It's been a while, but a lot has been happening! I've recently passed my written and oral preliminary exams, so I am officially a PhD candidate.
In celebration I've updated my website. Go check out what I've been up to!
https://t.co/IUNDPrQPpw
Making an appearance on the #badwebsite to let ya'll know that I updated my (better) website! Visit https://t.co/IUNDPrQPpw to find up what I've been up to!
I've been using Mendeley Desktop daily for years, & have an annotated library of thousands of pdfs. Today, I switched to Zotero. Here's a 🧵of tips on how to do this, if you're also tired of Elsevier's BS and want to make the switch w/minimal effort while maintaining workflow.
New podcast alert! My husband and other dear friends have worked so hard to bring this story to life. If you like fantasy, intrigue, and collaborative storytelling, this podcast is for you! #talespinners#podcast#DnD#rpg
https://t.co/g8t9Nkx1CH
Calling all families! Please take a minute to complete an important medical survey about Birt-Hogg-Dube symptoms in people with SMS: https://t.co/8EOAASR99S #SmithMagenisSyndrome#SMSResearch
Today we also celebrate Ellen Magenis, one of the co-discoverers of Smith-Magenis Syndrome, who passed away on this day six years ago. We would not be a community at all without her. Thank you, Ellen. You will always be part of the SMS family. #hugorbehugged
We know our caregivers take on a lot. For those who could use assistance, check out NORD's Rare Caregiver Respite Program! Up to $800/yr per caregiver https://t.co/QBaVZyufxL
Join us January 22nd at 7 pm EST for a webinar overview of the history of Smith-Magenis Syndrome, led by Ann Smith, M.A., DSc (Hon)! Ann co-discovered SMS, helped found PRISMS, and currently serves on our PAB. Register at: https://t.co/Y7h1TxvCwX
Sleep in children with Smith-Magenis syndrome- more research like this needed for this rare disorder where sleep disorders are so characteristic,severe and affect families so much @SmithMagenisUK https://t.co/sLgkDz3Ot8
It’s GivingTuesday! Consider donating to the @SMSResearchFoun —they’re doing great work for those affected by Smith-Magenis Syndrome. Donations are TRIPLED today thanks to matching by generous donors! https://t.co/FgajhHAbKi
Happy SMS Awareness Day! We celebrate #SMSAwarenessDay every November 17th, since the main chromosome affected in Smith-Magenis Syndrome is 17p11.2. Join us and learn more about SMS by visiting https://t.co/XQeekVad77!
Take a moment on #WorldMentalHealthDay to check out this great read on the impact caring for a child with a rare disease can have on the mental health of caregivers. Caregivers need care too!
We will be going live in about half an hour from our research symposium, with our keynote speaker Gianluca Pirozzi. Follow along with us on Facebook: https://t.co/sXC7v5ALty