Nita Aldridge

[Nita Aldridge @Sweetpea4853]

.@sentoddyoung Thank you for being an ALS champion! By supporting ACT for ALS, you are helping advance access to promising treatments and ALS research!

[Nita Aldridge @Sweetpea4853]

.@RepJimBaird Thank you for being an ALS champion! By supporting ACT for ALS, you are helping advance access to promising treatments and ALS research!

[Nita Aldridge @Sweetpea4853]

.@SenatorBraun Thank you for being an ALS champion! By supporting ACT for ALS, you are helping advance access to promising treatments and ALS research!

[No More Excuses ALS Watchdogs! @als_now]

Nothing magnanimous to say except 2022 must be the year *multiple* new drugs finally reach #ALS bodies. If not, #ALS will waste its best chance to transform- maybe for a decade. Can #ALS unify, and make access to ANY drug that is ready its #1 goal for 2022? #demandresults #ENDALS

[I AM ALS @iamalsorg]

.@BrainstormCell shared this data:

https://t.co/Fost3PmMQE

ALS is not a homogeneous disease that is the same in every person living with it. If a treatment proves safe and effective for some, it should move forward quickly to be accessible to those living today.

[Nita Aldridge @Sweetpea4853]

Hey @SenToddYoung why not join @SenatorBraun and help Hoosiers with ALS by sponsoring #S1813 #ACTforALS today. Veterans like you are twice as likely to get ALS. Thank you @SenatorBraun for your support.

[Brian Wallach @bsw5020]

There must be no silos when dealing with ALS or any other terminal disease. @DrOzdinler is a great example of how true collaboration works. #Together

[Jeff Fortenberry @JeffFortenberry]

So proud of Nicole, who tells the story of so many dashed hopes for people with the cruel disease of #ALS. Let’s drive the hope. @US_FDA #ACTforALS https://t.co/o03QEagniK

[Nita Aldridge @Sweetpea4853]

@WSJopinion Please help us. I am #DyingWaiting. I need #DrugsInBodies. The FDA is #ProtectingMeToDeath. PLEASE.

[No More Excuses ALS Watchdogs! @als_now]

@WSJopinion SHOCKING! PLEASE retweet amd SHARE! Go to "No More Excuses ALS Watchdogs" on FB for more!

[Nita Aldridge @Sweetpea4853]

Please help us. I am #DyingWaiting. The FDA is #ProtectingUsToDeath. We need #DrugsInBodies. PLEASE.

[Wall Street Journal Opinion @WSJopinion]

My husband and I fought for continued access to treatment and to improve an archaic regulatory pathway. He died waiting for change, writes Nicole Cimbura https://t.co/w1lklYHptl

[ALS ACCESS @brainmatters10]

@biogen Well it is time that you step up and help this severely underserved need. People with ALS, have been ignored for over 150 years. Countless millions have died. Step up and help now

[No More Excuses ALS Watchdogs! @als_now]

@biogen PLEASE SIGN to help demand access! And WHERE IS ALSA ON ASKING FOR THIS? Too busy trying to get its favorite supplement based drug approved so it can MAKE $$, that's where #ALS #ENDALS #fALS @alsassociation #ENDALS @FoxNews @cnnhealth @CNN @statnews

https://t.co/DRPD03zb8c

[No More Excuses ALS Watchdogs! @als_now]

@biogen "Our hearts break for all families impacted by ALS...." Translation: "NO, a sorry, we're gonna keep our $41B". So inhumane, yet so typical for #ALS. Hey @alsassociation, are 500 pALS who might be SAVED by a billion dollar company not even worth your bother to ASK? @statnews @CNN

[Jeff Fortenberry @JeffFortenberry]

For complex diseases like #ALS incremental progress is often monumental. But @US_FDA would rather OK a drug with a 3% benefit to every patient than one that helps 20% of patients substantively. It's hard to see how any ALS drug can get thru that gauntlet https://t.co/iAcRUcNnIG

[Jeff Fortenberry @JeffFortenberry]

My brother-in-law's death from #ALS connected me to so many courageous persons suffering from this cruel disease. The @US_FDA just shattered hope, not approving the treatment NurOwn because it only helped some. We can’t take much more. Is our government here to help?

[Sherry Quisenberry @sherryquis]

This is someone who “gets it.” Even he is dismayed by the lack of insight and support from the FDA and Dr. Woodcock. #ALS #DyingWaiting We need your HELP @POTUS @VP

[No More Excuses ALS Watchdogs! @als_now]

@alstexas @ALS_SanDiego @alsassociation @ALSMNDAlliance @alstexas @ALSA_MidAmerica @AlsOklahoma @ALSANorthernOH @ALSAOCC @ALSofGNY @ALSAMA @ALSAUNY @alsncchapter @ALSAGeorgia @ALSTDI @mndaustralia @ALSA_EC @WVALSA @ALSAMichigan @alsa_ri @ALSA_Nevada @ALSA_MNNDSD @ALSAChicago

[I AM ALS @iamalsorg]

It might look like a bunch of words, but the @US_FDA said it will accept a different standard to get treatments to the #ALS community. ALS is relentless. ALS is taking lives. It’s time the FDA came through on its word.
https://t.co/gQFmvKLe4s

[Greg @gregkochak]

If #NurOwn was a cancer treatment, it would be approved already.

#EndALS