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Lyme diet
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Lyme Disease
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Katebirch
Veteran Member
Joined : Sep 2013
Posts : 1265
Posted 12/6/2014 4:47 PM (GMT 0)
I was just given this email from the herbalist whose protocol I am about
to start. She was so nice to give me all this info for free and not charge me for a consult! So here is what she said- I will copy and paste it below. But my question to you all becomes- okay, I am willing to try this but then WHAT THE HECK CAN I EAT????
I have already (mostly) eliminated gluten- but I do eat dairy and eggs. I mean I eat cheese and drink some milk. Also I eat a ton of eggs. And all the GF products use eggs. So if I cut out dairy gluten and eggs, what the heck do I eat? I cannot realistically eat only brown rice quinoa oats veggies and meats. I mean, I could if it will save my health. What do you guys think???
•Gluten free diet for at least 6 months, reintroducing gluten containing food items one at a time with at least a full week between additions
•Eliminate refined sugars
•Restrict natural sugars
•eliminate peanuts
•eliminate soy
•eliminate dairy
•eliminate eggs
•limit fruit to one serving daily
•Eliminate fruit juices
•Eliminate iced drinks
•Eliminate excessively cold foods
Add:
•Coconut milk
•Coconut oil
•Oats
- Long cooking organic oatmeal
- Milky Oats in tea
•Quinoa
•Home made vegetable juices
•Warm water with fresh lemon
Garden Peace
Veteran Member
Joined : Sep 2012
Posts : 4191
Posted 12/6/2014 5:16 PM (GMT 0)
Eggs would be the hardest for me. I wonder why she's having you avoid them. Maybe because it's a common allergen? I'd suggest you ask her about
that. I can understand the other things she's having you eliminate.
Traveler
Elite Member
Joined : May 2007
Posts : 36573
Posted 12/6/2014 5:40 PM (GMT 0)
I would think she's checking for food allergies. My list was much longer, but I only had to go 2 months. When I started reintroducing foods is when I discovered - very rudely - that I was very allergic to soy, allergic to MSG, don't tolerate white potatoes or peanuts well at all.
You can add in quinoa - it's a seed that has "complete protein" (all 9 amino acids), Lentils ( I love red lentil chili!!), beans, switch to almond butter (don't expect peanut butter when you try it and it's pretty good!), use rice cakes for some things, rye crackers for some other things.
If you would like, we can start a whole thread on food for those on allergen elimination diets. I can list some of what I've done, and others can chime in too - who knows what we might be inspired to try!!
Katebirch
Veteran Member
Joined : Sep 2013
Posts : 1265
Posted 12/6/2014 5:56 PM (GMT 0)
I am actually feeling pretty inspired by this path that lies before me.Thanks to traveler's suggestion I have connected with this new path- I think I finally get this lyme diet thing I have been questioning so much, and am willing to give it a go. ANd Ifeel hopeful about
the herbal healing.
Pirouette
Veteran Member
Joined : Mar 2014
Posts : 6235
Posted 12/6/2014 6:04 PM (GMT 0)
ohh… I'm so sorry. But… welcome to my world.
I can't eat legumes (although I do sneak in hummus in very small quantities). No soy, no corn, no dairy, sugar, fruit, eggs, nuts, nothing processed, no grains at all.
Thanks to leaky gut, I have all of those food sensitivities and my diet for the past year, as prescribed, consists of chicken, beef, pork, steamed veggies and salad. It is HARD. But as with leaky gut, ANYTHING you eat—even the good, non-inflammatory stuff (quinoa) starts to show up on the food sensitivity tests. Once I realized this, I stopped obsessing and just started focusing on healing my gut.
Now, 75% of my diet is pure and follows protocol. But every now and then (certainly not two days in a row) I do add in other foods. Try eating the same meal, 3x a day, e-v-e-r-y day. As long as I don't feel any GI distress in doing so, I don't stress too much. I don't know if I'd recommend this to anyone else who has severe allergies or doesn't yet know what their sensitivities are—since I'm still having a tough time healing my gut, according to recent tests.
But also, I can't make myself crazy by battling food every single flipping meal. There are times when I don't feel well enough to make meals. And I have a tough time with a nonexistent appetite so if something actually sounds good to eat, I'm more apt to prioritize that over the restrictive diet. As long as I don't overdo it.
Hope you find a good approach.
-p
Traveler
Elite Member
Joined : May 2007
Posts : 36573
Posted 12/6/2014 6:04 PM (GMT 0)
What I found to be most helpful is to not expect to replace foods, but to discover new ones. Trying to replace peanut butter was really hard, until I realized that there was nothing that was going to taste or feel like peanut butter, so when I had accepted that, I know really enjoy the taste of almond butter better!!
It's a crash course, but there are tons of resources online!! And feel free to post about
this on this forum - I'm a bit surprised more don't go through the complete allergen testing like this more often.
Who knows how long I've actually been allergic to soy and never noticed the effects due to it being gradually brought into more and more products so my tolerance was trying to build - but once my body had the time to actually heal from exposure to it, WOW! I had a bad reaction!
You do have to learn to read labels - every time!! No product can be considered safe each time you buy it -especially if you find you really do have an allergy. So learn to take your time in the grocery store reading labels - it saves a lot of frustration at home!
Katebirch
Veteran Member
Joined : Sep 2013
Posts : 1265
Posted 12/6/2014 6:19 PM (GMT 0)
I eat almond butter anyway and have for decades :) love it. I love rice and beans. the hard part for me is giving up cheese- I LOVE cheddar chees on everything.
And now I eat tons of eggs since being GF. Before lyme I ate LOTS of bread and cheese, that is really my favorite foods.
So now I will eat: oatmeal, nuts, stir fries with meat and veggies, lots more veggies, beans and rice, quinoa, salads, home made soups, . Still gonna have my small morning cuppa coffee with a splash of 1/2 and 1/2 and a spoonful of maple syrup though :), fish, um . . . guess that is gonna have to be it. Anyway, it is only temporary and at this point I will do it if it gets me back into health.
( I think I can I think I can ).
Katebirch
Veteran Member
Joined : Sep 2013
Posts : 1265
Posted 12/6/2014 6:22 PM (GMT 0)
I forgot to add this part of the email she sent:
Exercise daily: Gentle walking, swimming, light strength training
Sauna: 3 times weekly
Hot Baths: 2-3 times weekly
Heat helps drive out the spirichete. May also cause some Herxheimer response, too.
CD3764
Veteran Member
Joined : Sep 2014
Posts : 4510
Posted 12/6/2014 6:41 PM (GMT 0)
Best of luck to you on this next path in your Lyme journey, KB!
For whatever it's worth, organic sunflower butter tastes very much like peanut butter and spreads very much like organic peanut butter.
Traveler
Elite Member
Joined : May 2007
Posts : 36573
Posted 12/7/2014 12:35 AM (GMT 0)
No, we don't have a recipe thread going, but I'm thinking it's time. I've asked Admin for a sticky thread for success stories, but haven't heard back from him yet. I think I'll ask for two - why not, right?
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