Yesterday’s approval of a new treatment option for people with #Alzheimer’s disease is incredibly exciting. It also means that accessible, accurate diagnostics are more important than ever. https://lnkd.in/ev38CZ3c
In her recent op-ed, newly appointed Danaher Executive Vice President for Diagnostics Julie Sawyer Montgomery describes the need for a vast, coordinated effort in the multifaceted fight against Alzheimer’s.
#speedoflife
Eating Marketing for Breakfast, Lunch and Dinner * Head of Marketing Food Ingredients Division Stern Wywiol Group * Marketing Manager for Mühlenchemie and Deutsche Back
For #WorldAlzheimersMonth, we are supporting Alzheimer's Disease International's mission to raise awareness and challenge the stigma that persists around Alzheimer’s disease.
This year’s theme, “Time to Act on Alzheimer’s,” reminds us of the tremendous, growing need for more reliable and sensitive diagnostic tests to accelerate drug development and enhance patient care.
Learn more about World Alzheimer’s Month: https://lnkd.in/eGsXmt4K#TimeToActOnAlzheimers#alzheimers
"I have scleroderma, so I'm asking you to say it." – Cynthia, dx 2021
Why #SayScleroderma? Many people are unaware of what scleroderma is and the impact it has on those affected. This lack of awareness can lead to delays in treatment and diagnosis, and hinder progress in finding a cure.
In this clip, Cynthia opens up about her difficult experiences seeking care for scleroderma and highlights the crucial need for awareness and education about this disease.
Thank you so much to Cynthia and her brother for making this project to spread the word about scleroderma. Watch the full video on our YouTube channel: https://bit.ly/3zfQ1AT
Though it's the last day of Scleroderma Awareness Month, let's keep the momentum going. Together, we can make sure scleroderma is heard until we find a cure. Learn more about how you can #SayScleroderma and get involved: https://bit.ly/45BgBR1#sayscleroderma#sclerodermaawareness#scleroderma#sclerodermaresearch#srfcure
Join us April 3 for an online event that will blow your mind! Did you know focused ultrasound is a therapy and delivery mechanism for #fibroids#cancer#Alzheimers#painmanagement — 170+ indications. It can break the blood brain barrier and can go right to the point of injury/illness. This life-saving technology has huge potential for #patients#healthcare — learn more on this Congressional Briefing!
Today we announced continued positive results for bemdaneprocel for the treatment of Parkinson's disease at 24 months. You can read the full press release here: https://lnkd.in/egENjFyw
BlueRock will be at #MDS2024 this weekend to talk more about our positive 24-month data from the bemdaneprocel Phase 1 clinical trial for the treatment of Parkinson's disease. Tomorrow, Dr. Harini Sarva will present two oral platform presentations at 1:30 PM ET. Additionally, you can visit Dr. Sarva and #BlueRocker Nauman Abid, M.D. at the poster session on September 29 from 1-3 PM ET.
#ParkinsonsDisease#CellTherapy#Congresses
February 29 is Rare Disease Day. There are limited treatment options and cures for patients battling their rare disease. Take a moment to learn about a rare disease today!:
Abeona Therapeutics, a clinical-stage biopharmaceutical company, is advancing gene-corrected epidermal sheets to treat recessive dystrophic epidermolysis bullosa. This genetic skin disorder makes the skin fragile and susceptible to chronic wounds.
The Ataxia Telangiectasia Children's Project works to find therapies and a cure for children with Ataxia-telangiectasia, a genetic disease that impairs muscle control and the immune system.
#rarediseaseday2024
This Rare Disease Day, listen to Dr. Karen Wiss talk about the possibilities and changing landscape of treatment for severe dystrophic epidermolysis bullosa (DEB) as we all work together to make a difference.
At Abeona, we are dedicated to advancing therapies for severe DEB. Our commitment to innovation is steadfast, and every story of patient courage fuels our pursuit of new advancements.
#WeFightEB#EpidermolysisBullosa#RDEB#SevereDEB#RareDiseaseDay
Very exciting! Thank you for sharing