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From Merek007:  I'm Always Here With You From Merek007:  I'm Always Here With You

03-19-2010 , 04:07 AM
Quote:
Originally Posted by daveT
Is this strictly a white blod cell problem (which white blood cell?), or is it related to osteo-blasts/clasts/cytes as well?
strictly related to Plasma Cells. bone damage results from osteoclasts being overactivated by the plasma cells.
From Merek007:  I'm Always Here With You Quote
03-19-2010 , 11:35 AM
Quote:
Originally Posted by Fishwhenican
While this sucks, Merek, I am glad that you have such a good attitude and feel a little bit honored that you would share something like this with all of us in the Lounge.

I think this will be a fascinating story to follow (with hopefully a good outcome) and I am sure there will be plenty of folks here who will follow and will care about how you are doing. I know I will.

Hang in there and keep up the good attitude. I do believe that a persons mental outlook can effect how they do with recovery from things like this and it sure looks like you have that part whipped.
Quote:
Originally Posted by BustoRhymes
Think it would be over the line to let Jewel Staite know you have cancer and your dying wish is to see her eat a strawberry in person?
This to both. I could have picked any number of other posters, but I think Fish wrote closest to what I would have done, but with less grammatical errors. As for Busto, it's great example of keeping a good attitude about things and get some other good things out of the situation.
From Merek007:  I'm Always Here With You Quote
03-19-2010 , 12:51 PM
Quote:
Originally Posted by Merek007

The old way was, find a bone marrow match(which was hard), suck their marrow with 2 ft long needles in a very painful way, inject marrow into donor and add rejection drugs by the bucket.... pray it works.

With this cancer. They give you drugs to make your stem cells leave the marrow and go to the blood. Then they filter your blood for 2-4 hrs a day for a week or so. Need to collect 9 million or so.
This is really interesting, Merek. I didn't realize that donor marrow was not used as much any more. I thought that all marrow transplants were from donors! That's really cool that you can harvest your own stem cells.

What kind of drug are they giving you to make your stem cells leave the marrow?


Quote:

They usually collect enough for two or three treatments just in case you learn to like it.
You are funny.

Quote:
The nasty bit is between the chemo and when the re-added stem cells graft. They take a couple of week to wander around and find a bone that meets their high accomadation standards. Until then you produce no blood cells of any kind.
So remind me how this works. These are blood stem cells that eventually hook up with a bone that they like and then they start producing blood? How do the blood stem cells get back into the bone? Or maybe they don't need to get back in the bone? I'm confused Sorry to ask such dumb questions . I just don't understand stem cells very well.

So for a couple of weeks you will be anemic and feeling run down?

How far away is the cancer center from where you live?
From Merek007:  I'm Always Here With You Quote
03-19-2010 , 03:04 PM
Quote:
Originally Posted by kudzudemon
merek-
My mom was diagnosed with multiple myeloma in 2002.She is about to celebrate her 73rd birthday, and was declared cancer-free in 2005. She had the stem-cell transplant/treatment you described.

She is a very spiritual woman, and you can take from that what you will. You may or may not be. Spiritual, I mean. Not a woman. Unless, you know, you want to be one. That will require further surgery. And I'll support you then, too. But that does not matter right now. What is of utmost ****ing importance (if I may quote Christopher Walken from "True Romance") is to maintain the positive mindset you have shown here, and keep in mind that the things they can do for you now, that they would not have been able to do even a decade ago, are nothing short of astounding, and you are going to be given the weapons to kick this thing squarely in balls, and leave it shriveled and groveling while you go on, eventually dying from a gunshot wound, killed at the age of 134 by a jealous husband.

Seriously, the survival rates from multiple myeloma have climbed due to this process. When my mom was diagnosed, I did some research, and it was somewhat less than heartening. But the strides that have been made are ridiculously encouraging.

You are going to be fine. Consider prayers and good vibes sent.
Thanks Kudz - the support has been great.
Hope your mom spends the next 40 years breaking hearts and kicking your ass when required.
---
Survival Rates - Cancer survival rates are always a bit of a statistical bull**** story as we are not all the same and the tech is ever changing.

When I first came back from getting the cancer word, I looked up Multilple Myeloma on the internet.......and had to sit down. The end of the first paragraph in Wikipidia said "50-55 months" fffffffff

BUT - First you learn many people diagnosed...don't get treatment. Myeloma usually shows up around 65 plus and saddly, many elderly are not healthy enough to take the treatments which are chemo and nasty drugs. If you can't take the treatment.....1-3 years.

But like Kudz said, I am lucky.
1990 - 3 year survival rate is 10%
2006 - 3 year survival rate is 90%.

Being slow, lazy and procrastinating about things saves me again. Yeah Ha.
From Merek007:  I'm Always Here With You Quote
03-19-2010 , 03:58 PM
I'll join in wishing the OP the best of luck.

By the way, this reminds me of the part of American Splendor, recounting Harvey Pekar's struggle with cancer, which he made into a graphic novel Our Cancer Year.

I wonder if it would be comforting to read that book?
From Merek007:  I'm Always Here With You Quote
03-19-2010 , 04:48 PM
Quote:
Originally Posted by katyseagull
This is really interesting, Merek. I didn't realize that donor marrow was not used as much any more. I thought that all marrow transplants were from donors! That's really cool that you can harvest your own stem cells.

What kind of drug are they giving you to make your stem cells leave the marrow?

So remind me how this works. These are blood stem cells that eventually hook up with a bone that they like and then they start producing blood? How do the blood stem cells get back into the bone? Or maybe they don't need to get back in the bone? I'm confused Sorry to ask such dumb questions . I just don't understand stem cells very well.
Stem Cells - are very cool. They live in the bone marrow and can become any kind of blood cell. As my Plasma Cells are now causing more trouble than Hobby and Dom at a wiffle-bat convention...they have to go. It seems a bit over the top, but the only way to deal with the trouble makers is poison everyone in the family. BUT if we save some of the Magical stem cells(which are not blood cells yet) they can eventually be put back and replace all the blood cells. Hopefully with fewwer "super breeding plasma cells".

So to actually answer Katys' question... By using a medication called a Granulocyte-Colony Stimulating Factor (G-CSF) (e.g. Neupogen®) the bone marrow is stimulated to increase the number of stem cells in the blood. A process called pheresis is then used to collect the stem cells from the blood. Pheresis is a fancy way of saying "everyday for a week we strap the paitent to a table for 2-5 hours, stick a large needle in his arm, suck his blood, filter out the tasty bits(stem cells) and put the rest back. When they have enough....they put them in the freezer... I think they treat them too, but not sure on that. Apparently stem cells keep better in the freezer than leftovers. They do collect enough for several transplants as often people need another, years later, and the Chemo makes a second collection difficult or immpossible(not sure on this)

I believe the same drug is used to make the Stem Cells collect in the bones and start working. The Colony Stimulating stuff.

Bone Marrow Transplants from youself vs others- two big issues seem to be "graft vs Host" and "effectiveness"
With your own stem cells there may be a slightly higher rate of "reinfection" but very low rate of rejection(Graft vs Host)

With other peoples stem cells....mortality rates go way up on transplants and so do complications. Your body will reject the cells as not your own and attack.

For reasons I have not be able to find, a few people can't use their stem cells.... hopefully not me. I think I have already had 5 people ofter bone marrow, even though they think it involves large needles, health risks and hosptiall stays.... I have good friends. What i really need is friends to drink Sangria with in Spain, Wine in Italy, Ozuo in Greece and margaritas anywhere...... but that is next year.



While I am trying to become a expert....expect errors

Quote:
Originally Posted by katyseagull
So for a couple of weeks you will be anemic and feeling run down?.
I wish.

Quote:
Originally Posted by katyseagull
How far away is the cancer center from where you live?
While I only live a 100 miles from Vancouver, it takes 4-6hrs due to big inlets surronded by high mountains The trip is drive 20 minutes, take a ferry for 50 minutes past waterfalls, mountains, whales and forest covered islands, drive for a hr+ on a narrow twisting road 2 lane road, another ferrry for 40 minuties and then 30-50 minutes to the hospital depending on traffic. With waiting, 4 1/2 hours on a good day, 6 hrs on a bad one. Or a 25 minute flight.
From Merek007:  I'm Always Here With You Quote
03-19-2010 , 05:26 PM
Quote:
Originally Posted by Merek007
At least between the Canadian Med system and my extra work insurance money is not a issue. Work insurnace is basicly paying 66% of wages tax free and the drugs. Med system pays for hospital and docs. So far it has cost me $20 in gas and a few stamps for insurance claims.
Jeez this is nice. In America, your diagnosis could result in financial ruin quite easily.
From Merek007:  I'm Always Here With You Quote
03-19-2010 , 06:18 PM
Quote:
Originally Posted by Blarg
Jeez this is nice. In America, your diagnosis could result in financial ruin quite easily.

I have read a few blogs/stories of people in the US. Some have been treated well by their insurance but one one guy had a 2nd bone marrow transplant turned down as "it didn't work the first time", but this is common with Multiple Myeloma.... The "failure of treatment" was he only got 6 years of healthy living before it came back?? wtf They did pay for another treatment, just refused the transplant.

Up here without the private work insurance I could still have gone on medical unemployment insurance for up to a yr($1,500 max per month) and you could still claim drug and other medical costs on your taxes as a deduction, but you would have had to pay up front.

If you are really poor...the welfare system would pay for most drugs and all medical costs.

Pay a bit more taxes...lose some of the life risk.
From Merek007:  I'm Always Here With You Quote
03-19-2010 , 06:48 PM
Here a significant medical problem could mean that you could lose your house, your retirement, and the lion's share of your personal income.
From Merek007:  I'm Always Here With You Quote
03-19-2010 , 06:57 PM
Quote:
Originally Posted by Blarg
Here a significant medical problem could mean that you could lose your house, your retirement, and the lion's share of your personal income.
This still happens here. It is just usually related to the reduced income and not medical costs.

No Insurance in the US would scare the crap out me. What does Insurance cost there?

Here the govt premiums are about $100 per month, depending on family and such. That protects you from all the big costs except drugs and is manditory.
From Merek007:  I'm Always Here With You Quote
03-19-2010 , 07:46 PM
Insurance can be pretty insane here. Also, they can drop you. And they regularly petition to do so. Not just in health insurance, but auto insurance, homeowner's insurance, etc. They petition the government to drop buyers merely on the basis of their being unprofitable. They've had many successes doing so here in California, for example, where the political campaigns have largely been funded by insurance companies and a lot of politicians go on to jobs in the insurance companies after their tenure, or come from there before election (or appointment).

$100 per month is nuts. Here you can easily spend $300 to $600 if you're single, healthy, and never go to the doctor. Many people pay twice that much and more. And that's to get a $2000 deductible or more.
From Merek007:  I'm Always Here With You Quote
03-19-2010 , 09:50 PM
Quote:
Originally Posted by Merek007

Here the govt premiums are about $100 per month, depending on family and such. That protects you from all the big costs except drugs and is manditory.
WTF?! That is insanely good considering how much it covers.
From Merek007:  I'm Always Here With You Quote
03-19-2010 , 09:54 PM
Quote:
Originally Posted by Merek007


While I only live a 100 miles from Vancouver, it takes 4-6hrs due to big inlets surronded by high mountains The trip is drive 20 minutes, take a ferry for 50 minutes past waterfalls, mountains, whales and forest covered islands, drive for a hr+ on a narrow twisting road 2 lane road, another ferrry for 40 minuties and then 30-50 minutes to the hospital depending on traffic. With waiting, 4 1/2 hours on a good day, 6 hrs on a bad one. Or a 25 minute flight.
What a great experience to go through on the way to and from something not so great. When I was going back and forth to chemo treatments as a kid I mostly rode in a car past cheese factories and feed mills.
From Merek007:  I'm Always Here With You Quote
03-19-2010 , 10:31 PM
Quote:
Originally Posted by BustoRhymes
WTF?! That is insanely good considering how much it covers.
I had to go check and make sure the numbers were right as my work pays.
------
BC Health Premiums
Monthly rates are $54 for one person, $96 for a family of two and $108 for a family of three or more. Effective January 1, 2010 monthly rates will change to $57 for one person, $102 for a family of two and $114 for a family of three or more. This covers all health costs, except drugs, glasses, dental(although it does cover emerg stuff but not fillings and such) or volunteer stuff like sex changes or larger boobs.

Now remember....we do pay 4-13% more in taxes than Americans, depending on income. But the taxes also provide other benifits such as free polar bear meat and architectural igloo instructions.
From Merek007:  I'm Always Here With You Quote
03-19-2010 , 10:35 PM
LOL

How do you take care of vision and dental expenses? Are those all out of pocket? So you are still paying a premium (for insanely good coverage) in addition to higher taxes?
From Merek007:  I'm Always Here With You Quote
03-19-2010 , 10:50 PM
Quote:
Originally Posted by BustoRhymes
LOL

How do you take care of vision and dental expenses? Are those all out of pocket? So you are still paying a premium (for insanely good coverage) in addition to higher taxes?

Oh yeah. Everything is not free. People get extra insurance to cover glasses, dental, physio, disablility(like I am on currently). Usually like the US, either work pays or there is some split between employees and employers. Deal with Billion Dollar insurance giants.

Now I have to go find a pay stub - I never even pay attention as to what that extra insurance costs..... Hum? Work must pay 100%. It is not on my income. Oh right, Med Insurance in Canada is no taxable. Now I have to ask our bookeeper.
From Merek007:  I'm Always Here With You Quote
03-19-2010 , 10:57 PM
Good luck, man. My father and 3 of his siblings died of cancer. It's such a bastard of a disease. Don't be afraid to use your "C'mon! One Time!".
From Merek007:  I'm Always Here With You Quote
03-20-2010 , 02:17 AM
First of all, I want to wish you the best. I've never really posted in the lounge, but I felt like I need to respond to your story. Keep up the positive attitude, it will undoubtedly help you overcome this.


Quote:
Originally Posted by Merek007
Apparently stem cells keep better in the freezer than leftovers. They do collect enough for several transplants as often people need another, years later, and the Chemo makes a second collection difficult or immpossible(not sure on this)

Chemotherapy is tough. As you already mentioned, there is no effective way to kill only the cancer cells. Chemotherapy is designed to kill off cells that divide rapidly. Unfortunately, cancer cells are not the only ones who divide rapidly, bone marrow cells also fall into this camp. Therefore, when you undergo chemotherapy your bone marrow cells are killed along with the cancer cells. This is why collection of stem cells for several treatments is necessary. After chemotherapy, the cancer cells will be gone, but so will some or all of your bone marrow cells. This makes future collection more difficult since you will have fewer cells. If, several years later, the cancer cells return to a high number you may need to once again undergo chemotherapy and have another marrow transplant.



For reasons I have not be able to find, a few people can't use their stem cells....


I looked into this a bid and didn't find a definitive answer. However, the National Cancer Institute stated that in order to use ones own stem cells they must be relatively free of cancer cells. (#12) This makes sense, since a large amount of cancer cells would cause the cancer to reappear quickly.



I'm not a doctor or other medical professional, at least not yet, but after reading your story I felt like looking into it.

All the best,

Jokes
From Merek007:  I'm Always Here With You Quote
03-20-2010 , 09:21 PM
It's been almost 24 hours since the OP posted in the thread. I hope he's ok.
From Merek007:  I'm Always Here With You Quote
03-20-2010 , 09:39 PM
Best wishes and best of luck Merek. Stay strong, and fight.
From Merek007:  I'm Always Here With You Quote
03-20-2010 , 10:15 PM
Quote:
Originally Posted by Matt Williams
It's been almost 24 hours since the OP posted in the thread. I hope he's ok.
Our Multiple Myeloma fact of the day

Depending on your condition they put you in different stages ( 1,2,3) and treat you differently

The one that got me was.......

Stage 1 - over 600 million plasma cells
Stage 2 - 600-1,200 million plasma cells
Stage 3 - over 1,200 million plasma cells

No real information here.....except those are really big numbers.

No wonder sh.t goes wrong with the human body. Seems more complex than required. ....ok. It is supposed to be a sefl-repairing system. Still.

Billions of independent cells all humping/splitting and rubbing up as against each other. No wonder some weird mutant cells get produced. Amazing it doesn't happen more. ..... although it probably does happen a lot. Just most the mutants are like your lazy cousin/friend, who would have to actually get off the couch to cause a problem. Lazy and unproductive saves us again.
---------
Monday I go to Cancer clinic and learn the "what treatment and when".....and yes I will be wearing the "I'm Not Dead Yet" T-shirt. I have always believed it is better to offend and apologize, than to never risk offending.

Derek
From Merek007:  I'm Always Here With You Quote
03-21-2010 , 12:07 AM
Quote:
Originally Posted by Merek007
Our Multiple Myeloma fact of the day

Depending on your condition they put you in different stages ( 1,2,3) and treat you differently

The one that got me was.......

Stage 1 - over 600 million plasma cells
Stage 2 - 600-1,200 million plasma cells
Stage 3 - over 1,200 million plasma cells

No real information here.....except those are really big numbers.

No wonder sh.t goes wrong with the human body. Seems more complex than required. ....ok. It is supposed to be a sefl-repairing system. Still.

Billions of independent cells all humping/splitting and rubbing up as against each other. No wonder some weird mutant cells get produced. Amazing it doesn't happen more. ..... although it probably does happen a lot. Just most the mutants are like your lazy cousin/friend, who would have to actually get off the couch to cause a problem. Lazy and unproductive saves us again.
---------
Monday I go to Cancer clinic and learn the "what treatment and when".....and yes I will be wearing the "I'm Not Dead Yet" T-shirt. I have always believed it is better to offend and apologize, than to never risk offending.

Derek
That shirt is definately your good luck charm. Don't leave home without it! I really do believe keeping a good outlook is a key factor of beating cancer. Don't ever lose it bro, ever.
From Merek007:  I'm Always Here With You Quote
03-21-2010 , 12:20 AM
Incredible read, I wish you the best of luck. I really admire your positive outlook - Christ - I'd be like Eeyore in this situation.
From Merek007:  I'm Always Here With You Quote
03-21-2010 , 11:19 AM
Thoughts with you on what is going to be an amazing victory in life, I'm sure.
From Merek007:  I'm Always Here With You Quote
03-21-2010 , 03:45 PM
It's been said here already, but your attitude pretty much rocks. I would assume if anyone can beat this thing, it would be someone with so much cool about it.

Sort of reminds me of Will Hunting's explanation about why he would choose the wrench:

"Because ^&#$ him, that's why."

I know everyone here is looking forward to hearing that you are winning the fight. Give it hell.
From Merek007:  I'm Always Here With You Quote

      
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