Fodmap Eating Plan
I will be starting on the fodmap eating plan next week and I'm looking for some suggestions about following this plan for the first four weeks. Did you have the guidance of a dietician? Did you find any books, recipes, YouTube videos that helped you? I'm also wondering how you went about the addition of foods after the four-week restricted period?
Any success stories (I'd really like to hear them). Anything that was particularly helpful or difficult for you?
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Understand all of this….I carry protein in my urine from my amyloidosis diagnosis that I had a stem cell transplant 15 yrs ago & my husband is diabetic. Going through tremendous fatigue right now….. I have hypothyroidism & wonder if that’s it or long term effects of having covid 2 times…. I called & can’t get into see my PC until Oct…..☹️
Under the guidance of a certified dietitian I followed FODMAP plan. The first think my dietitian had me do was download the Monash FODMAP app. I was advised to eliminate the foods I used that were rated red. My diet was rather bland. After a couple of months the reintroduction phase started. That lasted for quite a while. I have learned to monitor what I eat. Every once in a while my body lets me know that I have eaten something I shouldn’t have. My diet remains bland. I try to avoid processed and prepared foods. I mainly shop the perimeter of the grocery store.
I went through the process with the help of two sessions with the Mayo dietician. It is a meticulous process with big payoffs. Some have tried to do it on their own but I don’t recommend that. For me it’s a lifelong diet, with very few changes from the DASH/ Mediterranean diet we are on. There are two foods I have omitted for most of the time, with eating small portions if invited out for a meal. There are other foods that I use in small portions when cooking at home. Really the changes for me were not dramatic but a friend went through the same process at Mayo and she absolutely cannot eat any garlic. This is hard for her at restaurants. I have tried many things in my lifetime to solve my gastro problems. Nothing helped until FODMAP came along. My suggestion is to be patient, find a dietician trained in this, and enlist family and friends to be helpful during your time of discernment of what you can eat.
Thank you for your reply ~ I am just considering this Fodmap low diet. Please let me know how it goes. Was there a charge for the consult and follow up?
Thank you for your comments. I have decided to also go lactose free and gluten free. If you have suggestions re: Fodmap diet, please share.
How do you feel on the colestromine? Is it easy to take? My doctor has suggested it.
Thank you
I must admit gluten free and lactose free really helps. Easier to find good lactose free products or take a lactase pill than finding great tasting bread!
Gluten free baking though is fantastic!
I agree that lactose and gluten free seem to help. I’ve followed low FODMAP for about two months and use both the Monash U and Fig apps and totally endorse both. My GI diagnosed SIBO so I’ve just finished a two week course of Xifaxan. I refused to take Neomycin due to my mild tinnitus and my GI supported that decision. I had started some reintroduction but stopped when SIBO results came back since the GI told me to stay on low FODMAP while on the Xifaxan . I am debating at this point working with a dietitian. It’s costly since Medicare won’t reimburse for it. Also wondering if anyone in SoCal where I am or in Seattle area has used the IBS Treatment Center with Dr. Wangan, etc.?? Saw him on YouTube. Again very costly to pay out of pocket.
Totally understand you being hesitant to pay out of pocket for health care. But I bit the bullet and paid for functional medicine doctor. Best $ I’ve ever spent. She helped me tremendously!! Might I also suggest doing a food sensitivity test. That was one of the things that helped me the most.
What is a food sensitivity test? The breath test?