Dysphagia/difficulty swallowing and MS
Hi everyone, just reaching out to see if anyone has ever experienced worsening dysphagia/difficulty swallowing with their MS? My dysphagia has been steadily worsening to the point I can only have a full liquid diet (can't swallow purees without pain), with some small improvements from time to time over the past few years. Am I just a weird one or have others experienced similar with their MS? I would be so grateful if anyone is willing to share their experiences with dysphagia and MS, and any related suggestions to help me.
Thank you
Hi
,
We appreciate you reaching out.
Dysphagia is more common than you'd imagine among MS patients.
As we wait for others to chime in with their personal experiences, I like to share these two articles with you. The first one goes into great detail on dysphagia, including assessment and treatment options: https://multiplesclerosis.net/symptoms/swallowing-problems. The second is one of our patient leader's perspective and experience with dysphagia: https://multiplesclerosis.net/living-with-ms/trouble-swallowing-issues
Wishing you all the best, Doreen (Team Member)
