If someone you know has tardive dyskinesia (TD), you can be their champion
You may not have TD, but you might know someone who does
As a caregiver of someone living with TD, you may be taking on the responsibility of identifying and managing their condition.
Caring for someone with TD can be challenging. They may not realize that the uncontrollable movements they are exhibiting are signs of TD. Without fully understanding the scope of their condition, they may even reject seeking help.
However, you may be one of the few people who can positively influence this ongoing conversation. Use your role to make a difference.
Here are some tips for TD support:
Here are some tips for
Educate yourself on the cause and impact of TD
TD is associated with taking certain kinds of important medications, such as antipsychotics, for at least a few months
Know what TD looks like and how to recognize it
The uncontrollable movements of TD may appear in the lips, jaw, tongue, and eyes. TD can also affect the upper body, arms, hands, legs, and feet
Keep an eye out for signs and symptoms of TD
If someone you know is experiencing uncontrollable movements, they may not be aware of these movements. You can help them learn to recognize the condition and get the help they need
If you think someone you know may have TD, encourage them to talk to their doctor
If you think someone in your life may have TD, ask them if they would consider talking to their healthcare team about TD or related movement disorders
You may notice movements they don’t
If someone in your care starts to have uncontrollable movements, they may not be aware of them. They also may not know that help is available.
Caregivers need support, too
If you’re caring for someone with TD, make sure you’re not forgetting to take care of yourself as well! Studies show that caregivers often neglect their own health due to the challenge of caring for others.
Some ways to make sure you’re staying healthy include
- Getting plenty of sleep every night
- Maintaining a balanced, nutritious diet
- Resting when you’re sick
- Exercising regularly
“Shelly’s TD symptoms are physical, but it’s really the emotional and social aspects that affect us.”
HUSBAND OF SHELLY, LIVING WITH TD