Greetings all.
My husband was diagnosed with PPMS in December 2016. We went thru two years of being told that it was not MS because he did not have any lesions on his brain. He had a total meltdown at that time and became a quadriplegic within a couple months of his being diagnosed. He had to have two kidney procedures within a six month period that almost did him in. He was on hospice for eight months after those but has been off hospice and is relatively stable for the past six months.
Basically I would like to know how to improve his diet and try to get him to eat more. The meds he is on make lots of the foods he used to love unappealing to him now. Any suggestions? Thank you.