Monday, August 24, 2009

Cauliflower, Broccoli and Squash- Oh My

This has nothing to do with anything, just thinking about it. I have been trying to eat healthier for a LONG time, way before I got the MS diagnosis. It is a challenge though, especially when you have been a finicky eater throughout life. My tastes have grown somewhat over the years though, and lately I have been stepping up the pace on trying new foods. I have recently had squash on a couple of different occasions, and while it isn't something I would think about cooking, it actually wasn't bad. I put it on my "so-so" list for now, but will probably add it into my diet for variety. The same with cauliflower. They served me cauliflower on my first hospital stay in May. I ate it because it was on my plate, and I needed nutrition. I can't say I particularly enjoyed it, but again, it was so-so. On my second hospital stay they must have got a good deal on it, because I got cauliflower every day. And I ate it every day. I will probably add it to the rotation as well.

Broccoli I have eaten through the years, but only cooked. And it has to be chopped. Preferably in a casserole or something. I have tried it raw, at salad bars and such but that just doesn't do it for me. I guess I don't like the texture, it seems dry and crumbly and tastes like weeds?

For the MS'ers I am going to be adding some resources and links about diet going forward. Don't be afraid to research diet and I urge you to include dietary needs with your medical team to get their advice regarding your own particular situation.

About My Blog

This is my personal blog. It details my own personal experiences with MS, as well as other ramblings about my life. I am NOT a medical professional and cannot offer advice or opinions of a medical nature. If you need medical atention, please contact a physician or, in emergencies, your nearest hospital emergency room. MS has many faces, and every single patient has his or her own unique experiences and challenges.

The links I provide are things I think may be of interest to those with MS or their friends and family for further research, and does not constitute an endorsement.