Neurology and Neuromuscular Care Center - Diana Castro MD

Neurology and Neuromuscular Care Center - Diana Castro MD Our Mission
Neurology & Neuromuscular Care Center is a 501(c)(3) non-clinic. We accept all patients regardless of insurance or ability to pay.

Dr. Castro a board-certified neurologist and neuromuscular physician is an expert in clinical care and research

For inquiries, please email [email protected]
We do not monitor the messenger Our mission is to provide state-of-the-art compassionate care to children and adults with neuromuscular conditions. This model enables us to spend much more time with each patient. Our affiliation w

ith Neurology Rare Disease Center, an in-house private research facility, provides a unique opportunity to involve patients in the latest research protocols. Dr. Diana Castro
Dr. Castro, a board-certified neurologist and neuromuscular physician, is a pioneer in research and management of patients with Spinal Muscular Atrophy (SMA), Duchenne Muscular Dystrophy (DMD), Myasthenia Gravis, and Acquired Neuropathies, like Chronic Inflammatory Demyelinating Polyneuropathy (CIDP). Since completing training in pediatric neuromuscular medicine, Dr. Castro has conducted multiple clinical research trials in SMA, DMD, and Charcot-Marie-Tooth (CMT), among other conditions. Being an intricate part of developing innovative therapies for rare neuromuscular conditions is one of her biggest passions, along with the strong bonds she makes with all her patients and their families. This unique relationship with her patients drives her to continue searching for therapeutic options for them. In addition to managing a busy patient load and conducting research, Dr. Castro has had many peer-reviewed publications, book chapters and has given multiple national and international lectures in English and Spanish. She also sits on several national medical advisory boards and steering committees.

After more than ten years, Dr. Castro left academia with the objective of creating a non-profit private practice and research institute for neuromuscular conditions. The non-profit neuromuscular practice will have the capacity to offer care to all neuromuscular patients, including pediatric and adult patients, with or without insurance, as well as international patients.

June is Myasthenia Gravis Awareness Month. ❄️Myasthenia Gravis (MG) is a rare chronic autoimmune neuromuscular disease —...
06/02/2026

June is Myasthenia Gravis Awareness Month. ❄️
Myasthenia Gravis (MG) is a rare chronic autoimmune neuromuscular disease — and despite affecting over 700,000 people worldwide, it remains widely misunderstood and frequently misdiagnosed.

This month, our team is committed to educating our community about what MG really is, sharing the latest advances in diagnosis and treatment, and highlighting clinical research opportunities for our patients.

Follow along for updates

📩 Contact us at [email protected]
🔗 Learn more at NeuroMDCenter.com

There is meaningful progress in the treatment of Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) and related au...
05/27/2026

There is meaningful progress in the treatment of Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) and related autoimmune neuropathies.

From home-based immunoglobulin therapy to investigational agents targeting pathogenic antibody pathways, there are more options than ever for patients living with CIDP and related autoimmune neuropathies.

At the Neurology Rare Disease Center, we stay current on these advances and evaluate our patients for access to clinical research opportunities in neuromuscular disease.

🔬 Ask about our clinical trials: [email protected] or 972-999-1011
🔗 NeuroMDCenter.com/cipd

Did you know Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) is often misdiagnosed for years?Patients with CIDP...
05/19/2026

Did you know Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) is often misdiagnosed for years?

Patients with CIDP commonly report seeing multiple physicians before receiving the correct diagnosis. The symptoms — progressive weakness, numbness, balance problems — can mimic many other conditions.

If you have been told your test results are normal but something still does not feel right, a second opinion from a neuromuscular specialist may be the answer. We provide multi-disciplinary expert care to treat CIDP.

Contact us at [email protected]
Learn more at NeuroMDCenter.com

05/13/2026

Bella came to us as a patient at 10 years old with Guillain-Barre Syndrome (GBS), and we later found she had CIPD. Now she is thriving and working to help others with GBS as our Research Coordinator at the Neurology Rare Disease Center.

We celebrate you, Bella Herman, and we are lucky to have you as part of our team!

Contact us at [email protected]
Learn more at NeuroMDCenter.com

May is GBS/CIDP Awareness Month!Guillain-Barré Syndrome and Chronic Inflammatory Demyelinating Polyneuropathy are rare a...
05/10/2026

May is GBS/CIDP Awareness Month!

Guillain-Barré Syndrome and Chronic Inflammatory Demyelinating Polyneuropathy are rare autoimmune disorders that attack the peripheral nervous system — causing weakness, numbness, and in severe cases, paralysis. Yet despite affecting hundreds of thousands of people worldwide, they are frequently misunderstood and delayed in diagnosis.

The Neurology & Neuromuscular Care Center is a certified GBS/ CIDP Center of Excellence and is shining a light on GBS and CIDP this month. Follow along all month for education, patient stories, and the latest treatment updates.

🔗 Learn more at NeuroMDCenter.com

Leaders from healthcare, research, and industry recently came together at the Neurology & Neuromuscular Care Center for ...
03/12/2026

Leaders from healthcare, research, and industry recently came together at the Neurology & Neuromuscular Care Center for a Rare Disease Roundtable hosted in collaboration with BioNTX. The discussion focused on improving coordination in rare disease starting from earlier diagnosis to faster pathways to treatment.

We were honored to welcome Senator Tan Parker , who presented Dr. Diana Castro with an official State of Texas Recognition for her leadership in rare disease care and the opening of the new center.

Meaningful progress in rare disease will require stronger collaboration across institutions, better data sharing, and more connected clinical research. Conversations like this help move that work forward for patients and families across North Texas.

Thank you to everyone who joined us in advancing the future of rare disease care.

Algunos superhéroes no usan capa… usan valentía. 💙En clínica con este increíble guerrero de Duchenne que recibió terapia...
02/07/2026

Algunos superhéroes no usan capa… usan valentía. 💙

En clínica con este increíble guerrero de Duchenne que recibió terapia génica y continúa evolucionando de forma maravillosa. Momentos como este me recuerdan por qué impulsamos la ciencia con urgencia y con el corazón.Nunca dejen de tener esperanza.
Some superheroes don’t wear capes… they wear courage. 💙

In clinic with this incredible Duchenne warrior who received gene therapy and continues doing amazing. Moments like this remind me why we push science forward with urgency and heart. Never stop being hopeful.

I'm honored to be part of ' vital work in improving care for adult DMD patients - we're taking the first steps! 🥰.  Es u...
12/08/2025

I'm honored to be part of ' vital work in improving care for adult DMD patients - we're taking the first steps! 🥰. Es un honor ser parte de el trabajo vital de ‘s para mejorar el cuidado de adultos con DMD- estamos tomando el@primer paso 🥰

✨ A historic moment ✨Today we celebrate the first Chilean patient to receive Elevidys, the groundbreaking gene therapy f...
09/23/2025

✨ A historic moment ✨

Today we celebrate the first Chilean patient to receive Elevidys, the groundbreaking gene therapy for Duchenne muscular dystrophy. 💙

This is more than science — it’s hope, courage, and the promise of a brighter tomorrow. 🌍💪

✨ Un momento histórico ✨

Hoy celebramos al primer paciente chileno en recibir Elevidys, la innovadora terapia génica para la distrofia muscular de Duchenne. 💙

Esto es más que ciencia: es esperanza, valentía y la promesa de un mañana más brillante. 🌍💪

✨ Grateful to have joined the BioNTX meeting today at the Hilton Anatole in Dallas!I had the honor of speaking on the se...
09/17/2025

✨ Grateful to have joined the BioNTX meeting today at the Hilton Anatole in Dallas!

I had the honor of speaking on the session:
“Putting Patients First: Access and Business Strategies for Better Care.”

It was inspiring to stand alongside leaders who are committed to innovation, collaboration, and keeping patients at the center of every decision. Together, we explored how business strategies and access initiatives can work hand in hand to deliver better care for families living with rare conditions.

Thank you to BioNTX for creating such a powerful space for these conversations. 💙

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1651 Justin Road
Flower Mound, TX
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