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Medical Marijuana



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07/24/2007 09:29
CJ
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Just curious, are there any of you who have been given prescription for medical marijuana and if not would you consider it?

Personally, I would consider it, never having tried it before, but just reading up on the benefits vs. downfalls, it seems like a no brainer.

Your thoughts...

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07/24/2007 10:19
jaime1978
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CJ-

I don't think it's a bad idea honestly....although never been there myself. I know over in Europe, for dying cancer patients they give them heroin! Here everyone is so worried about addiction, but my thing is, "what about quality of life?" Here, you have a dying cancer patient, and they are afraid to give them morphine for god's sake....who cares if they get addicted...THEY"RE DYING!

So I guess if the option were there I may consider it...even on pain meds, my level is never below a 6....and that's a good day...which are very few and far between

Please do not take anything I say as medical advice. I am not a doctor.

~lyme disease support group leader~
please pm me with any special concerns
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07/24/2007 12:25
janieslife
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I may have cancer and I would ask for it as a matter of fact I would probablly demand it.

So YES it is a good idea.

Hi my name is Jane. I was diagnosed with Bipolar in 2003.
Later to be diagnosed with post tramatic stress P.T.S.D
I am married to a wonderful man who bless his heart thinks he can cure me and a 16 year old daughter that thinks that's funny.
Unfortunatly I have had many failed attempts at marriage and
A few seperations from this one.
But he keeps coming back.
Even on medication I have many problems that Doctors can't explain so maybe being here will help.
In 2003 the first real problem started I have always had depression and was treated for 15 years before 2003.
When I realized something had happen to me I was waking up in a Hospital.
No memory of why I was there and was too out of it to care for a few days.
When I got home I got some details of all that had happen to me.
Then they diagnosed me Bipolar but no one could explain the memory loss.
Since then I have days even weeks that I have no memory of what I did or where I go.
I seem to do everything normal to other people who are around me but the fear of maybe never coming back from the next one is always there.
From talking to others this is not from Bipolar and some Doctors say it could be from P.T S.D.
But no one knows how to treat it yet.
So Here I am trying to treat myself.
I am here to get help and advice for myself and to help others.
jane



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07/24/2007 12:27
jaime1978
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Jane.... just wondering if you have looked into lyme disease? This is a tricky one... and you would need to find an llmd for it.... they are hard to come by and expensive... please check your pm ....
Please do not take anything I say as medical advice. I am not a doctor.

~lyme disease support group leader~
please pm me with any special concerns
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07/25/2007 21:00
erleichda
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Jane, yes, it is entirely possible with PTSD. It sounds like you are not certain that you agree with the PTSD diagnosis, or maybe you haven't worked with anyone on it yet. Do you think that the diagnosis is accurate? Have you taken the DAPS?

Jaime has a point mentioning Lyme disease, too. Lyme has caused more havoc with my brain than the PTSD. My psych insists that my brain fog is caused by my PTSD. I used to think so. PTSD *can* cause physical changes in the brain. But last year, before I found out I had Lyme, I had four month's worth of cortisone shots. Since then, I've experienced significant changes in thinking and memory. My family tells me about things I've done that I swear never happened. And I insist that I've done things that I haven't. It's been horrible. Cortisone reduces activity of the immune system, which is what you need to fight Lyme. And although I've had PTSD for some time, this spike can only be explained by Lyme, since my PTSD was not triggered - but my Lyme was.

I don't mean to speak for Jaime, but you may be wondering why we are mentioning Lyme to you. You are in the Fibromyalgia forum, and most Lyme is initially misdiagnosed as fibro. I was misdiagnosed for 4 years. So, it's not as strange as you might think. Unless you just came here to comment on the medical MJ, since you said you might have cancer.

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07/25/2007 21:19
erleichda
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CJ - A few years ago, my father died a horrible, painful death by pancreatic cancer. I wished at the time that MJ were legal so that he would not have to suffer so. No one should have to die in that much pain and suffering.

They sent him home with Hospice when the doc couldn't help him anymore. They only supply pills. He could not keep them down. For the nausea, they gave him more pills which came right back up. They had nothing else to offer, no shots of morphine, nothing except by mouth. How great it would have been if he had been able to get pot. It would have helped with the nausea so that he could keep pain pills down. And it would have helped with pain.

The same was true with my sister-in-law. She died two months after my dad, and I got to watch years of her misery with both leukemia and lymphoma.

I don't want to get into a fight about what is safer, better, etc., but I do think that pot is more useful than alcohol and if that's legal, why not pot? I know that people believe it leads to harder drugs but I think that's only because it is illegal (so, since you took that first illegal step, you're more inclined to go further). I think that if it were legal, that reasoning is no longer true.

No, I am not a pothead. But I have watched enough suffering. Prescription meds are almost illegal because docs are even afraid to prescribe them to people who are dying. What kind of a society are we, where treating pain and suffering is illegal?

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07/26/2007 06:02
jaime1978
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Lori,

very well said. I have to agree whole heartidly. It is sad when people we love, and even ourselves suffer needlessly. There have been so many studies done even on prescription meds, that when taken properly, the risk of addiction is VERY low.... not saying your body doesn't become DEPENDANT...two different things here.

Thanks for explaining why I brought up lyme in the fibro forum Lori.... I too have been dx with fibro...MCTD (lupus, RA, scleroderma), and now possible lyme... they did a study of 50 fibro patients, all ended up having lyme.... they are starting to feel that fibro is a symptom rather than a disease itself....

Please do not take anything I say as medical advice. I am not a doctor.

~lyme disease support group leader~
please pm me with any special concerns


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07/30/2007 10:44
claireuk
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hello folks

i live in the uk and so quite near to amsterdam where it is legal, im planning on going for a lovely haze filled long weekend there soon! so yes i would take it, bring it on, mr brown....

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08/10/2007 13:43
bshapiro
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hi,

I live in California and use medical marijuana in addition to the usual fibromyalgia medications (40 mg methadone twice a day, 140 5mg oxycodone tablets per month for flare to use as needed).

My personal philosophy is that once you're told that you have to take narcotics for the rest of your life or live in horrible excruciating pain there really isn't much question that smoking a little (or a lot) of pot is beneficial both to your physical and emotional well-being. Physically it both helps counter act the nausea that comes with taking the opioids as well making the pain more diffuse. Overall it seems to provide another level of relief that helps me delay &/ or decrease my usage of things like adivan & Xanax.

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08/10/2007 13:44
bshapiro
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Post edited by: bshapiro, at: 08/10/2007 15:48
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