Community Member
7 days agoI have salivary gland cancer. Diagnosed and surgery last year. Now I have severe trismus and can barely open my mouth to eat.has anyone gone through this?
Community Member
7 days agoTrismus can be a challenging side effect following surgery in the head and neck area, and it's completely understandable to reach out for support from others who may have experienced similar difficulties. Many community members have found that working with speech therapists or occupational therapists who specialize in head and neck issues can be helpful, and there are often specific exercises and techniques that may provide some relief over time.
Community Member
3 days agoHi Vicki, Yes! I also have severe trismus. For my last surgery, they had to force it open to do their work! Now, I'm getting a device that I will use several times a day, to stretch it. I can't eat. I have a feeding tube for all my nutrition. There are specialists and devices for trismus. Your surgeon should inform you on the options. I wish I had known sooner... Best of luck to you, Barbara
Community Member
3 days agoI have had speech therapy and physical therapy. I’m on my third session of physical therapy. I also use a therabite device to try and stretch my mouth. I was doing better until I developed an infection after a second surgery. I’m now back to square one with my trismus.
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