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 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.

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

I left the University June 2022 to open a clinic to improve access and quality of care. Here we are 2 years later with t...
06/20/2024

I left the University June 2022 to open a clinic to improve access and quality of care. Here we are 2 years later with this amazing group of people. Missing Memo in the pic! Thanks for trusting me ❤️

May is international Guillian-Barré Syndrome (GBS) and Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) awarenes...
05/02/2024

May is international Guillian-Barré Syndrome (GBS) and Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) awareness month!
As a Center of Excellence for the treatment of GBS and CIDP, we want to spend the month of May educating and spreading awareness about these conditions and highlighting our patients who live with these disorders. Stay tuned all month for more information and resources on GBS|CIDP!

Yesterday we got to celebrate our wonderful admin, Sofia! From being the first smiling face people see when they walk in...
04/26/2024

Yesterday we got to celebrate our wonderful admin, Sofia! From being the first smiling face people see when they walk in the door to making sure everything runs smoothly behind the scenes, she has been such an integral part of the team & clinic. Thank you so much for all you do for us and the patients! ♥️

✨Check out this article on the Dallas Morning News! ✨We are so honored to be a part of Hudson’s care team for Duchenne M...
04/06/2024

✨Check out this article on the Dallas Morning News! ✨

We are so honored to be a part of Hudson’s care team for Duchenne Muscular Dystrophy. Hudson and his family has inspired us all with his bravery and resilience throughout his Elevidys journey, and we are excited to see all that is to come!

Copy the link below or check out the link in our bio for access

https://www.dallasnews.com/news/public-health/2024/03/31/a-race-against-time-one-familys-plight-to-treat-their-sons-rare-muscle-wasting-disease/?outputType=amp

04/06/2024

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Dallas, TX

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