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← Return to Severe pain eating 7 weeks post-RT
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Severe pain eating 7 weeks post-RT
Head & Neck Cancer | Last Active: 3 hours ago | Replies (45)Comment receiving replies
@ranchroad
Hi,
Cheezeyburgies are not in my vision. I get most of my nutrition in my feeding tube. Easy-peasy. The new normal is finding foods that work for you. It's really taking it in with trial n error. I'm almost 3 yrs out from SCC Tongue and one neck lympher. Radiation side-effects are long-lasting. There's hope and light in this journey. Lean on us. We all get it. Wishing you well.
Replies to "@ranchroad Hi, Cheezeyburgies are not in my vision. I get most of my nutrition in my..."
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@zenren14 Thank you for sharing that — it really helps to hear from someone further down the road. The “new normal” idea resonates a lot; I’m still in the thick of the trial-and-error stage and it’s been frustrating. Knowing that things can settle and that others have found what works for them gives me some hope. I appreciate the reminder to lean on this community — it means a lot right now. Wishing you continued healing and comfort, too.