You just clicked a link to go to another website. If you continue, you will leave this site and go to a site run by someone else.
It is possible that some of the products on the other site not be licensed for sale in Canada.
Your browser is out of date
With an updated browser, you will have a better Medtronic website experience. Update my browser now.
By choosing to accept, you acknowledge that you are a Certified Healthcare Professional.
Living With the Therapy
While intrathecal baclofen therapy may help improve your severe spasticity through medication, you play an important role in your own treatment.
The following guidelines will help you maximise the benefit from your baclofen pump:
Your doctor may recommend that you restrict activity for 6 to 8 weeks after your surgery. As you become more active, discuss your level and type of activity with your doctor. Follow his or her suggestions about work, sexual activity, travel, recreation, hobbies, and exercise.
Talk with your doctor if you perform any excessive or repetitive activities that may damage your programmable pump and catheter. Certain activities that can increase or decrease the flow rate of your pump are also potentially dangerous.
Tell your doctor if you plan to travel. If necessary, he or she will adjust your pump refills to prevent serious injury or death from a travel-related change in your treatment.
People who live or travel at high altitudes are often exposed to lower air pressures for long periods of time. This continued exposure can increase the flow rate of the pump. If your doctor determines an increase in flow rate might pose a significant risk to you, he or she can adjust your infusion prescription accordingly.
Tell your other doctors and your dentist about your baclofen pump before you have any medical or dental procedures. Certain procedures could affect your safety or the performance of the pump.
Electromagnetic interference from sources such as diagnostic ultrasound, mobile phones and microwave ovens is unlikely to affect your baclofen pump. However, there are exceptions. For more information consult the patient manual or ask your doctor.
Those who suffer from severe spasticity and their family caregivers can share experiences, offer support, and better understand the challenges of living with spasticity.
Advocacy groups offer further information, support, and volunteer opportunities for those affected by cerebral palsy.
Information on this site should not be used as a substitute for talking with your doctor. Always talk with your doctor about diagnosis and treatment information.