Swallowing difficulties
I have SFN and was recently diagnosed with a swallowing disorder called Oropharyngeal Dysphagia which weakens the throat muscles and makes it difficult to swallow. One of the risk factors for this condition is neurological or nervous system disorders. So my question is, can this swallowing condition be one of the effects of Neuropathy? Also I have always suspected my many years of Statin drugs has caused me to have neuropathy and since Statins are a known cause of muscle problems, I suspect my throat muscles are the latest victims of Statins. (I no longer take Statins.)
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I recently have begun having indigestion and some choking when I eat foods that are dry and acidic. I have been bothered for years but to lesser degree and was diagnosed with slatsky's disease about 20 years ago. I have never had stretching or dilation of the throat. I am wondering if anyone else has slatzky's disease and what treatment they have had?
Hi I’m a speech pathologist and speech pathologists deal with swallowing disorders (dysphagia). That’s mostly what I deal with at my job. Has your GI doctor done a full work-up? If not, he should. The burning you feel could be caused by reflux due to GERD. There is medication for this. Also I would suggest you have a modified barium swallow study, which is an easy non-invasive procedure. Also see an ENT who should do endoscopy to view your throat. Let me know how it goes!
I am having endoscopy on October 14 at Mayo. Really looking forward to answers. Thank you so much for your informative and thoughtful response.
Sorry to hear about your difficulties. Diagnostic studies you may benefit from:
- Modified barium swallow study which assesses swallow.
- Videostroboscopy which assesses the vocal cords.
- Esophageal manometry which assesses the esophagus' ability to push food down into your stomach.
Your symptoms are definitely something your physician needs to be aware of. They may want to refer you to a neurologist or other specialist.
Praying you find relief soon.
I see that you were first diagnosed with idiopathic neuropathy. Then when it moved down into your extremities, you were diagnosed with CIDP. Is there more to it that I missed?
Thank you for your response. I was evaluated by an ENT PA the other day. Scoped the nasal passages down to vocal cords. Possible mild acid reflux. Recommends Flonase each evening. Anti-reflux med morning and evening. Right now the swallowing/sinus problems are low on my list. The severe, chronic pain levels(8-9 daily) are my main concern. Three and a half years searching for answers. No real solutions. Even with meds, it's still pretty bad. I have been trying to get a trial of a spinal cord stimulator for three months. The wheels of medicine turn very slowly here in Delaware. Appreciate your prayers.
It is believed that I probably had CIDP ten years earlier when I got the sleepy symptoms in my finger tips, and after an incomplete diagnostic exam was given an idiopathic "diagnosis." It was after the symptoms started expanding that I "demanded" a more comprehensive exam to determine the cause, which led to the CIDP diagnosis.
Thanks. I guess the neurological tests I had done must have ruled our CIDP. The mystery continues.
If you have not been test for H-Pylori you should do so. Maybe they will check when you have your endoscopy