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#47145 08-23-2006 04:35 AM
Joined: Aug 2006
Posts: 23
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Joined: Aug 2006
Posts: 23
The MD Anderson nurses taught my husband to do mouth and neck exercises at the beginning of Rad Tx (IMRT) - we just finished week 4 (yeah!). He doesn't do them very often I think because he doesn't feel any changes in his muscles yet.

When does the tightness start? Is it during tx or afterwards as things heal?

Should I "make" him do these exercises? He has an app't with a speech therapist today - perhaps she'll discuss this with him.

#47146 08-23-2006 07:50 AM
Joined: Mar 2002
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OCF Founder
Patient Advocate (old timer, 2000 posts)
OCF Founder
Patient Advocate (old timer, 2000 posts)

Joined: Mar 2002
Posts: 4,918
Likes: 70
Not doing the exercises, for the facial muscles and those used in masticataion, will make it difficult to open his mouth fully when this is all over, for his neck it will leave him with a limited range of motion. He needs to get off his butt and do this stuff, because once trismus sets into the muslce groups it is very hard, if not impossible in some patients, to reverse. At the very minimum he should be concentrating on maintaining the ability to open is mouth using a Therabite or wooden tongue blades every day from the begining of treatment to months after it is over. It's tough to survive this cancer and then find out that you can't open you mouth enough to enjoy eating again when it's all over!!


Brian, stage 4 oral cancer survivor. OCF Founder and Director. The first responsibility of a leader is to define reality. The last is to say thank you. In between, the leader is a servant.
#47147 08-27-2006 12:41 AM
Joined: Aug 2006
Posts: 23
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Joined: Aug 2006
Posts: 23
What is Therabite - no one has mentioned this to us! Do we need a prescription or can we buy it at the drugstore?

#47148 08-27-2006 02:08 AM
Joined: May 2006
Posts: 720
Likes: 1
"Above & Beyond" Member (500+ posts)
"Above & Beyond" Member (500+ posts)

Joined: May 2006
Posts: 720
Likes: 1
Use the forum's search function (at the top of this page) to search for Therabite -- make sure you Search in All Open Forums. It's been discussed quite a bit, and you could PM or e-mail the folks who have used it to get their experience.

You can find additional information using the search function on the main OCF pages.

And here's the Therabite website .


Leslie

April 2006: Husband dx by dentist with leukoplakia on tongue. Oral surgeon's biopsy 4/28/06: Moderate dysplasia; pathology report warned of possible "skip effect." ENT's excisional biopsy (got it all) 5/31/06: SCC in situ/small bit superficially invasive. Early detection saves lives.
#47149 08-27-2006 05:24 AM
Joined: Jan 2004
Posts: 1,116
Patient Advocate (1000+ posts)
Patient Advocate (1000+ posts)

Joined: Jan 2004
Posts: 1,116
Just wanted to add that I am a firm believer in the Therabite device, I still use it (not every day though, I probably should), I went from not even being able to get one finger in my mouth to being able to get 3. My insurance did not cover the cost, but it was well worth it.
Carol


Diagnosed May 2002 with Stage IV tongue cancer, two lymph nodes positive. Surgery to remove 1/2 tongue, neck dissection, 35 radiation treatments. 11/2007, diagnosed with cancer of soft palate, surgery 12/14/07, jaw split. 3/24/10, cancer on tongue behind flap, need petscan, surgery scheduled 4/16/10
---update passed away 8-27-11---

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