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 newpatient@neuromdcenter.com
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 with 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.

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. 💙

💙 Today on World Duchenne Awareness Day, our hearts are with every child, teen, adult, and family facing Duchenne muscul...
09/07/2025

💙 Today on World Duchenne Awareness Day, our hearts are with every child, teen, adult, and family facing Duchenne muscular dystrophy.

This day is about more than awareness — it’s about love, courage, and community. Every smile, every step, and every victory matters. 🌍✨

We stand united with our patients and families — you inspire us daily with your strength and resilience. Together, we will continue to fight for hope, better treatments, and brighter tomorrows. 💪💙

HERE’S THE FLYER FOR THE UPCOMING CONCERT THAT BENEFITS THE NEUROLOGY AND NEUROMUSCULAR CARE CENTER WITH
03/27/2025

HERE’S THE FLYER FOR THE UPCOMING CONCERT THAT BENEFITS THE NEUROLOGY AND NEUROMUSCULAR CARE CENTER WITH

Had an incredible time at the live podcast for  at the  meeting. What a great experience, to have a live conversation wi...
03/25/2025

Had an incredible time at the live podcast for at the meeting. What a great experience, to have a live conversation with an patient and SMA mom of 2,

And thank you for the beautiful red suit!

Happy Holidays to all our patients and families. Thanks for trusting us with your care. We love what we do and it would ...
12/25/2024

Happy Holidays to all our patients and families. Thanks for trusting us with your care. We love what we do and it would not be posible without YOU ♥️

Thank you  !! For highlighting our patients and their fight!!
10/04/2024

Thank you !! For highlighting our patients and their fight!!

Melanie Sanford fought to get her son Hudson a breakthrough gene therapy to stop the progression of the fatal disease Duchenne Muscular Dystrophy. She rushed to get him access just days before he turned 7 and aged out of eligibility.

On this World Duchenne Awareness Day, let's come together to:* Raise awareness about DMD and its impact on families worl...
09/07/2024

On this World Duchenne Awareness Day, let's come together to:

* Raise awareness about DMD and its impact on families worldwide
* Support research efforts to find effective treatments and a cure
* Advocate for access to care and support services for those affected by DMD

Saturday September 7th, I will be giving a talk in San Antonio about research in SMA. Come and join us!
09/06/2024

Saturday September 7th, I will be giving a talk in San Antonio about research in SMA.
Come and join us!

Grab your headphones and listen to the first episode of the Life Takes Muscle podcast.​Join host Dr Diana Castro, a lead...
06/22/2024

Grab your headphones and listen to the first episode of the Life Takes Muscle podcast.​

Join host Dr Diana Castro, a leading SMA expert who has cared for hundreds of individuals living with . Dr Castro has conducted research, written many published papers, and given multiple national and international lectures. ​

Dr Castro will host a variety of guests living with SMA and HCPs involved in SMA care, providing key insights surrounding the muscle’s role in the disease. ​

Tune in to hear unique stories and perspectives from guests who are part of Life Takes Muscle. Episode 1 can be found at https://lnkd.in/ebAsTNGq

Address

2817 S Mayhill Road Suite 115
Dallas, TX
76208

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