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

Mosquito Magnetism


queenofhearts

Recommended Posts

queenofhearts Explorer

I'm wondering if there is a connection here, or if I'm dreaming...

All my life I've been a mosquito magnet, always more bites than anyone else in a group, piling on the repellent & still getting bitten.

I was noticing the other evening in the garden, I had not applied repellent, but the skeeters were flying around me but NOT BITING!!! I can NEVER remember seeing this happen before. I did get a couple of bites, but normally I'd have been covered with them.

Could it be that something in my metabolism has changed since going gluten free that no longer attracts the little devils? Has anyone else had this experience?

Will wonders never cease?!!?

Leah


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



Celiac.com Sponsor (A8-M):



BRUMI1968 Collaborator

I have had the same experience, though from quitting wheat two years ago. I still get bit now and again, but for the most part, no. It used to be I got bit ALL THE TIME, and my husband never did. It's tough to get him t shut screen doors.

but anyway, if you're dreaming, I'm having the same dream.

tarnalberry Community Regular

I'm still a bug magnet. I've got six bites on me from the 21 miles of hiking I've done the past four days. :-) (Which is incredibly low for me - I used bug stuff (oil of lemon eucalyptus) the first two days, but mostly I think the bugs in my new state don't know me yet.)

Matilda Enthusiast

..

ArtGirl Enthusiast

Ohhh... I sure hope I follow this pattern. I've always wondered why I get bit all over when others hardly at all. I've even considered moving to a condo so as not to have to work in the yard I get so tired of having bites all over me all summer long. :angry:

As I type this message I have 11 bug bites, a couple of them are doozies. This is from a couple days working in the yard - with repellant and having first sprayed the area with bug spray. I can't step outside for even a minute without at least one misquito bite. And every year I get at least two bites from some bug I've never been able to identify that raises a good sized blister that lasts for a couple weeks and then takes a couple more weeks to heal up, leaving a red patch on my skin for the rest of the season.

Looking forward to next year to see if the bugs leave me alone!

TCA Contributor

I haven't thought about it, but I"m the same way too. Never thought about it. I'm O+.

ArtGirl - could those bites be fire ants? That's the way they do me.

tarnalberry Community Regular

I'm O+ too, but so's my husband, who doesn't get bitten much at all.


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



Celiac.com Sponsor (A8-M):



ArtGirl Enthusiast
IArtGirl - could those bites be fire ants? That's the way they do me.

Do fire ants live in the midwest? We have a lot of ants - several sizes and colors.

I never know when I've been bit by this bug. It's usually the next day that an area the size of a quarter becomes hot and begins to swell. Then, the next day the area is red and the blister begins to form, swelling to about the size of a very large pea over several hours. So, you see, since the reaction is delayed it's very hard to tell what bit me. I've never seen an insect crawling on me. Usually the bite is on my legs and the back of my knees.

BRUMI1968 Collaborator
I'm O+ too, but so's my husband, who doesn't get bitten much at all.

My hubby is O and he NEVER gets bit. I'm A+ and I would always get bit (until last year!)

Green12 Enthusiast
My hubby is O and he NEVER gets bit. I'm A+ and I would always get bit (until last year!)

I'm also an A+ and I would always attract the bugs and get bitten. I just realized reading this post that this doesn't seem to be the case anymore, I haven't gotten bitten once this summer and I don't think I did last summer either. Hmmm, mystery?

I had read about this somewhere some time ago, the reason why some people attract the mosquitos while others don't and I can't remember what it was. I think it had to do with something in the blood, but not necessarily blood type...

BRUMI1968 Collaborator

I recall that sugar-eaters had more bites...but there was something else too......

corinne Apprentice

I'm A-. I'm really lucky and never get bitten by mosquitoes, but black flies (horrible nasty evil insects) love me. I got about 200 bites on my feet once when I was hiking in BC in Tevas. and had to call in sick the next day for work because my feet swelled so much I couldn't get my shoes on.

queenofhearts Explorer
Ohhh... I sure hope I follow this pattern. I've always wondered why I get bit all over when others hardly at all. I've even considered moving to a condo so as not to have to work in the yard I get so tired of having bites all over me all summer long. :angry:

As I type this message I have 11 bug bites, a couple of them are doozies. This is from a couple days working in the yard - with repellant and having first sprayed the area with bug spray. I can't step outside for even a minute without at least one misquito bite. And every year I get at least two bites from some bug I've never been able to identify that raises a good sized blister that lasts for a couple weeks and then takes a couple more weeks to heal up, leaving a red patch on my skin for the rest of the season.

Looking forward to next year to see if the bugs leave me alone!

My father in law talks of being bitten (or stung, actually) by blister beetles. Sounds similar to your reaction. Did they hurt? (His did.)

I'll be overjoyed if my mosquito luck holds out. I love gardening, & end up doing it in the hottest part of the day to avoid being devoured. (I'd rather be drenched in sweat than covered with bites.) It would be so wonderful if I can really enjoy outdoor evenings!

Leah

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,901
    • Most Online (within 30 mins)
      7,748

    tessycork47
    Newest Member
    tessycork47
    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
      Welcome to the forum, @Judy M! Yes, he definitely needs to continue eating gluten until the day of the endoscopy. Not sure why the GI doc advised otherwise but it was a bum steer.  Celiac disease has a genetic component but also an "epigenetic" component. Let me explain. There are two main genes that have been identified as providing the "potential" to develop "active" celiac disease. We know them as HLA-DQ 2.5 (aka, HLA-DQ 2) and HLA-DQ8. Without one or both of these genes it is highly unlikely that a person will develop celiac disease at some point in their life. About 40% of the general population carry one or both of these two genes but only about 1% of the population develops active celiac disease. Thus, possessing the genetic potential for celiac disease is far less than deterministic. Most who have the potential never develop the disease. In order for the potential to develop celiac disease to turn into active celiac disease, some triggering stress event or events must "turn on" the latent genes. This triggering stress event can be a viral infection, some other medical event, or even prolonged psychological/emotional trauma. This part of the equation is difficult to quantify but this is the epigenetic dimension of the disease. Epigenetics has to do with the influence that environmental factors and things not coded into the DNA itself have to do in "turning on" susceptible genes. And this is why celiac disease can develop at any stage of life. Celiac disease is an autoimmune condition (not a food allergy) that causes inflammation in the lining of the small bowel. The ingestion of gluten causes the body to attack the cells of this lining which, over time, damages and destroys them, impairing the body's ability to absorb nutrients since this is the part of the intestinal track responsible for nutrient absorption and also causing numerous other food sensitivities such as dairy/lactose intolerance. There is another gluten-related disorder known as NCGS (Non Celiac Gluten Sensitivity or just, "gluten sensitivity") that is not autoimmune in nature and which does not damage the small bowel lining. However, NCGS shares many of the same symptoms with celiac disease such as gas, bloating, and diarrhea. It is also much more common than celiac disease. There is no test for NCGS so, because they share common symptoms, celiac disease must first be ruled out through formal testing for celiac disease. This is where your husband is right now. It should also be said that some experts believe NCGS can transition into celiac disease. I hope this helps.
    • Judy M
      My husband has had lactose intolerance for his entire life (he's 68 yo).  So, he's used to gastro issues. But for the past year he's been experiencing bouts of diarrhea that last for hours.  He finally went to his gastroenterologist ... several blood tests ruled out other maladies, but his celiac results are suspect.  He is scheduled for an endoscopy and colonoscopy in 2 weeks.  He was told to eat "gluten free" until the tests!!!  I, and he know nothing about this "diet" much less how to navigate his in daily life!! The more I read, the more my head is spinning.  So I guess I have 2 questions.  First, I read on this website that prior to testing, eat gluten so as not to compromise the testing!  Is that true? His primary care doctor told him to eat gluten free prior to testing!  I'm so confused.  Second, I read that celiac disease is genetic or caused by other ways such as surgery.  No family history but Gall bladder removal 7 years ago, maybe?  But how in God's name does something like this crop up and now is so awful he can't go a day without worrying.  He still works in Manhattan and considers himself lucky if he gets there without incident!  Advice from those who know would be appreciated!!!!!!!!!!!!
    • Scott Adams
      You've done an excellent job of meticulously tracking the rash's unpredictable behavior, from its symmetrical spread and stubborn scabbing to the potential triggers you've identified, like the asthma medication and dietary changes. It's particularly telling that the rash seems to flare with wheat consumption, even though your initial blood test was negative—as you've noted, being off wheat before a test can sometimes lead to a false negative, and your description of the other symptoms—joint pain, brain fog, stomach issues—is very compelling. The symmetry of the rash is a crucial detail that often points toward an internal cause, such as an autoimmune response or a systemic reaction, rather than just an external irritant like a plant or mites. I hope your doctor tomorrow takes the time to listen carefully to all of this evidence you've gathered and works with you to find some real answers and effective relief. Don't be discouraged if the rash fluctuates; your detailed history is the most valuable tool you have for getting an accurate diagnosis.
    • Scott Adams
      In this case the beer is excellent, but for those who are super sensitive it is likely better to go the full gluten-free beer route. Lakefront Brewery (another sponsor!) has good gluten-free beer made without any gluten ingredients.
    • trents
      Welcome to the forum, @catsrlife! Celiac disease can be diagnosed without committing to a full-blown "gluten challenge" if you get a skin biopsy done during an active outbreak of dermatitis herpetiformis, assuming that is what is causing the rash. There is no other known cause for dermatitis herpetiformis so it is definitive for celiac disease. You would need to find a dermatologist who is familiar with doing the biopsy correctly, however. The samples need to be taken next to the pustules, not on them . . . a mistake many dermatologists make when biopsying for dermatitis herpetiformis. 
×
×
  • 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.