Natural Products Expo East 2013 Giveaway!!!

Expo East Giveaway
Expo East Giveaway

Natural Products Expo East 2013 Giveaway!!!

This blog post is embarrassing for me!

I went to Natural Products Expo East in September and have been meaning to get around to do this giveaway for you for weeks now. It seems like a day turned into a week, which turned into a month went way too quickly and time has certainly gotten away from me.

We are finally feeling like home in our new apartment. The walls are painted and we actually have a couch! Living on outdoor furniture for 3 weeks was taking a toll on us…

I’ll admit, I haven’t been very motivated to blog. I haven’t been motivated to do much of anything since we moved away from Columbus. I miss my friends, my clients and my business. I miss the familiarity of knowing how to get places and where everything is in the city. But, while a large part of me misses my old life, an even bigger piece of me loves my new life.

I’m getting out, meeting people, joining organizations and applying for part-time jobs. I started playing tennis, I joined a yoga studio and I’m working on lots of new projects with Andrew Cordova over at GF Magazine! Things are great and I’m starting to crawl out of my cave.

I feel I owe it to all of you, my loyal readers, to give you a fantastic giveaway filled with goodies and that is exactly what I am going to do…

So, how do you enter this amazing giveaway? Simple! Follow the instructions below in the Rafflecopter prize program and then see if you win on Sunday!

What’s in the prize pack? Tons of samples, information, goodies and PLC gear!!!!

International Celiac Disease Symposium 2013: Recap Day 1

International Celiac Disease Symposium September 23-25, 2013
International Celiac Disease Symposium September 23-25, 2013

Wow. Just wow. That is all I can say right now after my first day at the ICDS 2013.

I am forever grateful and thrilled I was able to attend this monumental event in Chicago. The information I learned already is so incredibly valuable and helps wade through much of the misinformation you find on the internet or hear through the grapevine.

The biggest thing I’ve learned so far is not to trust information found on the internet, even studies! They are filled with inaccuracies, small sample sizes or inconclusive information that can spread like wildfire. There are world-renowned celiac experts at this conference, sharing their findings, beliefs and information about celiac disease.

If you aren’t sure what the heck I’m talking about yet, the International Celiac Disease Symposium is a 3 day event held every 2 years in cities all over the world. Here is what the conference is all about directly from the ICDS2013 website,

“While the 15th ICDS meeting will continue to build upon the successes of 40 years of past ICDS scientific programs, the Chicago meeting is designed to address the interests of all of those affected by celiac disease and gluten-related disorders – from physicians and researchers to patients and clinicians to family and friends. The ICDS Chicago will present two distinct interactive educational tracks. The meeting will bring together the world’s top scientists and physicians to discuss the most recent scientific advances in managing and treating celiac disease and gluten-related disorders while a separate clinical forum will be held to further educate dietitians, clinicians, and patients.“

It’s impossible for me to share all the information I learned today into one blog post so I am going provide some information based on the major points of the discussions. If you head over to Twitter and do a #ICDS2013 search, there are hundreds, if not thousands, of tweets from the event that will blow your mind!

Here are some great things I learned today:

  1. We are not born with celiac disease. Genes, yes but the actual disease can develop at any age or stage of life.
  2. Women are diagnosed 2-3 times more frequently than men.
  3. When a biopsy is done, advocate and ask for 4-6 biopsy samples to be taken during the procedure. 2 is simply not enough.
  4. There is a major lack of follow-up with doctors and celiac patients – patients must advocate for their health and not only see their doctor for follow-up appointments, but work with a registered dietitian to ensure proper nutrition is being received by the celiac patient. There are inadequate follow-up visits, no assessment of compliance with diet, no follow-up biopsies are being done and inadequate f/u serology testing.
  5. Gluten alters bowel function in patients with irritable bowel syndrome if they are positive for the HLA-DQ2 or HLA-DQ8 gene but do not have celiac disease.
  6. Just because you have the HLA-DQ2 or HLA-DQ8 genes, it does not mean you have celiac disease.
  7. Celiac disease is seriously under diagnosed in men.
  8. There is not enough information to diagnose non celiac gluten sensitivity and no reliable information is available to determine how many people may be affected by this because screening is unknown as well.
  9. Small Intestinal Bacterial Overgrowth may be a problem in people who have similar symptoms as IBS or Celiac but aren’t diagnosed. There isn’t a lot of research on this but a hydrogen test is available. (Actually, this test is something I have at my house to take next week when I get back from the conference)
  10. A gluten-free diet should never be started prior to ruling out or being diagnosed with celiac disease.
  11. Doctors are still recommending a gluten challenge for people who have been gluten-free on their own merit or for other reasons and then need to be tested for celiac disease.
  12. If you have a first degree relative diagnosed with celiac disease, you should be tested.
  13. Support groups for children and adolescents are the best way to help them cope with their diagnosis. If you can’t find one, create one yourself. Sometimes we need to take these matters into our own hands in order to help the kids.
  14. Osteoporosis normalizes within 3 years of following a gluten-free diet of people with celiac disease.
  15. Failure to adhere to a gluten-free diet will cause continued bone density loss and contribute to osteoporosis.

The 4 out of 5 Signs Rule for having celiac disease – you should have 4 of 5 of these done in order to diagnosed celiac disease:

  1. Presence of signs and/or symptoms compatible with celiac disease
  2. Positive serology testing (TTG +/- EMA)
  3. Compatible HLA genes (DQ2 e/0 DQ8 positive)
  4. Positive internal biopsy with enteropathy (damage) typical of celiac disease
  5. Resolution of symptoms with a strict compliance with a gluten free diet

In total, my mind was filled with information and excitement to not only learn about celiac disease, but also to have safe foods to snack on and enjoy for 3 full days. Stay tuned for more information from tomorrow and Wednesday!

 

Dear Diary: I Think I’m Having a Tri-Life Crisis!

It’s a late night on our second full day of vacation and I’m sitting on our balcony, in the peaceful darkness, listening to the crashing of the waves with the sweet sound of cicadas chirping in the background. There’s a lot on my mind and keeping me awake.

When I think about the last few years of my life, the memories are filled with highs and lows, which seem like a never-ending roller coaster. Many of you may also think of your life in this manner too! I guess part of life is dealing the ebbs and flows as they come and developing the skills necessary to stand tall during the times of adversity. I’m proud to say I’ve gone through a ton of stuff and am still smiling and pushing forward to this day.

My first book coming out this fall is a self-help memoir about using these negative events, the lows as I would call them, to help propel you to the next chapter of your life. Looking back on all of the adversity throughout my lifetime, I realize that each one of these moments were life lessons to be used for the future. Sometimes though, you just want things to be easy.

I don’t want life to be easy, because I think frankly that would be pretty boring.

But, as I sit on a beautiful vacation, with my wonderful husband, in tears over all the changes we have going on in our life it really makes me wonder.. Am I doing something wrong?

Major life changes typically provoke thoughts and conversations that you didn’t even expect. I’m struggling with my sense of identity once we move to Washington DC next month. Who will I be there? What will I do? How will I fill my days?

Of course I will worry about my business in Columbus and our house we can’t sell. I’m sure I will have health issues to address and aches and pains to mend. The first few months will be filled with getting things settled in our new place, exploring the new city and making new friends. But, what happens after that?

I have an exciting opportunity to be whoever I want to be in a new town with new friends and create our new life, so why is this so stressful? Is it because I have too many options or am I having an identity crisis?

A Tri-Life Crisis? (I am in my 30′s so this is the term I’ve coined for struggling with your identity 30 years into life)

I know. I know. That’s ridiculous. (or is it?)

I will figure things out but right now I have a lot of things going on pushing me into panic mode! Never one to sit still, I will find things to fill my time. In a few months, my posts will be exciting and provide you will my fun gluten-free finds in the new city and some new opportunity that I found through my innate ability to network and connect with people.

But, I still can’t shake that feeling. The feeling of being the new girl in town and answering the question, “So, what do you do?”

I’m usually great at making major decisions and horrible at the small ones like, “where should we go for dinner?” or “What movie should we see tonight?”

In the end, it will all work out but for this moment I find myself questioning everything.

Gluten and Dairy Free Ice Cream Sandwich Recipe Guest Post

Well, I’m off to Hilton Head on vacation and have some wonderful guest posts lined up for you this week while I’m gone. The first comes from Tiffany Hinton with her fabulous gluten and dairy free ice cream sandwiches!
Enjoy!

Gluten and Dairy Free Ice Cream Sandwich Recipe Guest Post

Tiffany Hinton bio 
Tiffany Hinton is a Super Mom, Business Owner, Best Selling Author, and Gluten-free lifestyle expert!  Tiffany started writing several years ago, while going through treatments for infertility. Tiffany learned in 2009 she was gluten intolerant along with being lactose intolerant, turning her life up side down. Not know where to start and pre-made gluten-free items being too pricey. She started to experiment and explore cooking and baking; still wanting family favors to eat. With research and practice Tiffany can now turn any desirable recipe into gluten and dairy free, without sacrificing the taste.

Do you remember those hot summer days as a child where an ice cream sandwich brought the taste of chocolate and cold ice cream in an easy to hold treat… This was the first time my girls got to experience this wonderful memory from my childhood. As a Mom with 2 little girls who have gluten allergies and one who can not have dairy, it is always an adventure.

Do you remember those hot summer days as a child where an ice cream sandwich brought the taste of chocolate and cold ice cream in an easy to hold treat…
This was the first time my girls got to experience this wonderful memory from my childhood. As a Mom with 2 little girls who have gluten allergies and one who can not have dairy, it is always an adventure.

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Nummy, Nummy and Franki’s new word tasty!  The repeated request for chocolate and I knew these were a huge hit.
To make your own you will need the Brownie Bite Recipe from Gluten Free Mom Certified and the Dairy Free Ice Cream from Summer Thyme.  (both are fabulous cookbooks of mine)
Here is a link to the Ice Cream Recipe
and a short video with instructions

Tips for Handling a Bad Gluten-Free Dining Experience

What to do when you have a negative gluten free dining experience?
What to do when you have a negative gluten free dining experience?

What to do when you have a negative gluten free dining experience?

I travel frequently and love to try new places, despite living a gluten-free life. I put my health in the hands of strangers all the time but it never gets easier. The language barriers seem to be one of the hardest situations I encounter when explaining that I can’t consume gluten.

But through all the experiences, some are wonderful, positive and delicious and others leave little to be desired.

So, you had a bad gluten-free restaurant experience? Now what?

Anyone who lives a gluten-free lifestyle has survived a less than enjoyable experience in a dining establishment. Whether you deal with an agitated waiter or an uneducated kitchen staff, the experience still leaves a salty taste in your mouth. No one wants to go out to eat and have a great time, only to leave there a feel a gluten poisoning coming on to ruin the next few days of your week.

Most recently I entered into a dispute with a manager from a place I’ve eaten at before and received wonderful service from the girls working there, over their gluten-free menu. He told me it didn’t exist and when I asked for the orange menu from behind the bar with the gluten filled items scratched out on it, he told me the menu was exactly the same as the regular one. No kidding, I know it’s the same, but this one very clearly has it blacked out the items they can’t make safe for me and giant warnings about their chips not cooked in a dedicated fryer. He literally argued with me for 5 minutes about it before I just sat down and talked to my server about it.

I’ve been poisoned before and had a bad experience. Here are my tips on how to handle an unpleasant gluten-free restaurant experience.

  1. Try not to fly into an immediate rage or hysterics. While certainly you are emotional and for all the right reasons, now isn’t the time to go into antics. Compose yourself and ask to speak to the manager.
  2. Hopefully, the manager will offer to make it right or at least take care of your bill since they made you sick and it will end with them. But, sometimes you need to take it up the chain. One time I suffered from a horrible experience at an Asian themed restaurant where they served me an entire plate of regular sauced food and I was sick immediately. I barely made it out of there without changing my pants. The manager was less than sympathetic and assured me I received the correct meal. Clearly by my dash to the restroom before I even finished eating was a sign he didn’t know what he was talking about. I had no choice but to take it up a level.
  3. I wrote an email to the corporate office of the restaurant. I explained the situation in a calm, descriptive manner. When they didn’t respond within 48 hours, I wrote a blog post about my experience.
  4. The blog post was shared with their Facebook and Twitter pages and sure enough within 12 hours of the post, I received a message from them and spoke with their communications director who offered me a gift card in exchange for my experience.
  5. Then I wrote a review on Yelp and copied it to other sites with the corrected information about how they made the situation better and finally responded to the problem.

I am NEVER quick to write a bad review. I believe the business has the right to remedy the situation prior to it escalating to a negative review or blog post. When I write the review, I will mention the problem and then clearly explain how they decided to make the situation better.

If the manager and/or owner fail to respond to my attempts to get them to remedy the situation, then I will make it known very publicly about the situation and my attempts to offer them the opportunity to make things better.

Have I gone back to a restaurant after having a negative experience? Yes. But, if I have a problem on the second time, I can tell you it will be my last time eating there.

There are also times where I’ve gone to places that I loved because I always felt safe and they failed me. It happens everywhere and we need to always have our guard up.

 

Recipe: Clean and Gluten Free Rotisserie Chicken

chickendinner
Clean Rotisserie Chicken

Maybe I should have called this Fauxtisserie Chicken because it tastes like it but without cooking it the same way!

I’ve been pretty bored with our options lately at home and feel a rut coming on with dinners. In order to stop it, I found some ideas for clean gluten-free dinners and I’ll post them as we go each week. The first one was a home run and I’m thrilled to tell you about it!

I wanted to get a rotisserie chicken but I think we need to open our eyes to the hormones in those chickens and fillers to make them so cheap at the grocery stores. I guess technically this is a baked chicken but it looked and tasted just like a rotisserie so I’m going to call it that!

So, I ran over to Trader Joe’s to see what they had in the store that day. I found a small, organic, young chicken which weighed about 4.5 pounds. A little big for Aaron and I but I figured it would make great left overs.

Here’s how I made it

Ingredients

-Small Chicken – preferable hormone free and organic
-4 Tablespoons of coconut oil
-2 Tablespoons of fresh rosemary
-2 Garlic pieces – chopped or minced
-3 Tablespoons of unsalted grassfed butter – we use Kerrygold
-2 Tablespoons of lemon juice

  1. Preheat the oven to 350 degrees
  2. Clean the chicken with water and then put it in an oven save dish or roasting pan. I used a clear pyrex baking dish because that’s all I have to work with.
  3. In a small saute pan – I threw it on low heat and mixed the coconut oil, garlic, rosemary, lemon juice and butter for about 5 minutes to let the flavors mix together
  4. Once the chicken was clean I put it in the glass pan and grabbed a marinade brush to rub the dressing all over the chicken making sure it covered the whole surface and I poured the rest inside the chicken.
  5. Cook the chicken for 25-30 minutes per pound. My 4.5 pound chicken was done in about 75 minutes
  6. We let it cool for about 1o minutes prior to cutting
  7. It was served with broccolini that I baked and threw some kerrygold butter on after taking it out

I was delightfully giddy when my husband cut into the chicken and the juices streamed into the pan. I don’t care for the skin but it was crispy as you can see from the picture! It was amazing. It’s  very rare I venture out to try new things like this but I must say this was a home run. Something I will make in the future. It only took about 15 minutes to get ready so the cooking time took the longest.

Gluten Free Sausage and Wild Rice Recipe

Gluten Free Sausage and Wild Rice Recipe
Gluten Free Sausage and Wild Rice Recipe

Gluten Free Sausage and Wild Rice Recipe

Last night I made a random gluten-free version of a jambalaya with a few things we had in our kitchen and it turned out very clean and tasty! Who knew whole foods could taste this good and be this easy?

Ingredients:

1 cup Wild Rice
3 Trader Joe’s Jalapeno Chicken Sausage (yup they are gluten-free!)
1 cup Mushrooms
3 cloves Garlic
6  total of small red, yellow & orange Sweet Peppers
4 tablespoons grass-fed Butter
2 tablespoons of Olive Oil
2 cups Spinach
1 can Cannellini Beans

 

How to make:

  1. Make 1 cup (dry) wild rice. I mixed it with water but you can also mix with gluten-free broth to add some additional taste.  It takes about 45 minutes to cook so make sure you get in on the stove in advance.
  2. About 30 minutes after you put on the rice – Grab a sauté pan and put 4 tablespoons of butter, 3 cloves of fresh garlic, 2 cups of fresh spinach, 6 small sweet peppers chopped into bit size pieces, 1 can of navy beans, 1 cup of mushrooms and 3 sausages cut up into bite size pieces. Mix them all together really well and throw the lid on it for about 10 minutes.
  3. When the rice is done, make sure all the liquid is drained and mix the rice in the sauté pan. Be sure to mix all the ingredients in very well. I threw in a little bit of garlic salt to add some extra flavor.
  4. Perfect for lunch leftovers! Enjoy
Trader Joe’s Spicy Chicken Sausage
Trader Joe’s Spicy Chicken Sausage

Workout of the Week – July 8th 2013

wowjuly812
Workout of the Week

This weekend, I hit a number on the scale I thought I would never see again. I feel amazing but I don’t look the part, which is always a struggle for me in the fitness industry. I absolutely love my clients because they encourage and support me as much as I do them and they never judge me for what I look like because I have the knowledge and education to help them. They realize my health problems have taken a toll on my body and I continue to struggle with random things as they come up which is just part of living with a chronic disease.

For the past few weeks, I’ve been experimenting with different workouts and am realizing, shorter and more intense workouts are getting the job done without leaving me sore for a week and preventing me from getting a workout in the rest of the week. This is the most incredible feeling. It’s like when you are working on a puzzle but you can seem to find a key piece that’s holding up the rest of your board.

I’ve been playing around with foods as well and am realizing after an internal struggle of not wanting to give up corn and grains, I think they need to go bye-bye. I just feel better when they aren’t in my life. I’m less bloated and I feel like I have more energy. I need to stop fighting my body and go with the flow.

I’m very petite and adding 30 pounds to my frame is a lot of weight. It’s time to focus, create a goal board and stick to the program. Now I know what my limitations are and what works for me, I can finally create a program for myself that will trigger weight loss and help build lean muscle with a good diet and supplements.

My before pictures are taken and tucked away in a secret file. I think to hold me accountable I will post the progress pictures every other week. That will keep me in line with following the guidelines of my program along with allowing me to see results. What I’ve learned in the last 5 years, is you can’t use the scale exclusively to see results and I’m going to show you exactly what I mean in the next 3 months.

The past few weeks, I’ve limited my intake of sugar and am feeling pretty good! The cravings are going away which is something that happens if you can fight through the cravings in the first 10 days. Food will taste much better when you eliminate fake sugars and corn syrup from your life. It takes a bit of time for your taste buds to adjust but when they do, you will be pleasantly surprised!

I’m excited to take this journey with you. I hope I can inspire you to do the same!

I will post workouts throughout the upcoming weeks and an example of what I’m eating during the day to help you with ideas on getting fit yourself. I’m working on videos as well which I will post each week on the YouTube page, so make sure you subscribe!

 

25 Things I’ve Learned from Celiac Disease

25thingsaboutceliac

It’s been an incredible life long journey for me (and many of you) until I finally got the answers I needed for all my medical problems. It seems as if it were yesterday that I was sitting in a doctor’s office, waiting to be seen, only to leave disappointed and without any hope or answers for what was wrong.

Another doctor, another prescription and still no relief…

But the last few weeks, I’ve had some time to reflect and really think about what having celiac disease means to me and some of the major things I’ve learned over the last 18 months through my own personal experiences and the last 10 months as a blogger. If you have things you learned about gluten-free living or celiac disease, please feel free to post them in the comments so other readers know they aren’t alone!

  1. My celiac disease is not your celiac disease. I can’t emphasize this one enough! We all have different triggers and ailments so it’s incredibly important to pay attention to your own body versus what you hear from me or others on forums and websites.
  2. Celiac comes with other problems. Endometriosis, thyroid problems, arthritis and vitamin deficiencies for me!
  3. Vitamin & Nutrient levels should be tested on a regular basis to ensure you are supplementing properly to nourish your body with what’s missing.
  4. Gluten will make you feel crazy, act crazy, think you’re crazy and make you paranoid. It consumes you life and there are times when I just have to stop and think… at least it’s managed with food.
  5. It seems to be the only disease people don’t know enough about to tell me how to live my life. Now, gluten-free is another story but celiac disease usually doesn’t get too many unsolicited comments or advice from others.
  6. You have to be incredibly educated about celiac disease, living gluten-free and your body to be safe as much as possible.
  7. It’s essential to learn how to plan accordingly when traveling, dining out or anything out of the norm to prevent you from being stuck.
  8. A gluten-free emergency supply kit is a necessity not an idea.
  9. Poop can tell you so much about your eating habits and health of your body!
  10. I still learn about gluten in things and are surprised by it – tea bags are my most recent discovery!
  11. The gluten-free and celiac community is amazing and I am honored to be a part of it!
  12. I’ve come to realize that packaged gluten-free food is my worst enemy. For my health & my waist line – real foods is where it’s at!
  13. Celiac gave me the opportunity to see who my real friends are and learn the ones who care enough about me to always make me feel safe.
  14. Celiac and fitness is an interesting concept. I’m excited to come out with my program late summer!
  15. I’ve learned to accept the days when my body won’t cooperate and stopped beating myself up about feeling tired, having a headache or achy joints.
  16. Being curvy and healthy is more important than being lean and unhappy.
  17. Living gluten-free doesn’t have to be more expensive – you just have to plan better and eat clean to keep the budget tight.
  18. I’ve learned to look at life as a new adventure, instead of letting it stress me out every day.
  19. My family shouldn’t be burdened by my celiac disease, so I try to bring my own foods to events just to make sure I’m safe and not starving.
  20. Airports are the worst for living gluten-free and with celiac.
  21. Writing and blogging helps keep me sane and warms my heart when I’m able to help you too.
  22. There are no true gluten-free substitutions. Gluten free bread is not soft sourdough bread and it never will be. Gluten-free Oreos are not the ones I’ve learned to love over my lifetime an none can duplicate it either. I’m done trying to find substitutes and instead I’m learning to love new things instead.
  23. I’m proud to take charge of my health and not take no for an answer. I refused to accept that I didn’t have anything wrong with me and I was correct.
  24. I love my husband more now than ever. He has been the most amazing and supportive person through this and I certainly hit the husband lotto.
  25. I love my body more now than ever. All of it. All the problems. All the wonderful things people take for granted, I’ve learned to love and enjoy.

Comments

  1.  Sheryl Rex says:

    I have learned that ‘Gluten Guard’ meds, do NOT work on everything. It is easier just to go without.

     

    •  Rebecca says:

      What are “gluten guards?”

       

  2.  Atherton Baking Co. says:

    I’ve learned the GF is very supportive and generous. During a very low period I found Karen Morgan & Tim Lawson, they taught me how to be strong! The GF fam shares and supports all over the world! When you reach out, someone is always there!

     

    •  Rebecca says:

      I second that with the community! It is so true!!

       

  3.  Charlotte says:

    I’ve learned to be a better and more adventurous cook. I’ve learned that there is MORE to eat as a celiac than I ever ate pre-diagnosis and I was a pretty adventurous eater already even with a ton of allergies. I’ve learned to be my own advocate. I’ve learned that I have some AMAZING friends who support me and my GF life.

     

    •  Rebecca says:

      Those are awesome things! Thank you so much for sharing :)

       

  4.  Mindy says:

    I love the 25 things you have learned! Very inspirational for me! I still struggle with many things related to living with Celiac after almost 5 years of living gluten free.

    I also need to learn how to attend events without feeling so awkward when taking my own food. Right now one of my challenges is attending the service’s at church that offer crackers for the Lord’s supper practice. The preacher told me to just bring my own cracker’s. Still I dealt with a lot of guilt for awhile by not participating in the practice at church.

    I do still have days that I do not feel well mainly due to environmental allergies and other food allergies like dairy, soy, yeast and garlic which makes my eliminating other foods important.

    Am still trying to figure out how to get high protein (which of course helps the energy level) Not easy when I am not a huge meat person.

    Thanks for these wonderful comments!

     

    •  Chessie says:

      Mindy, I was diagnosed with celiac disease about a month ago (quite a shock) and I’m slowly climbing out of the deep hole of fatigue I was in. I hear you about protein, because I’ve been vegan for about a dozen years and most of the vegan “fake meats” out there are made with lots of wheat gluten. So, it’s beans, tofu, tempeh, nuts, and seeds for me. I think I can get enough protein, but it will take daily thought. It’s too bad you don’t do soy, but there are lots of other beans and legumes out there.

      Oh, how I loved stuff made with “vital wheat gluten” (i.e., deadly wheat gluten). But yeah, turns out there’s a reason why it didn’t agree with me so much.

      Rebecca, thanks for the 25 tips!

       

      •  Rebecca says:

        Chessie-

        Thanks for listing some other sources of protein! I think people automatically assume that you can only get it from meats.

         

    •  Rebecca says:

      Mindy if you eat eggs – Pasturized egg whites are a perfect way to get protein into your diet. They don’t taste like anything and are protein packed. I put them in my juice and shakes. You can buy them in larger packages which are much more affordable through places like Egg Whites International. They come frozen and then you just keep them in the fridge and use them as you wish.

       

  5.  Brittany says:

    Do you have a post somewhere explaining:

    “A gluten-free emergency supply kit is a necessity not an idea.”

    What is that?!

     

    •  Rebecca says:

      An emergency kit is something that you would want to have in case there is a disaster like a hurricane, power outage, tornado or fire. It should filled with gluten-free foods that you can consume in case you don’t have access to anything for a few days.

       

  6.  Angela says:

    Wow I had never thought about tea bags. Thanks for the tips!

     

    •  Rebecca says:

      You’re welcome!

       

  7.  Martin says:

    re12: Great to see more celiacs avoid processed food and look into the real food/paleo diet

     

  8.  Amanda Yoder says:

    Love this! So true and so relatable!

     

  9.  Kay Gaumer says:

    I’ve been gluten free since February of this year. It has be a challenge to adjust my diet. I am also allergic to dairy and most grains. I think your comment about making mew ‘friends’ and not trying to substitute gluten free products for old ‘friends’ is an excellent idea. I lean toward a vegetarian diet and buy organic and GMO free products. I also try to buy local as the products are fresher and tastier that way.

     

  10.  Sherry says:

    I am glad I found this blog. I can relate so much to what you said!