Head and Neck Cancer Support Group Meeting

Head and Neck Cancer Support Group Meeting

Thu, Jan 4, 2024
5:00pm to 6:00pm MT

Description

The Head and Neck Cancer support group meets monthly on Zoom the 1st Thursday of every month from 5:00 to 6:00 p.m. Arizona time (find your time zone). All are welcome.

This virtual group is open to patients (and caregivers) who are in any stage of their treatment journey with head or neck cancers. This group fosters a sense of community amongst survivors and allows participants to both receive and offer support.

To register, contact: Katie Lespron MSW, LMSW 480-342-4005 or Lori Klusovsky PA-C ENT 480-342-2890 for additional information.

Location

Online

Contact

Katie Lespron, MSW
Katie Lespron, MSW
Email: lespron.katherine@mayo.edu
Phone: 480-342-4005
Lori Klusovsky PA-C ENT
Lori Klusovsky PA-C ENT
Email: Klusovsky.Laura@mayo.edu
Phone: 480-342-2890

How to you deal without saliva and no taste?

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@kloseknit311

How to you deal without saliva and no taste?

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going through radiant I lost my taste and saliva was thick..... I had 30 treatments of rad. and the only thing for some reason I could eat fry'd eggs and home fries and peanut butter of which I could taste

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Has anyone on here had photon therapy for their neck cancer and were the results good?

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@cancerback

Has anyone on here had photon therapy for their neck cancer and were the results good?

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did u have surgery first...?

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@richardpaul

going through radiant I lost my taste and saliva was thick..... I had 30 treatments of rad. and the only thing for some reason I could eat fry'd eggs and home fries and peanut butter of which I could taste

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Taste is definitely temporarily compromised. Don't compare yourself to others because it all depends on where you were radiated and your body. The good news it is temporary and you will be back to normal or a new normal at least.
Keep forcing healthy soft foods with syrup, salts, miso glazes, avocados or whatever works to get your calories for the day. Stay focused on the end goal. It will return to normal. Hang in there!

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@richardpaul

did u have surgery first...?

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No, no surgery was proposed. this is a recurrence.

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@shielashepperd

Taste is definitely temporarily compromised. Don't compare yourself to others because it all depends on where you were radiated and your body. The good news it is temporary and you will be back to normal or a new normal at least.
Keep forcing healthy soft foods with syrup, salts, miso glazes, avocados or whatever works to get your calories for the day. Stay focused on the end goal. It will return to normal. Hang in there!

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your absolutely right.... it's been 2 years since my last day of Radiation treatment, I had the TORS surgery to remove my right tonsil and first lymph node. I had HPV. I see my ENT doctor every six months now. for follow ups.

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@cancerback

No, no surgery was proposed. this is a recurrence.

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may I ask u what type of cancer you had......mine was HPV of the right tonsil and the first lymph node

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metastatic cervival cancer to the supraclavicular node

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@richardpaul

going through radiant I lost my taste and saliva was thick..... I had 30 treatments of rad. and the only thing for some reason I could eat fry'd eggs and home fries and peanut butter of which I could taste

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I have Merkel carcinoma and have just completed 18 radiation treatments to the left side of my face and neck. My sense of taste has completely disappeared. So far nothing I try has any taste. I have heard taste will return and am hoping this is true! Thank you for sharing!

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