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

High Blood Sugar, Celiacs Scared And Confused...help!


gregbell232

Recommended Posts

gregbell232 Newbie

Hi all,

Need to know what to think because my docs are very confused right now. Short background... Diagnosed with T1DM in 2010 A1C=10 FBG=350, PCM sent me to emergency room. I accepted my fate as a T1D, but the emergency room physician was not convinced said my body was obviously making insulin and my bs was actually dropping following eating... Put me on IV for an afternoon sent me home with BS ~180. Over the course of a week my BS spiked back up and I lived in the 300s (and felt LIKE CRAP). This kept on for about two weeks. I remember very vividly after eating a Chili's coming back to work feeling very very shaken and dizzy, also pale as a ghost. I grabbed my meter and to my surprise my BS was 100! Remember I was not an any medication and was checked at 300 just that morning. From that time forward my BS was in the 40-80 range (yes with one 26). Went back to the doctors about 6 weeks later re-ran A1C=5.0. Endo said she had never seen anything like this! She re-ran every diabetic test she could think of, all came back stone cold normal...even low 60 after glucose challenge. She gave me a hug told me I didn't have diabetes and I did cartwheels out of her office!

Something though still did not seem right... I had had persistent stomach pains for about 1.5 years before and thought this was a great time to see if it was tied to the blood sugar issues. Endo Dx'd with celiac disease w/blood and biopsy. Mentioned that Celiacs could have been causing bizarre blood sugar spike.

Almost one year to the day (and after being strictly gluten-free), another blood sugar explosion! 385-400 for about two weeks then a random plunge to 100 and fine for another year...

Which brings us to today, my BS is 250 feeling crappy for the last week and thought I should check. Went to the ER as I was urinating like crazy and could barely sleep through the dry mouth. Put me on fluids again, pulled my record from the last two trips and said, well this is DEFINITELY not how T1DM works... you don't recover! Brought in internist and said nothing like he has ever seen. Maybe pancrease tumor, maybe thyroid, maybe finally T1DM taking over.

So I wait... feeling like crap hoping and praying that my BS drops to normal again. Asked for insulin to use temporarily and they laughed at me, saying they would never give insulin to a person with BS levels in the 200s. I have a CT scan of my organs tomorrow praying for an explanation that is NOT cancer.

Has anyone experienced anything like this? Honestly I am 31 years old and a military pilot (physically fit). This will be the end of my career if T1DM and I am supporting my wife and children. Scared to death!!!!! I know there are successful people with T1D who have normal lives, but I have NEVER heard of anyone with celiac disease+T1 (though I have heard it is very common).

I am basically accepting the T1DM and am looking for some inspiration and encouragement that I will be able to care for my family and have a decent standard of living if I expertly manage both. Anyone else out there????


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



Celiac.com Sponsor (A8-M):



Skysmom03 Newbie

My husband has both. He has had type 1D for almost 35 years and was diagnosed with celiac a year and a half ago. ( although he had severe damage to his intestines). He does live a normal life. He does have a pump but regardless of that he counts his carbs and doesn't eat gluteny products! There are lots of things he can have that he enjoys. He is not miserable by any means. He does have a harder time controlling his bs since the celiac but nothing too major.

gregbell232 Newbie

My husband has both. He has had type 1D for almost 35 years and was diagnosed with celiac a year and a half ago. ( although he had severe damage to his intestines). He does live a normal life. He does have a pump but regardless of that he counts his carbs and doesn't eat gluteny products! There are lots of things he can have that he enjoys. He is not miserable by any means. He does have a harder time controlling his bs since the celiac but nothing too major.

Thank you so much for your reply! Thanks for not slamming me for asking such a question. It is just more unknown... I knew scores of people w/celiac disease at my Dx so it didn't seem impossible to cope with. I know very successful people with T1, but just not both...

Honestly I have lived a strict diabetic diet since my first (apparently) misdiagnosis of type 1 <100 carbs/day. I have not even tasted a sugary or sweet treat in 2 years. To the extent that my PCM and dietitian threatened to send me to the shrink for an eating disorder (which honestly i believe I had) if I didn't eat more carbs and exercise less (triglycerides came in at 18). Some days I was at zero carbs just because I was so afraid of the BS shooting up again. I know I was running massive calorie deficits but was sooo afraid of DM that I was starving myself.

GFinDC Veteran

Hi Gregg,

There are other members on the forum with diabetes, but I don't know if it is T-1 or T2. It sounds lie you are doing a good job with the diet. I was going to suggest a Paleo type diet with limited carbs but you are already doing that. They say autoimmune diseases like to run in packs which just means it is not uncommon for people to get more than one. Dr, Peter Greens book Celiac Disease A Hidden Epidemic says there is some indication that autoimmune thyroid disease symptoms can improve on the gluten-free diet. Stretching that to diabetes doesn't seem entirely crazy, but it might be.

Some people say alpha-lipoic acid helps their glucose control. Metformin (commercial med) is also supposed to be good.

You may find some herbs or foods can affect your blood glucose levels even if they aren't carbs. Metformin is based on Goat's rue, an herb. So if one herb can affect blood glucose then others probably can also. Can you remember anything unusual you were eating during your "attacks"? It might help to keep a food log so you can look back and possibly identify foods that are potentially problems.

And thanks for serving our country! :)

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,855
    • Most Online (within 30 mins)
      7,748

    Tara M
    Newest Member
    Tara M
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
    • Me,Sue
      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
    • Francis M
      Thanks. Since the back and forth and promises of review and general stalling went on for more than six months, the credit company will no longer investigate. They have a cutoff of maybe six months.
×
×
  • 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.