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Posts posted by gerbil runner
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Ah, yes, makes sense. The only problem is, how can you see a clear ribbon? Chalk up another one for being the "invisible" cancer .
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That reminds me - does LC have an "official" color of ribbon?
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I did a quick web search for foundations that support LC research specifically, and this one looked pretty good.
http://www.lungcanceronline.org/foundation/mission.html
How about we compile a list of such organizations so we know how to get fundraising/memorial money to where it can actually help.
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Becky, the tapeworm analogy had me lol! Probably not the reaction we want, though .
One I discarded for much the same problem was "If smokers deserve lung cancer, a$$holes deserve hemorrhoids" or "If smokers deserve lung cancer, drivers deserve head-on collisions".
I always have to be on guard against foot-in-mouth disease .
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It's beautiful. So many of us want one...could it go in the online store as a t-shirt?
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Let's dream up some good slogans for Rick and Katie to use in the store, or for anyone else to use in their awareness-raising issues.
Here's one: "LUNG CANCER - NOT JUST FOR SMOKERS ANYMORE"
How about a chemo-friendly cap saying "Lung cancer sucks" (my 12-year-old son suggested this for my mom's hair loss)
"Tobacco tax for lung cancer, not politicians pay" (Could use "settlements").
"Lung cancer is cruel and unusual punishment"
"Nobody throws away lottery tickets before the drawing. Don't give up on lung cancer."
Anyone else?
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TAnn, glad you're out!
My mom spent Christmas in the hospital for much the same reasons. Bummer. And now she says, "The good news is, I'm in remission. The bad news is, I'm sleeping through it".
I agree - there's gotta be a better way!
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My mom had another interesting appt. with her oncologist. He wants to send her to Dana-Farber to see if she is a candidate for autologous (self-donated) stem-cell transplant. Her onc had consulted with a buddy now in Colorado whom he had practiced with for years. His opinion was to go for it. Mom would get at least 2 opinions before proceding.
Basically, the patient has stem-cells harvested and then endures a really tough, short course of chemo which wipes out the bone marrow. The previously-harvested stem cells are then replaced in the body. It takes about 3 weeks for the body to recover to "normal" disease-resistance.
Mom wants to do it if they'll take her - it's about the only course of treatment that has a real possibility of cure, according to the onc.
My brief research on the web (will do more) seems to indicate she would be part of a clinical trial.
Has anyone had this procedure? Looked into it? Known anyone who did it? Found any good information?
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Norme - I'm glad to see you posting. ((((((((HUGS)))))))))
I think Buddy was right. You are stronger than you know. I'm sure he's watching you.
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My dh had his birthday today - he's hit the speed limit! 55!
He's celebrating by snoring on the couch right now.
Becky - we're a May-December pair, too. Just about 20 years apart.
When we first met, one of Bob's friends commented "She's gonna kill you!" Another replied "What a way to go!"
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Zippy Apple-hiney reporting as ordered!
Dean - good to see ya!
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My favorite commentary is, notice how we castrate our male pets so they're possible to live with?
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I like it!
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Angie, prayers going out that Caitlin has nothing of interest going on in her eye. Hang in there.
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OhioKat, good to see you back!
Sorry to hear you're feeling "under the weather". What an appropriate saying - late winter weighs heavily on most of us!
Be good to yourself. You had major surgery not too long ago. And chemo can certainly be exhausting. My mom says "The good news is, I'm in remission. The bad news is, I'm sleeping through it."
Just think how much those nasty little c-cells are suffering through this .
Hope you feel some sunshine soon.
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DaveG:
My typical response to such comments is "Snip, snip" (think Lorena Bobbit).
My husband sometimes accuses me of male-bashing. Then I remind him that my ex is still walking the face of the earth, so I must be pretty forgiving at heart.
BTW - the legal summary of the Bobbit trials is: it's ok to rape your wife, but don't come crying to us if she cuts it off afterwards.
I'm the only female creature in this house, unless you count the 2 guinea pigs. Husband, 3 sons, 2 male cats and one male dog. So I gotta stick up for the females!
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Berisa, prayers going out for your father - and for you, too.
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Mmmmm, yummy!
Remember the chocolate patch? The directions said some people have so much chocolate in the bloodstream that it would be impossible for the transdermal patch to work properly. If the patch begins to melt, it must be consumed orally as soon as possible .
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C'mon, guys!
I like my dogs big (Mikey is 62 lbs. My last dog, Samantha the rottie, was 100 lbs.) I like my cats big - the smallest one I ever had was 12 lbs. when not fat. I love horses and ponies - someday I'll get one of my own.
We also have 2 guinea pigs which live in Danny's room (he's almost 4). Nice kids pets, low-maintenance lap-buddies.
I've also had gerbils and hamsters. Almost got a pet skunk as a kid.
I must admit, I envy the owners of small dogs who get to take them shopping in a bag.
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Holly, I'm sorry to hear Bill is struggling right now. Prayers going your way that he will be able to receive more treatment.
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Larissa, welcome (though we all wish you didn't have to meet us).
Set the statistics aside. My mom pushed her radiologist for some stats, and the ones he gave her ended up being compiled from the '70s and '80s!
Take it one step at a time. The first thing to do is get your mom into remission.
I know how you feel about distance. My mom is only 40 miles away, but because I have 3 sons (12, almost 4 and almost 2), it can be very hard for me to visit. The worst part is when my kids get colds, because I don't dare expose her to the germs. I do call every day to check in.
Don't let statistics - or even setbacks - scare you. Every patient is an individual. My mom spent 4 days on a ventilator before her diagnosis because her first bronchoscopy made her bleed. But now, she's had such a dramatic response to chemo that her onc is giving her radiation just like a limited case would be.
Take a deep breath and fasten your seat belt. LC can be a wild ride, but there are long-term survivors. Helping your mom take the best care of herself that she can will go a long way.
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MO, big prayers it ends up a "little" problem.
Nice to see your dr. is taking absolutely no chances, though.
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I looked up the pamphlet on ethyol at http://www.medimmune.com/products/htmlp ... tml#dosage and administration
It seems there is concern that it may lessen the effectiveness of the chemo. Although it is not stated as such, it lools like it's only approved where the chemo and radiation are primarily palliative.
Organizations for LC research funding
in ADVOCACY
Posted
That's the idea - post the organizations which fund LC treatment and research! Lots of people come here for info., so if we have a thread they can refer to quickly, it could really help!