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

Venting Slighty But I Do Still Wonder


Kylie

Recommended Posts

Kylie Explorer

Hello all,

Well i hate to sound whiney in my first post in this section, but seeing that i am the only Celiac in my family and i know no one who has Celiac, i feel very alone sometimes!! I was diagnosed almost three years ago and it was the best thing i ever did. I had been sick for months, lost close to 15 pounds but looked like i had gained close to 20 from all the bloating and swelling. The first year of being gluten free was a great time and I have the best gastro doc anyone could ask for, however, it only last a year. Since then, I have been hospitalized for random things, needed more and more biopsies, seen an infectious disease specialist, was paralyzed for close to two weeks and nearly failed my senior year of high school because I missed so many days of school. In a year I managed to contract a strain of mononucleosis (sorry for the spelling!) that landed me in the hospital because my tonsils swelled so much I couldn't breathe. I missed a month straight of school, was not able to celebrate Thanksgiving or Christmas, and to this day am still tired, sore, and pulling strains of the mono virus (Epstien Barr) up in blood tests. I have also needed my nose cauterized because I had such bad nose bleeds that I had to be sent home from school because I had lost too much blood. I seem to catch every cold that comes around (currently I have a cold, ear infection, and possible strep in the middle of the summer). The most interesting of them all however has to be the paralysis. I woke up one day with very sore legs which I thought were growing pains, I'm 5'8 and 18 years old and still growing. By two days later I could barely walk the 10 steps it took to walk to the bathroom. Because the pain was so bad, I managed to trip down the stairs and bruised my tailbone and sprained an ankle. The day after that, I could not get out of bed and had to use a wheelchair to get to my various doctors appointments to try and find out what was wrong. It did eventually go away after about two weeks but I am still having pain and on the occasional few days, I won't be able to walk because of the numbness and pain. And the grand finale to this whole saga (and probably the reason I am most distressed) is that I will have to have another colonoscopy on Tuesday (I had one a little over 2 months ago) because I have a bleed somewhere in my small or large intestine. This will be my third endoscopy/colonoscopy since my diagnosis! I am really getting tired of all of this, I have tested negative for Crohn's, Lupus, ticks, Lyme disease, various poisonings, and pretty much any disease you can think of. In a few weeks I will be tested for Chronic Fatigue Syndrome and hope that maybe it will shed some light on an answer. Does anyone else just seem to catch every cold, cough, disease, and never be able to get a handle on their Celiac? I follow the strictest diet that I maintain personally so that there are no mistakes. I eat a healthy diet and exercise regularly (that is when I can get out of bed). I am very fed up with feeling like I am 60 years old when I am only 18. Does anyone have any advice or a morale boost because I think I am about to lose it if I find out that one more thing is wrong but no one can explain why. Any help would be greatly appreciated, and my apologies for the rant, I am just looking for someone who understands.


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



Celiac.com Sponsor (A8-M):



confusedks Enthusiast

Ugh! I'm so sorry you're going through all of this! I am 17 and I am having a lot of physical problems also. Doctors have no idea what is wrong with me. They say it's one thing, but then they treat that problem and it doesn't work! I may have to have back/ SI joint surgery in a few months and am very worried! If you ever want to talk, you can email me knshore@hotmail.com or IM me knsgoestonz511

Kassandra

Feel Better!!!

tom Contributor
Hello all,

Well i hate to sound whiney in my first post in this section, . . . .

Hi Kylie,

Let me be the first of many to say there is never a need to apologize for or spend a moment worrying about sounding whiney.

Seriously.

. . . .. . I am very fed up with feeling like I am 60 years old when I am only 18. Does anyone have any advice or a morale boost because I think I am about to lose it if I find out that one more thing is wrong but no one can explain why. Any help would be greatly appreciated, and my apologies for the rant, I am just looking for someone who understands.

I remember a 3 month period where I was sure I'd aged 15-20 years. Or was it a 6 mo period? Memories weren't filed away properly for a time there.

I can relate at least a bit anyway. But I didn't go thru what you have or are still having to deal with.

I know it's natural to feel the need to apologize like u have, but don't u ever believe it's necessary - whether u write it or not.

Most of the people here have been thru some pretty rough times and are all more than willing to help when they can and sympathize when they can't. (And often both)

I wish I had more to offer right now. I think all I can add is that CFS isn't a real diagnosis - it's a symptom.

Something else is causing the fatigue.

There is an answer and it can be found.

Best of Luck, Kylie.

trents Grand Master

Kylie,

As others have said, you need to vent. Psychologically, its appropriate and healthy as you are grieving something - the loss of the normal energy, health and vigor that ought to come with youth. Don't give up, however, you may very well have it yet again.

Have you had any systematic allergy testing done? And does your (or your parents') insurance cover the services of a naturopathic doctor? I can't help but wonder if what you are suffering is tied to some toxicity problem or nutrient defficiency.

God bless,

Steve

Kylie Explorer

Thanks Steve, I haven't thought of that, but I will look into it. Currently the only relief I get is from going to acupuncture, the best hour of my life. Thanks to all for the support, I really appreciate it!

tom Contributor
Thanks Steve, I haven't thought of that, but I will look into it. Currently the only relief I get is from going to acupuncture, the best hour of my life. Thanks to all for the support, I really appreciate it!

Whew I was SO skeptical going into acupuncture out of pure desperation.

Walked out calling it magicpuncture.

Too too amazing! :)

loraleena Contributor

I would suggest a full thyroid panel including thyroid peroxidase antibodies. Hypothyroidism can cause a lot of body pain and fibromylagia. Also nightshade veggies can cause body pain as well. These include eggplant, potatoes, peppers and a few more I am forgetting (tomatoes to I think).


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



Celiac.com Sponsor (A8-M):



marciab Enthusiast

Interesting ... I was diagnosed with CFS / FM back in 1990 partly because my immune system had fallen apart and I would get an URI everytime I exerted myself. Actually in the first few months after contracting CFS / FM, I would get an URI everytime I stopped the antibiotics.

I also could barely walk any distance without my legs forgetting how to walk or feel too heavy for me to lift. My arms were too heavy for me to wash my hair without letting them rest for a few minutes and then trying again. This turned out to be either gluten ataxia or nuerological celiac and has gone away since eliminating gluten. I had a sleep disorder called nocturnal myoclonus (seizures when my body would go into REM) and insomnia which is gone now too. Headaches and pain from head to toe .... The list goes on ....

Bottom line, my body was falling apart too.

Since I went gluten, soy, dairy, corn, eggs and chemical free back in 2005, my symptoms have begun to go away, but I'm not sure I will recover. We'll see.

I wish I could tell you exactly what you need to do, but there are so many theories out there about CFS and so many people with different symptoms that it's not that simple. BUT, I understand that those of us with true CFS are overly sensitive to the things most people's immune systems can fight off. That's how we got the label "Canaries in the coal mine". The best thing you can do is to build up your immune system.

So, if you haven't already, I would recommend detoxing your body using herbs, treat for candida and eliminate to the best of your abilities all known allergens. I'd stick to the milder treatments though since we are known to overly react to all treatments. Weak herbal teas are easy on the body.

BTW, CFS is a real diagnosis, BUT current theory is that CFS is caused on an underlying problem such as undiagnosed celiac, Lyme, food intolerances, toxins, etc. etc. Undiagnosed celiac can definitely cause CFS as it robs the body of nutrients. BTW, How careful are you about gluten ? I am very sensitive and will get wiped out again if I have any contact with gluten. I'm still getting swollen lymph nodes and sore throats regularly too probably from dust mites.

So many people think that CFS is just fatigue but that isn't it at all. Chronic Fatigue is not the same as CFS. See the CDC criteria for CFS.

Open Original Shared Link

Good luck and don't settle for a diagnosis of CFS until all other avenues have been researched. The diagnosis of CFS / FM lead to my other symptoms being ignored. I was severely anemic and since the symptom is fatigue I wasn't tested. Many doctors have an attitude about the CFS / FM diagnosis too, so you won't get the respect other patients do either.

Take care ... Marcia

gfpaperdoll Rookie

you will find some answers & get better but you will also have to work on things that you can while the doctors are probing around etc. Make sure you do not have any damage from those scopes etc, you know not all doctors do those perfectly...

I whole heartedly support the posts re other allegens, you should explore an organic plain whole foods diet for a bit. go grain free, dairy free, soy free, egg free, nightshade family free (no potatoes) You can do this. You are young & you will heal quickly. If you are living at home & the house is not gluten free - there is a MAJOR PROBLEM for you. get your parents to read on here about cross contamination. The biggie in that situation is that there should never be any wheat flour in the house (or cake mixes etc) because that stuff poofs up gets in the air & you breath it in (it can get in the air conditioning ducts etc) & you will get sick. Also, you do not need to be eating out at this time, if you have to go somewhere take your food with you...

also start taking a B12 everyday. the sublingual is the kind that melts under your tongue & is supposed to the best absorbed for us...

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,929
    • Most Online (within 30 mins)
      7,748

    Mike Rowicki
    Newest Member
    Mike Rowicki
    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

    • lehum
      Hi and thank you very much for your detailed response! I am so glad that the protocol worked so well for you and helped you to get your health back on track. I've heard of it helping other people too. One question I have is how did you maintain your weight on this diet? I really rely on nuts and rice to keep me at a steady weight because I tend to lose weight quickly and am having a hard time envisioning how to make it work, especially when not being able to eat things like nuts and avocados. In case you have any input, woud be great to hear it! Friendly greetings.
    • Hmart
      I was not taking any medications previous to this. I was a healthy 49 yo with some mild stomach discomfort. I noticed the onset of tinnitus earlier this year and I had Covid at the end of June. My first ‘flare-up’ with these symptoms was in August and I was eating gluten like normal. I had another flare-up in September and then got an upper endo at the end of September that showed possible celiac. My blood test came a week later. While I didn’t stop eating gluten before I had the blood test, I had cut back on food and gluten both. I had a flare-up with this symptoms after one week of gluten free but wasn’t being crazy careful. Then I had another flare-up this week. I think it might have been caused by Trader Joe’s baked tofu which I didn’t realize had wheat. But I don’t know if these flare-ups are caused by gluten or if there’s something else going on. I am food journaling and tracking all symptoms. I have lost 7 pounds in the last 10 days. 
    • trents
      Welcome to the forum, @Hmart! There are other medical conditions besides celiac disease that can cause villous atrophy as well as some medications and for some people, the dairy protein casein. So, your question is a valid one. Especially in view of the fact that your antibody testing was negative, though there are also some seronegative celiacs. So, do you get reactions every time you consume gluten? If you were to purposely consume a slice of bread would you be certain to develop the symptoms you describe?
    • klmgarland
    • DebJ14
      I only went on the multi vitamin AFTER a couple of year of high dose, targeted supplementation resolved most of my deficiencies.  I was on quite a cocktail of vitamins that was changed every 6 months as my deficiencies resolved.  Those that were determined to be genetic are still addressed with specific doses of those vitamins, minerals and amino acids. I have an update on my husband and his A Fib.  He ended up in the hospital in August 2025 when his A Fib would not convert.  He took the maximum dose of Flecainide allowed within a 24 hour period.  It was a nightmare experience!  They took him into the ER immediately.  They put in a line, drew blood, did an EKG and chest Xray all within minutes.  Never saw another human for 6 hours.  Never got any results, but obviously we could see he was still in A fib by watching the monitor.  They have the family sign up for text alerts at the ER desk.  So glad I did.  That is the only way we found out that he was being admitted.  About an hour after that text someone came to take him to his room on an observation floor.  We were there two hours before we saw another human being and believe it or not that was by zoom on the TV in the room.  It was admissions wanting to know his vaccine status and confirming his insurance, which we provided at the ER desk.  They said someone would be in and finally a nurse arrived.  He was told a hospitalist was in charge of his case.  Finally the NP for the hospitalist showed up and my husband literally blew his stack.  He got so angry and yelled at this poor woman, but it was exactly what he needed to convert himself to sinus rhythm while she was there.  They got an EKG machine and confirmed it.  She told him that they wanted to keep him overnight and would do an echo in the morning and they were concerned about a wound on his leg and wanted to do a doppler to make sure he did not have a DVT.  He agreed.  The echo showed everything fine, just as it was at his annual check up in June and there was no DVT.  A cardiologist finally showed up to discharge him and after reviewing his history said the A Fib was due to the Amoxicillan prescribed for his leg wound.  It both triggers A Fib and prevents the Flecainide from working.  His conversion coincided with the last dose of antibiotic getting out of his system.  So, make sure your PCP understands what antibiotics you can or cannot take if susceptible to A Fib.  This cardiologist (not his regular) wanted him on Metoprolol 25 mg and Pradaxa.  My husband told him that his cardiologist axed the idea of a beta blocker because his heart rate is already low.  Sure enough, it dropped to 42 on the Metoprolol and my husband felt horrible.  The pradaxa gave him a full body rash!  He went back to his cardiologist for follow up and his BP was fine and heart rate in the mid 50's.  He also axed the Pradaxa since my husband has low platelets, bruises easily and gets bloody noses just from Fish Oil  He suggested he take Black Cumin Seed Oil for inflammation.  He discovered that by taking the Black Seed oil, he can eat carbs and not go into A Fib, since it does such a good job of reducing inflammation.   Oh and I forgot to say the hospital bill was over $26,000.  Houston Methodist!  
×
×
  • 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.