NeuroStar® TMS Therapy
FDA-cleared, non-medication depression treatment
(855) 940-4867
Medically reviewed on by
Regional Medical Director Greater St. Louis
Trauma, separation from loved ones, injury, extreme stress, and death are all potential hazards faced by military families. These pressures can lead to major depressive disorder for service men and women, as well as their loved ones. TMS can be an effective depression treatment for military families.
Depression can linger for members of the military long after their tours of duty are over. The U.S. Department of Veterans Affairs (VA) estimates that:
Many factors can increase the risk of depression for service men and women. These include:
The risk of depression also may increase for people with post-traumatic stress disorder (PTSD). The trauma they’ve experienced can trigger symptoms of depression, such as sadness, guilt, hopelessness, or insomnia. Some of the VA’s sobering statistics on PTSD and members of the military:
These issues aren’t limited to those who served. Loved ones and close relatives can also suffer from depression, especially during deployment. They may also struggle with PTSD if the enlisted member of the family experienced trauma or injury during military service.
Has your loved one acted differently since separating from active duty? Or are you feeling a gnawing anxiety with your partner on tour of duty? It’s helpful to know if depression is the cause. Watch for these signs:
Depression treatment for military families usually entails talk therapy (perhaps with a counselor who is also trained in treating PTSD) and/or antidepressant medications. Sometimes, it is also beneficial for military members to join a support group of fellow veterans where they can share their stories with others who have similar experiences.
TMS therapy for PTSD isn’t cleared by the U.S. Food and Drug Administration. However, TMS can be used to treat symptoms of major depressive disorder.
This can be an effective treatment method for members of the military and their families who haven’t gotten the results they want from medication or talk therapy. TMS can be used on its own or in conjunction with other treatment modalities.
The science behind how TMS works: An electromagnetic coil is placed on the patient’s scalp. It emits magnetic pulses, which turn into gentle electrical currents that stimulate targeted areas of the brain. Treatment sessions last about 18 to 40 minutes and take place over several weeks. Sessions take place every weekday for the first several weeks before tapering in frequency.
TMS for military members offers several benefits, including:
Plus, TMS for military members is covered by TriCare. This is the health insurance carrier for active duty service men and women, as well as family members, retirees, and members of the Reserve and National Guard.
Greenbrook TMS is honored to help military families find solutions for depression with TMS treatment. We understand the importance of supporting members of the military in their quest to improve their mental health. Our chief medical officer, Dr. Geoffrey Grammer, is a decorated Army colonel who served two tours of duty in Iraq. He also developed the Transcranial Magnetic Stimulation Program at Walter Reed National Military Medical Center as its chief of Inpatient Psychiatric Services. Contact us today to learn how we can help you and schedule your free consultation.
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NeuroStar Adult Indications for Use
The NeuroStar Advanced Therapy System is indicated for the treatment of depressive episodes and for decreasing anxiety symptoms for those who may exhibit comorbid anxiety symptoms in adult patients suffering from Major Depressive Disorder (MDD) and who failed to achieve satisfactory improvement from previous antidepressant medication treatment in the current episode.
The NeuroStar Advanced Therapy System is intended to be used as an adjunct for the treatment of adult patients suffering from Obsessive-Compulsive Disorder (OCD).
NeuroStar Adolescent Indications for Use
NeuroStar Advanced Therapy is indicated as an adjunct for the treatment of Major Depressive Disorder (MDD) in adolescent patients (15-21).
Important Safety Information
NeuroStar Advanced Therapy is only available by prescription. A doctor can help decide if NeuroStar Advanced Therapy is right for you. Patients’ results may vary.
The most common side effect is pain or discomfort at or near the treatment site. These events are transient; they occur during the TMS treatment course and do not occur for most patients after the first week of treatment. There is a rare risk of seizure associated with the use of TMS therapy (<0.1% per patient).
Visit neurostar.com for full safety and prescribing information.
Important Safety Information
What is the most important information I should know about SPRAVATO®?
SPRAVATO® can cause serious side effects, including:
Do not take SPRAVATO® if you:
If you are not sure if you have any of the above conditions, talk to your healthcare provider before taking SPRAVATO®.
Before you take SPRAVATO®, tell your healthcare provider about all of your medical conditions, including if you:
Tell your healthcare provider about all the medicines that you take, including prescription and over-the-counter medicines, vitamins and herbal supplements. Taking SPRAVATO® with certain medicine may cause side effects.
Especially tell your healthcare provider if you take central nervous system (CNS) depressants, psychostimulants, or monoamine oxidase inhibitors (MAOIs) medicine. Keep a list of them to show to your healthcare provider and pharmacist when you get a new medicine.
How will I take SPRAVATO®?
What should I avoid while taking SPRAVATO®?
Do not drive, operate machinery, or do anything where you need to be completely alert after taking SPRAVATO®. Do not take part in these activities until the next day following a restful sleep. See “What is the most important information I should know about SPRAVATO®?”
What are the possible side effects of SPRAVATO®?
SPRAVATO® may cause serious side effects including:
See “What is the most important information I should know about SPRAVATO®?”
Increased blood pressure. SPRAVATO® can cause a temporary increase in your blood pressure that may last for about 4 hours after taking a dose. Your healthcare provider will check your blood pressure before taking SPRAVATO® and for at least 2 hours after you take SPRAVATO®. Tell your healthcare provider right away if you get chest pain, shortness of breath, sudden severe headache, change in vision, or seizures after taking SPRAVATO®.
Problems with thinking clearly. Tell your healthcare provider if you have problems thinking or remembering.
Bladder problems. Tell your healthcare provider if you develop trouble urinating, such as a frequent or urgent need to urinate, pain when urinating, or urinating frequently at night.
The most common side effects of SPRAVATO® include:
If these common side effects occur, they usually happen right after taking SPRAVATO® and go away the same day.
These are not all the possible side effects of SPRAVATO®.
Call your doctor for medical advice about side effects. You may report side effects to Johnson & Johnson at 1-800-526-7736, or to the FDA at 1-800-FDA-1088.
What is SPRAVATO® (esketamine) CIII nasal spray?
SPRAVATO® is a prescription medicine used:
SPRAVATO® is not for use as a medicine to prevent or relieve pain (anesthetic). It is not known if SPRAVATO® is safe or effective as an anesthetic medicine.
It is not known if SPRAVATO® is safe and effective for use in preventing suicide or in reducing suicidal thoughts or actions. SPRAVATO® is not for use in place of hospitalization if your healthcare provider determines that hospitalization is needed, even if improvement is experienced after the first dose of SPRAVATO®.
It is not known if SPRAVATO® is safe and effective in children.
Please see full Prescribing Information, including Boxed WARNINGS, and Medication Guide for SPRAVATO® and discuss any questions you may have with your healthcare provider.
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