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T DM-1 Activism
Please post on other boards , its on Inspire. Approval is getting close. maybe this Fri. ? This FDA is dragging it out, probably developing a defense of their mis-handling of this drug since 2010. Some signs include recent quicker approval of lesser drugs , ones w/ smaller target populations. Lately, This FDA has promoted " Black Box Warnings " on chemo drugs. Everyone knows that cancer drugs have s/e, risks; this is an FDA PR ploy. A defense of their slowness since Pres. Obama took office . ( We at Our Her2Cancer Struggle (FB) are non-partisan, but we " call em as we see em " ). This FDA is deliberately playing up risk. " We had to take due diligence , etc. "
Some of you have asked us about advocacy for this drug, and how to be true Activists, working to change This FDA System. The opportunity will come soon. When the drug is FINALLY approved, anytime from now until Feb. 26th, we must Seek Publicity. To keep this from happening again. To make sure there are no conditions on appr that keep it from early Stage IV Survivors. Start right now to look up your local, nat'l media e-mails. TV first , then print. Your local / national reporters who cover cancer-related issues. When appr. comes , we will post a Press Release here. With the " Real Story" , not This FDAs' excuses. With our website, http//:stageivsurvivor.webs.com . If you haven't visited lately, we have added Christi Turnages' Avastin story, and Darlene Gants' Pertuzumab story. More examples of un-necessary suffering caused by This FDAs' anti- Stage IV agenda. At that time , send out the Press Release to your contacts in media. If you are on T DM-1, you are one of the lucky few, add your personal story. Keep it brief. This drug will tell its Own Story, just like original Herceptin did in '96.
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