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Mad about Lupron!

From: andrea (anonymous@obgyn.net)
Mon Oct 1 15:37:11 2007


It seems like most doctors out there push Lupron on us like used car salesmen, at least that's how I feel. They don't tell us the dangers of this drug and tell us that the effects will eventually wear off. This is not always the case, as you will read on these pages.

I read on one page, that once you've had Lupron injections, you are no longer allowed to donate blood. Now, what does that say? That it stays in your system forever? I just feel there is so much doctors don't tell us about Lupron.

I don't blame anyone for taking Lupron, as I know how desperate we are to get better and have our pain relieved and doctors make many of us feel like it is our last hope - which is NOT RIGHT! They don't tell us what all this drug is capable of doing to us, either.

I feel that doctors play on this desperation of ours to get well and feel they can talk us into taking anything, including things that may be dangerous and cause us even more pain or illnesses. They are risking our health, so they can get rich.

I just sent a friend of mine to my specialist to see about surgery. (I am just under his care for pain management right now.)

She has already been on 6 mos. of Lupron and has fibromyalgia, so I did not think he would even go near the suggestion of giving Lupron to her. Well, he did!!! He wants her to do 6 more months of this drug, when she is already extremely sick from it! Is he crazy? Can he not see how crappy she feels?

I am furious now and no longer want to go to this specialist for surgery. I only went to him because he is supposed to be one of the best and was recommended by a friend. When he mentioned Lupron to me, I said not for a million bucks would I take that! So, he dropped the subject and was not pushy about it. But with my friend, he was insistant.

I told my friend that I don't think she should do anymore Lupron. I think that doctors who push Lupron on their patients are immoral a-holes and I don't want them touching me. I don't know if I will ever find a doctor who I totally trust to do a lap on me now. I would go to Redwine in Oregon, but that is unaffordable.

New Links about Lupron:

http://www.ipetitions.com/petition/Depot-Lupron/signatures-8.html

http://www.mercola.com/2002/mar/6/lupron.htm

http://www.medications.com/se/lupron




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