NNRI

National Neuromuscular Research Institute is a global center for excellence in neuromuscular medicine, committed to research and clinical advancement.

[NNRI @NNRI_Research]

Living with a rare neuromuscular disease isn't easy. If these signs sound familiar, it may be time to learn about clinical trial options, especially if your current treatment isn't enough. #ALS #CIDP #myositis #neuromusculardisease

[NNRI @NNRI_Research]

New treatments don't start in pharmacies—they start in clinical trials. Participating could give you early access to emerging therapies for your #neuromuscular condition. See our link in bio to learn about our active trials and check your eligibility to participate. #ALS #CIDP

[NNRI @NNRI_Research]

Living with #CIDP shouldn't mean settling for "good enough." If your current treatment isn't providing the symptom control you hoped for, clinical research may offer another option to explore at NNRI, where Neuromuscular Medicine is all we do.

#ClinicalTrials #RareDisease

[NNRI @NNRI_Research]

Better treatments start with research. At NNRI, we're advancing medicine through clinical trials for rare neuromuscular diseases—and providing the compassionate, specialized care that leaves participants feeling truly cared for. Click our link in bio to see if you qualify.

[NNRI @NNRI_Research]

Where you decide to participate in a clinical trial can make a difference. Our team has been focused on rare neuromuscular diseases since 2015. Click the link in bio to see our active trials and find out if you are eligible to participate. #ALS #CIDP #MyastheniaGravis

[NNRI @NNRI_Research]

Clinical trials offer more than access to emerging therapies—they offer a way to take control, contribute to discovery, and help shape the future of care for rare neuromuscular diseases. Click to see if you qualify. #RareDiseases #Neuromuscular #ALS #CIDP #MyastheniaGravis

[NNRI @NNRI_Research]

Early symptoms of ALS vary from person to person and can be very subtle and easily dismissed. If you are noticing these symptoms, seeking evaluation from a neurologist or a specialized neuromuscular center is an important first step. #ALS #ALSAwareness #Neuromuscular

[NNRI @NNRI_Research]

🎗️ June is Myasthenia Gravis Awareness Month. Join us in raising awareness, supporting patients and caregivers, and promoting research for this rare autoimmune neuromuscular disease. Together, we can make a difference. #MyastheniaGravis #MGAwarenessMonth

[NNRI @NNRI_Research]

ALS, known as Lou Gehrig’s disease, is a progressive neurological disorder affecting muscle movement. This ALS Awareness Month, NNRI stands with patients, families, and caregivers while supporting continued research and innovation in neurological care. 💙

#ALSAwarenessMonth #ALS

[NNRI @NNRI_Research]

Big shout out and thank you to all of our incredible nurses and nurse practitioners at NNRI and ANC! We’re so grateful for all that you do and proud to celebrate you this week!

Happy Nurses Week! 👩‍⚕️👨‍⚕️

#NursesWeek #HealthcareHeroes #NurseAppreciation

[NNRI @NNRI_Research]

We’re excited to announce a new ALS clinical trial now enrolling at NNRI. We’re honored to support progress in ALS research—an area where innovation is deeply needed. #ALSResearch

To learn more, visit out new website:
https://t.co/M65nqtbUNt
OR visit
https://t.co/CKZZ1Pf02B

[NNRI @NNRI_Research]

On Doctors’ Day, we’re proud to recognize Dr. Reddy and Dr. Hussain for their compassion, skill, and tireless dedication. The care and guidance you provide to our rare disease patients throughout their journeys make a profound impact. Thank you for all that you do!

#DoctorsDay

[NNRI @NNRI_Research]

Today we’re recognizing Manzi, our amazing research assistant! Your positive attitude, strong work ethic, and willingness to help without hesitation make a difference every single day. Thank you always lending a helping hand. We appreciate you!

#EmployeeRecognition

[NNRI @NNRI_Research]

On March 10, we recognized Histopathology Professionals Day and took a moment to celebrate the incredible work of our Histotechnician, Britni.

Thank you, Britni, for your hard work, attention to detail, and commitment to excellence. We’re grateful to have you on our team!

[NNRI @NNRI_Research]

As a research assistant at NNRI, Mayra has shown incredible dedication and work ethic every day. We’re so proud to see her start nursing school and can’t wait to see the impact she’ll make as a nurse.

Thank you for all that you do, Mayra!

#FutureNurse #NursingJourney

[NNRI @NNRI_Research]

Today, we stand with the millions of individuals and families affected by rare neuromuscular diseases. To our patients, caregivers, researchers, and partners: we see you, we support you, and we remain committed to accelerating progress.
#RareDiseaseDay #RareDiseaseAwareness

[NNRI @NNRI_Research]

We are proud to share that Dr. Hussain has been elected President of the Texas Neurological Society! This prestigious honor recognizes Dr. Hussain’s outstanding leadership and dedication to advancing neurological care. Thank you for all that you do! #TexasNeurologicalSociety

[NNRI @NNRI_Research]

Shoutout to Emma for her hard work and dedication in reaching this Rainbow Study milestone. NNRI only works because we have incredible employees like you. Thank you for all you do!

To learn more about the Rainbow study:
https://t.co/7rVz2y9mrp
https://t.co/QykzIWGqKO

[NNRI @NNRI_Research]

With no cure, research is vital. NNRI is conducting research to better understand this condition and exploring potential treatment options through clinical trials.

Learn more about NNRI's studies: https://t.co/7rVz2y9mrp

#ALSResearch #ClinicalTrials #RareDisease

[NNRI @NNRI_Research]

A platform study for Myasthenia Gravis is now at NNRI. We look forward to being a part of this research.🔬🧬

More information here:
https://t.co/Ps7Sgf1GlF

To learn more or request additional information, please visit our website: https://t.co/7rVz2y9mrp