Latest tweets patientchat


RT @abrewi3010: .We need more opportunities like this for patients to tell their story. It’s also a great opportunity to fight silos. Stage…
.We need more opportunities like this for patients to tell their story. It’s also a great opportunity to fight silo… https://t.co/5QKEhU67e9
Do you have a pacemaker and apple phone12? Keep The magsafe charger not at your bedside.. Those with pacemakers alr… https://t.co/IGaqba8cfL
RT @carlyflumer: T1: It all starts with sharing your story. Whether it be on social media, through a blog, or an organization, that’s advoc…
RT @darlakbrown: I'm looking forward to the next #patientchat, "Let's Talk Mental Health" on Feb. 5 at 10am Pacific. A topic near and dear…
RT @darlakbrown: I'm looking forward to the next #patientchat, "Let's Talk Mental Health" on Feb. 5 at 10am Pacific. A topic near and dear…
RT @MightyCasey: T2: I'm bad, I'm nationwide. Srsly, tho, I'm kinda everywhere. My core communities are #bcsm + @BeLikeLight, I'll show up…
RT @christie_health: Hi everyone! Christie here from the Hudson Valley in NY. I'm the founder of How to Talk to Your Doctor and a public he…
RT @myraredisease: For my rare disease #scimitarsyndrome there isn’t a specialist resource so they next best area to look at is #congenital
@patientchat I request another doctor or nurse.
RT @patientchat: Join us for a “Let’s Talk Mental Health” Empowered #patientchat on Friday, February 5th @ 10 AM PT| 1 PM ET! https://t.…
RT @ohhiialexa: CT: Every #patientchat makes me realize more and more how I wish pharma/medical science/medical schools/etc had more patien…
RT @MightyCasey: T3: My go-to resources are ProPublica's Surgeon Scorecard for common surgical procedures (joint repl etc.). Also a big fan…
RT @myraredisease: Joining the rare disease community is one big step, chatting to others in similar situations to you, establishing what y…

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