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.

Meet Jennifer Avelar  one of the people helping move our research mission forward.As Head of the Clinical Research Depar...
08/20/2026

Meet Jennifer Avelar one of the people helping move our research mission forward.

As Head of the Clinical Research Department at the Neurology Rare Disease Center, Jennifer helps coordinate the work behind clinical studies and keeps the research process moving with care, precision, and purpose.

Research is not only about protocols.

It is about people, communication, and creating better opportunities for patients and families.

We are proud to have Jennifer as part of the team behind the mission. 💙

08/20/2026

La oportunidad no debería depender de dónde vives.

Una de las cosas que más amo de nuestro trabajo en investigación es poder recibir pacientes de otros países, incluyendo familias de Latinoamérica.

He trabajado con pacientes de Argentina, México y otros lugares que, de otra manera, tal vez no tendrían acceso a ciertas oportunidades de investigación.

Cuando un estudio y su protocolo lo permiten, hablamos con las compañías y buscamos maneras de reducir barreras, incluyendo apoyo con algunos costos de viaje.

No siempre es sencillo. Pero vale la pena intentarlo.

Porque para mí, la investigación también significa crear acceso.

Y una familia no debería quedarse fuera de una conversación solo por vivir lejos.

Más acceso. Más información. Más oportunidades.

NRDC

08/18/2026

Yo puedo conocer la enfermedad. Pero ustedes conocen a su hijo.

Conocen sus cambios, sus noches difíciles, sus miedos, sus señales y esas pequeñas cosas que nadie más ve. Por eso admiro profundamente a las madres y padres de niños con enfermedades raras.

Viven atentos. Preguntan. Luchan. Aprenden. Y siguen adelante incluso en los días más difíciles.

Como médicos, nuestro trabajo no es hablar por encima de ustedes. Es escucharlos, trabajar con ustedes y hacer todo lo posible para que la vida de sus hijos sea un poco mejor.

Ustedes son una parte esencial del equipo de cuidado. ❤️

08/17/2026

Why We Built Neuro-MD Center Differently

When I created Neuro-MD Center, I wanted to make care easier to access and easier to navigate.

NNCC operates as a nonprofit clinical center, while NRDC focuses on clinical research.

In rare disease, time matters. Patients should not have to wait months for care or feel lost inside a complicated system.

We built this center to feel different:

More access. Less friction. More human care.

Because patients with rare diseases already carry enough.

08/11/2026

When the System Makes You Forget Why You Started

There was a moment when I realized how easy it is for physicians to get lost in the system.

You are running all day.
Your autonomy gets smaller.
Someone else decides what “productivity” should look like.
Success becomes how many patients you can see—not always the quality of the care you can give.

And slowly, you can lose yourself inside that structure.

I think that is part of why burnout is so common.

For me, discovering a different way of thinking about care was a revelation.

It felt exciting to learn again.

To imagine something outside the usual model.

To remember that medicine can still be creative, human and built differently.

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

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1651 Justin Road
Flower Mound, TX
75028

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