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Families In Jacksonville Nc


bear6954

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bear6954 Apprentice

Just looking for some families in jacksonville nc area. My son was diagnosed in May and I have yet to meet another person with celiacs. It would just be nice to have some local support and discuss things!


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MySuicidalTurtle Enthusiast

Here are some North Carolina groups:

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dreamindarlin Rookie

Hi,

I'm in Asheville NC.

Guest elysealec

Hi.

How old is your son? Our family is in Kure Beach. That's not too far from Jacksonville. The kids go to school in Wilmington. I have celiac disease as well as my 11 year old daughter. I also believe me my 10 year old son has it as well. He went gluten free over the summer and feels so much better. He doesn't want to have to eat gluten again in order to be tested, so I am leaving the choice to him.

Vicki

  • 2 weeks later...
SAHM2one Contributor

my son and I are both gluten free, we are in Havelock

  • 1 year later...
MinRalph Rookie

Hi! I live in Jacksonville, NC and also haven't met anyone else with Celiac here. I was diagnosed in 2003 (age 17) and have been living (or at least trying to live) gluten-free since then. My sister also has it. Thanks for posting, I never would have known there was anyone here with it too!

Shess0816 Apprentice
Just looking for some families in jacksonville nc area. My son was diagnosed in May and I have yet to meet another person with celiacs. It would just be nice to have some local support and discuss things!

Hello! My mom and my little sister are just getting ready to start the gluten free diet. They live in Wilmington, which if I remember is around an hour away. I live in Nebraska, so I'm not much help, but I have given them a lot of information, meal plans, etc... to help them out. It's so hard when you're first starting off and you feel kind of isolated!! I totally understand!


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  • 10 months later...
seeleeak Newbie

Hi!

I am so happy to find someone else in Jacksonville with Celiac disease.(Not that I'm glad you have it. lol) I thought I was the only one. I was just diagnosed in February. Any ideas you may have for gluten-free shopping or restaurant suggestions will be greatly appreciated. Our supply here seems to be pretty limited. I usually just cook everything I eat other than fresh veggies and fruit.:(

Heidi S. Rookie

Hi!

I am so happy to find someone else in Jacksonville with Celiac disease.(Not that I'm glad you have it. lol) I thought I was the only one. I was just diagnosed in February. Any ideas you may have for gluten-free shopping or restaurant suggestions will be greatly appreciated. Our supply here seems to be pretty limited. I usually just cook everything I eat other than fresh veggies and fruit.:(

My sister and her daughter live in Sneads Ferry, right near Jacksonville both are gluten-free. Her daughter is going into first grade! Let me know if you want to meet, she is excellent at gluten free cooking!

quincy Contributor

My sister and her daughter live in Sneads Ferry, right near Jacksonville both are gluten-free. Her daughter is going into first grade! Let me know if you want to meet, she is excellent at gluten free cooking!

I am staying in Wilmington visiting my sister for a few weeks and returning home soon.I found several places that catered to Celiacs. One was a food co op called Tidal Creek. They are located on Oleander. They label all their shelves to indicate the item is gluten-free. Their salad bar dishes are all indicated if gluten-free and warnings not to mix utensils. Another place is Lovey's Market in Landfall shopping center. Their salad bar also lists ingredients as gluten-free free or not.

Harris Teeter has a good selection of gluten-free foods as well. THey even carry the gluten-free beer which is very good.

hope that helps...!

seeleeak Newbie

My sister and her daughter live in Sneads Ferry, right near Jacksonville both are gluten-free. Her daughter is going into first grade! Let me know if you want to meet, she is excellent at gluten free cooking!

Thanks! I could really use some tips for baking and frying. The recipes and commercial mixes I have tried so far taste fair, but are VERY dry. The flour seems to fall right off and end up burned in the bottom of the pan.

seeleeak Newbie

I am staying in Wilmington visiting my sister for a few weeks and returning home soon.I found several places that catered to Celiacs. One was a food co op called Tidal Creek. They are located on Oleander. They label all their shelves to indicate the item is gluten-free. Their salad bar dishes are all indicated if gluten-free and warnings not to mix utensils. Another place is Lovey's Market in Landfall shopping center. Their salad bar also lists ingredients as gluten-free free or not.

Harris Teeter has a good selection of gluten-free foods as well. THey even carry the gluten-free beer which is very good.

hope that helps...!

Thank you!! I will have to make a trip to Wilmington soon. I appreciate your help. I can't wait to try these places.
  • 2 months later...
semperwife Newbie

I am in Jacksonville, NC

My son was 7 when he was diagnosed and is now 14.

Would love to meet other families~

  • 1 month later...
rmhodgdon Newbie

Hi!

I am so happy to find someone else in Jacksonville with Celiac disease.(Not that I'm glad you have it. lol) I thought I was the only one. I was just diagnosed in February. Any ideas you may have for gluten-free shopping or restaurant suggestions will be greatly appreciated. Our supply here seems to be pretty limited. I usually just cook everything I eat other than fresh veggies and fruit.:(

There aren't too many places in Jacksonville itself. There is a small health store in the New River Shopping Center that offers a few gluten-free items. Food Lion on Piney Green Rd offers a good selection, Walmart also now offers gluten free items. If you are willing to travel Harris Teeters, Loveys and Tidal Creek in Wilmington offer gluten-free items.

As for restaurants, the best in town I have found so far is Outback Steakhouse, they have a dedicated gluten-free menu. Also Olive Gardens now offers a gluten-free pasta meal. Longhorn steakhouse also claims to offer gluten-free dining but I have not tried them yet. Just be sure to remind them that you do not want bread. Sometimes the waitresses that pack the food in take out bags forget and include the bread.

  • 2 years later...
JennCo Newbie

We are in Jacksonville and have a 9 yr old daughter with Celiac.

  • 3 years later...
mynxr Rookie

Hi,

I know this thread is old but I'm in Swansboro.  My husband and I moved here almost 6 years ago and I was diagnosed with Celiac 3 years ago.  I can't find a support group, meetup group or anyone else that has Celiac even close to me.  I would happily drive to Jacksonville or host a group if people are willing to come to Swansboro.  I've learned a lot during the past three years but still have trouble with groups, dining, out etc.

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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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