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We Cannot Wait: FDA Needs to Act on ALS realclearhealth.com/articles/2021/… By the FDA refusing to approve NurOwn they are literally murdering ALS patients who could survive. The FDA needs to do what's right by approving NurOwn so ALS patients have a chance to live. Approve NurOwn now!

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@Michell62614519 @SenatorBurr @ThomTillis @JimInhofe @SenJoniErnst @SenatorWicker @SenBillCassidy @SenKevinCramer @SenatorRounds @MarshaBlackburn @SenatorBraun @MilitaryTimes @NavyTimes @starsandstripes Senators, FDA, please don't doubt for a second that NurOwn is a life-saving treatment for ALS patients. Postings like Matt Bellina's are true and it represents the ONLY treatment available today that can save the lives of my son and hundreds of other ALS patients. APPROVE IT NOW!

@DrWoodcockFDA Great. You care more about saving my pet than saving my son. How about caring about saving his life and the lives of thousands of ALS patients by approving NurOwn. Every day you delay in doing so is one more day that ALS patients suffer and eventually die. Approve NurOwn now!

@US_FDA I applaud you for helping COVID and Alzheimer patients but I don't understand why you continue ignoring pALS who benefitted from NurOwn. Their testimonials tell the real story that it is an effective treatment. Do what's right and humane, stop making excuses. Approve NurOwn now!

Just read on STAT+ web page that Lilly seeks speedy approval for its Alzheimer drug after only a Phase 2 trial and @DrWoodcockFDA is "not concerned" about criticism. How about approving Brainstorm's NurOwn for pALS too! End the delay, approve NurOwn now and no one will complain!

@als_now @sandymorris333 @SenatorBraun @DrWoodcockFDA @FDACBER Father's Day is coming and those fathers battling ALS need NurOwn now so they'll be able to be spend years not just weeks with their children. Delaying NurOwn is cruel and heartless. A few FDA decision makers can make it happen, PLEASE, stop the delay and save ALS fathers now!!!

This was this AM. THANK YOU to @SenatorBraun for telling the #ALS truth. Patients remain dumbfounded at the denials by @DrWoodcockFDA and @FDACBER that SAFE, EFFECTIVE ALS drugs exist NOW that could be encouraged to apply for approval. #NUROWN #AMX0035 youtu.be/mbrs_4RAQoc

Help support ALS expanded research: helpmayuri.com via @tawheed

@alsadvocacy @statnews Amazing article about ALS patients ongoing battle for the right to live. In addition to Amylyx, let's not forget how the FDA caused Brainstorm to suddenly postpone its NurOwn expanded access effort as well. pALS shouldn't keep being told to just go home and prepare to die.

@DrWoodcockFDA I appreciate you wanting to save lives by seizing products with kratom, but now why don't you show that you really care about saving thousands of more lives by approving NurOwn for ALS patients now so they too can be given the opportunity to live. Please , NO MORE EXCUSES!!!!!

As ALS Awareness Month passes by the only people who really care are pALS and cALS. If politicians and FDA officials did they'd stop delaying the approval of treatments and do something meaningful to save pALS lives before the month ends. But unfortunately, they won't! SO SAD!!!

Hundreds of pALS send and resend tweets to politicians and FDA leaders pleading for approval of these treatments. Weeks pass, but nothing changes, and more pALS continue declining and die. Yet those not approving these treatments sleep peacefully at night, so disgraceful!

@als_now @US_FDA @biospace @WSJopinion @DrWoodcockFDA @SecBecerra @PattyMurray @SenatorBurr @FrankPallone @cathymcmorris @RepAnnaEshoo @brettguthrie @MinoSean @Chance4Lisa @ThurmanTough @FinishALS @JeffFortenberry I read hundreds of tweets to politicians and FDA staff from pALS pleading for treatments. As long as insurance and pharma lobbyists keep discouraging politicians and FDA officials from approving treatments nothing will ever change. Hold a #ALShearing and end this injustice now!

@als_now @US_FDA @biospace @WSJopinion @ThurmanTough @Chance4Lisa @MinoSean @alsnewstoday @JeffFortenberry @DrWoodcockFDA @FinishALS Hundreds of pALS send and resend tweets to politicians and FDA leaders pleading for approval of these treatments. Weeks pass, but nothing changes, and more pALS continue to decline and die. Yet those not approving these treatments sleep peacefully at night, so disgraceful! #ALS

@iamalsorg This is an inspiring story, however those with the power to approve ALS treatments, and others who read success stories like Sally's, shouldn't be led to believe that the majority of pALS can do what she did. Achieving dreams & normalcy isn't possible without approved treatments.