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

My Baby & Husband Have Celiac... Need Advice


gatakat

Recommended Posts

gatakat Newbie

Hello all:

I just found this website and I am very glad I did. My husband was diagnosed with Celiac about 4 years ago. He has been struggling with it ever since. He cheats here and there (and pays for it)... he has the most difficult time accepting the fact that he cannot eat gluten (being Italian and not being able to eat regular pasta KILLS him). Even though I think corn pasta tastes great, he disagrees. When he was first diagnosed, I found VERY little gluten-free items in our area... and now, there is so much stuff out there, which I am grateful for. But nothing prepared me for what happened next.

My son was born in October and when he was just 8 days old, he started having wretched diarrhea. It lasted 20 days. (it was an awful time and test after test and hospitalization after hospitalization were causing major stress in our lives when we shoudl have been enjoying our beautiful boy). After MANY negative test results, the doctor said the only way to really test for Celiac was through Endoscopy which I said no too since he was soo little and needed to be put to sleep. *he did have a Colonoscopy but was awake during it*. Then suddenly, the best thing ever happened. We learned of this new, state-of-the-art gene testing that is only performed in California.... Ofcourse, we did it. SURE ENOUGH, POSITIVE FOR CELIAC. Strangely enough though.... it was BOTH my husband and I who were carriers and thus, my son's Celiac is FAR WORSE than my husband's Celiac. I have never showed symptoms but now I know I carry the gene.

My son is now 8 1/2 months and I am stressing about.. all foods he comes in contact with. He is getting teeth now and I'd like to know what finger foods I can give him... since obviously cheerios and cookies are out of the question. I worry about how HARD some gluten-free foods can be since, he has only 1 tooth...

Any advice you can give a new mom is greatly appreciated.

All my love

Sussie


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



Celiac.com Sponsor (A8-M):



Worriedtodeath Enthusiast

I would stick with natural fruits/veggies for a long time. There is a yahoo group called silly yaks that has lots of kid recipes on it icluding gold fish crackers. You could make your own teething biscuits. There is a cheerio sub called Perky o's. We make lots of cookies and i even just made a cookie cake that a little one could probably gum. Leave out the chocolate chips and it would probably be soft enough but hard enough to hold shape in those little baby hands you could make some gluten-free bread and cut that into strips and toast it.

I cut veggies into itty bitty cubes and then boiled them until they could be squished but still held their shape when touched. I fed mine that which seemed to satisfy their need to feed themselves. we didn't know about Celiac until later so I did the normal course of finger foods so I don't have much insight into that first year gluten free.

HTH

Stacie

RiceGuy Collaborator

My only thought is that any grains at such a young age seems a bit early to me. I mean, wouldn't celery or something be better for teething? Maybe I shouldn't try to make suggestions though, as I'm no expert in feeding infants. I don't know...all the things I can think of that are tough enough to gnaw on might also get stuck in an infant's little throat.

But for finger foods in general, how about some fresh raw garden green peas? Also blueberries (oh, the stains!), raisins, figs, cut green beans, cucumber slices, melon slices, boiled & cubed sweet potato or squash, etc. I suppose sunflower seeds are too small, but if you mash up some figs or other sticky fruits, and press a bunch of seeds into that, it might make a tasty snack bar. Come to think of it, I'd add shredded coconut, and eat it all myself LOL!

I'm sure someone more experienced and thus qualified will have great suggestions for you.

AliB Enthusiast

Have a look at the Pecanbread website. It has some great ideas for food for children who need to eat basic. It's aimed for children with ASD but the info is extremely useful for everyone.

Don't worry about feeding your little one too much in the way of gluten-free baked and sweet stuff - I think the longer we hold off giving them the sugary stuff the less of a taste they develop for it. My youngest grandson at 4, unlike his older brother, has never liked fruit and veg and would happily live on chocolate biscuits if he had half a chance. I wish they had never been given to him. You don't miss what you've never had! We love our kids and want to spoil them, but sometimes we really 'spoil' them if you get what I mean!

My eldest grandson who is 7 loves fruit and veg. I have a series of photos of him when he was not much older than your baby, sat in his highchair in our garden chomping on strawberries and grapes cut in half. I have framed them as the expressions on his face were just fantastic!

Try giving him soft little french beans, french fries (and sauces to dip them in), cooked carrot sticks, banana, soft boiled egg to dip the fries in (good co-ordination thing!), pieces of cooked chicken (try chopping it fine, seasoning, adding an egg, forming into little balls and fry for a few minutes gently, moving them round the pan so they don't get too crispy and hard) and chunks or slices of cheese if he's dairy tolerant, sliced pear, pieces of rice cake or little snack-a-jacks, gluten-free toast with peanut butter, jelly or spread, cooked sweet potato chunks, etc.

We always think of finger foods being dry and hard but they can also be moist and soft - as long as they can be picked up by chubby little fingers, it doesn't matter what they are, and getting messy is all part of the fun!

I remember sitting in the dining room with Connor next to me in his chair and the little tinker kept leaning over and pinching my string beans off my plate and scoffing them! He thought it was a great game!

peetred Rookie

What about arrowroot cookies? Can't celiacs have arrowroot? I am not sure, but I bet there is a gluten free alternative if the ones in the store are not already gluten free.

slmprofesseur Apprentice

My baby/toddler does mostly fruits (and a few )veggies. Bananas, mangoes, melons, pineapple etc. We leave Gluten-free cereal in the church nursery for him.

  • 1 month later...
theceliachusband Rookie

Hi there,

I feel for you and the dilemma at hand. Both my wife and daughter are Celiacs.

Let me be radical here and though I agree with other posters who advise against grains at such early age, we gave our daughter Cocoa Pebbles when she was little. To replace the Cheerios.

In terms of Pasta, let me tell you about Brown Rice Pasta from a company called Rizopia. It is made in Canada.

I am from Austria and LOVE pasta. We have exclusevly switched to Rice Pasta and let me tell you (or your husband), it is the closest you will ever get. It is brilliant.

:)

Peter, The Celiac Husband

Hello all:

I just found this website and I am very glad I did. My husband was diagnosed with Celiac about 4 years ago. He has been struggling with it ever since. He cheats here and there (and pays for it)... he has the most difficult time accepting the fact that he cannot eat gluten (being Italian and not being able to eat regular pasta KILLS him). Even though I think corn pasta tastes great, he disagrees. When he was first diagnosed, I found VERY little gluten-free items in our area... and now, there is so much stuff out there, which I am grateful for. But nothing prepared me for what happened next.

My son was born in October and when he was just 8 days old, he started having wretched diarrhea. It lasted 20 days. (it was an awful time and test after test and hospitalization after hospitalization were causing major stress in our lives when we shoudl have been enjoying our beautiful boy). After MANY negative test results, the doctor said the only way to really test for Celiac was through Endoscopy which I said no too since he was soo little and needed to be put to sleep. *he did have a Colonoscopy but was awake during it*. Then suddenly, the best thing ever happened. We learned of this new, state-of-the-art gene testing that is only performed in California.... Ofcourse, we did it. SURE ENOUGH, POSITIVE FOR CELIAC. Strangely enough though.... it was BOTH my husband and I who were carriers and thus, my son's Celiac is FAR WORSE than my husband's Celiac. I have never showed symptoms but now I know I carry the gene.

My son is now 8 1/2 months and I am stressing about.. all foods he comes in contact with. He is getting teeth now and I'd like to know what finger foods I can give him... since obviously cheerios and cookies are out of the question. I worry about how HARD some gluten-free foods can be since, he has only 1 tooth...

Any advice you can give a new mom is greatly appreciated.

All my love

Sussie


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



Celiac.com Sponsor (A8-M):



Lisa Mentor

"My son was born in October and when he was just 8 days old, he started having wretched diarrhea. It lasted 20 days..."

I don't understand how a child as young as 8 days can have diarrhea associated with Celiac, unless he is reacting to your breast milk.

HiDee Rookie
My son is now 8 1/2 months and I am stressing about.. all foods he comes in contact with. He is getting teeth now and I'd like to know what finger foods I can give him... since obviously cheerios and cookies are out of the question. I worry about how HARD some gluten-free foods can be since, he has only 1 tooth...

Any advice you can give a new mom is greatly appreciated.

All my love

Sussie

Baby MUM-MUMs are awesome. Made of rice, gluten-free, very easily gummed and dissolved in a baby's mouth (with or without teeth). My Wal-Mart carries them in the baby food isle but they are also on Lame Advertisement. They have a regular flavor and a vegetable flavor. My toddler has been eating them since she started on rice cereal, she loves them. They are a great snack for babies and kids when you are on the go and not a bad price.

Juliet Newbie

Other things besides Baby Mum-Mums that we used with our daughter (those mum-mums weren't available at the time :( ):

Health Valley Rice and Corn chex like cereal (however, now you can just use regular General Mills Rice Chex) slightly crushed up - they easily dissolved in her mouth by 7 months

fresh, homemade gluten free bread (try these links: Open Original Shared Link or Open Original Shared Link

cooked very soft arborio rice (clumps together nicely, but still very mushy)

Gerber Wagon Wheels

And of course, all the pureed fruits and vegetables you can stuff down that mouth of theirs!

Amyleigh0007 Enthusiast

My 11 month old only has two teeth so the foods I give her must be easy to chew (gum) also. I bought a food grinder and she eats almost everything that we do. She really likes mac and cheese (Tinkyada elbow noodles, Velveeta, milk). I cut the noodles in half. I also bake sweet potatoes and let them cool. Then I press the inside into little balls so she can pick them up. I also do that with carrots. I steam organic baby carrots, grind them in the food grinder and press them into little balls. They are formed enough for little fingers to pick up but very easy to chew (gum).

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - cristiana replied to Scatterbrain's topic in Sports and Fitness
      5

      Feel like I’m starting over

    2. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      8

      My only proof

    3. - Wheatwacked replied to Jmartes71's topic in Coping with Celiac Disease
      8

      Related issues

    4. - NanceK replied to Jmartes71's topic in Related Issues & Disorders
      8

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,299
    • Most Online (within 30 mins)
      7,748

    Philbin
    Newest Member
    Philbin
    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

    • 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.  
×
×
  • 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.