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ALS Advocacy
@
alsadvocacy
Stanford MedX ePatient Scholar
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ALS = Lou Gehrig's Disease Thought it had been cured by now? Still no known cause. Still no cure. Still no treatment. Still quickly fatal. Still outrageous.
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77.473
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1.637
Pratim
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8.540
Osobe koje vas prate
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ALS Advocacy
@alsadvocacy
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Many thanks.
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ALS Advocacy
@alsadvocacy
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Agree with Corey on thanks for the ALS Caucus.
And NIH funding!
I'll be talking to him next week about those plus CDC ALS Registry concerns.
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ALS Advocacy
@alsadvocacy
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STAT
@statnews
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The drug has been tried, tested — and failed. Repeatedly. So why did CODA Biosciences just buy it? buff.ly/2ShYdHT
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ALS Advocacy
@alsadvocacy
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2 h |
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Thanks!
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ALS Advocacy
@alsadvocacy
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ALS Advocacy
@alsadvocacy
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Not much on neurological diseases.
? twitter.com/pfizer/status/…
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ALS Advocacy
@alsadvocacy
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ALS is unsafe.
When data safety monitoring boards view data in a trial looking for "unsafe" situations, do they ever consider that people on therapy who are improving or stable are a lot safer than those not getting the therapy?
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| ALS Advocacy proslijedio/la je tweet | ||
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Maurice
@MauriceOnTW
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20 h |
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Nice slide on #genetherapy capacity vs potential demand in NIH talk pic.twitter.com/dO55YyVgf6
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| ALS Advocacy proslijedio/la je tweet | ||
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Girl Travelin Alone
@CathyStandish
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A memory from the days of little boys, Christmas trees and our first tiny house.
When talking #ALS we were “lucky” - at diagnosis our kids were grown.
So I continue. To hope. To fight (not argue) for an #ALS treatment.
A cure.
#WednesdayMotivation #EndALS pic.twitter.com/mRoEtYZwRo
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| ALS Advocacy proslijedio/la je tweet | ||
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Brian Wallach
@bsw5020
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There is not a red state version of ALS and a blue state version of ALS. There is only ALS.
There is not a pro-ALS group and anti-ALS group, there is 1 movement to end ALS.
We speak with different words but seek the same future. We fight for each other and will be the cure.
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ALS Advocacy
@alsadvocacy
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Worth taking 2 minutes to read this in detail before deciding that this is a panacea for ALS... 2 minutes are all it will take.
Executive Order on Advancing American Kidney Health whitehouse.gov/presidential-a… via @whitehouse
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ALS Advocacy
@alsadvocacy
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Link? Thanks.
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PBS NewsHour
@NewsHour
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4 h |
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“80 percent of the raw materials used by American drug companies to make generic drugs come from China,” reports @davidjlynch to.pbs.org/2SdXJCw
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ALS Advocacy
@alsadvocacy
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4 h |
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healthforum.wsj.com/attendees/
Scroll down to "c" -- Nobody titled "caregiver."
Scroll down to "p" -- Nobody titled "person with _____"
I know people w ALS and caregivers who would add value to this conference and would would learn a few things, too.
#NothingAboutUsWithoutUs
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ALS Advocacy
@alsadvocacy
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.@WSJhealth @WSJ @PhRMA Do you provide any scholarships for patients and caregivers for this significant conference? You are missing important stakeholders and experts in the conversations. Thank you. healthforum.wsj.com
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ALS Advocacy
@alsadvocacy
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Jeff Bam Bam Schmeltzer - wrbiradio.com/2020/02/03/jef… #ALSobit
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ALS Advocacy
@alsadvocacy
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#ALSobit Hamburg Township Trustee Jim Neilson dies after battle with Lou Gehrig's Disease livingstondaily.com/story/news/202… via @livingstondaily
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ALS Advocacy
@alsadvocacy
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Thank you, @bubbawatson Bubba Watson commits to the 2020 Travelers Championship wfsb.com/news/bubba-wat… via @WFSBnews
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ALS Advocacy
@alsadvocacy
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8 h |
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CytRx Corporation Highlights Updated Arimoclomol Milestone Guidance Provided by Licensee Orphazyme A/S | BioSpace biospace.com/article/releas… #jobs
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