a restrictive airway. I wonder how many organ failures are caused from neglected nerve damage? Cristopher reeves could have used some help. From what i have read preventing the injury is the only thing available. once you have the injury forget getting medical help. with five minutes allocated to you from the doctors you will run out of breath prior to saying what you are experiencing. If i had not put on my hard hat i would have been instantly dead. Instead i have suffered for decades.maybe amino acids can repair some nerve damage?
Scientists have been looking at the fertilizers for at least 30 years. As a biologist and anatomy and physiology instructor that they may be on to something with the brain trauma. We are learning that it is extremely devistating to the nervous system especially with repeated trauma.
Ron - the world of medical research does not orbit around cancer.
Traci - Your brain orbits around Uranus.
Ouch, another zinger from the Ron-man...
Hey Ron G F Y
I will when i am done with your mom.
"Ron - the world of medical research does not orbit around cancer"
I never said it did!
The world of medical research does not revolve around what Lou Gehrig died from either.
ron-1902603, you're suspended for a day for violating #1 of the Code of Honor.
"Lou Gehrig may not have had Lou Gehrig's disease"
wow
The medical information behind this revelation is explained quite well even a layman like me nods in agreement.
Which brings me to the other puzzlement tickling my brain.
Was Lou Gehrig's disease ever really Lou Gehrig's?
The disease that used to be formally known as Lou Gehrig's disease.
Never really was Lou Gehrig's disease.
But something else. A disease that needs a new name.
Lou Gehrig didn't bring this disease into this world upon his birth, or spawn it in during his life.
Just like a cold or flu isn't your's or mine it just is.
Never claim it.
Now, now children - play nice.
So funny that the Times is just reporting this. About 10 years ago, my physician told me he learned this in med school. My father suffered from this horrible disease 25 years ago and virtually no progress has been made since. I truly believe if they can crack this case, it will lead to so many other discoveries. I think Gehrig will always with it be associated no matter what.
My father died in the mid 70's of what was diagnosed as ALS but now I have to wonder. He was in an automobile accident in which he received a serious whip lash and his neck did not get better. Then came the other symptoms. He also servered in Europe for the duration of WW11. Interesting that they don't autopsy people who die from ALS. The have never found a genetic marker either.
Meant served. sorry
My sister was diagnosed with ALS about nine months after a really serious fall. I have learned that returning servicemen have twice the incidence of ALS as the general population - Congress now considers it a combat-related illness - so this trauma connection makes perfect sense. Perhaps, now that stem cell research is a viable option, we can make progress on this. Thanks for the info!
Does this mean Big Lou was a fraud?!?
It means his doctor was a quack.
It means that medicine has made some advance since 1939.
My father died of ALS 20 years ago. He had been diagnosed 8 months before he died. It's a horrible disease; not being able to move, swallow, or blink his eyelids. And although ALS doesn't create pain, all the results of the ALS did-bedsores, hunger, thirst, dry eyes, emotional and mental. He was claustrophobic and said it was like being in a casket with your eyes open. Panic most of the time.
Was the diagnosis wrong? I don't know. But that is why they call it "practicing medicine", no one, even doctors, can be 100% correct all the time. Did the doctor and health staff do everything they could to make my father as comfortable as he could be? Yes. Do Ihope that a cure will be found? Every minute of every day as I think of my three sons and their future.
It may no longer be ALS but it still seems to be 'Lou Gehrig's Disease.' And it should serve as a heads-up warning to parents whose children start contact sports at such an early age today--and that includes soccer which so many people think is benign compared to football.
Being a nurse and watching people die from this disease, I cannot fathom a doctor making this type of mistake. It is a disease that follows a fairly common progression. With that said, no matter what it was, let the poor man rest in peace. A great man passed away tragically. Let's leave it at that.
If we left everything at that, the practice of medicine would still be at the Stone Age level. Research into causes, manifestations and progression of diseases all contribute to the knowledge needed to find treatments and hopefully ways of preventing many of the devastating diseases man is vulnerable to.
My Mom was diagnosed with ALS over 50 years ago (after many many misdiagnoses since it was rare). I was 12 yrs old when she passed. It was seriously debilitating and terrible for her. Cindy - no one else in our family has come down with this disease and among our family we have 40+ year old children - no symptoms on any of us. My Mom was diagnosed at about 42 - passed away at 46-47 years old. Hope this helps allay some fears for you and your family Cindy2223407.
I was diagnosed 7 years ago, and I tell people everyday that I am "pass the expiration date" so don't make me mad!!!! Since the average life span is 3-5 years, but in some cases it is 30 or more years. I hope they are able to find some relief for everyone that suffers with this awful disease, as well as the family members who must suffer along.
Oh Abby, I am so sorry for your diagnosis, and hope you pass many more expiration dates!!! Be well and I know how much you and your family are suffering from this terrible disease. I am glad to see your comments about making you mad tho. I honestly feel that people who have this attitude, make it work for them.
Thanks, I go back to the Mayo Clinic tomorrow, and once again will be told that I am "past my expiration date' (lol) I have twin daughters that are seniors in high school this year. I just hope I am able to see them both graduate in June, and enroll in college. Ron is just an immature joke, that needs to take his energy and go something positive with it instead of trying to make people mad. I can at least say that today is a good day, and I hope nothing or no one changes my attitude today!!!!!!
How sad Lou Gehrig died of someone elses disease
My dad was diagnosed with ALS in 1975 and died mercifully within 14 months. He had been a career shipbuilder who performed heavy physical labor on a daily basis. Watching him waste away, not being able to lift a spoon, swallow, or speak was the most horrific thing that I have ever witnessed. But his mind was alert until the end. To all of you " a** hole posters" making those asinine remarks, I sincerely hope that neither you, nor any friend or family member, is ever diagnosed with ALS.
can we remember this is a terrible disease,that takes many good people,rip marlin.
The headline could have read,
Lou Gehrig may have had Lou Gehrig's disease
My comment was valid on post #1
My sister-in-law died of ALS a couple of years ago, maybe a couple of years after a head injury.
My husband's grandmother's maiden name was Gerig (different spelling, but probably same ancestor), and that family was from the same area of France where ALS was first identified.
Should I be concerned about a possible genetic connection?
at your next physical ask the doctor to do a blood test. check for alpha 1 deficiency this lack of an important enzyme can cause nerve damage an paralysis if left untreated for decades. easy fix add protease enzyme to your body. they sell it in powder an capsules. If you have a lot of constipation beware that is a symptom. using a microwave to cook your food kills the enzyme natural in the food that is needed to properly metabolize the food. Russia banned microwave because it is very bad for the health. the united states should ban microwave ovens also. in my opinion it is the number 1 cause of cancer. it stops the food from providing nurishment to the body.
My father suffered for 3 years with ALS before he died. He wasn't in any physical pain but he was in mental torment. His body was reduced to that of a helpless baby while leaving his brain sharp as a tack. I wish ALS had also affected his brain so he wouldn't have been aware of just how bad his physical condition was. I also watched my mother die of cancer. Given the choice, I would rather suffer an extended, painful cancer death than suffer one day with ALS. I cannot believe the stupidity of some these posters. FORGIVE THEM LORD, FOR THEY NO NOT WHAT THEY ARE TALKING ABOUT.
PS. About 6 years before he was diagnosed with ALS he was in a bad car accident and had a severe head injury.
"I would rather suffer an extended, painful cancer death than suffer one day with ALS."
I hope you never suffer with any disease.
Thank you, Ron. My grandfather always told me that I was supposed to overlook people like you because they haven't had a proper upbringing.
Your welcome, Tricky. I was told the same about people like you.
My grandmother had something like this disease. She gradually became paralyzed. She was a very active, rambunctious and energetic person before the disease. I am glad that she did not linger excessively.
I may someday get the disease, whatever it is, because I sustained a severe head concussion as a child. Knowing that you have something like this is a good recommendation for Dr. Kevorkians actions. I think people should have the right to voluntarily end their lives if they are not comfortable with what is left of their lives. Regardless of the inconvenience and loss of income for medical parasites and life insurance companies.
I agree with you. we have mercy to put dogs,cats an other animals to sleep. why so unmerciful to people? let the sick person decide when an how. as for me i have been paying for life insurance to leave something to my spouse so i will linger on till policy term ends or i do.
well,excuse me! There was no advance tests in 1939 and the medical field was just getting started.But as for ALS...two of my classmates died from it and it does exist.And the sight of it isnt pretty.She was in a closed coffin,so was he.They wasted away to nothing.To come out about this 60 years later shows that the American people want something else to talk about and I am getting tired of hearing about that oil spill and Tiger Woods.The world is changing and we must be aware of other events in the Middle East.It is very dangerous over there now and so far no reporter has had the guts to say so....who is next? Michael Jackson? Please let me read more stories that are important and stop worrying what happened 60 years ago especially when you were not there.
you missed the ENTIRE point of the story. Contact sports, military injuries, etc cause trauma that may lead to a disease that mimics ALS. Lou Gehrig was one of the first people to bring the disease to the publics attention. Now his fame may help bring the attention necessary to research not only ALS, but also this trauma based neurological disorder. It didn't happen 50 yrs ago, it happens everyday to a person and their family....I can't imagine how devastating it must be to a family....if you didn't like this story, go to another blog and comment there!
I totally agree deb, in this story they are basically saying that his death could have been caused by a trauma that mimics A.L.S. Lou Gehrig is the one that the disease was named, they are just letting the public know that his death could have been caused by something other then A.L.S. My grandmother died from A.L.S in 1971, it is very rare for women to get this disease. The more research for A.L.S and trauma neurological disorders or any disease should be researched, the medical field and technology has come so far since then, granted there hasn't been a cure found for A.L.S but the difference between the two diagnoses can be determined with more research.
There is no cure for ALS.So why cant they work on one?
That is where the research comes in.
yeah well first thing you have to do is figure out what it is that you're trying to cure. Much like cancer, HIV, etc., that's not a trivial question. The article is basically hinting that they may not know what ALS really is. When one is trying to find a cure, knowing the cause is a big plus. Maybe they'll rename the S to syndrome rather than sclerosis.
It is an unfortunate condition. Whether Lou had the disease or not means little or nothing at this time. I am sure in some way he is thankful that his memory lives on and that he might have contributed to advancing the research via the use of his name.........The "Iron Man" of Baseball still lives on to this day.......