Atualização do abaixo-assinadoNOBODY SHOULD BE LEFT TO SUFFER IN PAINLET’S GET THIS SEEN & SIGNED
Kimberly PlattRochester, NY, Estados Unidos
27 de nov. de 2024

We hit and passed the 200 goal! We are almost halfway to the next goal! This needs to be shared as far and as wide as possible!

On TikTok, my username is @_galaxy_kim_  in case you’re wanting to see more of what this all means. I have two playlists that are of utmost importance! The first is “petition for change.org”. BUT, also the playlist titled “fight for pain treatment”. There are a ton of videos and there is a very large reason why. All of this petition is because of all of that fight! 

This is all of our cries for help! Check the comments of those videos as well to see how many of us are suffering; needlessly! Anyone that can get this to the most eyes possible would be of eternal gratitude in ways I cannot explain! 

Pain patients are dying because they aren’t believed or because of the restrictions placed upon practitioners by the government agencies. It won’t let me make the DEA a decision maker. The CDC doesn’t even offer to send an email!  People have got to start seeing that this is absolutely NOT the way to go! Any doctor that is still using 2016 guidelines is incorrect as well. There have been a few changes since then. 

Too many people have been suffering in agony in their beds because of a fear that the media and government and big pharma planted into you. Open your eyes! There are so many people that have so much to give to this world and we are in our own pain prisons! Let doctors treat accordingly. Stop the stigma! 

To vilify a class of drugs while glorifying another is wrong. The one glorified leaves permanent damages to every patient’s entire nervous system! But because it costs more, so we are going to push that? When did it change from prevent and heal to diagnose and treat?

Pain medication, when used adequately to treat an acute issue, will drastically drop the possibility of chronicity! But it HAS TO BE ADEQUATE!! And patients need to be believed when they are in so much pain. MMEs mean nothing without genetic reasoning to back it up.  They don’t allow you to get the genetic testing to prove how you metabolize certain families of medications. Insurance won’t cover it. Wonder why…

Please keep up the good work! The louder we get the better. None of us get to a point of euphoria. Please remember that. Thank you again for all efforts thus far, and to come! 

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