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

Develop Celiac Disease At 35


uruboy02

Recommended Posts

larry mac Enthusiast

Diagnosed at 55, after 2 years sick and three doctors.

Am convinced the "trigger" was this chain of events:

1) Got bad cold.

2) Went to Doctor, got antibiotics.

3) Cold got better, but got major bad GI problems.

4) Went back to Doctor, diagnosed with C-Diff., got powerfull antibiotics to fight C-Diff.

5) C-Diff cured, but GI symptoms, albiet milder than C-Diff, started probably a few months later and continued 2 years until diagnosed with Celiac by blood tests, endoscopy, and biopsies. Got miraculously better same day went on gluten-free diet.

best regards, lm

  • 2 weeks later...

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



Celiac.com Sponsor (A8-M):



songwrtr54 Newbie

I figured it out myself at 57. Had a horrible time last year. Super high blood pressure and all my teeth are gone. This happened all in a period of approx. 1 year. Avoiding gluten now for only about six weeks and have now stopped by high blood pressure medication. I am on the Gerson eating program. Dr. Gerson solved it all in the 1920's. It's all about diet. I wish I had known this earlier.

Financialman Newbie

Unfortunatly Celiac disease doesn't recognize or care about your age. Since it is a genetic disease it can lie dormant for many years until a "triggering event" sets it off. That is what happened to me and I am well past 35. The good news is you can manage it and it is getting better everyday with all of the many gluten free food companies that are popping up everywhere. Stay connected to this forum and ask your questions. There are a lot of knowledgable people on this forum that can help you get through this. Good Luck! :D

  • 2 weeks later...
Juls Newbie

I was diagnosed finally at 52. I am having a really horrible time figuring out what I can and can't tolerate. I am at the point where I would rather feel hunger than the pain of eating something "bad". It is a real battle, as you all very well know. It started with a carb-free diet last June, (but I know I have had it for years looking back). I was trying to encourage my daughter, 21, to lose a few pounds, and I needed to lose a few anyway. After 20 pounds I weighed less than I had in years and was very happy. Went back to carbs, and wow, it was awful. I have lost another 30-35 since then, and am still losing. Even some foods that are gluten free seem to bother me. I also have RA, anxiety, depression (which I am on meds for), psorasis, and many other obvious Celiac symptoms. Exhaustion, and my hair is falling out. I'm sure these symptoms are nothing new to most of you, but I am really getting discouraged. I ended up in the ER in December for the most excruciating stomach pain I have ever had in my lifetime, and last night it was almost as bad. The Dr. gave me pain pills, but I really don't want to be taking any more meds than nescessary. Does anybody else have stomach "pain"? And if so, what has helped alleviate it? I will take any advice! Thanks for reading!

hnybny91 Rookie

I started having severe symptoms at 36 but looking back I think I may have been some form of gluten sensitive since childhood.

mommysboys2 Rookie

Thank you for the welcome! That is exactly what I am dealing with! I am taking liquid vitamins, liquid iron for severe anemia, and a high protein liquid supplement throughout the day to try to repair muscle damage. Also B12 injections.. I have been SO weak, depressed, and have very sore joints and muscles, so my lifestyle has taken a huge left turn over the last year. My guy friend was so disappointed that I didn't get a ski pass, but it isn't worth it! I bought one last year and skied one time. I need to get my body back! I sure thank you for the encouraging words.... I look forward to getting better and learning from this site..... Thank you!

I was wondering...do you have to lose weight in order to have gluten sensitivity or celiac disease?

mushroom Proficient

No, some gain quite a bit of weight because their bodies save everything, they are so starved of nutrients.


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



Celiac.com Sponsor (A8-M):



TB4me2000 Newbie

I'm joining in--I find this thread rather reassuring. Good to know I'm not the only one wondering where the heck this came from.

I'm 23, graduated from college last May, got my first job this past September. New city, first apartment, first job (make that a super stressful job with a crazy boss) and a nervous stomach somehow landed me in serious pain for the few months leading up to my birthday. I had settled into work and figured it couldn't be nerves tearing my stomach to shreds every day like clockwork 20 minutes after I ate just about anything. Did a little research and went gluten-free the week before my birthday. I felt better within 24 hours. Hurrah! No way in heck am I ever going back to that way of life again.

(Thanks to all of you, by the way, for sharing your stories and advice. It's ever so helpful to hear about other people's experiences and to realize you're not alone.)

  • 1 month later...
Luddie Newbie

Thank you for the welcome! That is exactly what I am dealing with! I am taking liquid vitamins, liquid iron for severe anemia, and a high protein liquid supplement throughout the day to try to repair muscle damage. Also B12 injections.. I have been SO weak, depressed, and have very sore joints and muscles, so my lifestyle has taken a huge left turn over the last year. My guy friend was so disappointed that I didn't get a ski pass, but it isn't worth it! I bought one last year and skied one time. I need to get my body back! I sure thank you for the encouraging words.... I look forward to getting better and learning from this site..... Thank you!

I think the vitamins and minerals will certainly help. I, too, have the sore muscles and joints and it doesn't help my piano playing at all because it's mostly in my shoulders and wrists. A bit of neuropathy, too. I'm a very active, multi organization volunteer person who was diagnosed with celiac only 4 years ago, when I was 73! Talk about surprise!! It was awful. I finally let go and went with the flow and tried to laugh about what symptoms would appear "tomorrow", I suffered from what I call "migratory" pains. Anyhow, that is slowly getting better but not being able to jump in and out of the car and get my work done is truly frustrating. Not eating various forbidden foods really doesn't bother me very much. Just my two cents worth. As you heal your gut, you will feel better!

chefsands Newbie

I got it at 28, my father at 68, my sister at 38, my niece at 1 and nephew at birth. Stress brought it on for me :(

  • 2 weeks later...
GlutenFreeJess Newbie

I was diagnosed with Celiac at age 28. I think it's a common misconception that Celiac only occurs in childhood, which is why so many people go un or mis diagnosed.

Monael Apprentice

It's funny, I am 46 and figured it out for myself after many years of being told I had IBS. So many different symptoms have disappeared or have improved I can't believe it. I don't even WANT my old favorites that have gluten.

But looking back, I also wonder how long I had this. I was very anemic starting when I was a child. And the IBS has been around for so long I forgot when I didn't have it. Now by eating no gluten I have not had diarrhea except a couple of times I ate things I didn't realize had gluten in them.

I don't even know what my trigger was.

  • 2 weeks later...
NinaSA Newbie

Ask your dr about iron IV. I was and currently am severly anemic and always tired. When my iron is low it feels like I have to use every ounce of energy to do ordinary tasks. With the iron IV my levels return to normal within two weeks. Much faster than the months oral iron can take. I am also on liquid iron to try to maintain a good level. It is amazing how my life can completely turn around within only to weeks. I literally felt like a new person!!!! Just got another IV today looking forward to feeling better. You may not need it more than once but I also have a bleeding disorder. My dr said it's a double whammy. Don't absorb it and can't keep it. Good luck and I hope you feel better soon!

  • 3 weeks later...
josh052980 Enthusiast

I turn 31 on Sunday, and just went gluten free. I'm 5 weeks in and feeling so much better. Looking back, there's been signs all the way back into my early teen years, but they were never an issue so I just overlooked it.

Coleslawcat Contributor

I was 31 when I was diagnosed. I was largely asymptomatic, or so I thought. It wasn't until after I went gluten free that certain things I thought were normal (regular headaches, frequent random nausea, joint pain, fatigue) actually weren't normal and were caused by celiac. Looking back I'm nearly positive I've had this since I was 21 and had a severe case of mono.

Fire Fairy Enthusiast

I'm pretty sure mine dates back to age 27 and the year 2001. I had two personal crisis surrounding the week of September 11th and I think the stress was too much for my body and activated the Celiac Disease. I had already had some issues (mostly migraines) but that was when I really got sick.

Karla01 Apprentice

I am 44, was diagnosed last August, I had symptoms for 5 years,but thought they were all realated to working nightshift and the stress of being a nurse. I think it would have been easier being diagnosed as a child. As an adult I miss so many things I used to eat.

jemms Apprentice

No, some gain quite a bit of weight because their bodies save everything, they are so starved of nutrients.

I am 35 as well and recently found out about my gluten intolerance...am hoping to get results back from endo this week regarding Celiacs. Anyways, I could not lose weight for the life of me, I gained 60 lbs after my daughter was born in 2006 and I couldnt understand why. I tried everything to lose it but it just didnt matter. Now, the weight is coming off like crazy. It is reassuring to know that some people do gain weight from this. I felt like such a failure because I was close to 250 lbs. I would explain to my doctor that I wasnt eating much and still gaining. She would look at me like I was lying and tell me to exercise more. It is so nice to finally have answers!!!

NoodleUnit Apprentice

Similar story here...

I've just turned 40 and pretty much that was when the celiac disease got triggered. I've always had symptoms I guess. I remember eating 4 slices of toast when I was a teenager after school and being unable to fight the urge to fall asleep. I've always had a troublesome stomach but just assumed everyone did and didn't complain as much as me :)

Then I got a massive infection, 5 months of antibiotics and BOOM I can't so much as look at gluten now. I'm fairly convinced it's the antibiotics wiping out my gut flora which did it for me. As is my neurologist. Annoyingly, my GP seems to think that my symptoms are unusual for celiac disease but from coming on this forum and doing a lot of research I know that it's very common. He put me on the wrong path for months imo.

  • 6 years later...
ldh84 Newbie

I am 33 and just diagnosed with celiac in July 2017. I am gluten free but still suffering from costocondritis and stomach acid issues. I am also dealing with some neurological things like pins and needles in my left shoulder blade that come and go. No deficiancies right now that we know of othwr than vitamin D which I have a prescription for. My symptoms were not bothersome until right after my first child and then everything fell apart. 

Ennis-TX Grand Master
10 hours ago, ldh84 said:

I am 33 and just diagnosed with celiac in July 2017. I am gluten free but still suffering from costocondritis and stomach acid issues. I am also dealing with some neurological things like pins and needles in my left shoulder blade that come and go. No deficiancies right now that we know of othwr than vitamin D which I have a prescription for. My symptoms were not bothersome until right after my first child and then everything fell apart. 

Your posting on a thread with a previous response from 2011, try starting a new thread. On your issues you mention no deficiency but I most attest that the pins and needles correlates to B-vitamins or magnesium both of which effect nerve response and can trigger this symptoms. It might not even show up as a deficiency on test but you will find supplementing to get rid of the symptoms. Everyone is different with different levels and needs of things. I would try a full spectrum B-vitamin making sure to have niacin in addition to it, I found Liquid Health Neurological Support and the Stress & Energy formula in combination 1 tbsp each 3 times a day to contain what I needed. Magnesium since you do not show issues of constipation and I assume you have a daily BM we might skip over the citrate version and go to the glycinate version as a first suggestion. Try Doctors Best powdered form 1 scoop in the evenings. You will notice very deep sleep with vivid dreams as a side effect, pins and needles and cramping/achey muscles should lessen. If your on PPIs they make it where you body can not use both b-vitamins, magnesium, and iron in the ways it is meant to. We have a fellow member who might be able to address getting you off them.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,543
    • Most Online (within 30 mins)
      7,748

    yfuvhg
    Newest Member
    yfuvhg
    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

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.