Save Liz Nevra
@SaveLizNevra
Get updates and help Nevra Liz meet her housing and healthcare needs for Ehlers-Danlos Syndrome #EDS #CCI #POTS #MCAD #PMDD #LongCovid #MECFS. #MillionsMissing
🚨 Only *9 more days* before August rent is due, I need 832.33£ or $1,131.18 This is an emergency, I’m at risk of homelessness, I could not survive being unhoused Please RT/engage! 🚨 My friend Annie made this Rent PayPal: paypal.com/paypalme/SaveL… GFM: gofundme.com/f/save-nevra
Please help my dear friend if you can 💙 If you can't, please RT.
I have 10 days before August rent is due, I need 832.33£ or $1,131.18 This is an emergency, so few people have donated recently, I’m at risk of homelessness, I could not survive that Please boost/engage! 🚨 Rent PayPal: paypal.com/paypalme/SaveL… GFM: gofundme.com/f/save-nevra
Please donate if you can. Likes and RTs are also important! She deserves a safe place to live and recover.
I have 10 days before August rent is due, I need 832.33£ or $1,131.18 This is an emergency, so few people have donated recently, I’m at risk of homelessness, I could not survive that Please boost/engage! 🚨 Rent PayPal: paypal.com/paypalme/SaveL… GFM: gofundme.com/f/save-nevra
I have 10 days before August rent is due, I need 832.33£ or $1,131.18 This is an emergency, so few people have donated recently, I’m at risk of homelessness, I could not survive that Please boost/engage! 🚨 Rent PayPal: paypal.com/paypalme/SaveL… GFM: gofundme.com/f/save-nevra
July update here! Please RT, QT, comment for engagement Been such a hard month, I need to move into safer housing but am so sick now from mould and water damage So grateful for your help ❤️🩹 💜 Rent PayPal: paypal.com/paypalme/SaveL… ❤️ GoFundMe: gofundme.com/f/save-nevra 🧵 1/3
If you’re seeing my posts mourning multiple friends with MECFS and Long Covid who’ve died, and want to help — Please engage with mutual aid posts! I boost, comment, support, help fundraise for many yet folks ignore them Nevra and others need our help to survive! Be the change
July update here! Please RT, QT, comment for engagement Been such a hard month, I need to move into safer housing but am so sick now from mould and water damage So grateful for your help ❤️🩹 💜 Rent PayPal: paypal.com/paypalme/SaveL… ❤️ GoFundMe: gofundme.com/f/save-nevra 🧵 1/3
Bridget Denise Jhanne Elmear Jana Sharon David Klara Lena Loes Lauren Céline Kara Jane Andrea Daniela Melanie Lisa Maeve And so many more 💙 #MEKills
This is devastating. @Bridget_OShea’s last experience was not being believed and being dismissed by her own mother just before she died. It’s what this community goes through over and over. I hate this world
I called my mom. I told her I'm afraid I'm going to die. Her response? She hung up. 😫#MECFS
I’m so sorry we lost you, Bridget, and that your family was not more supportive of your needs 💔 will miss you
Researchers from Stanford University just published a study identifying oxidative stress as a central, shared biological feature in both Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and Long COVID. • Significant metabolic abnormalities were found in both #MECFS…
EBV antibody test can predict MS years before symptom onset…body develops antibodies against a specific part of an EBV protein called EBNA-1- these antibodies then mistakenly cross-react with myelin-related proteins to drive MS. multiplesclerosisnewstoday.com/news-posts/202…
German Health Minister: “We should invest 1 billion in #MECFS research. The disease costs us 30 billion per year. Young people are taking their own lives, so great is their suffering. Now Trump has cut research funding.. Without significantly more research, there is no hope.”
Wir sollten 1 Milliarde für ME/CFS Forschung investieren. Die Krankheit kostet uns 30 Mrd. pro Jahr. Junge Menschen bringen sich um, so stark ist ihr Leid. Jetzt hat auch noch Trump die Forschung gekürzt. Ohne deutlich mehr Forschung gibt es keine Hoffnung spiegel.de/politik/deutsc…
#MEAction has announced the 2025 Severe ME Artists Initiative, celebrating artistic talents for #SevereMEDay on Aug 8th. People with Severe ME are invited to showcase their creativity through literature, photography, illustration, and more. buff.ly/lI797rW