Top Tweets for #MOGProject
Today we present the story of our MOGDog, Newcastle, a guide dog and MOG Project Champion!
Read the story here:
https://t.co/rMTkxBJtIP
#MOGDog #MOGProject #MOGAD #MOG #blinddog #blind #MOGProjectChampion
Cynthia was finally diagnosed with MOG-Ab disease in 2018 and has since not had any flares. She co-founded The MOG Project at SRNA along with 3 other individuals.
Read Cynthia's full story: https://t.co/cu3vwzd0Ky
#MOGAwareness #MOGabdisease #MOG #SRNABlogs
#MOGProject
Do you or someone you love live with MOG-Ab disease? Share your story and become a TMA Hope Ambassador! Consider joining us as an advocate as Julia Lefelar has: https://t.co/dehk0rJ6bH
#TakeInitiativeTuesday #MOGAwareness #MOG #MOGProject #RareDiseases #rare
Swan Hunter completes Modular Offshore Grid Cable Storage Load-in
https://t.co/MnKRsbI6Ul #SwanHunter #MOGproject #offshore #ModularOffshoreGrid #LivingStone #CableLayVessel
It's hard to believe that the MOG Project's partnership with the TMA is already one year old! Let's look back on our first podcast on MOG Antibody-Associated Disease: https://t.co/KZQl3TLUT4
#ThrowbackThursday #MOGAwareness #MOGProject #rare #RareDiseases #MOG
The MOG Project at the TMA would like to know what ideas you have about how we can help bring awareness to MOG-Ab disease. #WelcomeWednesday in with your thoughts on how we can help the MOG community!
#MOGAwareness #MOG #MOGProject #Rare #RareDisease
Bring in MOG Awareness week by attending the 2019 Maryland Walk-Run-N-Roll! If you can't attend, consider celebrating this #MotivationalMonday with a donation to support rare neuroimmune disorders: https://t.co/DTtNXxJvkt
#MOGAwareness #MOG #MOGProject #Rare #RareDisease
This #MotivationalMonday during #MOGAwareness week, we want to highlight the #MOGProject members, who worked with the TMA to add this disorder to the spectrum of rare neuro-immune disorders the TMA advocates for. Read more here: https://t.co/M3YUDDZhYE #MOG #RareDiseases #rare
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