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Grand Wizard
Picture of MaxJerz
Posted
There was a column in the New York Times about chronic pain sufferers and their caregivers. Hopefully this link will work: Chronic Pain: A Burden Often Shared

I know parts of this rang true for me, especially about the guilt and lashing out.

Found this on The Daily Headache, a blog written by a woman in Seattle who suffers from migraines and chronic daily headache. Her blog entry linking to the NYT article.


-MJ

my blog: http://rhymeswithmigraine.blogspot.com/

“HOPE CAN GROW FROM THE SOIL OF ILLNESS!”
This is the theme of 2008’s National Invisible Chronic Illness Awareness Week in September. Drop by and find out ways to encourage a friend, be encouraged yourself, and spread the word.
http://www.InvisibleIllness.com

"What will you do, if it does not turn out how you expect?"
"I do not know. Nor shall I worry about it until it happens. I still have an action left to take; until I have exhausted it, I shall not despair." - Robin Hobb, Assassin's Quest



 
Posts: 2121 | Location: western WA | Registered: 06-01-2007Reply With QuoteEdit or Delete MessageReport This Post
Community Manager
Guru
Picture of Nancy Bonk
Posted Hide Post
Hi MJ,

This is exactly the information and education we talk about on this forum everyday. Is it better coming from the NY Times???
 
Posts: 2596 | Location: New York | Registered: 01-11-2007Reply With QuoteEdit or Delete MessageReport This Post
Forum Moderator
Wizard
Picture of JamieHOST
Posted Hide Post
quote:
Originally posted by Nancy Bonk:
Hi MJ,

This is exactly the information and education we talk about on this forum everyday. Is it better coming from the NY Times???


I agree, Nancy, that we talk about it every day. But, imho, every person that is touched by this article; that reads this article and sees themself and isn't here yet, for them, it might just have been the article that they needed just to know that they weren't alone. Hey, whatever works to give more people a fighting chance, I think, as long as the facts are correct, mind you, is wonderful.

Perhaps it also could help a non pain sufferer identify more with what we go through. One step at a time, but, having greater numbers of allies can be a big step. It's worked before in other movements...

Ok, so, I'm talking w/o reading the article. Perhaps I should have done that first. But honestly, I'm in a lot of pain right now, and reading is not something that's coming easy to this muddled brain.

If the NYT article said something absolutely stupid, please disregard my plug for the coverage. (eek)


Jamie
Forum Moderator



 
Posts: 1780 | Location: north carolina | Registered: 01-12-2007Reply With QuoteEdit or Delete MessageReport This Post
Grand Wizard
Picture of MaxJerz
Posted Hide Post
Nancy, you are absolutely right that this information isn't anything new, that we talk about it on here all the time. My main point in posting it was because it's nice to see some write-ups about it in a large publication. Sort of like that migraine column that one of their writers did a few months ago.

I apologize if my intention was misinterpreted. Jamie put it well, that there are a lot of migraineurs and chronic pain sufferers, as well as their caretakers, out there that haven't found a support network like what we have now. I know I am very thankful both for this forum and for my boyfriend, who shares a lot of the burden of this disease.


-MJ

my blog: http://rhymeswithmigraine.blogspot.com/

“HOPE CAN GROW FROM THE SOIL OF ILLNESS!”
This is the theme of 2008’s National Invisible Chronic Illness Awareness Week in September. Drop by and find out ways to encourage a friend, be encouraged yourself, and spread the word.
http://www.InvisibleIllness.com

"What will you do, if it does not turn out how you expect?"
"I do not know. Nor shall I worry about it until it happens. I still have an action left to take; until I have exhausted it, I shall not despair." - Robin Hobb, Assassin's Quest



 
Posts: 2121 | Location: western WA | Registered: 06-01-2007Reply With QuoteEdit or Delete MessageReport This Post
Community Manager
Guru
Picture of Nancy Bonk
Posted Hide Post
MJ, I owe you an apology. My comment was a bit "snarky" and I'm sorry Flower.

The NYTimes article was a good one, and Jamie is right, if it brings more attention to people in pain and their caregivers all the better.
 
Posts: 2596 | Location: New York | Registered: 01-11-2007Reply With QuoteEdit or Delete MessageReport This Post
Master
Posted Hide Post
MJ,
Thanks for sharing the article. I agree with what Jamie said. I just can't articulate exactly that at this migraine moment. Skillet


Sherry



"Be kind, for everyone you meet is fighting a hard battle." ~ Plato c. 427-347B.C.
 
Posts: 305 | Location: GA | Registered: 01-18-2007Reply With QuoteEdit or Delete MessageReport This Post
Grand Wizard
Picture of MaxJerz
Posted Hide Post
quote:
Originally posted by Nancy Bonk:
MJ, I owe you an apology. My comment was a bit "snarky" and I'm sorry Flower.

The NYTimes article was a good one, and Jamie is right, if it brings more attention to people in pain and their caregivers all the better.


No hard feelings, Nancy! Smiler


-MJ

my blog: http://rhymeswithmigraine.blogspot.com/

“HOPE CAN GROW FROM THE SOIL OF ILLNESS!”
This is the theme of 2008’s National Invisible Chronic Illness Awareness Week in September. Drop by and find out ways to encourage a friend, be encouraged yourself, and spread the word.
http://www.InvisibleIllness.com

"What will you do, if it does not turn out how you expect?"
"I do not know. Nor shall I worry about it until it happens. I still have an action left to take; until I have exhausted it, I shall not despair." - Robin Hobb, Assassin's Quest



 
Posts: 2121 | Location: western WA | Registered: 06-01-2007Reply With QuoteEdit or Delete MessageReport This Post
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    Migraine Community  Hop To Forum Categories  MyMigraineConnection  Hop To Forums  4 Partners, Families, Friends    chronic pain article in the NY Times

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