Joined July 2024
201 Photos and videos
Pinned Tweet
Replying to @iamalsorg
Ok. So now let’s cut the #ALS BS! Act for ALS is ONLY to give access. Dont oversell it “HUGE strides towards ending ALS”. That’s unfair immoral to pals cals to ALWAYS grossly overstate everything! Shameful ! Let’s actually see what the report said below 👇👇👇
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Hiw is this
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#mnd @mndassoc #als see 👇 u r fuckin morons! Why? U don’t even know ur fucking disease! U don’t want to set a precedent BUT ur too fucking thick/clueless to realize another Tx like Torsefen will take DECADES . Many of you heathy idiots may be dead by that time. No f’ precedent!
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#ALS #MND I studied this savage beast for 6y 24/7 spanning decades! ALL of it & 1000s of posts. Conclusions: 2 many. BUT “awareness” for the “masses” DOESN’T work. Polls show it’s still dismal. It’s 2 rare. Ppl can’t relate. & how many ppl can name former advocates w/out Google?
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ScienceMatters retweeted
Replying to @GrimzyNews
Does that "police officer" really believe that or is he just parroting what his bosses are telling him to say or is he just a pussy that's afraid to be called out for "politically incorrect" speech? In either case, he's not fit for the job.
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#als #mnd @bsw5020 @iamalsorg @alsassociation question! Read this. Do you actually know of Scleroderma, IPF, PAH, Amyloidosis, Ehlers-Danlos syndrome, GPA? Most of us Clueless. I am. So are the masses about #ALS. Same reaction as you now. Rare=unknown. ZERO way to change that!
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#als #mnd the truth about ALS. It is rare, thankfully ! I don’t believe in deceit !
Replying to @CathyStandish
Sadly (thankfully ) it’s rare. #ALS strikes 1-2 out of 100k yearly. ALZ strikes ~150 per 100k per yr! Thats 9,900% more frequently than ALS!! 😳😳 Some pals say that the population must not be led to think it’s rare bc they donate. I find deceit abhorrent no matter the disease.
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#als #mnd @bsw5020 and @iamalsorg you have sod there are “breakthroughs” coming since 2020! 👇
15 Sep 2025
We're launching our Push for Progress campaign to accelerate ALS research, expand treatment access, & secure $1BN in federal funding over 3 years. ALS is at a tipping point CLOSE to new treatments, but thousands will lose access unless we TAKE ACTION @ iamals.org/progress
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I hope @iamals takes stock after 5 years of ACT4ALS or renewal in 2027 (?) to see how many EAP drugs were approved. My educated guess. Zero. ALS gets $200My in research. Pittance. ALZ gets ~3.5By! 16x more! ACT is what pals “want” but isn’t what ALS “needs”. It needs research $
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ScienceMatters retweeted
I hope @iamals takes stock after 5 years of ACT4ALS or renewal in 2027 (?) to see how many EAP drugs were approved. My educated guess. Zero. ALS gets $200My in research. Pittance. ALZ gets ~3.5By! 16x more! ACT is what pals “want” but isn’t what ALS “needs”. It needs research $
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This. Is. Beautiful…. Pride ! @PrabhdeepReform bless you! UK is a beautiful country.
🇬🇧 Our flag is our pride. I had the privilege of serving this great nation in the British Army. On Civvy Street, I continued my service by standing up for our communities—fighting against draconian policies like the ULEZ expansion, Food Poverty, Cost of living Crisis, Net Zero Fantasy. 👉fight2survive.org No lefty, so called liberal, or anyone else needs to tell me why I hoist this flag!!! I earned it. I served it. I stand proud with it and I’ll always defend it. #BritishArmy #ProudBrit #UnionJack @TiceRichard @Nigel_Farage @Towler @reformparty_uk
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Fucking vile, ugly, unsightly, dehumanizing, savage disease! #als #mnd
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#als #mmd completely decimate families, tear fathers and mothers away from their young children, destroys relationships, and these fucking people talk about miracles with ALS and living their best life insanity! Fucking toxic positivity
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Anyone who says loving with #ALS #mnd is “living the best life” is FOS!
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Jesus f’ing Christ is #ALS #MND so f’ing brutal and hard to look at !!! Such a vicious, savage, dehumanizing pig of a disease !!!
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I’m very selective to who I give kudos to in #ALs #MND world. But kudos! Love Dr Rothstein btw. Kudos bcuz for decades most in ALS “community” keep repeating same old “what” BUT NEVER the “Why”. 🙏
13 Aug 2025
Announcing Champion Insights: a remote study on why elite athletes and military face higher ALS rates. At home steps and one blood draw. Data flows to Neuromine to speed discovery. Learn more 👉 answerals.org/2025/08/13/uni… #ALS #AnswerALS #ALSTDI #AugiesQuest #OpenScience #EndALS
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#als #mnd so broke blocked me when I suggested a while back that her overly positive posts were tone deaf to the advanced pals. Over 6y I’ve seen countless slow progressors start off cheery and then taper off as broke has. Massive change in her posts. Massive. That was my point
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Imagine even the #CFL #Montreal #Als team is more known the #ALS the killer beast! That says a lot!
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What else are they gonna say they need to be funded they need money and they can’t go around being doing gloom but the reality is this type of talk was heard. 10 years ago 15 years ago some 20 years ago and what counts are #als results not process. Enuf lipstick on a pig
We asked #ALS researchers how they're feeling about the future of #ALSResearch. The overwhelming answer: optimism and excitement about progress with real-world impact. The Annual Meeting Impact Report drops tomorrow. 📩 Sign up now to get it first: bit.ly/3GGRGTT
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Fuck do I despise the terms #ALS #mnd “community , tribe, and anything of the like”. F’ing vile. Gross. WTF wants to be part of that shit! Give me a f break !
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#ALS #MND has taken everything from me. To those who portray the vile disgusting disease with smiles, laughs, bibs, socks, moons, bull fucking shit toxic positivity you ARE fucking insane and I will personally fucking dress you down online your crazy, delusional. Denial fucks!
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