Frustrated Writer · @frustratedwriter
50 followers · 79 posts · Server mstdn.social

I did not know that today was . Last year I had an done on my brain for something else. Then I find out that I was born with an . Or . The Corpus Callosum is the fibrous part of the brain that connects and communicates between the two . This is a rare disease that can cause developmental delays, learning disabilities, and eating difficulties to name a few.

#hemispheres #agenesisofthecorpuscallosum #corpuscallosum #underdeveloped #mri #RareDiseaseDay

Last updated 2 years ago

GPTrending · @GPTrending
14 followers · 1044 posts · Server mstdn.social

: Dr. Jacob Adashek of Johns Hopkins Kimmel Cancer Center discussed research on tumor mutational burden and checkpoint molecules -Experts call this a breakthrough in cancer research! GPTrending.com/#/?date=2023-03

#oncologyleaders #mednewsweek #cancerresearch #RareDiseaseDay

Last updated 2 years ago

UC Santa Cruz Science · @ucscscience
129 followers · 47 posts · Server mstdn.social

Today, on , we’re sharing a couple ways that @ucsc is advancing research for treatments of rare diseases.

1. The Millhauser lab recently gained insight on a new way to develop treatments for the the rare genetic disease cystinosis.

2. Michael Stone & team have been working to examine disruptions to the processing of RNA in the cell. They developed an RNA Rescue challenge that invites players to solve puzzles & advance therapeutics.

We recognize there is still a long way to go❤️

#RareDiseaseDay

Last updated 2 years ago

UC Santa Cruz Science · @ucscscience
156 followers · 77 posts · Server mstdn.social

Today, on , we’re sharing a couple ways that @ucsc is advancing research on treatments for rare diseases.

1. The Millhauser lab recently gained insight on a new way to develop treatments for the the rare genetic disease cystinosis.

2. Michael Stone & team have been working to examine disruptions to the processing of RNA in the cell. They developed an RNA Rescue challenge that invites players to solve puzzles & advance therapeutics.

We recognize there is still a long way to go❤️

#RareDiseaseDay

Last updated 2 years ago

Claire C · @wildflowersandpixels
22 followers · 42 posts · Server mastodon.scot

It's so I wanted to share my own rare disease, Lime Girdle Muscular Dystrophy (LGMD).

#RareDiseaseDay

Last updated 2 years ago

GPTrending · @GPTrending
14 followers · 1033 posts · Server mstdn.social

Great interview with Dr. Jacob Adashek discussing his abstract on the correlation between transcription expression and multiple checkpoint proteins on GPTrending.com/#/?date=2023-02

#researchspotlight #johnshopkins #cancerresearch #RareDiseaseDay

Last updated 2 years ago

Sachin Rawat · @sachinxr
333 followers · 49 posts · Server mas.to

On , a reminder that while individual rare diseases are rare, collectively over 5% of the world population has a rare disease.

Add the family and friends who support rare disease patients and the number of people impacted by rare diseases makes them a fairly common burden. A burden that countries shouldn't ignore any longer.

Newborn screening doesn't solve everything, but it will go a long way in improving rare disease diagnosis and care.

#RareDiseaseDay

Last updated 2 years ago

Sachin Rawat · @sachinxr
331 followers · 47 posts · Server mas.to

On , a reminder that while individual rare diseases are rare, collectively they over 5% of the world has a rare disease.

Add the family and friends who support rare disease patients and the number of people impacted by rare diseases makes them a fairly common burden. A burden that countries shouldn't ignore any longer.

Newborn screening doesn't solve everything, but it will go a long way in improving rare disease diagnosis and care.

#RareDiseaseDay

Last updated 2 years ago

Judith Sleeman · @JudithSleeman
16 followers · 8 posts · Server mastodon.scot

RT @MNDScotland
Today is .

Although motor neuron disease is considered a , it's not as rare as you might think.

Around 1 in 300 people will develop and with no cure, that means 1 in 300 people will die because of MND.

Please retweet! 💙

#rarediseaseday2023 #MND #raredisease #RareDiseaseDay

Last updated 2 years ago

Vivienne Dunstan · @vivdunstan
721 followers · 668 posts · Server mastodon.scot

Today is , so here’s a link to my writeup about the 1 in a million or so, primary cerebral , I’ve lived with since 1994. Inflammation in the blood vessels in my . In my case never gone into remission and . vasculitis.org.uk/living-with-

#progressive #brain #vasculitis #disease #RareDiseaseDay

Last updated 2 years ago

#SCIENCEMATTERS · @ottawatts
571 followers · 890 posts · Server mstdn.social
C. Harris Floudas · @chfloudas
70 followers · 378 posts · Server mstdn.social

For 4th year, a meeting which addresses a significant information gap for patients with olfactory neuroblastoma

RT @NCICCR_SurgOnc@twitter.com: Are you ready for 2023?
4th Annual Olfactory Neuroblastoma meeting hosted by Dr. Nyall London @NCIResearchCtr. Virtual and in-person attendance on February 25, 2023.
More at shorturl.at/ACR26
@NIH @theNCI @NIDCD twitter.com/NCICCR_SurgOnc/sta

#RareDiseaseDay #oncology

Last updated 2 years ago

jOhn Wallace RareDisease · @WallaceRD
27 followers · 768 posts · Server mastodon.scot

RT @AddisonsUK@twitter.com

We're joining @RareDiseaseUK@twitter.com to get a Google Doodle for on 28 February 2023!

Get involved, show the power of rare & send an email to doodleproposals@google.com using @RareDiseaseUK@twitter.com's email template.

Visit their website for more info⤵️ twitter.com/rarediseaseuk/stat

🐦🔗: twitter.com/AddisonsUK/status/

#RareDiseaseDay

Last updated 2 years ago