Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×

  • 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 Celiac.com!
    eNewsletter
    Donate

Can't Get Over The Flu

Sarah B

By Sarah B
in Coping with Celiac Disease

Recommended Posts

Sarah B Apprentice
Sarah B
Posted

I have been gluten free for about a year now.

I am a teacher which means I am around little kids and all their germs. Usually when I get sick and can get over it without having to get medicine for it. It runs its couse of two weeks and it is gone. But this year I had a terrible cough and tiredness for about 3 and a half weeks before I finally went to the doctor. She gave me antibodics for the flu and slowly but surely 4 and a half weeks later, I think I'm almost over it.

I also have a staff infection that I've been trying to get rid of for about 5 months now and it hasn't gone away completly yet.

Has anybody else found that after they have gone gluten free they are having a hard time getting over sicknesses?

Link to comment
Share on other sites
Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):

Celiac.com Sponsor (A8-M):


pricklypear1971 Community Regular
pricklypear1971
Posted

Nope.

Have you had your thyroid checked and been checked for Hashimoto's?

I was sick all the time before I started thyroid meds. Now, it's quite rare (except for those mysterious gluten things).

Link to comment
Share on other sites
sariesue Explorer
sariesue
Posted

Have you been tested for MRSA? It's no longer just in hospitals it's everywhere. And it does not heal on it's own and is resistant to many antibiotics. If it is MRSA you may need IV antibiotics or an extensive course of oral antibiotics. If left untreated MRSA is very dangerous not to mention very contagious.

Link to comment
Share on other sites
lovegrov Collaborator
lovegrov
Posted

The true flu does not respond to antibiotics. It's a virus, not a bacteria.

richard

Link to comment
Share on other sites
Skylark Collaborator
Skylark
Posted

The true flu does not respond to antibiotics. It's a virus, not a bacteria.

How is your comment supposed to be helpful? She clearly got secondary bacterial bronchitis. Doctors don't give antibiotics for flu.

Sarah, I have trouble getting well when I'm hypothyroid. The staph infection may be metihcillin resistant (MRSA). Has your doctor cultured it to find out what antibiotic might work to kill it?

Link to comment
Share on other sites
Sarah B Apprentice
Sarah B
  • Author
Posted

How is your comment supposed to be helpful? She clearly got secondary bacterial bronchitis. Doctors don't give antibiotics for flu.

Sarah, I have trouble getting well when I'm hypothyroid. The staph infection may be metihcillin resistant (MRSA). Has your doctor cultured it to find out what antibiotic might work to kill it?

I feel like the amoxicillin is working... and I read online that yeah, many doctors percribe it for secondary bacterial bronchitis. I went to a urgent care center because I was worried I had strep. the docter there was very impersonal and I probably should have asked a lot of questions because she didn't tell me anything.

I finally got another appoint with my dermatologist this thursday so I'll see what she says. I just wanted to make sure none of this had anything to do with nutrients not being obsorbed.

Link to comment
Share on other sites
Celtic Queen Explorer
Celtic Queen
Posted

Have you taken amoxicillin several times before? I ask because my body has built up an immunity to it. I had taken it many times for sinus infections and the last time I went through 2 rounds of it without any effect. I had to be switched to another drug.

I saw a documentary on the problems with people becoming resistant to antibiotics and it said that amoxocillin, as well as zithromycin, were two of the most common ones people are building resistances to becuase they're prescribed so often.

Link to comment
Share on other sites
Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):

Celiac.com Sponsor (A8-M):


Sarah B Apprentice
Sarah B
  • Author
Posted

No, I don't usually take medicine

Link to comment
Share on other sites
lovegrov Collaborator
lovegrov
Posted

How is your comment supposed to be helpful? She clearly got secondary bacterial bronchitis. Doctors don't give antibiotics for flu.

Sarah, I have trouble getting well when I'm hypothyroid. The staph infection may be metihcillin resistant (MRSA). Has your doctor cultured it to find out what antibiotic might work to kill it?

Skylark, I was responding to this line from her post: "She gave me antibodics for the flu." I was simply trying to point out to anybody who didn't know that you DON'T take antibiotics for the flu.

Now please explain how your comment to me was supposed to be helpful.

richard

Link to comment
Share on other sites
Sarah B Apprentice
Sarah B
  • Author
Posted

Skylark, I was responding to this line from her post: "She gave me antibodics for the flu." I was simply trying to point out to anybody who didn't know that you DON'T take antibiotics for the flu.

Now please explain how your comment to me was supposed to be helpful.

richard

All your comments were very helpful. Thank you.

Link to comment
Share on other sites
frieze Community Regular
frieze
Posted

Have you taken amoxicillin several times before? I ask because my body has built up an immunity to it. I had taken it many times for sinus infections and the last time I went through 2 rounds of it without any effect. I had to be switched to another drug.

I saw a documentary on the problems with people becoming resistant to antibiotics and it said that amoxocillin, as well as zithromycin, were two of the most common ones people are building resistances to becuase they're prescribed so often.

not splitting hairs....but I doubt your body became "immune" to the ABT, but that the bacteria causing the infection did. Also, a fair number of sinus infections are fungal, or at least they are co infections.

Link to comment
Share on other sites
Celtic Queen Explorer
Celtic Queen
Posted

Sorry. I'm not in the medical field, so I probably did explain it wrong. My bacteria are immume to amoxicillin :D Unfortunately this was a while ago when I had a doctor who would prescribe antibiotics for almost anything and I didn't know better. Now I'm much more conservative about taking them. But the damage has already been done.

Link to comment
Share on other sites

Archived

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

Go to topic listing
  • Celiac.com Sponsor (A19):


  • Member Statistics

    • Total Members
      121,224
    • Most Online (within 30 mins)
      7,748
    Suzi374
    Newest Member
    Suzi374
    Joined
  • Celiac.com Sponsor (A20):

  • Forum Statistics

    • Total Topics
      120.3k
    • Total Posts
      1m
  • Celiac.com Sponsor (A22):



  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • Suzi374
      Lots of tests

      By Suzi374 · Posted

      And I’m anaemic, however I’m also female and vegetarian. I had an iron trans a couple of years ago however it’s starting to dwindle and taking supplements doesn’t seem to work. I can’t seem to absorb it. 
    • Suzi374
      Lots of tests

      By Suzi374 · Posted

      Hi, I attended a neurologist appt last Tuesday, which I nearly cancelled, due to ongoing numbness and tingling in toes to mid foot. One of the first things he asked was ‘are you celiac’. I’m not. He thought all reflexes were ok but at the last minute decided on nerve conduction tests which were low normal. He was a little confused as he felt they should be better and tried a new set of probs, all the time, giving me multiple shocks which were not enjoyable lol. Anyway, he’s now ordered tests for myeloma, and all the vitaminy things that so many of you mention on here, also tests looking for autoimmune responses. I already have Hashimotos. Interestingly, to me, but maybe someone out there can relate or knows more than i do, although I was a nurse, but ED not ‘weird symptoms’  nurse. Anyway back to the interesting thing, I took duramine in 2013 to lose weight which caused a massive panic attack when I stopped taking it and half my hair fell out. I only took it for a week but it was horrible and I regret it. It triggered ongoing panic attacks which are horrendous. So I feel like I’m a bit crazy. Then in 2020 I had this sudden onset of horrible pain when trying to eat a cinnamon roll. It continued and I lost around 20 kgs. I had two gastroscopes and a colonoscopy and they were all normal. I scored a barium swallow and CT angiogram. All normal. The pain subsided a little but I was left with reflux and an awful feeling that I couldn’t get air when I ate some foods. This was not anxiety.  The anxiety was separate and I still maintain this. This was something to do with eating. It was like the air was thick but I wasn’t short of breath. I just had the sensation I was, then it triggered anxiety. Anyway, I had other weird things- couldn’t bend knees to shave legs in shower lol. Knees felt stiff and swollen but they weren’t. Knee WOUld swell up randomly but mri showed minimal issues. A bit of a meniscus degeneration but insignificant. Then the buzzing sensations in my head, the feeling like someone was stabbing me with something sharp. So now, I pre empted his tests, although I don’t think I’m celiac because it should have come up on gastroscopy, I’ve gone off gluten. Since Tuesday last week so 9 days. Since then I don’t appear to be as constipated, I realised I got through today without a nap and I’m not tired, maybe it’s just today and not related but I get very tired normally and sleep straight after work often, I can bend my knees and shave my legs lol, the buzzing vibrating has gone from my head, I had to call and ambulance as my heart decided we were off on a run, but we weren’t running and I’ve been a bit twitchy at bed time when trying to sleep, reflux is improving, I did get the weird suffocating feeling a bit when eating today but not as bad normall. Tingling and numbness still present and I felt like it moved up my legs a bit today but I’m a bit jittery. So I don’t know if it’s celiac disease or a gluten intolerance but I think, and it may be wishful thinking because my symptoms do make life a bit challenging, but maybe I’m feeling better. I don’t feel as cloudy. My thinking feels crisper. Like there’s no buzzing and I’m not fighting to break through the cloudiness now. I hope so much that this may help me feel a bit better moving forward. It would be a miracle as I really have struggled to work and parent and keep the house clean and I’m always anxious and exhausted.  If you get this far, please tell me if you you can relate to any of the above. Oh and tonsils out 5 years ago but before that antibiotics multiple times a year, sometimes intramuscular because they were so bad.  Op was meant to take 30 mins, it took 1.5 hours due to size of them. 
    • Peace lily
      Would like to gain weight

      By Peace lily · Posted

      Im still not gaining weight I’m on a gluten free diet . And still having issues with constapation started priobiocs figured it would help been over two weeks . I guess it’s going to be a long road for me .
    • Smith-Ronald
      Lymph nodes

      By Smith-Ronald · Posted

      Enlarged lymph nodes in neck and groin with celiac are not uncommon. They can take time to reduce even after going gluten-free. Monitoring is key.
    • Random.user556
      I think I might be celiac?

      By Random.user556 · Posted

      Hello! I’m sorry in advance for the long post!   Over the past few months I’ve been having a lot of issues with my stomach and have recently been referred to a Gastroenterologist. I’ve had stomach pain and issues since I was a baby. I had bad constipation (still do) and couldn’t tolerate most formula as a baby. When I was around 8 I started experiencing a lot of lower abdominal cramping (just below the belly button) and ended up missing a fair amount of school because of this. It would start about 2 hours after eating breakfast and I’d have lower abdominal cramps and feel nauseous . After a visit to my family doctor it was brushed off as separation anxiety.. or as the doctor put it “I was just a kid who wanted to stay home from school”. This stomach pain persisted all through my elementary and high school years. In fact I still experience it to this day and I’m now 24. Along with this my doctor believes I have a form of disautonomia called POTS (Postural Orthostatic Tachycardia Syndrome). I frequently feel unwell and exhausted. I also experience Raynaud’s phenomena especially during the winter months or when I’m sick. I also can not tolerate heat for the life of me.. although I’m not entirely convinced my symptoms are from POTS. The last few years I’ve also started experiencing frequent chronic sinus infections up to 5 a year most of which I require antibiotics for… Up until two years ago I have never had allergies or sinus problems. Back to my stomach issues… The last year I have been experiencing lots of stomach bloating and discomfort especially at night.. this has led to a few nights of 3am vomiting.. my doctor tested me for H. Pylori which was negative as well as full work ups to test my kidneys, liver, pancreas, gallbladder.. all of which were normal. At this time he also started me on Rabeprazole 20mg twice daily which is a Proton pump inhibitor (PPI) … as he believes it could be GERD. The PPI has not helped at all and I have since been moved down to once daily which I wait for a referral to a Gastroenterologist for an endoscopy as well as an abdominal ultrasound to verify I have no gallstones.. The pain I feel in my abdomen feels very heavy right around my bellybutton and frequently is accompanied by nausea and occasionally I also experience sharp stabbing like pain left of my belly button. I began tracking my symptoms, what I’m eating and bowel habits on an app called “My IBS” which track’s symptoms and flags foods that could be potential triggers.. all of my flagged potential triggers seem to be gluten related foods like pasta and breads. I asked to be tested for Celiac as I have an uncle with it. My doctor only sent for TtG IGA.. no other tests. My results came back negative at “<0.5 U/ml” the reference range being “ <12 U/Ml”. I am aware that total IGA should of been ordered as well but my doctor is confident we have ruled out celiac so I guess I will have to wait for the Gastroenterologist for more testing.. The other red flag for me is I have a rash that shows on both my knees and recently I have developed a similar rash behind both of my ears, on my neck and into my scalp.. there is dozens of small red and skin coloured lesions that sort of? resemble pimples but have a “head” and don’t pop (yes, i know don’t pop your pimples!) they are also itchy and sore.. I have tried washing and scrubbing them with antibacterial soap and body wash to no avail as well as ensuring I rinse my neck thoroughly after a shower, keeping my neck dry, frequently changing pillowcases and even keeping my hair off my neck as much as possible … it doesn’t have any effect on it.  In your experience does this sound like I could be experiencing celiac? I’ve debated going gluten free to see if my symptoms persist or begin to clear up.. any suggestions or help is appreciated! 
×
×
  • Create New...