Susan Baker @KSalsFighter
KS farm girl passionate about promoting awareness about Familial FTD ALS bepic.com/susanbaker Wellsville, Kansas Joined May 2009-
Tweets2K
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The town hall with BrainStorm Cell Therapeutics is coming up on Tuesday November 7th. Sign up here, where you can also submit your questions in advance -- and for those who can't make it to the town hall, it will be recorded! iamals.org/action/brainst…
Ady was a selfless, beautiful soul who fought for all of us. What he accomplished in his life is simply incredible. I cannot even imagine how much more he would have changed the world if he had more time. Today I am heartbroken. I am also sending all the love to Rachael and…
Ady was a selfless, beautiful soul who fought for all of us. What he accomplished in his life is simply incredible. I cannot even imagine how much more he would have changed the world if he had more time. Today I am heartbroken. I am also sending all the love to Rachael and…
Please take the few mins to watch. Two #MamaBears, that I proudly stand beside. @BellinaDeb @Smithstrongmom1 wlwt.com/article/asl-tr… @US_FDA @iamalsorg @alsagoldenwest @ComCareALS @everything_als @klink52 @nicolecimbura @BridgetRebecca4 @kks69okie @aVoice4ALS @FarberStacy…
97% of respondents would recommend the ALS Clinic Advisor survey to fellow #ALS patients & their caregivers. If you haven't already, please take the survey today! #EndALS @Team_Thriving @R1_Crew
If you’ve already seen this touching video about a mom & her sons refusing to let ALS alter their vision of his wedding day, consider sharing please. If this is the first you’ve seen it, consider sharing please. And then perhaps say a prayer of gratitude: goodmorningamerica.com/living/video/s…
#WeeklyWebinars are back this week with updates from the HEALEY ALS Platform Trial. Register here: partners.zoom.us/webinar/regist… @alsassociation @ALSTDI @MDAorg @NEALSConsortium @LesTurnerALS @alsone_official @everything_als
Wow! Rob Burrow: Living with MND is on the National Television Awards shortlist. This is for every single family living with the disease. 🥁 #proud Vote here for your favourite: nationaltvawards.com Look at @Rob7Burrow and his family’s reaction…
Cath’s 2024 #Eyegaze Calendar for #MND - a method of creating artwork using only your eyes. Each image takes Cath around 8 hours to make which is why each calendar costs £8 👁️ 📆 Preorder yours now: etsy.com/uk/shop/Caths2…
We cannot let dramatic Federal spending cuts harm the ACT for ALS appropriations that this community has fought for. Use this action to send a prepopulated Tweet to your Congresspeople encouraging them to maintain the proposed funding of $75m for EAP. iamals.org/action/appropr…
My badass Map Master Rhymes (@Team_Thriving ) on @CBS @kcalnews! I love this channel & its staff (am I 90 years old calling it a channel?) cbsnews.com/losangeles/vid… #NurOwnNow #Sept27AdComm @NewsJuan @suziesuhkcal @JeffVaughn @Patharveynews #kcal
THIS is real. #NurOwnWorks #NurOwnNow. The only agenda @BellinaMatthew has, is to save his own life, so he can watch his children grow up. It is what we all want. @FDACBER @iamalsorg @nicolecimbura @FarberStacy @klink52 @BridgetRebecca4 @bsw5020 @kks69okie #ALS @BellinaDeb…
THIS is real. #NurOwnWorks #NurOwnNow. The only agenda @BellinaMatthew has, is to save his own life, so he can watch his children grow up. It is what we all want. @FDACBER @iamalsorg @nicolecimbura @FarberStacy @klink52 @BridgetRebecca4 @bsw5020 @kks69okie #ALS @BellinaDeb…
"Making this product available to patients while validation of this retrospective analysis is carried out seems warranted. Our patients will be the ultimate beneficiaries." -Dr. Appel, one of the world's preeminent ALS researchers
Given rapid deteroriation that occurs with #ALS, patients do not have luxury of time to wait for P3 trial data to emerge. People will not live to see an opportunity for treatment should approval be delayed. Sincere hope & plea that you will vote to approve #NurOwn @DrCaliff_FDA
Thankfully for #ALS patients some 501(c)3 organizations and advocates like @iamalsorg still exist that remain unbiased and willing to speak the truth. And who fully embrace @FDA flexibility- including for the upcoming and most consequential decision for most #ALS patients ever.
#ALS patients, seen this one yet? Don't miss it! Or if you already have, watch it again. #nurownworks @alsassociation @Nightline @TEDx @mndassoc #ENDALS youtu.be/0KYK6A0j49s?si…
Thank you, @MinoSean. This post says it all. Please share far and wide and take the 2 minutes to watch this video. @FDACBER #NurOwnPreservesFunction #NurOwnNow #NurOwnWorks @BellinaDeb @klink52 @kks69okie @BridgetRebecca4 @FarberStacy @nicolecimbura @aVoice4ALS @iamalsorg…
Thank you, @MinoSean. This post says it all. Please share far and wide and take the 2 minutes to watch this video. @FDACBER #NurOwnPreservesFunction #NurOwnNow #NurOwnWorks @BellinaDeb @klink52 @kks69okie @BridgetRebecca4 @FarberStacy @nicolecimbura @aVoice4ALS @iamalsorg…
"FDA’s risk-benefit calculation in ALS must be different than it is for therapies developed for non-life-threatening conditions. There is almost no risk worse than imminent death from ALS." #NurownIsSafe #NurOwnWorks
Brian Wallach @bsw5020
159K Followers 3K Following Dad, husband, activist, entrepreneur, unlikely movie star, living with ALS, a currently fatal disease.
I AM ALS @iamalsorg
26K Followers 799 Following I AM ALS is a patient-led movement revolutionizing how to end disease with our sights set squarely on ALS.
AZ Latina ☮️🌊�.. @aVoice4ALS
4K Followers 5K Following Political Junkie. Advocate for Enviro Justice, Foster Care, Gun Safety, DEI, Amyloidosis, PD, ALS & Rare Diseases. Love LA Sports. I block disrespectful people.
Sandra Abrevaya @sabrevaya
21K Followers 4K Following Wife to @bsw5020. Mama to spunky girls. Caregiver. CEO & Co-founder @synapticure. Co-founder @iamalsorg. Executive Producer @noc_film. All in on curing ALS.
ALS Advocacy @alsadvocacy
12K Followers 2K Following 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.
Leanne Yacyshyn @leanne_yacyshyn
9K Followers 1K Following Wife. Mom of 2 teens. Former elementary school teacher. Canucks fan. Living with ALS and waiting for the day it is no longer terminal.
Sandra W. Marlowe @sandrawmarlowe
3K Followers 1K Following Married to the love of my life. Christ follower. Mom of five. Mimi to 14! Entrepreneur. Diagnosed with Bulbar ALS 3/30/2020. Fighting to live.
Shah Minokadeh, M.D. @MinoShah
4K Followers 730 Following Anesthesiologist -Johns Hopkins Hospital Pain Management -UC San Diego Now battling ALS & FDA regulatory rigidity for 100% fatal ALS
Lisa's Legacy for ALS @LisaLegacy4ALS
2K Followers 908 Following Lisa Stockman Mauriello fought for Expanded Access to an ALS treatment. Lisa passed away 8.4.21. Honor Lisa’s legacy by advocating for change for ALS.
Jamie Smith @JamieLW8
4K Followers 567 Following Mother I Widow I Pediatric Respiratory Therapist Fighting for reform in health care and research for ALS.
ALS TX DAD @AlsDads
2K Followers 894 Following USAF Vet, Father of 4, background in Healthcare Management and Disaster Response Management, ALS (pALS) Advocate (views & comments are my own)
SOD1 EndALS @CEHaddadNP
2K Followers 2K Following #ALS #fALS #SOD1 In the fight to save my family from ALS. Twin mom. Nurse practitioner. grieving daughter - 8/30/22 lost mom #33 in our family
Deb Paust @PaustDeb
1K Followers 723 Following Blessed mom, lover of snow, I AM ALS Organizing Associate, old fashion enthusiast and trying to be the change I wish to see in the world. #GoodTrouble
Mandi @RunningMama0522
2K Followers 1K Following
ALS Uncensored 🏴�.. @ScottsFight
2K Followers 1K Following Scott Craig. ALS Uncensored podcast. Digital Artist. AI Student. Typing with my eyes. Living Impossible! #ALSUncensored #ALS #EyeGazeArtist #AI
ALS ACCESS @brainmatters10
2K Followers 2K Following Fighting for a cure for ALS/MND/ and it’s variants. Fighting daily for many years, for ALS drug access. Sod1 Gene carrier.
Mike Harrington @Shankapotomas
3K Followers 929 Following Just a dude with ALS. Not dead yet, though.
No More Excuses ALS W.. @als_now
4K Followers 1K Following ALS advocate fighting for transparency, access to effective therapies, and ensuring ALS patients aren't victims of weak drug pharma gouging. YT: ALSNewsNow
Nicole Cimbura @nicolecimbura
1K Followers 2K Following
Laura Turner @LauraT24668
0 Followers 531 Following
Nyx @Nyx1185249
4 Followers 761 Following
David Ali @davidiali
358 Followers 407 Following MND advocate and supporter and working towards a world free from ALS/MND. Views/RT my own
PetalDance @dance_peta30706
36 Followers 1K Following
Rosesmat @Rosesmat145721
28 Followers 2K Following
Julie Michaelson @JuliepkMichaels
24 Followers 773 Following Found different beauties from all US states 🙀 Ready for a 1 on 1 meeting Nudes in profile! Watching this https://t.co/8qpaUgveJI
McNathe @McNathe20525
12 Followers 382 Following
Elin Adcock @elin_adcock
86 Followers 263 Following An ALS/FTD advocate and a vintage VW enthusiast, I am here to amplify voices, support caregivers, change healthcare policies and hoping to #endALS #fight2endALS
Make money easily @1cfWafB7dIllQsw
12 Followers 617 Following MEXC focuses on financial management, stocks, cryptocurrencies, digital assets and investments. Currently, new users can get free dollars when they sign up.
Margaret Sullivan @Margaret8674612
496 Followers 4K Following INTERPOL Global Cyber Programme aims to reduce the global impact of cybercrimes and protect communities.
DD Frederick @af_chief1970
2K Followers 3K Following Retired AF CMSgt. Husband, Father, Brother. Traditional Catholic, Constitutional Conservative Trump supporter. Please,🚫 DM, 🚫Porn.
SYNGAP1 Global Networ.. @SyngapNetwork
3K Followers 3K Following Global #SYNGAP1 @cureSYNGAP1 🇺🇸🇬🇧🇪🇺 @Syngap1A 🇦🇷 @SyngapAus 🇦🇺 @OSyngap1 🇨🇦🇫🇷 @syngap1Germany 🇩🇪🇦🇹@syngap1italia 🇮🇹 & 🇪🇸🇮🇳🇯🇵🇸🇪🇨🇭
Vivian Fry @VivianFry19054
92 Followers 3K Following
Rachel @rachel_MND
315 Followers 688 Following East Midlands Area Support Coordinator for @mndassoc interested in Health Psychology, Forest Bathing, carers support & volunteering
Dr KT Wong @drktwong
50 Followers 58 Following Retired pharmacist. Living with #MND since 2015. Usually post artworks of collaboration with my art therapist Kate. 🎨
ellen maugeri @EllenMaugeri
52 Followers 405 Following
Bill P Fights @WilliamP_Sr
132 Followers 338 Following Love my family and God bless the USA 🦅. Whiskey on the rocks. In the fight of my life. I hate ALS!!!!
pat wharton @Pjwharton80
578 Followers 617 Following fighting MND with everything I got 👊👊,blessed with a beautiful wife and four amazing children and 1 beautiful granddaughter xxx. love u all forever and ever x
Olga y su gemELA @Olga_Allende_T
1K Followers 1K Following Una santanderina en Zaragoza. La ELA ha irrumpido en mi vida sin pedir permiso. Maleducada!!!
Tal Gazanda @Tal_Gazanda
138 Followers 363 Following
Dr. Teresa L Clounch .. @DrTLCH2H
708 Followers 3K Following AssocVPSL&DOS&DiversityOfficer|AKA|Founder of HeadStartToHooding #H2H #DrTLCSpeaks She/Her Tweets are mine.
Jackson @lifewithALS
1K Followers 699 Following Mum of 2 wonderful boys. 3 cats. Diagnosed August 2022 with ALS determined to fight and stay strong until a cure is found. Forever hopeful 🧡💙🧡💙
Jordan @AnnmarieMND
586 Followers 890 Following Fighting to find a cure for Motor Nerones Disease! https://t.co/aOnxCOQQXK
Kristen #endals @titan1ium
230 Followers 227 Following Quiet but Loud. Educator| fuck als | I fight for sensible gun laws | trying to stick to my personal values on this platform.
Scorpio Services @ScorpioServKC
38 Followers 179 Following Happy to Clean for Kansas City and Surrounding Areas. Shine Bright with Professional Cleaning!
Betty’s Brigade Fou.. @No_More_ALS
347 Followers 530 Following We Are… the Betty’s Brigade Foundation ________ We Are… Fighting ALS Together _________________ - to raise ALS awareness & funding
NeuroSense Therapeuti.. @NeurosenseT
538 Followers 269 Following A Clinical stage Biotech company. Advancing novel therapy for ALS and neurodegenerative diseases. Nasdaq: NRSN $nrsn
Eileen Kelley @Eileen123Kelley
76 Followers 987 Following
Amy Stiens @StiensAmy
76 Followers 197 Following Battling a Terminal Illness. ALS. Trying to spread awareness about this awful disease . A wife, mom of 3 amazing kids. I love watching @Bengals @Reds . ❤️
Donald Davis @atcyyc
898 Followers 595 Following Proud father of 2 children on the spectrum! Retired Air Traffic Controller, Pilot,Sailing,#endALS,#autism aware, #f*ck Cancer, #RA, #Chiara,Conservative
Katie Feroz-Potts @klferoz
550 Followers 2K Following
Kasandra Foster @KasaAFoster
165 Followers 796 Following
MSWarriorHNYPT4HTSCT�.. @jakemar711
1K Followers 2K Following 🧡HEALTHisWealth🧡🥃 Sassenach 🥃 ITTY BITTY WEE ONE. MS: no one gets it until they get it. Want my beautiful life back💋😘#NervGen #EBVcausesMS
Raydyez @raydyez54482
60 Followers 343 Following
MND Lincolnshire @MNDLincs
98 Followers 105 Following Supporting those and their families living with Motor Neurone disease in Lincolnshire. Find us also on Facebook and Instagram
Philip Moore @philipmoore933
330 Followers 1K Following Dreams still come through only if you believe.
car128 @crayne128
232 Followers 317 Following homesteader, lover of sustainable living, hater of ALS for stealing it all away from me, and for threatening to steal my family from me. We need NurOwn now!
Brian Wallach @bsw5020
159K Followers 3K Following Dad, husband, activist, entrepreneur, unlikely movie star, living with ALS, a currently fatal disease.
Kelsie Snow @kelsieswrites
61K Followers 1K Following Storyteller, writer, podcaster @sorryimsadpod, ALS advocate, widow, mom, dual citizen (🇨🇦🇺🇸). Instagram & TikTok: kelsieswrites
I AM ALS @iamalsorg
26K Followers 799 Following I AM ALS is a patient-led movement revolutionizing how to end disease with our sights set squarely on ALS.
AZ Latina ☮️🌊�.. @aVoice4ALS
4K Followers 5K Following Political Junkie. Advocate for Enviro Justice, Foster Care, Gun Safety, DEI, Amyloidosis, PD, ALS & Rare Diseases. Love LA Sports. I block disrespectful people.
Sandra Abrevaya @sabrevaya
21K Followers 4K Following Wife to @bsw5020. Mama to spunky girls. Caregiver. CEO & Co-founder @synapticure. Co-founder @iamalsorg. Executive Producer @noc_film. All in on curing ALS.
ALS Advocacy @alsadvocacy
12K Followers 2K Following 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.
Leanne Yacyshyn @leanne_yacyshyn
9K Followers 1K Following Wife. Mom of 2 teens. Former elementary school teacher. Canucks fan. Living with ALS and waiting for the day it is no longer terminal.
Sandra W. Marlowe @sandrawmarlowe
3K Followers 1K Following Married to the love of my life. Christ follower. Mom of five. Mimi to 14! Entrepreneur. Diagnosed with Bulbar ALS 3/30/2020. Fighting to live.
Shah Minokadeh, M.D. @MinoShah
4K Followers 730 Following Anesthesiologist -Johns Hopkins Hospital Pain Management -UC San Diego Now battling ALS & FDA regulatory rigidity for 100% fatal ALS
Mayuri Saxena @Mayuri_Saxena
9K Followers 607 Following 39yo living with ALS on Life support. Author. Creative Director. Advocate. Dreamer. Public Servant. ALSFRS 1/48 https://t.co/vibJSKdIl4
Seth Poling @SethPoling10
5K Followers 392 Following Wild & Wonderful WV. FSU grad. Married to @erika_poling , Father to Liam & Bayler, ALS Warrior & advocate. #EndALS Founder of @project_seth
Sarah Nauser @SarahNauser
12K Followers 515 Following Dominating ALS one day at a time. “Love the life you live and live the life you love” Go Royals! #FightLikeAGirl
Lisa's Legacy for ALS @LisaLegacy4ALS
2K Followers 908 Following Lisa Stockman Mauriello fought for Expanded Access to an ALS treatment. Lisa passed away 8.4.21. Honor Lisa’s legacy by advocating for change for ALS.
Jamie Smith @JamieLW8
4K Followers 567 Following Mother I Widow I Pediatric Respiratory Therapist Fighting for reform in health care and research for ALS.
ALS TX DAD @AlsDads
2K Followers 894 Following USAF Vet, Father of 4, background in Healthcare Management and Disaster Response Management, ALS (pALS) Advocate (views & comments are my own)
SOD1 EndALS @CEHaddadNP
2K Followers 2K Following #ALS #fALS #SOD1 In the fight to save my family from ALS. Twin mom. Nurse practitioner. grieving daughter - 8/30/22 lost mom #33 in our family
Deb Paust @PaustDeb
1K Followers 723 Following Blessed mom, lover of snow, I AM ALS Organizing Associate, old fashion enthusiast and trying to be the change I wish to see in the world. #GoodTrouble
Mandi @RunningMama0522
2K Followers 1K Following
Claire Ryan @ClaireRyanSport
7K Followers 4K Following Producer @BBCBreakfast - RTS SJA Awards. Rob Burrow: Living with MND, Kevin Sinfield: Going the Extra Mile, Marcus Rashford: Feeding Britain’s Children.
SYNGAP1 Global Networ.. @SyngapNetwork
3K Followers 3K Following Global #SYNGAP1 @cureSYNGAP1 🇺🇸🇬🇧🇪🇺 @Syngap1A 🇦🇷 @SyngapAus 🇦🇺 @OSyngap1 🇨🇦🇫🇷 @syngap1Germany 🇩🇪🇦🇹@syngap1italia 🇮🇹 & 🇪🇸🇮🇳🇯🇵🇸🇪🇨🇭
Jake Tapper @jaketapper
3.1M Followers 11K Following Dad; husband; anchor of @TheLeadCNN & @CNNSOTU; author of The Outpost, The Hellfire Club, The Devil May Dance, and All the Demons Are Here
Jerome Tang @CoachJTang
48K Followers 1K Following Lover of Jesus, Careylyen, Seven, and Aylyn Tang ... @KStateMBB Head Men's Basketball Coach … EMAW!!! #BeReadyFamily
KSU Foundation @KSU_Foundation
5K Followers 2K Following The KSU Foundation is K-State's strategic partner for philanthropy. Tweets from our president & CEO Greg Willems are signed - GW.
Mark Styles @MarkrStyles
511 Followers 540 Following Living with Kennedy's Disease. Supported by a hard working, unpaid carer. Unpaid carers must be visible and valued.
Betty’s Brigade Fou.. @No_More_ALS
347 Followers 530 Following We Are… the Betty’s Brigade Foundation ________ We Are… Fighting ALS Together _________________ - to raise ALS awareness & funding
ellen maugeri @EllenMaugeri
52 Followers 405 Following
Carmel Grant @cdgrant6472
124 Followers 74 Following An original Derry Girl - now waging the battle as a volunteer against Motor Neurone Disease. Proud Mum of two sons and Nan to my beautiful granddaughter
Dr KT Wong @drktwong
50 Followers 58 Following Retired pharmacist. Living with #MND since 2015. Usually post artworks of collaboration with my art therapist Kate. 🎨
Jayne Harler @dfc4ever
152 Followers 396 Following Early retired civil servant.Married to Graham, wife, mother, grandmother.Mother of a recently diagnosed MND warrior 2022. Supporter of Dartford FC.
APPG on Motor Neurone.. @APPGonMND
756 Followers 150 Following This is not an official feed of Parliament. It has not been approved by either House. APPGs are informal groups of Parliamentarians with a common interest.
Alli Anthony @AlliAnthony2
150 Followers 217 Following Proud to be working for the Motor Neurone Disease Association
Patients United2EndMN.. @united2endmnd
458 Followers 73 Following We are a group of patients, working to support the drive for a cure for MND.
Jennie Starkey @StarkeyJennie
481 Followers 320 Following Mum of 4, educator, PhD student, diagnosed with MND Sept 2021. recently retired. Raising MND awareness through humour (sometimes dark) with my blog.
Olga y su gemELA @Olga_Allende_T
1K Followers 1K Following Una santanderina en Zaragoza. La ELA ha irrumpido en mi vida sin pedir permiso. Maleducada!!!
Katie Feroz-Potts @klferoz
550 Followers 2K Following
Kasandra Foster @KasaAFoster
165 Followers 796 Following
Tal Gazanda @Tal_Gazanda
138 Followers 363 Following
PA Rare Disease Advis.. @PARareDisease
786 Followers 638 Following To improve the quality of life for all those affected by rare diseases in Pennsylvania.
Ed Slater @edslater
22K Followers 2K Following Living with ALS/MND. Former Rugby Player for Gloucester and Leicester. Charlton Ath fan. No particular order 🙂
pat wharton @Pjwharton80
578 Followers 617 Following fighting MND with everything I got 👊👊,blessed with a beautiful wife and four amazing children and 1 beautiful granddaughter xxx. love u all forever and ever x
Live Like Lou @LiveLikeLou4
784 Followers 446 Following Leaving ALS better than we found it #ONWARD #LiveLikeLou
César Pulex 🇬🇹.. @PulexCesar
427 Followers 2K Following I have met great loss. I lost my son🕊💙 to Amyotrophic Lateral Sclerosis ALS ELA w/C9orf72 February 26 2022 #forever18 #tooyoung #Madridistaforever #Forever12
Jordan @AnnmarieMND
586 Followers 890 Following Fighting to find a cure for Motor Nerones Disease! https://t.co/aOnxCOQQXK
heavy_sara @heavy_sara
1K Followers 235 Following ģ𝕒Ｍέ𝐑 * ALS fighter * twitch streamer * ĤⓊмⓐ𝐍 & 𝕕𝕠𝕘 mom * whiskey drinker * 𝖒𝖊𝖙𝖆𝖑𝖍𝖊𝖆𝖉
DEB-MNDWARRIOR @DEB_MNDWARRIOR
944 Followers 909 Following https://t.co/k61gquuj0Z Hairdresser,Mother of 3 World just tipped upside down with a diagnoses of MND/ALS 💔
Jackson @lifewithALS
1K Followers 699 Following Mum of 2 wonderful boys. 3 cats. Diagnosed August 2022 with ALS determined to fight and stay strong until a cure is found. Forever hopeful 🧡💙🧡💙
Kristen #endals @titan1ium
230 Followers 227 Following Quiet but Loud. Educator| fuck als | I fight for sensible gun laws | trying to stick to my personal values on this platform.
Eileen Kelley @Eileen123Kelley
76 Followers 987 Following
Gop Debate @GopDebate
5K Followers 84 Following Hello, we are interested in GOP Debate. Are you? Then follow us!
Ajay Sampat, MD @Sampat_md
476 Followers 37 Following Father, husband, son, and brother. Clinical educator and neurologist. Person living with ALS.
AMA Ed Hub™ @AMAEdHub
12K Followers 2K Following The official online #education platform of the @AmerMedicalAssn for #CME, medical research, industry trends and more. RT ≠ Endorsements. #AMAEdHub #MedEd
ᴊᴀɴɪᴇ🫧 @plainJaniexx
2K Followers 2K Following you can’t have everything, where would you put it? #GoTiges #FightMND #FuckALS #Fight4Jon 💛🖤
Amy Stiens @StiensAmy
76 Followers 197 Following Battling a Terminal Illness. ALS. Trying to spread awareness about this awful disease . A wife, mom of 3 amazing kids. I love watching @Bengals @Reds . ❤️
Nick✌🏻❤️ @NickMayerik
15K Followers 5K Following #Eddiesinfantry #CHD #BillsMafia #IUBB Mike McCready enthusiast! #PearlJam… ACE certified fitness coach
MSWarriorHNYPT4HTSCT�.. @jakemar711
1K Followers 2K Following 🧡HEALTHisWealth🧡🥃 Sassenach 🥃 ITTY BITTY WEE ONE. MS: no one gets it until they get it. Want my beautiful life back💋😘#NervGen #EBVcausesMS
TetraMouse @TetraMouse
334 Followers 1K Following I design & manufacture computer peripherals & gadgets for persons with disabilities. Improving my products & the quality of life for my customers since 2005.
MND Lincolnshire @MNDLincs
98 Followers 105 Following Supporting those and their families living with Motor Neurone disease in Lincolnshire. Find us also on Facebook and Instagram
Prof.Dr İdrisoglu @HAidrisoglu
259 Followers 3K Following
car128 @crayne128
232 Followers 317 Following homesteader, lover of sustainable living, hater of ALS for stealing it all away from me, and for threatening to steal my family from me. We need NurOwn now!
Gene Therapy @GeneTherapy_SN
3K Followers 902 Following Scientific journal providing peer-reviewed research and commentaries on gene and cell therapies
Naty Berhane Yifru @NatyYifru
92K Followers 976 Following I work in capacity building, career development & Public Relations. I admire consistency & decency. I yearn for justice, peace, happiness & truth for all.
Seifesilassie Gebreme.. @SeifGebre
184K Followers 399 Following Passionate about the powerful Axumite Empire that shaped the history, religion & culture of Horn of Africa. #StopWarOnTigray #TigrayGenocide #TigrayCantWait
This very good girl is 15 years old and may never see K-State lose the Sunflower Showdown
K-State football players seemed to appreciate this Sunflower Showdown victory more than any other during its 15-game winning streak over KU. For good reason. This rivalry finally has some juice. Cooper Beebe said it was one of the best road environments he's been a part of.
I'm in Lawrence today to watch @KU_Football and @KStateFB battle it out in the Sunflower Showdown. I will be channeling Donna Kelce come Monday -- wanting both of her children to win and knowing at the end of the game, she will both celebrate and console.
🎶 Rockin' around the #Christmas tree #sweatshirt Get it now 👉 msixapparel.com/products/rocki…
I appreciate being a guest of @KState & @UnivOfKansas for the 💜🌻Super Stressful Sunflower Showdown.🌻💜 I shared the day with my daughter - a K-State grad who will graduate from KU Law in May. That’s 20 years of Kansas public education for her! #ksleg #ksed
Sunflower Showdown winners
The Sunflower Showdown did not disappoint on Saturday evening: trib.al/dKUKXmG
Chris Klieman's opening statement after K-State's 15th straight Sunflower Showdown victory.
Congratulations to @KStateFB on your victory in tonight's competitive Sunflower Showdown! Enjoy another year with the Governor’s Cup.🌻
DEUUUUCEEEE!! @C_Vaughn22
Wreckin' ball 💥 @C_Vaughn22 📺: FOX & NFL+ → bit.ly/3Rgu6R7
Yesterday, I celebrated 12 years sober while successfully defending my PhD. To think that at 15yo, I was relearning how to speak following a TBI and at 22yo I was dying from OUD. No matter how things seem, it’s always possible to start over and rebuild. I am humbled and grateful.
I just told my partner: Babe, I joined Costco today. His response wow you really are middle-aged woman.
I joined Costco today to buy one item. Just. One. Item. I didn’t even make it past the first display on the other side of the welcome door. Toothpaste. The kind I like. $25 for five packs. I left with $500 worth of items. They sell gas. The line was so long it looked like what…
Tbh neither can I
Cannot get over the fact that baby Tallulah Willis just looks like a very displeased Bruce Willis
Yes yes yes it’s the way
when i interviewed tallulah willis, she said she presses oil into her skin post-shower and then puts on a robe and having done that tonight i must agree that it’s simply luxurious
NIH study found that specialized PET Scan can ID loss of norepinephrine in the heart, which "predicts & precedes the loss of #dopamine in the brains" of people who develop #LewyBody #Dementia & #Parkinsons. #EndPD #ParkinsonsResearch #Neurotwitter vist.ly/hqgp
We have a new episode for ALS Caregivers & Beyond. In Episode 9: The Need to Belong, we explore how our ALS life has changed how we fit in this world of ours. rss.com/podcasts/als-c…
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