Asst Professor of BioEng, UC San Diego | #SexDifferences 🤝 #Biomaterials | LatinXinBME Cofounder | CZI Science Diversity Leader | NIH Director’s New Innovator | WHISDEM Center Co-Director for Women’s Health | 🇨🇴🇺🇸🏳️🌈
https://aguado.eng.ucsd.edu/
VP for Research, T.H. Smoot Professor
Depts Chemical and Biomolecular Engn, Pathology, Oncology, INBT
Johns Hopkins University
3D multi-omic, CAR T therapy, cell migration and mechanics
Lab: https://wirtzlab.johnshopkins.edu
Modular #Biomaterials Lab // bleats by PI: Dr Lesley Chow (she/her) // Lehigh University MSE & BIOE // #BLM 🏳️🌈 ally // Assoc Ed npj Regenerative Medicine // thechowlab.com
We grow fat..in the lab. PI: Evangelia Bellas,PhD (she/her) 🇬🇷🇺🇸. #AdiposeTissueEngineering #fatchat #EngineeredFat. 🌈✊🏻✊🏽✊🏿
Weyerhaeuser Associate Professor of Chemical Engineering & Bioengineering, University of Washington | User-Programmable Biomaterials | Photochemistry | Optogenetics | Protein Engineering
http://www.coledeforest.com
Cellular biophysicist at NC State. My lab combines approaches from physics, biology, and engineering to ask how biological molecules self-assemble into cellular-scale machinery that transduces force and performs mechanical functions.
Interested in
history, disability, politics, chronic illness. Loves animals, dry white wine, chocolate and my bed. Irish. Actually Autistic,
ADHD, ME sufferer. Cat and dog person. @shurlookit in the bad place
A global network of people empowering one another to fight for equity for myalgic encephalomyelitis. Home of the #MillionsMissing linktr.ee/meactnet
#pwME #MyalgicEncephalomyelitis #LongCovid #MECFS #ChronicIllness #DisabilityJustice
Sharing info on COVID since the start of the pandemic.
#COVIDisNotOver #COVIDisAirborne #MaskUp😷
UK charity dedicated to supporting people with Long Covid
• Support • Research • Advocacy • Education •
www.longcovid.org
https://linktr.ee/longcovidsupport
📧info@longcovid.org
A group of physiotherapists with a special interest in Myalgic Encephalomyelitis (ME) with the aim to improve physiotherapy management for people with ME
Find out more at physiosforme.com
In-depth analysis of research on myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). Formerly known as ME/CFS Skeptic.
https://mecfsscience.org/
Chronically ill & disabled person with lots of personal opinions, who sometimes likes a hat. Occasionally an advocate for PwME, gamer and proudly on the Autism spectrum. I’ve low tolerance for ignorance and assholery so if you come for a fight, expect one.
Hello, welcome :)
This Invisible Illness: my first long form documentary photography project, about ME/CFS a complex & challenging health condition - like Long Covid.
https://linktr.ee/andrewgifford.photography
Bristol, UK. 335.42 ppm. He/him/oi.
2001 PVFS 'Recovered' to 90% by 2006. Sepsis 2013 resulted in M.E. / relapse. Brain/fitness not 'what it used to be'. Beloved Lisnakill Myles-Happy Hound himself 🌈
Disabled by very Severe Post-COVID ME/CFS. Not always able to use phone. Bedridden. Unable to Speak.
I care.
Ⓐ💚, (FR/DE/EN, but posts in english)
Clinging onto the ledge above the abyss.
Irish Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Association
NB: Posts should not be considered advice
Registered Charity Number 20100254
CHY 22039
#MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #PwME. Some #LongCovid items also
ME/CFS San Diego, a 501c3 public charity, is working locally to raise awareness of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), to help educate healthcare workers and researchers, to increase access and support for ME/CFS patients.
ME/CFS ist eine schwere körperliche Erkrankung, die bisher kaum erforscht ist. Wir setzen uns für die Interessen der Erkrankten und mehr Forschung ein.
mecfs.de
