Allyson Bontempo, Ph.D. (@acbontempo) 's Twitter Profile
Allyson Bontempo, Ph.D.

@acbontempo

Postdoc Research Fellow @Rutgers_NJMS | @RutgersCommInfo alum | Patient-clinician #communication | #Diagnosis | #Invalidation | #Endometriosis | Stay curious.

ID: 1133749050166173697

linkhttps://www.allysoncbontempo.com/ calendar_today29-05-2019 14:56:52

1,1K Tweet

749 Followers

527 Following

Neseret Bemient (@journeyofhope4u) 's Twitter Profile Photo

I trust those who are willing to question authority. Those who have invested so much of their life to discover they were wrong and are willing to admit it. It's those brave souls that people call "sh*t disturbers", "trouble makers" - and "the crazy ones."

COVID-19 Longhauler Advocacy Project (@c19lh_advocacy) 's Twitter Profile Photo

Hello #LongCOVID Team! In 2022, 44% of respondents in a #C19LAP survey said they had applied for #SocialSecurity #Disability. We are re-evaluating the experience of the U.S. #LongCOVID community when it comes to applying for Social Security Disability. We are asking everyone

#MEAction Network (@meactnet) 's Twitter Profile Photo

#MEAction’s narrative activity study with Mayo Clinic opens today! We’re looking for people with #MECFS or #LongCOVID with #PEM to share their experiences. The survey will be open from 5/24/2024 to 6/23/2024. Learn more & find out if you’re eligible here: surveys.mayoclinic.org/jfe/form/SV_2a…

#MEAction’s narrative activity study with <a href="/MayoClinic/">Mayo Clinic</a> opens today! We’re looking for people with 
#MECFS or #LongCOVID with #PEM to share their experiences. The survey will be open from 5/24/2024 to 6/23/2024.
Learn more &amp; find out if you’re eligible here:
surveys.mayoclinic.org/jfe/form/SV_2a…
Allyson Bontempo, Ph.D. (@acbontempo) 's Twitter Profile Photo

I think people underestimate the power of a clinician saying “I don’t know.” It leaves space for a reality in which patients’ symptoms can still exist. 🎗️

Allyson Bontempo, Ph.D. (@acbontempo) 's Twitter Profile Photo

#MedTwitter: In the DSM-5 (the mental health version of the ICD-10), it is explicitly stated that somatic symptom disorders CANNOT be diagnosed solely based on the absence of medical evidence, yet this seems widely practiced by physicians. Does the ICD-10 state differently?

Allyson Bontempo, Ph.D. (@acbontempo) 's Twitter Profile Photo

The status of one of my papers submitted to a journal has been “awaiting reviewer selection” for the past month. Has this happened to anyone before? Any advice? PhD Voice - Independently Run PostdocVoice #academia #publishing

Julie Sullivan (@curelongcovid) 's Twitter Profile Photo

Research study opportunity at Mass General Hospital: ME/CFS and post-COVID ME/CFS- survey blood draw and MRI to study the underlying cause of cognitive control impairment in these conditions. More info here: rally.massgeneralbrigham.org/study/mocci

Allyson Bontempo, Ph.D. (@acbontempo) 's Twitter Profile Photo

Really excited to see the NIH Women's Health update on women’s health research recognize #symptominvalidation experienced by females during their diagnostic odysseys, including in #endometriosis, at #ARM24.

Really excited to see the <a href="/NIH_ORWH/">NIH Women's Health</a> update on women’s health research recognize #symptominvalidation experienced by females during their diagnostic odysseys, including in #endometriosis, at #ARM24.
Allyson Bontempo, Ph.D. (@acbontempo) 's Twitter Profile Photo

Check out a #research opportunity on the #diagnosis journey for black and brown women and women identified people in the US with #lupus and #endometriosis some collaborators from Baylor and I are studying.

Check out a #research opportunity on the #diagnosis journey for black and brown women and women identified people in the US with #lupus and #endometriosis some collaborators from Baylor and I are studying.
Allyson Bontempo, Ph.D. (@acbontempo) 's Twitter Profile Photo

As someone who considers themself an advocate of ME/CFS and of patient legitimacy more broadly, I cannot express how angry this makes me.

As someone who considers themself an advocate of ME/CFS and of patient legitimacy more broadly, I cannot express how angry this makes me.