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

Becoming A Chemist And Frustrated!


DinaB

Recommended Posts

DinaB Apprentice

Hello all,

I don't post here often, but I am here regularly as I think most of you know more than some doctors. I believe in what I read here and take this site very seriously.

My one major complaint is that since I started having allergies and symptoms to allergies, I've done so much research I feel like I can be a chemist, or a nutritional expert of some kind. The most frustrating part is that once I feel I have it all worked out and KNOW what I can and cannot have, some little thing will creep into my world and cause all sorts of reactions - - leading me to become a detective again.

The FDA doesn't make it any easier either. If everything could just be labeled simply, we would not have to spend numerous hours researching and contacting manufacturers to dissect every ingredient where it originates from.

I was operated on last Tuesday. I spent two miserable days in the hospital itching, rashes and completely out of my mind. Turns out I was having a reaction to the anitbiotics as well as the pain killers. Every time I had to try a new pain killer, there was me or my husband looking it up online to make sure it was gluten/lactose/soy/egg free. I couldn't even have regular anesthesia because it contains egg and soy. I had to use an older anesthesia which takes a longer time to get out of your system and has lots of unpleasant side effects.

My husband had to bring a cooler of food as well as sheets and blankets for the hospital bed, as I also have a horrible fragrance allergy. Every time someone came in my room to take vitals they were swimming in perfume. Finally a note was posted on my door and the only people allowed in were my husband, doctor, and nurse -- all had to be perfume/cologne free.

Sorry for ranting and raving, but I am finding it thoroughly exhausting trying to keep my environment "free" of irritants. Every I turn around I find more and more things that cause a reaction to me. Do any of you find that the more you food and items you eliminate the more you become overly sensitive to things or is it just me?

What also worries me, as well as my family is what happens if I ever need to be hospitalized and NEED pain killers. I went through three and my doc gave up. I was in severe pain for three-four days cold turkey after major surgery...is this normal?

Truly frustrated and tired of playing a detective.


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



Celiac.com Sponsor (A8-M):



lovegrov Collaborator

I truly feel for you and your problems, but you also have to realize that only a very tiny miniscule itsy-bitsy percentage of people are faced with what you're faced with. For instance, I can't eat gluten but have no allergies to anything else. Labeling every single ingredient as to exactly what goes into it and where it all comes from (both of which can change constantly) would cost manufacturers a good deal and raise the price of everything significantly. Some products would have to increase the size of the package simply to accommodate the label (or else you'd have to carry a magnifying glass). It's just not practical.

richard

ravenwoodglass Mentor

I just got off of a long phone call with a drug company making sure a script I was given was gluten free. I agree with you that the makers of food and drugs really need to label with more accuracy and hopefully someday that will be a reality. We need to know what is in our food and in our drugs and IMHO there is no reason why that should not be done. Makers need to know what is in the ingredients that are used in a product and those ingredients need to be disclosed. If they can use allergy labeling for eggs, soy, dairy, wheat etc. there is no reason that other gluten ingredients can not be disclosed. This is particularly important with drugs as IMHO far to many times the ingredients that cause side or adverse effects with drugs are not the drugs themselves but the binders and allergans that are used in them. I am sorry you went through this and I would suggest that you continue to research and try to get a list of painkillers and antibiotics that you will be able to tolerate and give them to your doctor and also carry it in your purse in case of emergency. In additon the FDA has an area on it's website to notify them of adverse reactions to drugs that people are given. You should go to that website and notify them of the reactions you had and the reason you had them. If everyone who was made ill by a binder or vehicle that was in a drug did that it might help them develop alternatives that less people would have those reactions to. I realize that different people react to different substances but even if they just got gluten out of our meds it would make a big difference.

ang1e0251 Contributor

I wonder if a local compounding pharmacy could make you medicines you could tolerate. If you could work with your doctor while you are well to find a pain killer or two you could tolerate that was specially formulated just for you, it would go far helping you in an emergency.

mamaw Community Regular

Hi Dina

I feel your pain!I can not have any narcotics as my throat sweels shut in minutes... gluten-free or not.

I have had two major surgereries plus one about 40 minutes long.... no narcotics. I can tolerate versaid ( not a narcotic) & that is it. I feel everything & know & feel every cut the doctor makes, the drilling & so on. I just pray & pray . I always tell the doctors to work fast & make no mistakes. I take no pain medicine after except for tylenol with codiene, which puts me to sleep. Other than that it is like drinking water. My recent last procedure the doc asks if I drink, I said no & he suggested I start!!!! Whiskey may have to become my best friend...........

I'm also one that can not tolerate hospital bed sheets, hives instantly. I never thought of taking my own I figure they would tell me they are not santized & wouldn't permit it. I will try if ever I need in a hospital again. Hoping not!

Our hospital has next to nothing for gluten-free & they don't care.. so we too carry a gluten-free food supply & water as I don't drink city water....they have allowed my husband to heat my gluten-free food in a micro....

I react to planet earth so I'm with you , no smoke, no perfume, no pumping gasoline. My husband calls me a sniffer dog as I can detect things way before anyone else...

I'm told there are a few of us super sensitive beings in the world!

blessings

mamaw

DinaB Apprentice

Thanks everyone for posting and the ideas. I guess I've been in total denial about being "super sensitive" as it's another label I didn't want to give myself.

Something to make you laugh...I've been home from the hospital since last Thursday. I have to say the first days being home and not being on pain meds were the worst. However, feeling better and able to bend (stitches across abdomen) I decided to shave. Well, the maker of the razors decided to change it's "moisture strip" and add a vitamin oil to it. We order these razors in bulk as my husband shaves his head, and the cost is much cheaper to us. We never noticed the new packaging. Two days ago I developed a rash under my arms and down my legs. Going out of my mind. I realized yesterday when I went to open the new razors and they were marked "new" all over the place. Once I showered and reshaved I was fine.

The point is I know that companies are able to change their packaging at any time, BUT, if I didn't find out here on this site that Vitamin E is derived from wheat, I'd be beating my head against a wall still trying to figure out what is causing my symptoms.

All I am asking for is clear labeling. Is something is derived from wheat, then just say it!

ravenwoodglass Mentor
Thanks everyone for posting and the ideas. I guess I've been in total denial about being "super sensitive" as it's another label I didn't want to give myself.

Something to make you laugh...I've been home from the hospital since last Thursday. I have to say the first days being home and not being on pain meds were the worst. However, feeling better and able to bend (stitches across abdomen) I decided to shave. Well, the maker of the razors decided to change it's "moisture strip" and add a vitamin oil to it. We order these razors in bulk as my husband shaves his head, and the cost is much cheaper to us. We never noticed the new packaging. Two days ago I developed a rash under my arms and down my legs. Going out of my mind. I realized yesterday when I went to open the new razors and they were marked "new" all over the place. Once I showered and reshaved I was fine.

The point is I know that companies are able to change their packaging at any time, BUT, if I didn't find out here on this site that Vitamin E is derived from wheat, I'd be beating my head against a wall still trying to figure out what is causing my symptoms.

All I am asking for is clear labeling. Is something is derived from wheat, then just say it!

just a short note on the shaving products. I have had good luck by shaving immediately after I shower while the hairs are still soft and I don't have to use any shave cream at all.


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



Celiac.com Sponsor (A8-M):



mysecretcurse Contributor

I can relate a lot, especially to:

My one major complaint is that since I started having allergies and symptoms to allergies, I've done so much research I feel like I can be a chemist, or a nutritional expert of some kind. The most frustrating part is that once I feel I have it all worked out and KNOW what I can and cannot have, some little thing will creep into my world and cause all sorts of reactions - - leading me to become a detective again.

I'm going through this atm and have gone through it many times. It sucks so bad. For me, I always start thinking I am developing some other food intolerances and then nope, later on I usually find out there was gluten in something. Usually something that shouldn't have gluten in it at all. So annoying.

I really feel for you on the fragrance thing. :( You couldn't be around me, I love perfume. That must be really hard.

DinaB Apprentice
I can relate a lot, especially to:

I'm going through this atm and have gone through it many times. It sucks so bad. For me, I always start thinking I am developing some other food intolerances and then nope, later on I usually find out there was gluten in something. Usually something that shouldn't have gluten in it at all. So annoying.

I really feel for you on the fragrance thing. :( You couldn't be around me, I love perfume. That must be really hard.

The fragrance thing came out of no where. I LOVE perfume! I love my hair to smell pretty, I love my clothes to be soft and smell nice. Everything we use smells like nothing. It is so sad and I hope it doesn't last long. I guess we all have our issues to deal with, but the one thing I appreciate is being able to log on here and see that I AM normal and there are plenty of people out there with my same issues.

Be well.

  • 2 weeks later...
RollingAlong Explorer

Shortly after I went gluten-free, the allergist told me I was allergic to formaldehyde and phenols (ie fragrances.)

For what it is worth - In the last 6 months I started having more and more problems with fragrances, that is, the allergies seemed to be getting worse.

In the last month, I have become much less sensitive. I've only made 2 changes - more vitamin D (I had tested as a bit low) and taking probiotics.

hope this helps.

DinaB Apprentice
Shortly after I went gluten-free, the allergist told me I was allergic to formaldehyde and phenols (ie fragrances.)

For what it is worth - In the last 6 months I started having more and more problems with fragrances, that is, the allergies seemed to be getting worse.

In the last month, I have become much less sensitive. I've only made 2 changes - more vitamin D (I had tested as a bit low) and taking probiotics.

hope this helps.

That is interesting about the Vitamin D. I will have to try that. However, I am allergic to yogurt and all probiotics. I tested against all of those chemicals and nothing came up. All of it is mostly inhaled.

RollingAlong Explorer

It would be interesting to know if the vitamin D plays a role for you. I hope you will post back to this thread. Good luck!

DinaB Apprentice
It would be interesting to know if the vitamin D plays a role for you. I hope you will post back to this thread. Good luck!

I'm curious as to what kind you take. Since I have other allergies, it has to be free of Milk, Gluten, Egg, Soy, etc. I haven't had much luck finding vitamins at all. Lots of hidden ingredients.

RollingAlong Explorer

I have not checked these products for anything except gluten. I have used various combinations of these three:

Biotech Vitamin D3-50 (50,000 IU - 100 Caps)

Carlson Solar D Gems Vitamin D3 4,000 IU Soft Gels

Carlson Vitamin D Drops -- 2000 IU - 11 mL

I have read that some peope absorb the oil based forms of vitamin D better. I read this on the Heartscan blog. I've also read that you can take vitamin D only once a week and that's ok. So the 50k capsules aren't as crazy as they look at first. I read that at the Vitamin D Council website.

Good luck finding a product that works for you, vitamin-d wise, and I hope this helps with the fragrance sensitivities.

ghostcat Newbie

I wanted to respond to the pain killer part. When I was 17 I had major oral surgury (both my jaws were cut in half and it was approx 6 hour surgery? not sure it was a long time ago,) but I've always just vomited my brains out on pain killers. When I woke up in the hospitol they had a tube down my nose to my tummy to stop me from vomiting and had some pain killers in my IV, but again limited, to stop me from vomiting because my jaws were wired shut. When I went home, I had NO pain killers, jaws wired together. I actually do not remember the pain so much, overall I was pretty miserable....but I lived through it. That's just my experience anyway, you're not alone.

I do think Dr.'s overmedicate A LOT and I think the body has many natural ways of coping and healing. I know it's not a miracle cure or as good as the real thing (REAL DRUGS!), but I do put a lot of stock in things like meditation, natural alternatives and a positive mental attitude in dealing with pain. I think we're brain washed as patients to expect things from our own bodies and tune out what we're really feeling. In the last few years I had needed a root canal and of course, couldn't take pain killers and vomited my way through a few different antibiotics. They had to stop mid-way through drilling so I could puke! When they got me on an antibiotic that didn't make me sick (something they normally prescribe to cats? who knows....it seemed really old and obsolete? lol!) and they managed to drill into my tooth and relieve the pressure, I was fine and didn't even need a pain killer if I could have taken one. The local anastesia wore off and I was stuffing my face that night, but to hear it from the dentist......I should have been a lot of pain.

Hello all,

I don't post here often, but I am here regularly as I think most of you know more than some doctors. I believe in what I read here and take this site very seriously.

My one major complaint is that since I started having allergies and symptoms to allergies, I've done so much research I feel like I can be a chemist, or a nutritional expert of some kind. The most frustrating part is that once I feel I have it all worked out and KNOW what I can and cannot have, some little thing will creep into my world and cause all sorts of reactions - - leading me to become a detective again.

The FDA doesn't make it any easier either. If everything could just be labeled simply, we would not have to spend numerous hours researching and contacting manufacturers to dissect every ingredient where it originates from.

I was operated on last Tuesday. I spent two miserable days in the hospital itching, rashes and completely out of my mind. Turns out I was having a reaction to the anitbiotics as well as the pain killers. Every time I had to try a new pain killer, there was me or my husband looking it up online to make sure it was gluten/lactose/soy/egg free. I couldn't even have regular anesthesia because it contains egg and soy. I had to use an older anesthesia which takes a longer time to get out of your system and has lots of unpleasant side effects.

My husband had to bring a cooler of food as well as sheets and blankets for the hospital bed, as I also have a horrible fragrance allergy. Every time someone came in my room to take vitals they were swimming in perfume. Finally a note was posted on my door and the only people allowed in were my husband, doctor, and nurse -- all had to be perfume/cologne free.

Sorry for ranting and raving, but I am finding it thoroughly exhausting trying to keep my environment "free" of irritants. Every I turn around I find more and more things that cause a reaction to me. Do any of you find that the more you food and items you eliminate the more you become overly sensitive to things or is it just me?

What also worries me, as well as my family is what happens if I ever need to be hospitalized and NEED pain killers. I went through three and my doc gave up. I was in severe pain for three-four days cold turkey after major surgery...is this normal?

Truly frustrated and tired of playing a detective.

lisa25 Rookie
I'm curious as to what kind you take. Since I have other allergies, it has to be free of Milk, Gluten, Egg, Soy, etc. I haven't had much luck finding vitamins at all. Lots of hidden ingredients.

I have been researching vitamins and found that Solgar's Vitamin D3 is free of yeast, soy, gluten, and dairy. It doesn't say free from egg, but doesn't look like it is in the ingredients unless it is disguised as something else. If you go to their website they have images of all their product's labels that lists what it is free of. I haven't tried these yet, but plan to.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,957
    • Most Online (within 30 mins)
      7,748

    Dogdad21
    Newest Member
    Dogdad21
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.