Time to #AdapttoALS! Its been getting harder to wear button up pants these days, which leads to extra time getting ready and certain anxiety in public restrooms. the other night I was in front of the urinal for so long that by the time I finished zipping up, the crowded restroom had entered in was nearly empty. So I decided to go into uniqlo and get these tapered stretchy pants with an elastic waistband. It needed to be done, I had to face facts that wearing normal pants is not going to be an option without having someone there to zip and button me up. Does it suck? Yes, of course. But the faster I can adapt and move on, the faster I can go back to enjoying life. #ALS #mnd #MNDaSG #MACNotDefeated #macvsmnd #livingwithals #positivity #uniqlosg #keepmoving
Kobe & Jordan Acrylic on card, A2 sized Dm me or check out @artistsagainstmnd 's website for details #painting #acrylic #basketball #kobe #kobebryant #jordan #michaeljordan #mnd #als #artistsagainstmnd
Belirtileri nelerdir? Başlangıç belirtileri her hastada aynı olmaz. Genellikle bir kolda ya da bacakta güçsüzlük hastanın fark ettiği ilk belirti olur. Örneğin, kalem tutmak, düğme iliklemek, anahtar çevirmek zorlaşır; ya da hasta yürürken tökezler. Bazı hastalarda ise hastalık, konuşma veya yutma güçlüğü şeklinde başlar. Hastanın kendisi ya da yakınları peltek, genizden konuşma fark eder. Kaslarda seyirme ve ağrılı kramplar bu belirtilere eşlik edebilir. Kontrol edilemeyen ağlama ve gülmeler olabilir. Mayıs ayı #ALS FARKINDALIK AYI kapsamında, toplumu bu trajik hastalığın ciddiyeti konusunda bilgilendirmek için her gün paylaşım yapacağız. Lütfen gönderilerimizi paylaşarak bize destek olun hep birlikte hastalarımızın sesi ve nefesi olalım 💐 #Als #mayisayialsfarkindalikayi #alsawarenessmonth #alsduranakadarmücadeleyedevam #StopALS #benalsninfarkindayimyasen #sesimvenefesimol @alsmnhturkiye @nadirhastaliklaragi @acurareclub @saglikbakanligi @nadirhastaligim @nowhaber.tr #alshastalığı #alsmnhderneği
Vi har fået tapas tilbage på menukortet! 🤩 Hvem ønsker du at spise tapas sammen med? 🥳 Tapas bestående af: Minicroissant med hjemmelavet hønsesalat Riskugle med chilimayonnaise Lakseruller med flødeost Canapé med grillet gedeost 2 slags charcuteri Ostestænger, oliven & pesto Brød & knækbrød Kage kr. 179,- Reserver bord nu på tlf. 7447 1222, eller på [email protected] #augustenborg #sønderborg #fjordhotelaugustenborg #als #nordals #sønderjylland #restaurantsvanen #svanen #augustenborgfjord #hotel #restaurant #food #passion #velbekomme #tapas
Güzel bir Trabzon kursundan kareler... ✔ ERC- İleri Yaşam Desteği Uygulayıcı Kursu & İYD Kursu. ✔ 27, 28 Nisan / April 2024, Ankara, Turkey. The ALS Provider Course has done in Trabzon. Many thanks for all participants and instructors of ERC. #iyd #als #cpr #kurs #course #resusitasyondernegitürkiye #TurRC #turkishresuscitationcouncil #erc #eğitim #education #türkiye #turkey
AIS Windows offers a comprehensive range of doors and windows in uPVC and Aluminium substrates. * Customisable windows with acoustic-soundproof , energy efficient and water-resistant solutions. * Anti- pollution and smog resistant * Durable and hassle-free installation #AlS #AlSWindowschennai #verleezdecors #chennaiwindows #upvcwindow #aluminiumwindows #doorsandwindows #chennaiarchitects #upvc #aluminium #heatresistant #peaksummer #windowsolution #chennaibuilders #architectsofchennai
MOEDERDAGACTIES VOOR ALS Een mooi bloemetje in een vaas of een heerlijke moederdagstaart. Ook dit jaar heeft Jeanet van Holsteijn (ALS Patiënte) weer twee mooie acties opgezet om geld op te halen voor Team Sjaan. Samen duiken zij op 10 augustus het water De Lee in om geld op te halen voor onderzoek naar ALS. #als #zenuwspierziekteals #alocalswim #alocalswimwestland #moederdag #bloemen #taart #goeddoel
【LIVE配信】今日21時からM's channel YouTube LIVE配信やりまーす！！ 翔ちゃんねる セカンドチャンネルURL https://youtube.com/@shochannel24?si=B-hoBFWI1XU0yBIs M's channel公式LINE ID 19750121 Instagram URL M's channel公式アカウント 翔 https://instagram.com/mschannel2020 TikTok URL 翔 www.tiktok.com/@ms.channel59 Amazonほしい物リスト https://www.amazon.jp/hz/wishlist/ls/DAUZVX4EDNIM?ref_=wl_share #病気 #トーク #国指定 #難病 #ALS #筋萎縮性側索硬化症 #YouTube #翔ちゃんねる #セカンドチャンネル #病院 #面会 #制限 #施設 #呼吸 #肌荒れ #乾燥 #呼吸器 #誤嚥性肺炎 #緊急 #息ができない #痰 #肺 #処置 #LIVE #配信 #生
孫たち大集合 GW後半 孫たち４人が集合 孫たち連れて近くの公園へ 楽しかったー♪ かみさんのブログを更新しました ぜひ覗いてみてくださいね！ 検索ワード 奈津美ばあばの日々 ALSを生きる .:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.: Date: 2024.05 Location: Unzen City Japan Gear: Canon EOS R6 Lens : RF 50mmF1.8 Edit: Lightroom .:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.: PhotoBase ありよし : blog https://www.photobase-ariyoshi.com/ ALSを生きる https://www.natchan-als.com .:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.:.: #als #筋萎縮性側索硬化症 #九州ぐらむ #raw_japan_ #西日本の絶景 #アイシテルウンゼン #雲仙の休日 #kyushugram #my_amakusa #photo_nihonbungei #my_eos_photo #canon_eos_r6 #雲仙市に住もう #うんぜんぐらむ #出張撮影 #出張カメラマン #photographer #海が見えるおうち写真館 #孫たち #百花台公園
Belirtileri nelerdir? Başlangıç belirtileri her hastada aynı olmaz. Genellikle bir kolda ya da bacakta güçsüzlük hastanın fark ettiği ilk belirti olur. Örneğin, kalem tutmak, düğme iliklemek, anahtar çevirmek zorlaşır; ya da hasta yürürken tökezler. Bazı hastalarda ise hastalık, konuşma veya yutma güçlüğü şeklinde başlar. Hastanın kendisi ya da yakınları peltek, genizden konuşma fark eder. Kaslarda seyirme ve ağrılı kramplar bu belirtilere eşlik edebilir. Kontrol edilemeyen ağlama ve gülmeler olabilir. Mayıs ayı #ALS FARKINDALIK AYI kapsamında, toplumu bu trajik hastalığın ciddiyeti konusunda bilgilendirmek için her gün paylaşım yapacağız. Lütfen gönderilerimizi paylaşarak bize destek olun hep birlikte hastalarımızın sesi ve nefesi olalım 💐 #Als #mayisayialsfarkindalikayi #alsawarenessmonth #alsduranakadarmücadeleyedevam #StopALS #benalsninfarkindayimyasen #sesimvenefesimol @alsmnhturkiye @nadirhastaliklaragi @acurareclub @saglikbakanligi @nadirhastaligim @nowhaber.tr #alshastalığı #alsmnhderneği
Our puppies have been busy baking delicious cupcakes! What have your MND puppies been up to? If you'd like a baking buddy of your own, adopt an MND NSW puppy now at https://www.online.mndnsw.org.au/collections/plush-toy/products/mnd-puppy Every puppy you adopt helps us raise vital funds to support people living with MND, their carers and families. #ALS #MND #mndnswpuppies #adoptapuppy #baking #cupcakes #MNDNSW #puppy
Non nobis solum nati sumus – Non solo per noi stessi stiamo nati. #esserci #suem #118 #emt #padovaemergenza #prontoconselve #bls #ambulanza #soccorritore #esserci #echovictor #day #work #volontarisoccorritori #nurse #als #randevu #elisoccorso
We as ALS team always concern about solving issues of Farmers… #HappyToHelp #tanzania #ALS #AnimalCare #ashishlifescience #Animalpharma #poultryfarming #animalhealth #livestockfarming #nutrition #ProfitableFarming #follow #knowledgesharing #sharepost
Sunset ในวันเมฆหนา 🌤️ #Amwaytrip #extraordinary #extraordinarylife #travel #ALS #Amppafit
In honor of ALS Awareness Month this May, we are proud to introduce our latest creation: the ALS Cause Candle, featuring the uplifting fragrance of Lemon Drops. Proceeds from each candle sold will go to ALS ARIZONA, an organization tirelessly working to improve the lives of ALS patients and their families. 🍋Lemon Drops: Let this exquisite blend of lemon, mint, and vanilla take you on a sensory journey. With every inhale, experience a burst of sunshine, and with every exhale, find solace and contentment. From the tangy notes of lemon to the sweet embrace of vanilla and sugar crystals, this fragrance is a celebration of life’s simple pleasures and cherished memories. Top: Lemon, Citron Zest, Orange Pulp Middle: Mint Sprig, Sea Salt, Lemongrass Bottom: Vanilla, Sugar Crystals Together, let’s shine a light on ALS and show our unwavering support for those bravely battling this relentless disease. Join us in spreading awareness, sharing hope, and making a difference, one candle at a time. #als #miabellacandles #alsarizona #lemondrops #wixnaromasmb #candles #candlesofinstagram #handpouredcandles
Keller Army Community Hospital recognizes May as Amyotrophic Lateral Sclerosis (ALS) Awareness Month. ALS is also known as Lou Gehrig’s Disease. Keller seeks to increase awareness of ALS and of the severe physical, emotional, and financial burdens it creates for people living with the disease and their families. ALS is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord. There is no cure for ALS yet. Motor neurons reach from the brain to the spinal cord and from the spinal cord to the muscles throughout the body. They govern voluntary movements and muscle control. ALS causes these motor neurons to degenerate over time until they eventually die. When the motor neurons die, the brain can no longer initiate and control muscle movement. When voluntary muscle action is progressively affected, people may lose the ability to speak, eat, move, and breathe. ALS was identified in 1869 by French neurologist Jean-Martin Charcot, but it became more widely known internationally in 1939 when it ended the career of baseball’s most beloved players, Lou Gehrig. For many years, ALS was commonly known as Lou Gehrig’s Disease. For more information on ALS, go to the ALS Association page at https://www.als.org/. @als #ALS #ALSInThisTogether
【拡散希望】 いよいよ、今月の26日に迫ってきました！！ 「重い障害があるから…」 「呼吸器など医療依存度が高いから…」 だから、病院や施設で過ごすしかないんだ…… そんなことはありません‼️‼️ じゃあ、どうすればいいの？？ その答えが26日に聞けます👍 しかも、当事者の方達が実際に話してくれるので、説得力が違います！ ぜひぜひ、たくさんの当事者さん、ご家族、多職種の方に聞いて欲しいです！！！ 一人でも多くの方に講演会のことを知って欲しいので、どなたも拡散して頂いて構いません。というより、拡散して下さい！お願いします🙏 参加出来ない方も、当日、LIVEで視聴が出来ます👌 視聴用のQRコードとURLも記載しておくので、お気軽にご参加下さい！ https://vimeo.com/event/4273771 宜しくお願いします🙇♀️ #重度障害 #重度訪問介護 #自薦ヘルパー #広域協会 #難病 #長野県 #佐久市 #ALS #筋ジストロフィー #脊髄損傷 #拡散希望 #長野市 #上田市 #新潟県
Behind every great WOMEN is another WOMEN 🔥🔥💪 #dreamteam #teammugusari #als #paris #europe #amway #amwaybusinessowner #enterpreneur #fyp #fyppppppppppppppppppppppp #viral #trending #france #dreamcometrue #cityoflove #travel #women #womenempowerment
The trial is planned to launch later this year. If positive, data will be used to back an application for approval. Link in our bio to read. #ALS #AmyotrophicLateralSclerosis #ALSDisease #ALSTreatment #ALSResearch
amazing start to #ALS Awareness Month @alsunitedchi #alsunitedchi #alsawareness #endals
IN THE NEWS: Our May eNewsletter is in your inbox now or you can view it online! This month, we celebrate #ALS Awareness Month! Learn more about the ways that you can show your support and take action. Explore compelling and diverse stories from #ourALScommunity and key facts about ALS. Please proudly share your commitment to our mission priorities by posting on social media and tagging "@youralsnetwork". Let’s #cureALStogether! Please check our calendar for upcoming events and online connection groups this month and beyond. And be sure to visit the News and Stories which serves as a valuable resource for timely updates about ALS, our community, and ALS Network. Find out about our efforts in ALS research, care services, advocacy, and important news and resources. Read it today and share it with others! bit.ly/2024-05-eNews
3 YEARS 201 Days If you are looking to help spread awareness for ALS please contact Mitch Shaver and for $35.00 you can Rock the same hat that I’m wearing in my videos 👍🏻 Keep fighting Mitch Shaver because Your Not Alone In The Fight !! For those of you who don’t know, my friend Mitch Shaver is currently battling ALS so all of my push-ups will be in his honor. Mitch has the heart of a Lion and is a fierce competitor which is why he continues to fight and is unwilling to give in to this terrible disease. Keep fighting brother. We Love You!!! #MLSVERSESALS #keeppushingforward #ALS #ALSofMichigan #TeamGarbo Thank you all who have been following my post. I’ve continue to do my 25 pushups and posting them here. I also want to do them to bring awareness to ALS also know as Lou Gehrig’s Disease I’m hoping it will get people to read my post and possibly bring awareness to PTSD and ALS This all started by me being nominated by Pastor Dean Smith for a 25 push-ups for 25 days challenge to raise awareness for PTSD (Post Traumatic Stress Disorder), anxiety and depression which drives people to take their own lives. IT’S OK NOT TO BE OKAY. Let's make sure that everyone knows how important mental well being is and if you need to reach out know you are not alone and we are here for you. Don't be afraid to speak out.
𝐀𝐋𝐒, or 𝐀𝐦𝐲𝐨𝐭𝐫𝐨𝐩𝐡𝐢𝐜 𝐥𝐚𝐭𝐞𝐫𝐚𝐥 𝐬𝐜𝐥𝐞𝐫𝐨𝐬𝐢𝐬 is a progressive and incurable nervous system disease that causes a loss of muscle control and eventually paralysis. There is no known cure, but treatments can help manage symptoms. Together, let’s raise awareness to ALS this month. #oneauscare #ndis #ndisprovider #ALS #Australia #Melbourne #Adelaide
⚠️⚠️⚠️1 EM CADA 400 PESSOAS DESENVOLVERÁ ESCLEROSE LATERAL AMIOTRÓFICA 🟥Dificuldade em estimar o número exato de pessoas com ELA devido a disparidades nos relatórios de dados entre países e incertezas nos diagnósticos. 🟥Estudos indicam que cerca de 1 em cada 400 pessoas desenvolverá ELA durante a vida. Homens têm maior probabilidade de serem diagnosticados com ELA do que mulheres. 🟥A idade também influencia a probabilidade de desenvolver ELA, com riscos aumentando com a idade. 🟥Limitações nos dados disponíveis, principalmente da Europa, sugerem a necessidade de estudos adicionais em diferentes populações. 🟥Apesar de ser considerada uma doença rara, a ELA tem uma prevalência significativa, com um risco de 1 em 400 ao longo da vida. 🟥Maior conscientização sobre o risco de 1 em 400 poderia incentivar investimentos em pesquisas para encontrar tratamentos para a ELA. Curta, comente e compartilhe! COMPARTILHEM!!! A ESCLEROSE LATERAL AMIOTRÓFICA NÃO É TÃO RARA ASSIM! Siga: @falandodaela #als #amyotrophic_lateral_sclerosis #escleroselateralamiotrofica #elabrasil #epidemiologia
2024.5.4 この間前の職場の先輩がアロマタッチをやりに来てくれた😄 雨で遠い中ありがとうございました🙇♀️✨ やる前は体が重くてだるさがあったけど、 やってもらってからは体が一気に楽になった気がした🥰 その後先輩と色んな話してバイバイしてから 夜ご飯作り始めたんだけど、 なんとなーく右腕が上がりやすく感じた👀！ ずっとじゃなくて少しの間だけだったけど嬉しかった😭💕 普段もできるように2つ作ってくれて 毎晩旦那に背中をやってもらい… 朝と昼は自分で足裏にやってる☺️ アロマタッチするようになってから 朝起きた時の体の重だるさが全く違う😊 まじでありがたい😭✨ #ALS #筋萎縮性側索硬化症 #絶対負けない #絶対勝つ #ドテラ #アロマタッチ #最高 #ありがとうございます #1日1日 #大切に #楽しもう
Helt omöjligt att somna inatt. Massor mä tankar som far och flyger. Så klockan två petar jag mig upp och går ner och äter. Macka och ett glas mjölk brukar kunna funka. Igår var jag på läkarbesök för en uppdatering kring sjukdomsförloppet och mitt mående över lag. Min läkare tycker att jag ser välmående ut. Ja jag är pigg och lever på så mycket jag bara hinner och orkar blir mitt svar. Han hade glädjande nyheter att komma med. Jag fyller kriterierna för en fas2-studie i Lund som ska dras igång inom kort. Är inte helt hundra mä vad det riktigt innebär än så det får jag återkomma mä. Iaf så känns det positivt att äntligen matcha något jag kanske kan ha nytta av. Trots att jag är positiv och hoppfull i min ALS så är det alltid påfrestande känslomässigt att vara på sjukhuset. Där blir det så himla nära och sant! Trots att jag är stark och inte är så påverkad än så vet jag aldrig om min sjukdom är smygande el tvär. Den kan plötsligt göra helomvändning och kanske kan jag helt enkelt inte svälja en dag när jag vaknar el lyder inte mina armar mig. Att bli påmind om det är smärtsamt och särskilt som jag verkligen har bestämt mig för att leva fullt ut medan jag fortfarande kan. Jag är inte rädd för sanningen men att leva i mitt luftslott är mycket roligare och tryggare. När vi väl är hemma har jag tänkt att ta hand om alla medelhavsväxter som jag övervintrat i förrådet under växtlampa. Nu var det dags. Behöver plantera om en del . Mina händer är fumliga och med lyften blir min balans förvirrad över extra tyngd att ha koll på. Ett litet felsteg och fallet är där. Handfallen trillar jag bakåt i en pallkrage. Jag tar mig envist upp och fortsätter men då är det dags igen. För många krukor överallt och jag gör en felbedömning och tappar balansen. Denna gången framåt . Det går liksom inte att räta upp sig när väl kroppen tappat det. Mina armar och händer orkar inte längre vare sig ta emot mig el trycka ifrån för att komma på benen. Denna gången blir jag liggandes ihopkrupen och tårarna rinner och det gör ont i armar och knän. Sen kommer peter springandes och undrar varför jag inte kan vänta så han kan hjälpa mig. Han håller om mig och för första gången forts. I kommentarerna..
With only 2 more days until our Live Like Lou Hit-A-Thon, your donation makes the biggest difference. Help support ALS with the donation link in our bio.💙⚾️ #livelikelou #als #phideltatheta #donate
Vento 2.0 gli 💣 . . . . . . . . . #mundofierrero🔥 #fierrosalpiso🔥 #als #alsopi #playa #planchado #rebajados #remachadosalsopi #vento #vw #vwgolf #volkswagen #alemania🇩🇪 #alemania #gli #galvez
Join us at Kauffman Stadium on Sunday, June 2, for the @kcroyals' #LouGehrigDay game against the @padres! Before the game, we'll join our friends from the @permobilfoundation for a special presentation to an ALS family on the field. ⚾ The Blue Moon Taproom, located in the right field at Kauffman Stadium, has been reserved for Live Like Lou, Permobil, and our friends from Lou Gehrig's fraternity, Phi Delta Theta. 🥳 Your ticket includes access to the taproom, food, beverages (alcohol and non-alcoholic), and the ability to watch the game from this section. 🌭🍺 Gates open at 11:40 a.m. Get tickets through the 🔗 in our bio. #livelikelou #als #lougehrig #lougehrigsdisease #mlb #baseball #LG4Day
Here is this week's most read article featured on our #ALSNewsToday website! Are you caught up? Link in our bio to read. #ALS #AmyotrophicLateralSclerosis #ALSDisease #ALSTreatment #ALSResearch
Op bezoek bij Bernadette #lourdes #alsawareness #ALS #reizen #wheelchairlife #fightmind #motorneuronedisease #lougehrigsdisease #remedie #rayban #disabled #france
May is ALS awareness month!! My mom was diagnosed with ALS around July 2023 & started treatment without her insurance help around September. Because it took awhile for her to get her treatment the disease progressed quickly & took most function from her left leg. Since she’s been on Qalsody she hasn’t progressed much further.. thank God🙏. She is currently in a wheelchair most of the time to get around. My mom has a rare genetic mutation of ALS called (Sod1 A5V). This is actually what my grandfather Ron passed away from, he passed after 7 short months of having the disease. It’s a very aggressive form of ALS. Our mission is to help spread the word. The last time there was a lot of donations to the studies of ALS was during the ice bucket challenge. Here is a link to donate to research for ALS : https://donate.mn.als.org/give/326358/#!/donation/checkout It’s a dream of my moms to travel the world. My family & I are going together as much as we possibly can. If you wish to donate to my mom I have a link attached to my profile to help with her travel & health expenses. We appreciate & love all that have help us thus far.🙏🙏❤️ If you wish not to donate please share the last picture to spread awareness about ALS. #alsawareness #alsawarenessmonth #als
THANK YOU Papaw Randy and Ted Duty ! I know this was a big job (much bigger than Amazon led us to believe)! You guys are truly such a huge blessing in my life! But what a great addition and now I’m able to enjoy the outdoors a little more! 💙💙💙 #EndALS #wheelinforals #nowhiteflags #nottodayals #Godsgotthis #teamjacobwv #ALS #ion363 #Jacifusen #ALSawareness #joshua1v9 #ButGod @racingforals @osuwexmed @marshall_health
3 of my favorite timepieces - Omega Speedmaster Ed White 321, A Lange & Sohne Lange 1, and Rolex Day-Date (from left to right) #omega #speedmasteredwhite321 #als #lange1 #rolex #daydate #icebluedial
🚧 Afinal, obra sem autorização do condomínio poderá ser demolida? Arrasta para o lado que eu te conto 👉🏼 Qual sua opinião sobre a decisão? ⚖️ ALS Advocacia Associada #obra #demolicao #condominio #direitoimobiliario #regracondominio #irregularidadeconstrucao #direitocivil #ALS #ALSadvocacia
内覧会に来ていただいた方への御礼にデ カルネロ カステのいいとも会マーク入りカステラをお配りしました♪ 次回から、いよいよ内部のご紹介をしていきたいと思います♪ #通所リハビリテーション #松阪市 #decarnerocaste #ケアカフェ #パーキンソン病 #als、
🚧 Afinal, obra sem autorização do condomínio poderá ser demolida? Arrasta para o lado que eu te conto 👉🏼 Qual sua opinião sobre a decisão? ⚖️ ALS Advocacia Associada #obra #demolicao #condominio #direitoimobiliario #regracondominio #irregularidadeconstrucao #direitocivil #ALS #ALSadvocacia
HELLO! Do you have your STRONGER WITH MOE CHICKEN BBQ tickets yet? Only $20 and ALL MONEY goes to the ALS ASSOCIATION OF UPSTATE NY! Great food, great raffle items, and don't forget the CORNHOLE TOURNAMENT! #als #UntilTheresACure #findacure #cornhole #fightals #fundraiser #donateforacause #alsawareness #chickenbbq #cornholetournament #Donation #CureALS #hope
Exciting News! Live Like Lou is thrilled to launch Lou's Crew! Inspired by the crew that wrapped their arms around Lou Gehrig and supported him upon receiving his fatal ALS diagnosis, you too can join the team to promote ALS awareness, raise money for ALS research, and leave ALS better than we found it. Raise $444 during the calendar year, and earn a well-deserved spot as a proud member of Lou's Crew. Join Lou's Crew members ⭐ Whitney and Wynter who are hosting a lemonade stand ⭐ Gehrig and Giada who are continuing to participate in Live Like Lou events ⭐ Jeff Lyster who is raising money on his run across Kansas Together, let's make a difference and create positive change in our ALS community. Are you up for the challenge? Join Lou's Crew today through the 🔗 in our bio. #livelikelou #als #alsawareness
🚨𝐈𝐫𝐨𝐧 𝐏𝐡𝐢 #𝟐𝟏𝟏𝟗 🦹♂️ - Creed Roschyk (@creedroschyk) ⚔️ - Ohio Eta (@cwruphidelt) 💰 - $1,000 💪🏼 - Lifts for Lou Weightlifting Competition 📆 - 193rd Iron Phi of 2024 Join us at www.ironphi.org. #ironphi #livelikelou #phideltatheta #phidelt #ALS #lougehrig #lougehrigsdisease
Amyotrophic lateral sclerosis (ALS), formerly known as Lou Gehrig’s disease, is a neurological disorder that affects motor neurons, the nerve cells in the brain and spinal cord that control voluntary muscle movement and breathing. As motor neurons degenerate and die, they stop sending messages to the muscles, which causes the muscles to weaken, start to twitch (fasciculations), and waste away (atrophy). Eventually, in people with ALS, the brain loses its ability to initiate and control voluntary movements such as walking, talking, chewing and other functions, as well as breathing. ALS is progressive, meaning the symptoms get worse over time. The U.S. Food and Drug Administration has approved several drugs for ALS that may prolong survival, reduce the rate of decline, or help manage symptoms. However, there is currently no known treatment that stops or reverses the progression of ALS. Early symptoms include: Muscle twitches in the arm, leg, shoulder, or tongue Muscle cramps Tight and stiff muscles (spasticity) Muscle weakness affecting an arm, a leg, or the neck Slurred and nasal speech Difficulty chewing or swallowing As the disease progresses, muscle weakness and atrophy spread to other parts of your body. People with ALS may develop problems with: Chewing food and swallowing (dysphagia) Drooling (sialorrhea) Speaking or forming words (dysarthria) Breathing (dyspnea) Unintended crying, laughing, or other emotional displays (pseudobulbar symptoms) Constipation Maintaining weight and getting enough nutrients #medical #medicine #doctor #health #healthcare #hospital #doctors #covid #medicalstudent #neet #surgery #medstudent #medschool #medico #science #medicalschool #pharmacy #surgeon #anatomy #nursing #love #PD #Parkinson #MS #multiple_sclerosis #ALS #Amyotrophic_Lateral_Sclerosis
Heading into the weekend with a sweet treat! Look closely, these ones say make ALS history We hope this weekend is whatever you need it to be! #sweettreat #mnms #weekendvibes #friyay #saturdayvibes #saturdayfun #inspiration #weekend #sundayfunday #flashesofdelight #ALS #LouGehrigsDisease #icebucketchallenge #makeALShistory
🚨𝐈𝐫𝐨𝐧 𝐏𝐡𝐢 #𝟐𝟏𝟏𝟖 🦹♂️ - Simon Cohen (@simon.cohen15) ⚔️ - Ohio Eta (@cwruphidelt) 💰 - $1,000 💪🏼 - Lifts for Lou Weightlifting Competition 📆 - 192nd Iron Phi of 2024 Join us at www.ironphi.org. #ironphi #livelikelou #phideltatheta #phidelt #ALS #lougehrig #lougehrigsdisease
“I hope that other people with ALS will see – don’t give up.” This #MemorialDay, we honor the memory of Scott, a post-911 #Veteran who battled #ALS while fulfilling his bucket list. Start an #HonorYourHero fundraiser in memory of your hero via the link in our bio.
8 miles done today with @codyrigsby. But more importantly we have raised over $4,000 for The ALS Association . I am BLOWN away by the love and support of our community, friends, and family. Let’s keep this momentum going!! If you haven’t already please consider donating! Hey @onepeloton you match my ending donation amount and I match my miles?! Help me in supporting The ALS Association @als ❤️ Link to the FB fundraiser is in my bio. #als #alsawareness #alsawarenessmonth #peloton #pelotonmoms #pelotoncommunity
May is ALS Awareness Month ❤️ Living with ALS can be incredibly challenging, but plant medicine is offering new avenues of relief and comfort for many patients. 🙌 For those battling ALS, the symptoms can be overwhelming - from muscle stiffness and spasms to pain and difficulty sleeping. But plant medicine has shown promise in alleviating these symptoms, providing much-needed relief and improving quality of life. 💫 Research suggests that alternative plant medication can help manage muscle spasticity, reduce pain, and enhance sleep quality - all crucial aspects of managing ALS symptoms. 🛌💊 With the guidance of healthcare professionals, many patients are exploring plant medicine as part of their treatment regimen. It's not about getting high, it's about finding relief and comfort in the midst of a difficult journey. 🌱💚 If you or a loved one are battling ALS, consider discussing these options with your healthcare provider to see if it could be a helpful addition to your treatment plan, as ALS is a qualifying condition for this treatment alternative in the State of Mississippi. At Bragg Canna, we're here to help you #MakeYourselfComfortable and – together – we can explore new paths to comfort and hope 🫶 💪 #ALSawareness #HopeAndHealing #jackson #pearl #tupelo #ms #mississippi #patientsfirst #patienteducation #ALS #AmyotrophicLateralSclerosis #LouGehrigsDisease #BraggCanna #thesipp #thesip #mmjms
May is ALS Awareness Month ❤️ Living with ALS can be incredibly challenging, but plant medicine is offering new avenues of relief and comfort for many patients. 🙌 For those battling ALS, the symptoms can be overwhelming - from muscle stiffness and spasms to pain and difficulty sleeping. But plant medicine has shown promise in alleviating these symptoms, providing much-needed relief and improving quality of life. 💫 Research suggests that alternative plant medication can help manage muscle spasticity, reduce pain, and enhance sleep quality - all crucial aspects of managing ALS symptoms. 🛌💊 With the guidance of healthcare professionals, many patients are exploring plant medicine as part of their treatment regimen. It's not about getting high, it's about finding relief and comfort in the midst of a difficult journey. 🌱💚 If you or a loved one are battling ALS, consider discussing these options with your healthcare provider to see if it could be a helpful addition to your treatment plan, as ALS is a qualifying condition for this treatment alternative in the State of Mississippi. At Bragg Canna, we're here to help you #MakeYourselfComfortable and – together – we can explore new paths to comfort and hope 🫶 💪 #ALSawareness #HopeAndHealing #jackson #pearl #tupelo #ms #mississippi #patientsfirst #patienteducation #ALS #AmyotrophicLateralSclerosis #LouGehrigsDisease #BraggCanna #thesipp #thesip #mmjms
Do you experience fasciculations, or muscle twitching? See why it happens and how you might be able to help it. Link in our bio to learn more. #ALS #AmyotrophicLateralSclerosis #ALSCommunity #LivingWithALS #ALSAwareness
Each May during #ALSAwarenessMonth, we come together to shine a light on people living with ALS. People like Shelby, who was diagnosed at just 22 years old. Even as she faces the challenges of living with the disease, Shelby is finding ways to advocate for change, not just for herself, but the entire #ALS community. Read her story: https://bit.ly/Shelby-ALS ( #LinkInBio)
Last weekend Kayleigh, Ashley and Kieran got just a little bit muddy when they smashed the 5k Wolf Run! The team took on the challenge in memory of Kayleigh's Mom, Dawn, who had MND. "Mom was my world and losing her was hard for all the family. She was the glue that kept us all together. She was very determined to raise money and awareness for MND, so we try our best to continue what she started." They raised over £500 for her Tribute Fund 💙 ______________________ #mnd #als #motorneuronedisease #awareness #fundraisers #charity #mndhero #wolfrun #tributefund #teamwork #challenge #fundraising #fundraisingchallenge #tcs #teammnd
Our “JOEY O ALS” walk T-shirts are available for pre-order now. You can place your order through the link in our bio, located under LinkTree. The first slide, you'll see the actual color of the shirt, while the second slide features images of each design. Men’s sizes range from S to 5XL at $20 each, Women’s V-neck sizes range from S to 2XL at $20 each, Youth sizes range from XS to XL at $12 each. #als #WALKALS #donate #alsawareness #alssupportthecause
🚨𝐈𝐫𝐨𝐧 𝐏𝐡𝐢 #𝟐𝟏𝟏𝟕 🦹♂️ - Eliot Wagner (@eliot.wagner15) ⚔️ - Kansas Gamma (@ksuphidelt) 💰 - $1,003 💪🏼 - 4.44-Mile Run + 44 Push-Ups, Sit-Ups, Squats 📆 - 191st Iron Phi of 2024 Join us at www.ironphi.org. #ironphi #livelikelou #phideltatheta #phidelt #ALS #lougehrig #lougehrigsdisease
𝗦𝘁𝗶𝗰𝗵𝘁𝗶𝗻𝗴 𝗔𝗟𝗦 𝗵𝗲𝗲𝗳𝘁 𝗵𝗼𝗼𝗽 𝘃𝗼𝗼𝗿 𝗱𝗲 𝘁𝗼𝗲𝗸𝗼𝗺𝘀𝘁 𝗲𝗻 𝗱𝗲 𝗱𝗼𝗼𝗿𝗯𝗿𝗮𝗸𝗲𝗻 𝘃𝗮𝗻 𝗱𝗲 𝗮𝗳𝗴𝗲𝗹𝗼𝗽𝗲𝗻 𝗷𝗮𝗿𝗲𝗻 𝗺𝗼𝘁𝗶𝘃𝗲𝗿𝗲𝗻 𝗵𝗲𝗻 𝗺𝗲𝗲𝗿 𝗱𝗮𝗻 𝗼𝗼𝗶𝘁 𝗼𝗺 𝗱𝗼𝗼𝗿 𝘁𝗲 𝗴𝗮𝗮𝗻! Inmiddels weten veel mensen dat het Meerdaags Wandelevenement Venray zich ook inzet voor dit belangrijke doel en wij vinden het van groot belang dat mensen daarom meewandelen. Hoe meer mensen meedoen, hoe meer we ophalen, en hoe meer we kunnen bijdragen aan het realiseren van een wereld zonder ALS. @stichtingalsnederland zet zich in voor het bestrijden van de dodelijke ziekte ALS. Met jouw hulp financieren ze wetenschappelijk onderzoek naar de oorzaak en behandeling van ALS, PSMA en PLS. Hun inzet gaat verder dan alleen onderzoek; ze streven ook naar een betere kwaliteit van zorg en leven voor patiënten en hun naasten. Jouw steun is essentieel, en dankzij acties zoals het onze, hebben ze al grote vooruitgang geboekt. Meld je dus hier aan https://wandelevenementvenray.nl/inschrijven en zet je ook in voor een wereld zonder ALS ❤️. @volgers #ALS #Onderzoek #Steun #Vooruitgang #wandelen #wandelenindenatuur #wandeleninnederland #gezond #trainen #wandeltocht #nederland #bewegen #bewegenisgezond #vierdaagse #limburgsepeel #kennedymarssomeren #4daagse
Quem assopra as velinhas dos 5 anos de ALS hoje é o Diego, nosso Supervisor de Contas! 🎉 Seu profissionalismo e sua dedicação agregam um valor enorme para a #OneALS. Essa placa é um merecido reconhecimento por tudo isso. Que venham mais anos de sucesso e realizações. #ALS #rightsolutions #rightpartner #equipeexcepcional #5anosdeALS #placasquinquênios
My good family friend Louis Del Ray was diagnosed with Amyotrophic Lateral Sclerosis (ALS) also known as Lou Gehrig’s Disease. We are supporting here at Northern Vintage Vibez, spreading awareness for the him and the ALS foundation to raise money for his cause. Also rocking his cool t shirts. Please if you have anything you’d like to donate visit his go fund me it would be greatly appreciated 🖤 https://www.gofundme.com/f/lous-als-keeponbuzzin-fundraiser?utm_campaign=p_cp+share-sheet&utm_medium=more&utm_source=customer&utm_term=undefined ☝️
#tilva #tilvastålsmycken #smyckedesign #jewellrydesigns #stålsmycken #stalsmykker #stainlesssteeljewellry #jewellry #personligasmycken #ringar #armband #halsband #necklace #örhänge #webshop #smycke #ring #halsband #sweden #hockey #borjesalmingalsstiftelse #als #borjesalming #börjesalming #borjesalmingfoundation #swedishdesigned #eriksberg