Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

All You Celiacs Hiding In Tacoma/puyallup


Thx4noticingMe

Recommended Posts

Thx4noticingMe Newbie

My daughter (18 yr) was dianosed and tested August 2005 and I hid in denial until my endoscopy was done in Jan 2006. No more denial for either of us and a much better lifesytle has begun. Once in a while we go through a typical mourning period for one of our old favs, but the pain free life style offers much to be thankful for.

Now I work at grocery store that has a great nutrition center with gluten free products. The head of that department calls me over whenever a new person has discovered they have celiac. And the word has spread and other locations in Pierce County call me regarding gulten-free products or questions that customers have. I am far from being a pro at this, although I do lots of homework regarding my new lifestyle.

I meet people all over Pierce County who have this or have family members but refuse to explore it or give it a good shot. It is unforturnate that Pierce County does not have support groups. Seattle has many bonuses for celiacs, but since our traffic really stinks it makes it very difficult for us to enjoy those extras.

I would like to hear from some of you and know if a support group would be viable in Tacoma/Puyallup.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



BRUMI1968 Collaborator

I grew up in Tacoma - went to Sunset Elementary (then moved to Harbor so went to Gig Harbor High School) and then moved back and lived near Wright's Park for a few years. It seems I keep moving north - first to Seattle, then to Whidbey Island, then to Sedro-Woolley, and now to Bellingham. My parents and sister live in Tacoma - I'm trying to get them to be tested. My mom is having her mom tested in a few days - then is that's positive, she'll do it.

Anyway, good luck to you. Obviously I'm not up on the support groups - but the national support group, what are they called, have a listing. You might want to Private Message "Nini". If you go to "members" and then hit "n", you'll find her. She has a Newbie pack that might well contain the info you need.

At which store do you work?

Thx4noticingMe Newbie
I grew up in Tacoma - went to Sunset Elementary (then moved to Harbor so went to Gig Harbor High School) and then moved back and lived near Wright's Park for a few years. It seems I keep moving north - first to Seattle, then to Whidbey Island, then to Sedro-Woolley, and now to Bellingham. My parents and sister live in Tacoma - I'm trying to get them to be tested. My mom is having her mom tested in a few days - then is that's positive, she'll do it.

Anyway, good luck to you. Obviously I'm not up on the support groups - but the national support group, what are they called, have a listing. You might want to Private Message "Nini". If you go to "members" and then hit "n", you'll find her. She has a Newbie pack that might well contain the info you need.

At which store do you work?

Sorry it has taken so long to respond. I just returned from Eastern WA. My father had a large tumor removed from his neck. He is fine.

It seems that the Tri-cities has a larger group of Celiacs because the stores cater to our needs. I've discovered many new products.

By the way work for Fred Meyer.

It looks like you have lived in just as many places in the PNW as I have. Seattle and West Seattle as a young child. Burien during elementary and jr. high. Federal Way and Salem in high school. And just to round things out, I lived in Tacoma, Federal Way (Redondo) and now Puyallup/Sumner area during my adult years.

Thank you for the response and the information.

  • 2 weeks later...
Christina62 Newbie

-Thx4noticingMe - I'm from puyallup area, I actually worked at Fred Meyer's on 176th last summer. I was diagnosed w/celiac a few years ago, but I have never been able to stay gluten free. I am trying to find a new doctor, my doctor dosen't seem to know much so if you know of a good doctor that would be great! I really wish there was a support group around here so I could meet other people who are going through the same thing. I've been wanting to go gluten free, but it seems so hard to do if you have any tips please let me know. I hope I hear back from you. Thanx

lonewolf Collaborator

I don't live in Tacoma or Puyallup, but I am close by in Federal Way. Just wanted to chime in. I would love to have a support group in the area and wanted to start one, but my life has been too busy to take on one more thing.

Sorry Christina62, I don't know of a good doctor - I'm doing this on my own. There's a good naturopath in Fife named Dr. Data that's good with giving help with nutrition and diet. She's covered by most insurance and might be a good place to start.

  • 3 weeks later...
Thx4noticingMe Newbie

Christina and Lone Wolf.. glad to hear from you. Chistina... I understand the difficulty of staying on a gluten free diet. However, the way you feel after following the diet is extremely worth it.

Finding a good doctor and a knowledgeble dietician is very difficult. My oldest daughter saw the top gastro doc at Mary Bridge and after the biopsy, we were handed a two page hand out of foods that were no-no's. It was printed in 1985. After speaking with the Gluten Intolerance Group in Seattle, we found out much of the info was out dated. My daughter is also diabetic and recently became very ill and had a hospital stay for over five days. Large print on her chart...NO GLUTEN/DIABETIC... what do they bring her for dinner? A turkey sandwich (with wonder bread). :( She sends it back and they tell her the kitchen is now closed and tried to give her instant chicken noodle soup and saltine crackers. :angry: So much for the medical knowledge of celiac. The ironic side of this whole story is when the hospital dietician came to her room and asked her what she could eat. She simply stated to her, "You're the dietician, you tell me." ;)

I went to Digestive Health Specialists in Puyallup. My doctor was knowlegeble about celiac and after my biopsy he spoke with me and confirmed diagnoses. However he did call me four days later at 7 p.m. explaining that I was very malnourished and he was very concerned. He never seen such a case. Kinda scary huh? :unsure: This is what happens when a diagnoses goes undiscovered for many years. It is also an example of what happens when you don't follow a celiac diet.

Now here is the bad news... ususally after diagnoses and biopsy the doctor doesn't have much to do with you again for about a year and re-tests you. You can go to dieticians, but that is also shot in the dark sometimes. Keeping in touch with others and asking questions is your best bet. The other important is to have family and friends who are supportive because this is a life changing condition. Restaurants, potlucks at work, even going to other peoples houses for meals or any length of time can be challenging.

Well speaking about food, I'm hungry.

  • 2 weeks later...
seattlecdfriend Rookie

lonewolf.. I'm interested in contacting your Fife naturopath. How long have you been going, what have you learned/benefited, etc. Thanks.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



lonewolf Collaborator
lonewolf.. I'm interested in contacting your Fife naturopath. How long have you been going, what have you learned/benefited, etc. Thanks.

I've been seeing her for about 9 years. She's really good and takes the time to listen to you. She's not super knowledgeable about Celiac, but she's well-versed in nutrition. She doesn't push supplements either. I gotta run, but PM me if you want her name and more info.

There's also a good naturopath in Federal Way that a friend really likes. My friend has Celiac (and a bunch of other food intolerances) and has been really happy with her.

  • 1 month later...
Emily4u Newbie

I would love to start a support group. Currently I am between Sumner and Orting. I am a former member of the Bellingham Gluten Intolerance Group. Every year they had a gluten-free Christmas cookie exchange, a 3 course dinner night, cooking classes, field trips to gluten-free stores, etc... Also if anyone wants wondeful gluten-free food like: crutons, stuffing, sauces, scones, cookies, breads, buns, beer, pies, etc... there are two cafes in Vancouver BC that are wonderful and well worth the trip Panne Rizo and The Rice Bakery. Whole Foods in Bellevue is also wonderful because they have frozen pie crusts, breads, cakes and many other great items (Even some in the Bakery!). I think it would be great if we could start a group. Maybe meet once a month? e-mail me smlemily@gmail.com

Flotenspieler Newbie

Hi my fellow Puget-Sounders!

I live near Des Moines. There used to be a gluten intolerance group in this area, but I think they moved elsewhere recently. I was just diagnosed with gluten intolerance in August by Dr. Stephen Wangen. He has an office at Swedish Medical Center in downtown Seattle. Here's a bit about him from his website:

"Dr. Stephen Wangen is a board certified physician specializing in the identification and treatment of food allergies to improve your health. He has first-hand experience with food allergies, having been diagnosed with a gluten intolerance (wheat allergy) in 1996. He has since developed a comprehensive program to diagnose and work with food allergies and the multitude of potentially associated conditions.

Because food allergies have become a major (but under-recognized) factor in causing chronic disease, Dr. Wangen is focusing his practice on natural methods to deal with food allergies and related conditions and nutritional deficiencies."

He's extremely knowledgeable about celiac/IBS/food allergies and so much more. He spends a lot of time with his patients getting very thorough medical histories from them. Here's the link to his website if anyone wants to learn more about his practice: Open Original Shared Link

Meanwhile, if you hear of any gluten intolerance/celiac support groups cropping up in my neck of the woods, please post it here and thanks in advance! :D

  • 5 months later...
Emily4u Newbie

Hello everyone. I am going to have a support group meeting at the Puyallup Public Library on Tuesday April 24th from 7-8:30pm. Everyone is welcome. There will be good resources and gluten-free treats. The Puyallup Public Library is located in downtown Puyallup in the back of Pioneer Park at the intersection of Meridian and Pioneer. GIG will be e-mailing its members about the group. If you have any questions or concerns please e-mail me at smlemily@gmail.com.

  • 7 months later...
Smacd Newbie

Hi, I have met and talked with the Freddies health section manager. My family has truly appreciated how much Freddies has done for the Celiac community.

My husband and I have experimented with baking gluten-free breads, cookies, quick breads, muffins, pizza and have had great success. I want to open a South Sound gluten-free bakery and coffee shop next year. However, we need a two things: one is support for the community - letters of support, stating that as a consumer you would patronize such an establishment. The other thing I need is a business partner. I am looking for someone who would like to in with me on this venture, who is willing to put in the time that it takes to do a business. My email is scottandshila@msn.com.

lonewolf Collaborator
My husband and I have experimented with baking gluten-free breads, cookies, quick breads, muffins, pizza and have had great success. I want to open a South Sound gluten-free bakery and coffee shop next year.

Where in the South Sound area? I'm in Federal Way and would definitely like to see a GOOD gluten-free bakery in the area. I bake a lot myself, so would only go occasionally for treats for my kids when I was busy or for a fun trip out. I've thought of doing the same thing, but don't have any business sense whatsoever.

Archived

This topic is now archived and is closed to further replies.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Hmart replied to Hmart's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Is this celiac?

    2. - trents replied to Hmart's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Is this celiac?

    3. - klmgarland replied to klmgarland's topic in Dermatitis Herpetiformis
      10

      Help I’m cross contaminating myself,

    4. - DebJ14 replied to Jhona's topic in Introduce Yourself / Share Stuff
      30

      Does anyone here also have Afib

    5. - Hmart posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      2

      Is this celiac?


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,925
    • Most Online (within 30 mins)
      7,748

    Linda Stark
    Newest Member
    Linda Stark
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Hmart
      I was not taking any medications previous to this. I was a healthy 49 yo with some mild stomach discomfort. I noticed the onset of tinnitus earlier this year and I had Covid at the end of June. My first ‘flare-up’ with these symptoms was in August and I was eating gluten like normal. I had another flare-up in September and then got an upper endo at the end of September that showed possible celiac. My blood test came a week later. While I didn’t stop eating gluten before I had the blood test, I had cut back on food and gluten both. I had a flare-up with this symptoms after one week of gluten free but wasn’t being crazy careful. Then I had another flare-up this week. I think it might have been caused by Trader Joe’s baked tofu which I didn’t realize had wheat. But I don’t know if these flare-ups are caused by gluten or if there’s something else going on. I am food journaling and tracking all symptoms. I have lost 7 pounds in the last 10 days. 
    • trents
      Welcome to the forum, @Hmart! There are other medical conditions besides celiac disease that can cause villous atrophy as well as some medications and for some people, the dairy protein casein. So, your question is a valid one. Especially in view of the fact that your antibody testing was negative, though there are also some seronegative celiacs. So, do you get reactions every time you consume gluten? If you were to purposely consume a slice of bread would you be certain to develop the symptoms you describe?
    • klmgarland
    • DebJ14
      I only went on the multi vitamin AFTER a couple of year of high dose, targeted supplementation resolved most of my deficiencies.  I was on quite a cocktail of vitamins that was changed every 6 months as my deficiencies resolved.  Those that were determined to be genetic are still addressed with specific doses of those vitamins, minerals and amino acids. I have an update on my husband and his A Fib.  He ended up in the hospital in August 2025 when his A Fib would not convert.  He took the maximum dose of Flecainide allowed within a 24 hour period.  It was a nightmare experience!  They took him into the ER immediately.  They put in a line, drew blood, did an EKG and chest Xray all within minutes.  Never saw another human for 6 hours.  Never got any results, but obviously we could see he was still in A fib by watching the monitor.  They have the family sign up for text alerts at the ER desk.  So glad I did.  That is the only way we found out that he was being admitted.  About an hour after that text someone came to take him to his room on an observation floor.  We were there two hours before we saw another human being and believe it or not that was by zoom on the TV in the room.  It was admissions wanting to know his vaccine status and confirming his insurance, which we provided at the ER desk.  They said someone would be in and finally a nurse arrived.  He was told a hospitalist was in charge of his case.  Finally the NP for the hospitalist showed up and my husband literally blew his stack.  He got so angry and yelled at this poor woman, but it was exactly what he needed to convert himself to sinus rhythm while she was there.  They got an EKG machine and confirmed it.  She told him that they wanted to keep him overnight and would do an echo in the morning and they were concerned about a wound on his leg and wanted to do a doppler to make sure he did not have a DVT.  He agreed.  The echo showed everything fine, just as it was at his annual check up in June and there was no DVT.  A cardiologist finally showed up to discharge him and after reviewing his history said the A Fib was due to the Amoxicillan prescribed for his leg wound.  It both triggers A Fib and prevents the Flecainide from working.  His conversion coincided with the last dose of antibiotic getting out of his system.  So, make sure your PCP understands what antibiotics you can or cannot take if susceptible to A Fib.  This cardiologist (not his regular) wanted him on Metoprolol 25 mg and Pradaxa.  My husband told him that his cardiologist axed the idea of a beta blocker because his heart rate is already low.  Sure enough, it dropped to 42 on the Metoprolol and my husband felt horrible.  The pradaxa gave him a full body rash!  He went back to his cardiologist for follow up and his BP was fine and heart rate in the mid 50's.  He also axed the Pradaxa since my husband has low platelets, bruises easily and gets bloody noses just from Fish Oil  He suggested he take Black Cumin Seed Oil for inflammation.  He discovered that by taking the Black Seed oil, he can eat carbs and not go into A Fib, since it does such a good job of reducing inflammation.   Oh and I forgot to say the hospital bill was over $26,000.  Houston Methodist!  
    • Hmart
      The symptoms that led to my diagnosis were stomach pain, diarrhea, nausea, body/nerve tingling and burning and chills. It went away after about four days but led me to a gastro who did an upper endo and found I had marsh 3b. I did the blood test for celiac and it came back negative.  I have gone gluten free. In week 1 I had a flare-up that was similar to my original symptoms. I got more careful/serious. Now at the end of week 2 I had another flare-up. These symptoms seem to get more intense. My questions:  1. How do I know if I have celiac and not something else? 2. Are these symptoms what others experience from gluten?  When I have a flare-up it’s completely debilitating. Can’t sleep, can’t eat, can’t move. Body just shakes. I have lost 10 pounds since going gluten free in the last two weeks.
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.