So, here it is:
I can't drink with the medication I take, but if I did, that would have to be cut too. Man, do I miss my famous summertime daiquiris! I didn't get a single one this year, and I could really go for one right about now. I don't drink Coke, or any soft drinks at all. Coming from a complete Coca Colaholic, that was hard, but it was done, and I might have one every now and again, but nothing like morning noon and night like I used to. It was seriously the only thing I ever drank! Caffeine= bad for liver mmkay?
We cut out red meat, so, NO beef, anything. Ever. We use ground turkey or pork (Sprouts has some awesome ground pork) Anything we buy as in pasta's, rices, or breads, I make sure are whole grain, or whole wheat. We eat lots of fish and chicken. The more fish for me, the better for my joints (supposedly) HEB has some of the best salmon burgers! Fruits and veggies are just as important too. We do not do corn or bananas since they seem to backup the little one and give her more agony so they do more harm than good. There are only 2 vegetables she will eat; green beans and peas! HAS to be Le Sueur peas. I swear, that girl...I kid, if that's what it gets for her to eat them, then Le Sueur is what she will get! We have also re-evaluated our dairy intake. Not so much for us, but for Baby Bear and her poor tummy problems(She goes to the GI next month). I also have an issue with dairy and have noticed more inflammation and joint tenderness when I have had dairy. Like my chicken spaghetti the other night! So we do it all in moderation, a lot of moderation. Soon enough, I should be dairy free as well. At least until MY stomach gets back in order. I stay off the fried foods and away from the fast foods as much as possible because those oils are NOT good for my liver to be processing. Olive oil is much better, so that is what we use.
There you have it, in a nutshell. No, I am not on a "diet" I don't think is for everyone or anyone trying to lose weight. But, if you do have liver issues, you may want to give it a try. I have already seen my counts go down, and pray they get back to normal soon!
On another note I just took my 3rd dose of Humira. I take it every other week, while I still inject the methotrexate once a week. I have not had many pain free days, but I am nowhere in near as much pain as I used to be. I still have my good days and bad days. The Humira stops the crippling effects that RA can cause. I am still tired all.the.time and I cannot stand it! A good thing is that my eye has not flared since I have been on the methotrexate, so I will take it, no matter how much I hate the stuff.