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Lisa's Legacy for ALS Profile
Lisa's Legacy for ALS

@LisaLegacy4ALS

Followers
2K
Following
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Media
199
Statuses
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Lisa Stockman Mauriello fought for Expanded Access to an ALS treatment. Lisa passed away 8.4.21. Honor Lisa’s legacy by advocating for ALS.

Summit, NJ
Joined March 2021
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@LisaLegacy4ALS
Lisa's Legacy for ALS
3 years
Remembering Lisa with affection, admiration and love today on the one year anniversary of her passing. We honor her courage and legacy. Lisa you continue to guide and inspire. You are a Northstar shining bright for all fighting ALS. #endALS . Join the fight at @iamalsorg
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@LisaLegacy4ALS
Lisa's Legacy for ALS
2 days
RT @CathyStandish: There are no party politics involved with ALS. “No two people experience ALS the same way. ” That is why research for a….
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@LisaLegacy4ALS
Lisa's Legacy for ALS
4 days
RT @Jeanc9orf72: Please share !.
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@LisaLegacy4ALS
Lisa's Legacy for ALS
4 days
RT @YourALSguide: Learn more at #als
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@LisaLegacy4ALS
Lisa's Legacy for ALS
8 days
RT @CathyStandish: If you have a moment today, please consider taking this survey from the Vanderbilt ALS Research Center. Your participati….
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@LisaLegacy4ALS
Lisa's Legacy for ALS
8 days
RT @alsadvocacy: I sure didn’t see this one coming… Neurizon Therapeutics has entered into a global licensing deal with Elanco Animal Healt….
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@LisaLegacy4ALS
Lisa's Legacy for ALS
23 days
RT @iamalsorg: The #LongitudePrizeOnALS has launched! 🙌 This global, $10M challenge prize will drive AI-led innovation to transform drug di….
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@LisaLegacy4ALS
Lisa's Legacy for ALS
25 days
There are some special people in the ALS community. Such an honor and privilege to work with one of the best. Thank you for the 🌻🌻.
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@LisaLegacy4ALS
Lisa's Legacy for ALS
27 days
RT @alsadvocacy: This. .
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@LisaLegacy4ALS
Lisa's Legacy for ALS
28 days
RT @AhmadAlKhleifat: Today is #GlobalMNDAwarenessDay. MND isn’t incurable, it’s just underfunded. Research gives hope. Funding makes it pos….
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@LisaLegacy4ALS
Lisa's Legacy for ALS
29 days
RT @kelsieswrites: It’s been awhile friends. ❤️ . An all-new episode of Sorry, I’m Sad, brought to you by the ALS Society of Alberta. https….
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@LisaLegacy4ALS
Lisa's Legacy for ALS
1 month
We hate that this t-shirt has to exist but we love the creativity behind it. Our friend Ed created it as he works to bring about change for all battling ALS. Now please follow the alien's request and complete an ALS Clinic Survey today.
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@LisaLegacy4ALS
Lisa's Legacy for ALS
1 month
We feel so fortunate to have had the opportunity last night to view a new documentary about Dr. Bedlack and several people living with ALS. Each person is such an inspiration as they use their hopes and dreams to fight ALS. Thank you all for sharing your stories.
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@LisaLegacy4ALS
Lisa's Legacy for ALS
2 months
RT @MindyUhrlaub: Holy moly! A positive Kirkus review! If you haven't picked up a copy of Last Nerve yet, please go to my website, https://….
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@LisaLegacy4ALS
Lisa's Legacy for ALS
2 months
RT @stevehaberstroh: Today is 5th Annual #LouGehrigDay across @MLB. For a refresher on how it came to be, please watch the below by @OTLon….
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@LisaLegacy4ALS
Lisa's Legacy for ALS
2 months
RT @ALSMNDAlliance: Applications now open! The Patient Fellows Program is back for the 36th International Symposium on ALS/MND. 🌐 Apply by….
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@LisaLegacy4ALS
Lisa's Legacy for ALS
2 months
RT @iamalsorg: We are in need of women living with ALS to join our Peer Support program as mentors! Learn more about this program and apply….
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@LisaLegacy4ALS
Lisa's Legacy for ALS
2 months
RT @iamalsorg: The flag photos from the ALS Community Summit are ready! While it was our heartfelt intention to photograph each flag, human….
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@LisaLegacy4ALS
Lisa's Legacy for ALS
2 months
RT @iamalsorg: Our webinar about the role of palliative care in ALS is tomorrow, May 29! There's still time to sign up to learn more about….
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@LisaLegacy4ALS
Lisa's Legacy for ALS
2 months
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@LisaLegacy4ALS
Lisa's Legacy for ALS
2 months
RT @End_The_Legacy: Our friend , co-founder , and champion Mindy Uhrlaub has taken her talent for the written word and put it towards shari….
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