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Any Fellow Cd's In Nc


Lisa

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lizard00 Enthusiast

I'm another Raleigh-ite :)

Momma Goose, we had some friends that used to live in Edenton. It's beautiful there. I grew up in southeastern VA, Suffolk. It's about a hour to Edenton (if I remember) and about an hour and a half to the OBX. I miss being so close to the ocean...

Liz


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Lisa Mentor
I'm another Raleigh-ite :)

Momma Goose, we had some friends that used to live in Edenton. It's beautiful there. I grew up in southeastern VA, Suffolk. It's about a hour to Edenton (if I remember) and about an hour and a half to the OBX. I miss being so close to the ocean...

Liz

Yup, that would be us. :D PM me about your friends, perhaps we know them. Raleigh really is a small town, you know. We send our kids to go to school there and they never want to leave. Well, some appreciate "home".

lizard00 Enthusiast

Where do your kids go to school?

When I first moved here from Suffolk, I though this place was HUGE!! But my husband and I have been here 4 years now and doesn't seem so big anymore. It's big enough for me... of course everything is very compartmentalized, so you really never have to go more than 5 miles from your home if you don't want to. I have two groceries within walking distance, a drug store and a gym... along with quite a few eateries. What else do you need? lol

Your kids will appreciate home as they get older. It probably seems small to them now, but there's nothing quite like home. :)

lmthoma Newbie

Those living in Hendersonville, NC- I am the manager at Potenza, an italian restaurant downtown, and we just started a gluten-free menu that includes pastas. My younger brother has celiac so I know how difficult it can be to go out to eat. I am not trying to shamelessly promote my restaurant but I do want to let people know that there are options out there and more and more people are becoming aware of celiac disease. I would love feedback on what peoples needs are when they are dining out.

  • 3 months later...
nikken007 Rookie

Hi,

I live in Cary and have been gluten free for at least 3 months. My husband has a gluten intolerance and I highly suspect I do as well. I have no proof, except I feel a lot better! I do have 2 genes for celiac/gluten intolerance. I also have a sister who diagnosed herself with Celiac. We both had the enterolab test. The results were very surprising to us.

I want to let you Raleigh area people know there is a Celiac group that meets once a month at Rex hospital. It's the third thursday of each month. There will be a break for a month and then start back up July 17.

Breila Explorer
Hi,

I live in Cary and have been gluten free for at least 3 months. My husband has a gluten intolerance and I highly suspect I do as well. I have no proof, except I feel a lot better! I do have 2 genes for celiac/gluten intolerance. I also have a sister who diagnosed herself with Celiac. We both had the enterolab test. The results were very surprising to us.

I want to let you Raleigh area people know there is a Celiac group that meets once a month at Rex hospital. It's the third thursday of each month. There will be a break for a month and then start back up July 17.

Hi, I was at the meeting last night, were you there?

I'm in Garner, btw.

nikken007 Rookie

Yes, I was there. I was on the end of the table. I have brown, below the shoulder hair. I had a brown sweater and an olive green shirt. I was a little late and sat next to the new lady in pink.


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Breila Explorer
Yes, I was there. I was on the end of the table. I have brown, below the shoulder hair. I had a brown sweater and an olive green shirt. I was a little late and sat next to the new lady in pink.

Ah yes, I was new, sitting at the other end of the table, short hair and a blue tank top.

Guest digmom1014

Hi-

Just chiming in, I live in Matthews, south of Charlotte. There is an active Charlotte celiac group that I have not been able to meet with yet.

Has anybody been to the Celiac Cookie House in Cornelius? I am trying convince myself to make the drive. I have been sugar-free, dairy-free, egg-free for 4 months and am not sure I feel comfortable introducing those items again. I went gluten-free in Jan. after many years of being sick.

  • 2 months later...
Stormycubs Newbie
Hi, I was at the meeting last night, were you there?

I'm in Garner, btw.

Hi all-

My name is Brandy and I just met Amy at the mall today and she was talking about the rex group. My daughter is 6 and we found out she had celiac when she was 3ish. I have been looking for others around so I am so interested in the rex group. We live in Holly Springs. Can you give me all the info as to where the group meets and the time. I know the next meeting is tonight and I hate that I wont be able to make it. But hopefully I can make the next one. Thanks so much and its so nice to know there are others around going through the same stuff. I can't wait for Kendall to get home from school so I can tell her about the group!!!! :D :D :D :D

Ridgewalker Contributor
Hi all-

My name is Brandy and I just met Amy at the mall today and she was talking about the rex group. My daughter is 6 and we found out she had celiac when she was 3ish. I have been looking for others around so I am so interested in the rex group. We live in Holly Springs. Can you give me all the info as to where the group meets and the time. I know the next meeting is tonight and I hate that I wont be able to make it. But hopefully I can make the next one. Thanks so much and its so nice to know there are others around going through the same stuff. I can't wait for Kendall to get home from school so I can tell her about the group!!!! :D :D :D :D

Well, I got all excited seeing Holly Springs at first... There is a little town called Holly Springs that's just a hop, skip, and a jump from us- We live in Pilot Mountain/Pinnacle. I have two boys, ages 5 and 7. But then I remembered there's a bigger town called Holly Springs down near Raleigh. I bet that's the one you're referring to... Oh well. There are a handful of Raleigh members here, so others should chime in soon! :D

MinRalph Rookie

Hi everyone :)

I live in Jacksoneville, NC and have celiac disease. I have just recently heard of more people who have or know someone who has celiac disease or wheat allergies. It seems to be becoming much more well known, which I find pretty cool. Our local stores actually have a few gluten-free products in them!

Anyway, I just wanted to throw myself out there :D

  • 1 month later...
Guest elysealec
I am also in Wilmington and would love to meet other celiacs in the area. I was just diagnosed this week.

Holly

I live in Kure Beach and am in Wilmington every day. I know of one other celiac in the area. I am sure there are many more. We were talking about getting a gluten free dinner club together. Any interest?

Vicki

  • 6 months later...
KristynRCP Newbie

Hello I was Dx with celiac disease at end of December. I am from Rocky Mount, NC... there is no gluten-free stuff here.. no restaurants or anything.. I have a birthday coming up and I am looking for a gluten free cake.. any ideas from anyone? Im not good at the gluten-free cooking yet..so im looking for a bakery or something like that.....There is no support group here either.. wish i could get one started .....

Kristyn

Lisa Mentor

Kristyn,

I am not from Rocky Mount, but I'm not far. Do you have a Food Lion, if so they have a health food section which carries Pamela's Cake Mixes. Make them as you would a regular cake and I would dare anyone to tell the difference. Pillsbury Frosting often has gluten free choices, you just have to read the label. Wal Mart has many options for gluten free. It's out there, ya just have to find 'em.

The best support you will find in your area is right here on C.com.

bear6954 Apprentice

For anyone in Jacksonville, NC, White Oak Bakery makes gluten free cakes and cookies. You need to call and special order and they are expensive. However, I got a gluten-free cake for my son and it was wonderful. He was so happy to eat cake with everyone else. It brought tears to my eyes!

  • 4 weeks later...
sedkins Newbie

Hello. I am new to this board, but have been gluten-free/CF for about 3 years. My son (11) was recently diagnosed as likely having celiac disease, although he has been gluten-free off and on for about 3 years. We are looking for a support group, particularly one where he might be able to meet some other kids his age because he is really struggling with being "different." We are located in Lumberton, south of Fayetteville.

  • 2 months later...
TotalKnowledge Apprentice
Dear Lisa B.,

I am celiac in Wilmington, NC. Have you heard of any fellow celiacs in this area. I have only been gluten free since Aug 2006 and really haven't found anyone to relate to.

Thanks for your help!

Have a Happy 4th!

Mary Katherine Talley

There is a relatively new support group that is held and Lovey's once a month. I have only been to one meeting, but there were a several people there. They have a sign-up sheet there at the information table right when you come in next to the cafe seating.

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    • cristiana
      Hi @Scatterbrain Thank you for your reply.   Some of these things could be weaknesses, also triggered by stress, which perhaps have come about as the result of long-term deficiencies which can take a long time to correct.   Some could be completely unrelated. If it is of help, I'll tell you some of the things that started in the first year or two, following my diagnosis - I pinned everything on coeliac disease, but it turns out I wasn't always right!  Dizziness, lightheaded - I was eventually diagnosed with cervical dizziness (worth googling, could be your issue too, also if you have neck pain?)  A few months after diagnosis I put my neck out slightly carrying my seven-year-old above my head, and never assigned any relevance to it as the pain at the time was severe but so short-lived that I'd forgotten the connection. Jaw pain - stress. Tinnitus - I think stress, but perhaps exacerbated by iron/vitamin deficiencies. Painful ribs and sacroiliac joints - no idea, bloating made the pain worse. It got really bad but then got better. Irregular heart rate - could be a coincidence but my sister (not a coeliac) and I both developed this temporarily after our second Astra Zeneca covid jabs.   Subsequent Pfizer jabs didn't affect us. Brain fog - a big thing for people with certain autoimmune issues but in my case I think possibly worse when my iron or B12 are low, but I have no proof of this. Insomnia - stress, menopause. So basically, it isn't always gluten.  It might be worth having your vitamins and mineral levels checked, and if you have deficiencies speak to your Dr about how better to address them?    
    • knitty kitty
      @NanceK, I do have Hypersensitivity Type Four reaction to Sulfa drugs, a sulfa allergy.  Benfotiamine and other forms of Thiamine do not bother me at all.  There's sulfur in all kinds of Thiamine, yet our bodies must have it as an essential nutrient to make life sustaining enzymes.  The sulfur in thiamine is in a ring which does not trigger sulfa allergy like sulfites in a chain found in pharmaceuticals.  Doctors are not given sufficient education in nutrition (nor chemistry in this case).  I studied Nutrition before earning a degree in Microbiology.  I wanted to know what vitamins were doing inside the body.   Thiamine is safe and nontoxic even in high doses.   Not feeling well after starting Benfotiamine is normal.  It's called the "thiamine paradox" and is equivalent to an engine backfiring if it's not been cranked up for a while.  Mine went away in about three days.  I took a B Complex, magnesium and added molybdenum for a few weeks. It's important to add a B Complex with all eight essential B vitamins. Supplementing just one B vitamin can cause lows in some of the others and result in feeling worse, too.  Celiac Disease causes malabsorption of all the B vitamins, not just thiamine.  You need all eight.  Thiamine forms including Benfotiamine interact with each of the other B vitamins in some way.  It's important to add a magnesium glycinate or chelate supplement as well.  Forms of Thiamine including Benfotiamine need magnesium to make those life sustaining enzymes.  (Don't use magnesium oxide.  It's not absorbed well.  It pulls water into the intestines and is used to relieve constipation.)   Molybdenum is a trace mineral that helps the body utilize forms of Thiamine.   Molybdenum supplements are available over the counter.  It's not unusual to be low in molybdenum if low in thiamine.   I do hope you will add the necessary supplements and try Benfotiamine again. Science-y Explanation of Thiamine Paradox: https://hormonesmatter.com/paradoxical-reactions-with-ttfd-the-glutathione-connection/#google_vignette
    • Wheatwacked
      Your goal is not to be a good puppet, there is no gain in that. You might want to restart the ones that helped.  It sounds more like you are suffering from malnutrition.  Gluten free foods are not fortified with things like Thiamine (B1), vitamin D, Iodine, B1,2,3,5,6 and 12 as non-gluten free products are required to be. There is a Catch-22 here.  Malnutrition can cause SIBO, and SIBO can worsen malnutrition. Another possibility is side effects from any medication that are taking.  I was on Metformin 3 months before it turned me into a zombi.  I had crippling side effects from most of the BP meds tried on me, and Losartan has many of the side effects on me from my pre gluten free days. Because you have been gluten free, you can test and talk until you are blue in the face but all of your tests will be negative.  Without gluten, you will not create the antigen against gluten, no antigens to gluten, so no small intestine damage from the antigens.  You will need to do a gluten challange to test positive if you need an official diagnosis, and even then, no guaranty: 10 g of gluten per day for 6 weeks! Then a full panel of Celiac tests and biopsy. At a minimum consider vitamin D, Liquid Iodine (unless you have dermatitis herpetiformis and iodine exasperates the rash), and Liquid Geritol. Push for vitamin D testing and a consult with a nutritionist experienced with Celiack Disease.  Most blood tests don't indicate nutritional deficiencies.  Your thyroid tests can be perfect, yet not indicate iodine deficiency for example.  Thiamine   test fine, but not pick up on beriberi.  Vegans are often B12 deficient because meat, fish, poultry, eggs, and dairy are the primary souces of B12. Here is what I take daily.  10,000 IU vitamin D3 750 mg g a b a [   ] 200 mg CoQ10 [   ] 100 mg DHEA [   ] 250 mg thiamine B1 [   ] 100 mg of B2 [   ] 500 mg B5 pantothenic acid [   ] 100 mg B6 [   ] 1000 micrograms B12 n [   ] 500 mg vitamin c [   ] 500 mg taurine [   ] 200 mg selenium   
    • NanceK
      Hi…Just a note that if you have an allergy to sulfa it’s best not to take Benfotiamine. I bought a bottle and tried one without looking into it first and didn’t feel well.  I checked with my pharmacist and he said not to take it with a known sulfa allergy. I was really bummed because I thought it would help my energy level, but I was thankful I was given this info before taking more of it. 
    • Wheatwacked
      Hello @Scatterbrain, Are you getting enough vitamins and minerals.  Gluten free food is not fortified so you may be starting to run low on B vitamins and vitamin D.   By the way you should get your mom checked for celiac disease.  You got it from your mom or dad.  Some studies show that following a gluten-free diet can stabilize or improve symptoms of dementia.  I know that for the 63 years I was eating gluten I got dumber and dumber until I started GFD and vitamin replenishment and it began to reverse.  Thiamine can get used up in a week or two.  Symptoms can come and go with daily diet.  Symptoms of beriberi due to Thiamine deficiency.   Difficulty walking. Loss of feeling (sensation) in hands and feet. Loss of muscle function or paralysis of the lower legs. Mental confusion. Pain. Speech difficulties. Strange eye movements (nystagmus) Tingling. Any change in medications? Last March I had corotid artery surgery (90 % blockage), and I started taking Losartan for blood pressure, added to the Clonidine I was taking already.  I was not recovering well and many of my pre gluten free symptoms were back  I was getting worse.  At first I thought it was caused a reaction to the anesthesia from the surgery, but that should have improved after two weeks.  Doctor thought I was just being a wimp. After three months I talked to my doctor about a break from the Losartan to see if it was causing it. It had not made any difference in my bp.  Except for clonindine, all of the previous bp meds tried had not worked to lower bp and had crippling side effects. One, I could not stand up straight; one wobbly knees, another spayed feet.  Inguinal hernia from the Lisinopril cough.  Had I contiued on those, I was destined for a wheelchair or walker. She said the symptoms were not from Losartan so I continued taking it.  Two weeks later I did not have the strength in hips and thighs to get up from sitting on the floor (Help, I can't get up😨).  I stopped AMA (not recommended).  Without the Losartan, a) bp did not change, after the 72 hour withdrawal from Losartanon, on clonidine only and b) symptoms started going away.  Improvement started in 72 hours.  After six weeks they were gone and I am getting better.  
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