Supporting Families. Saving Lives.
It can take a while to get an appointment with a SADS expert, and it can take even longer to get some test results back, such as genetic testing results.
Here is a list of things you do to stay safe and healthy while you are waiting for your appointment.
Follow the Drugs to Avoid List If there is a chance you have a SADS condition, make sure you don’t take any drugs that could make your condition worse:
Learn CPR, and know where the AEDs are If you or someone in your family might be at risk of a sudden cardiac arrest, make sure everyone in the family knows CPR, and notice where AEDs are.
Check your Health Insurance Check to see if your policy will cover medically necessary diagnostic and treatment options. Consider getting Life Insurance Many patients have difficulty qualifying for life insurance, and some health insurances once they have a diagnosis from their doctor. Consider getting a plan before your diagnosis.
If anyone in your family has symptoms, urge them to get screened immediately. If a family member is fainting, is diagnosed with epilepsy, there is a strong family history or has other warning signs for a SADS condition, don’t wait until you are diagnosed, have them get screened by an expert immediately
Avoid triggers for SADS conditions:
Learn about treatment options: The main aspects of treatment involve:
Medications Beta Blockers Left Cardiac Sympathectomy Dennervation (LCSD) ICDs
- If you are anxious about a diagnosis, you might be on the internet doing research. There is a lot of incorrect and scary information on the internet. Make sure you only get your information from trusted sources such as the SADS website, the Mayo Clinic website, and other information from your doctor.
- Contact the SADS Foundation with questions, we have a friendly staff who are happy to answer any questions you might have, or direct you to medically accurate answers. 1-801-272-3023