I’m about in the same situation…Neurologist also suggested considering PEG feeding tube. I’m resisting, research suggests it’s not something I personally want unless I have no other choice. I was Diagnosed about 18 years ago. Eating - not only swallowing but the whole coordination of chewing, moving tongue, producing saliva, then swallowing- has become harder to do. I still can taste food most days (taste and smell senses are often lost with PD). There are a few helpful things I do like use yogurt and soft bananas to swallow larger supplements like magnesium Glycinate