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

B12, Pernicious Anemia, Celiac Disease, Iron Levels


Oma81307

Recommended Posts

Oma81307 Newbie

Hi! I've been celiac diagnosed for almost 2 years. I started the b12 injections shortly after being diagnosed and I am suppose to be down to once a month. (i'll get to that in a second). However last time my Iron/b12 was checked my b12 was 464 which is 64 over where dr wants it minimum. Iron however was a 12. They want that a 50. I took a round of repliva for 6 weeks. Iron still tested 12. They gave me another round of Repliva and scheduled a shot. Then all of a sudden it was like my energy went from decent. TO NOTHING. I couldn't get up. I wanted to sleep. I did work harder previous to this. Did I just over work myself to where the anemia symptoms kicked in or what? This was on a sat/sun that I became so drained I came home early from work. Slept 4 hours. When I woke up still not much energy. I knew that Monday I had a iron shot scheduled. On Tuesday after having the shot I cried. I really thought this would do like the b12 and give me energy at least for a time. It did not. All it did was make me want to sit up instead of lay down. I finally realized it was a few days till my monthly b12 shot so I checked with my best friend who is a RN and she agreed to go ahead and take it. All of a sudden ZOOM! I was up and gone. We decided maybe until I got the iron up I should take my b12 a little more often. Odd part is the b12 has helped me feel energy but I still feel weird. I have nausea, headaches, I feel like the top half my body wants to go go go and the other half wants to lay down. I have chills up my spine, I'm really cold, then pouring a sweat. I did find out there was some foods I was eating that contained glueten. Now I know why the iron isn't going anywhere. So rearranged my diet again. I just guess i'm curious why the b12 got me going with the iron so low and could the injection of b12 and the iron so low be interacting against one another. :huh:


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



Celiac.com Sponsor (A8-M):



TrillumHunter Enthusiast

The iron shots don't work like b-12. It takes some time for new blood cells to be made using the iron you've been given. I started on iron infusions about two weeks ago. I've had one partial, due to an allergic reaction, and two full infusions. I would say yesterday is the first time I noticed any change. My hands and feet are warm and it's easier to breath. But no real boost as of yet. I take the b-12 injections as well. I had one yesterday and it does give a more immediate affect. It doesn't give me energy so much as take away the nerve pain I get.

I would say you can't really evaluate the effectiveness until you get your diet free of gluten. Gluten causes me to have that deep, deep fatigue that rest doesn't relive. Work hard to take care with your diet.

HTH

MaryJones2 Enthusiast

Correcting anemia doesn't happen in a matter of weeks when your iron levels are so low. It takes months to correct and six weeks isn't really enough time to see much improvement. As Trillium mentioned gluten zaps any energy that I have and even with treatment I didn't see my iron levels start to improve until I was 100% gluten-free. I also had chills, sweats, etc. until my ferritin passed about 50. Hang in there and keep taking your iron pills. It's a slow improvement but eventually you'll get there.

Oma81307 Newbie
Correcting anemia doesn't happen in a matter of weeks when your iron levels are so low. It takes months to correct and six weeks isn't really enough time to see much improvement. As Trillium mentioned gluten zaps any energy that I have and even with treatment I didn't see my iron levels start to improve until I was 100% gluten-free. I also had chills, sweats, etc. until my ferritin passed about 50. Hang in there and keep taking your iron pills. It's a slow improvement but eventually you'll get there.

how do you work like this? i work for burger king and am a store manager. I can't function. Also, if i go to er and tell them i have all this would they consult a hemoglobin dr and perhaps do iv's or blood transfusion to correct?

Ms. Skinny Chic Explorer

I have pernicious anemia/ iron anemia also...

Ms. Skinny Chic Explorer
I have pernicious anemia/ iron anemia also...

PS. My levels used to be very low, but my b 12 is currently @ 1300.

It was @ 3000 4 months ago.. It wasn't nowhere near that 5 years ago..

I was seriously ill... My hematologist wanted to give me iron injections too.

My hematologist had me taking B-12 every month for 6 -12 ms. My pernicious anemia is miraculously improving.. My iron improved also...

Pernicious Anemia is a lifelong illness, but it can improve..

How often are you taking your injections and at what dosage????????

024Mandy Newbie
Hi! I've been celiac diagnosed for almost 2 years. I started the b12 injections shortly after being diagnosed and I am suppose to be down to once a month. (i'll get to that in a second). However last time my Iron/b12 was checked my b12 was 464 which is 64 over where dr wants it minimum. Iron however was a 12. They want that a 50. I took a round of repliva for 6 weeks. Iron still tested 12. They gave me another round of Repliva and scheduled a shot. Then all of a sudden it was like my energy went from decent. TO NOTHING. I couldn't get up. I wanted to sleep. I did work harder previous to this. Did I just over work myself to where the anemia symptoms kicked in or what? This was on a sat/sun that I became so drained I came home early from work. Slept 4 hours. When I woke up still not much energy. I knew that Monday I had a iron shot scheduled. On Tuesday after having the shot I cried. I really thought this would do like the b12 and give me energy at least for a time. It did not. All it did was make me want to sit up instead of lay down. I finally realized it was a few days till my monthly b12 shot so I checked with my best friend who is a RN and she agreed to go ahead and take it. All of a sudden ZOOM! I was up and gone. We decided maybe until I got the iron up I should take my b12 a little more often. Odd part is the b12 has helped me feel energy but I still feel weird. I have nausea, headaches, I feel like the top half my body wants to go go go and the other half wants to lay down. I have chills up my spine, I'm really cold, then pouring a sweat. I did find out there was some foods I was eating that contained glueten. Now I know why the iron isn't going anywhere. So rearranged my diet again. I just guess i'm curious why the b12 got me going with the iron so low and could the injection of b12 and the iron so low be interacting against one another. :huh:

Hi, I just wanted to let you know that I know exactly how you feel. about a year and a half ago when I was diagnosed with ceilac my iron was at 2, B-12 and hemagloben or how ever you spell it were also extremely low, and I had no idea at the time. I was so used to sleeping all the time and having no energy I didn't know anything was wrong. Now when I look back I should have noticed that there was something going on. I would sleep for at least 10 hours a day and take naps. If I fell asleep during the day It would take my boyfriend 30 mins to wake me up. I was always talking in my sleep and I would appear to wake up(sit up and talk) but still be sleeping. Sometimes He wouldn't be able to wake me up so he would just carry me up to bed. I couldn't do any exercise. I would fall asleep when we had friends over, at the movie theatre, and a bunch of other places. It took me months to get my iron up to normal levels. I used pills, they never did put me on injections. anyway be patiant It will come along. good luck


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



Celiac.com Sponsor (A8-M):



I hate gluten Apprentice

I am at the begining of my b12 injections. I had to beg for them to even test me for low vit. Every time I read a post like this it reminds me how not alone I really am.

Oma81307 Newbie
PS. My levels used to be very low, but my b 12 is currently @ 1300.

It was @ 3000 4 months ago.. It wasn't nowhere near that 5 years ago..

I was seriously ill... My hematologist wanted to give me iron injections too.

My hematologist had me taking B-12 every month for 6 -12 ms. My pernicious anemia is miraculously improving.. My iron improved also...

Pernicious Anemia is a lifelong illness, but it can improve..

How often are you taking your injections and at what dosage????????

I take one insulin syringe full of b12 once a month. though i took those extra shots i am now drained again. it was like go go go go go go and crash and burn. I went to er on saturday the 7th. didn't help. they couldn't get the results on the iron back till monday. I waited and waited missing work. I finally got aggravated and got my results from the er myself. iron was 47. i called my regular dr and got in with her by then i had sore throat and just felt lousy. she put me off for the rest of the week and said that she was calling it bacteria and viral and put me on predinsone steriod pack and zpak antibotic. by thursday my throat and stuff better but not energy. My doctor for celiac had never called back. so i called and spoke with a supervisor and they were like we don't know why they didn't call you but your dr wants you off work until she sees you. (which is today) so she checked the test the other places (er, reg dr) had run and said "no one tested your iron saturation" we will get that tomorrow when you come in." so we'll see what they find

wild fisher Rookie
Correcting anemia doesn't happen in a matter of weeks when your iron levels are so low. It takes months to correct and six weeks isn't really enough time to see much improvement. As Trillium mentioned gluten zaps any energy that I have and even with treatment I didn't see my iron levels start to improve until I was 100% gluten-free. I also had chills, sweats, etc. until my ferritin passed about 50. Hang in there and keep taking your iron pills. It's a slow improvement but eventually you'll get there.

What is Ferritin? I checked my last test result and i was at 5 and my iron saturation level was 9%. My Dr. did say i was anemic (iron deficiency) but didn't put me on any thing or say much about it so i left it alone. Now that i read this thread i'm thinking i should go back in.

Oma81307 Newbie
Hi, I just wanted to let you know that I know exactly how you feel. about a year and a half ago when I was diagnosed with ceilac my iron was at 2, B-12 and hemagloben or how ever you spell it were also extremely low, and I had no idea at the time. I was so used to sleeping all the time and having no energy I didn't know anything was wrong. Now when I look back I should have noticed that there was something going on. I would sleep for at least 10 hours a day and take naps. If I fell asleep during the day It would take my boyfriend 30 mins to wake me up. I was always talking in my sleep and I would appear to wake up(sit up and talk) but still be sleeping. Sometimes He wouldn't be able to wake me up so he would just carry me up to bed. I couldn't do any exercise. I would fall asleep when we had friends over, at the movie theatre, and a bunch of other places. It took me months to get my iron up to normal levels. I used pills, they never did put me on injections. anyway be patiant It will come along. good luck

Hey thanks for your input. But they have now decided my iron, b12 is okay. they are waiting on celiac levels to come back i have NO idea what that does and my white blood count is up. I am going to my reg dr today to hopefully get some answers. I've absolutly crashed. I've not worked in a week and a half. other than about 5 hrs. I'm so tired. Taking a shower wears me out. At my gi dr I talk more to the nurses than i do my dr and they are not helping. She wrote me a note for work stating that i could work if i felt like it and don't if i don't. and that this was due to iron deficiancy. well now they called and said iron is fine. and they are waiting on celiac test i said what does that mean. well it could be the reason you feel the way you do. HELLLOOOOOOOO. what does it test. I did find out I was eating foods i wasn't suppose to. they didn't say wheat barley or rye so i thought them to be safe. ha! so i'm learning all over again. i'm going to start kicking butt and taking names i can't take this anymore. I have extreme exhaustion, bone pain, muscle pain and spasms, light headed, little sparks in front of my eyes at times, over all i feel like i have the flu that won't go away. i'm an 80 year old in a 34 year old body! ick. help. ever heard of the celiac level?

mimommy Contributor
I have extreme exhaustion, bone pain, muscle pain and spasms, light headed, little sparks in front of my eyes at times, over all i feel like i have the flu that won't go away. i'm an 80 year old in a 34 year old body! ick. help. ever heard of the celiac level?

Are you sure it's not a "Celiac PANEL"? That is the name of at least two tests used to diagnose celiac disease--tissue transglutaminase (ttg) and total IgA.

Oma81307 Newbie
Are you sure it's not a "Celiac PANEL"? That is the name of at least two tests used to diagnose celiac disease--tissue transglutaminase (ttg) and total IgA.

yep that's what it was. and it was elevated. they don't want to do anything about it. however my regular dr says it is nothing to do with celiac. he's run a bunch of test.. we'll see

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,962
    • Most Online (within 30 mins)
      7,748

    AlissaW
    Newest Member
    AlissaW
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • 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.