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

Omg...i Might Be On To Something


Rachel--24

Recommended Posts

Green12 Enthusiast
In fact, more people with Lyme gain weight than lose.

I would have never guessed that. I thought it would be the opposite!

I am trying something different with foods, trying to eat as much variety as possible instead of doing my usual 7-10 (or so) safe foods over and over again.

I'm working on the stress response with food, the pattern that sets in when you ingest the same thing when your body is under stress- then the food becomes the stress.

I'm able to eat a lot more foods than most here, it seems. I do ok with fresh food in it's natural state so so far it's going ok.


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



Celiac.com Sponsor (A8-M):



  • Replies 33.4k
  • Created
  • Last Reply
CarlaB Enthusiast

That's probably because so many of us have Lyme, but thought we had celiac. Just because of the website that brought us together, we are the ones who lost rather than gained. :)

Over on LN, many talk about how much they've gained. I read the statistics once, I think it was 70-80% gain.

I'm glad your new diet strategy is working well. :) I'm looking forward to having a kitchen back ... and getting my braces off! My braces prevent me from eating a lot of foods that I normally would eat -- raw stuff, salads, etc.

AndreaB Contributor
I'm able to eat a lot more foods than most here, it seems. I do ok with fresh food in it's natural state so so far it's going ok.

Sounds good. Keep us updated.

Carla,

Will things be done enough for Thanksgiving?

CarlaB Enthusiast
Carla,

Will things be done enough for Thanksgiving?

Yes. :) There will still be some painting that is incomplete, and they didn't have enough tile for the backsplash, so we're waiting on that .... since it's stone, it will also need to be sealed .... but other than that, it will be done.

On the other hand, we'll be moving our stuff in it late Tues./early Wed., so we're cutting it close.

My dad is sick, so he just cancelled .... that makes it a little easier ... between my herx this week and cutting it close with the kitchen, it takes the pressure off ... he was our only visitor this year. Now, if I can't get to cooking till Friday, who cares? LOL

melmak5 Contributor

This is a fly-bye...

I am not sure if anyone has mentioned, but FYI - chocolate is fermented, so for persons with mold issues, it might not be the best.

Personal Update

- Heart monitor is comic gold - I have now got people convinced they modeled the ipod after it

- Upper GI stuff is better, lower is worse, the bleeding is back as is the C/D dance

- I have an appointment with a new GI at a new hospital for December 3. If my current doesn't think rectal bleeding deserves a returned phone call, nothing will get her attention.

confusedks Enthusiast

So, the never ending doctor journey continues!!

We went to the GI and she truly doesn't think I have celiac. She thinks I have a small bowel bacterial overgrowth and confirmed an IBS diagnosis!!!!!!!!! I asked her what causes IBS and she said "STRESS!" OMG, I could have killed her! She was very thorough, etc. but she's not looking at the whole body picture.

She said that it's not an emergency to get the Iron IV's (what the heck does she know...last I checked she was a GI Dr., NOT a hematologist!) because my Hemoglobin is fine.

She also said I may have lymphocitic colitis (I will research this later to see more about it). She ordered a hydrogen breath test to confirm the SBBO and then ordered a 10 course of abx, 2 pills 3 times a day!!! UGH!

I am really frustrated because she wants me to do the abx first, then do the iron IV's to see which one makes me feel better, but I think she thinks her area of specialty is more important than the blood stuff.

We are now waiting to see which course of action to take first...abx or IV?! She told us to call the hematologist and see what he says, but I told my mom to have the hematologist call her because we do not have medical degrees and we are unfit to decide which needs to happen first!

As of now, we are waiting for both dr's to talk to each other. She said in the long term, she is going to want to do an endo./colon. and may have me go back on gluten. SHe said "since you're already feeling crappy, why not put gluten back in your diet so we can diagnose you!" ARGH!

To say the least, it was frustrating. She also said that since I have grown fine, I couldn't have celiac...so wrong!

Kassandra

AndreaB Contributor
My dad is sick, so he just cancelled .... that makes it a little easier ... between my herx this week and cutting it close with the kitchen, it takes the pressure off ... he was our only visitor this year. Now, if I can't get to cooking till Friday, who cares? LOL

Friday would be good too. If it's just the family they'll understand.

So, the never ending doctor journey continues!!

I feel so bad for you and these doctors. :angry:

I would think the IV's are much more important.

I thought you had problems with abx.

Personally I'd do the IV's, get your lyme testing done (through Igenex) and head to the LLMD for the battery of tests they run. Lyme could very well be causing all that's going on with you and all the bandaids won't fix it.


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast

Kassandra, what abx is she talking about? I thought you couldn't take abx?

I would get the iron IV's to help with the symptoms and go see the LLMD for determining the treatment protocol. You may want to keep these other doctors which are covered by insurance, but let the LLMD direct. He will see the big picture rather than a bunch of seemingly unrelated health issues.

Andrea, we all cook together .... everyone has their job .... so if it's not till Friday, it'll be because of all of us! But I think we'll be able to pull it together for Thursday. :)

confusedks Enthusiast

Andrea,

I agree, this is all a bunch of BS!!!! Apparently the abx aren't absorbed through your blood... or some part of your body that causes the allergic reactions. I have no idea...I may go into anaphylactic shock...lol! Who the hell knows?!

Carla,

The abx is rfaximin. I have no idea what to think of all of this. Now my mom is holding onto the idea that it might all get better with the proper treatment of the SBBO. UGH!

Kassandra

CarlaB Enthusiast

Kassandra, I had the SSBO, too. In your case, especially, I'd try the non-abx route for the bacterial overgrowth ... I took Cipro for 21 days, and I felt much better on it, but as soon as I got off, the GI issues returned.

If you just take an abx to get rid of the bacteria, but don't try to completely restore the balance in the intestine, then it will just come back when you stop.

I was taking VSL#3, a very strong probiotic, along with the Cipro .... it still wasn't until I used herbs that I felt better.

BTW, Humaworm takes care of all the bad bacteria that I had in my intestine ... I wish I found it in the beginning of treating the dysbiosis .... it's cheaper than buying all the herbs separately.

If I were you, I'd get on a good probiotic, Humaworm for 30 days, and see the LLMD ... plus the iron IV.

Your mom needs to understand that a bullseye rash is diagnostic of Lyme, and until you fix the underlying cause of your body being so out of balance, you are not going to get better.

Maybe showing her the ILADS website and Dr. B's guidelines would help convince her.

CarlaB Enthusiast

Kassandra, Here is an article that we've posted before, but it's a good one. Open Original Shared Link

It mentions the use of Rifaximin to help with GI issues in Lyme. Maybe it's a good one to print out for your mom.

confusedks Enthusiast

Carla,

Thanks for the link. That is interesting...so you're saying that her stupid SBBO dx could be a co-infection of Lyme?! :o

I am so frustrated with all of this. Also, could you give me a link to Dr. B's guidelines? I don't know if I have ever seen/read that.

I am just in awe of everything...talk about disillusioned with the medical community! :angry: My mom talked to my hematologist and he is saying he still thinks I need the IV's ASAP!! He wants to know why the GI thinks that what she wants to treat is more important than my "critically" low ferritin. Also, my total iron has dropped from 102 to 73 in 3 weeks! This will get out of hand if we wait much longer.

Kassandra

P.S. Where did you get the probiotic?

CarlaB Enthusiast

I'm not saying it could be a coinfection, rather a manifestation of Lyme ... it IS Lyme. GI symptoms were a HUGE part of my Lyme Disease. Looking back over the years, anytime I had a Lyme flare, I had GI symptoms first. It was only within the past two months that I've healed from the GI issues ... treatment for both the dysbiosis and the Bartonella.

Many on LN seem to have GI issues from bart.

Dr. B's guidelines are at www.ilads.org.

I get VSL#3 at their website ... no one near me carries it. It's very expensive .... it has 450 billion bacteria ... Theralac is another GREAT one, a lot less expensive, but only has 20 billion bacteria, which is a LOT compared to the ones you buy in the store.

I think you need the iron, too ....

CarlaB Enthusiast

duplicate post

CarlaB Enthusiast

I'm not saying it could be a coinfection, rather a manifestation of Lyme ... it IS Lyme. GI symptoms were a HUGE part of my Lyme Disease. Looking back over the years, anytime I had a Lyme flare, I had GI symptoms first. It was only within the past two months that I've healed from the GI issues ... treatment for both the dysbiosis and the Bartonella.

Many on LN seem to have GI issues from bart.

Dr. B's guidelines are at www.ilads.org.

I get VSL#3 at their website www.vls#3.com ... no one near me carries it. It's very expensive .... it has 450 billion bacteria ... Theralac is another GREAT one, a lot less expensive, but only has 20 billion bacteria, which is a LOT compared to the ones you buy in the store.

I think you need the iron, too ....

AndreaB Contributor
BTW, Humaworm takes care of all the bad bacteria that I had in my intestine ... I wish I found it in the beginning of treating the dysbiosis .... it's cheaper than buying all the herbs separately.

Does dysbiosis have anything to do with parasites?......or is that just your situation.

Mitch has mild reflux and I am willing to get the humaworm for him if it will help.

My mom talked to my hematologist and he is saying he still thinks I need the IV's ASAP!! He wants to know why the GI thinks that what she wants to treat is more important than my "critically" low ferritin. Also, my total iron has dropped from 102 to 73 in 3 weeks! This will get out of hand if we wait much longer.

You need to get those IV's done! What's the holdup? Still the insurance and PICC line? I thought you'd been approved. Now that this appointment is out of the way will your mother get you in to get the iron IV's?

CarlaB Enthusiast
Does dysbiosis have anything to do with parasites?......or is that just your situation.

Here's the link to the info on parasites at Humaworm ... Open Original Shared Link

It has bacteria listed as a parasite ... among other things ... like mold, yeast, protozoa, etc.

I would tend to think if you have a bacteria overgrowth, it doesn't exist alone.

confusedks Enthusiast

More news...the Hematologist said that it can wait 2-3 weeks, but NO longer. So I am going tomorrow to get the hydrogen breath test for the SBBO. We are also in the process of finding out which abx I am allergic to. My pediatrician's office is getting my chart out of storage and we should get copies within the next day or two. The nurse at Cedars Sinai today was shocked that I don't wear a medi-alert for my abx allergies. She said we needed to get them.

The reason the IV's are being postponed is BEYOND me! I have no idea...it's not a money thing because everything has been approved. The GI wants to see if this makes me feel better.

Carla, Do you know...if I take these abx is it possible I'll have a herx? Are there only certain abx that cause herxes? I didn't mean to sound rude when I said about the coinfection, I meant it more in a "I might be onto something" way. :)

Kassandra

CarlaB Enthusiast

You didn't sound rude at all ... I knew how you meant it and didn't even think of it in a different way than "I might be onto something!"

You could herx from an abx .... but I don't know if you will on that one .... I Googled it earlier ... it seems it's used for traveler's diarrhea and it stays mostly in the digestive tract.

I think what you're dealing with is a GI doctor thinks the GI aspect is more important and the Blood doc thinks the blood is more important .... I'd pick the blood .... I don't think fixing your GI issues will be as cut and dry at the GI doc thinks ... based on my experience, it has taken me a couple months to fix the GI tract even after I knew the problem.

confusedks Enthusiast

I agree. She thinks I am going to go on the abx and feel better. For all we know, I was put on ones similar to these when I was a kid and I reacted. There are so many unkonwns it is crazy. The hydrogen breath test sounds grueling...you btreathe into a bag every 15 minutes for anywhere from 90 minutes to 3 hours!!!!! YUCK! They give you this sugary solution you have to drink before you breathe into the bag. Also, I have to fast...

Okay, I am glad you didn't read into that the wrong way. I am in such a frustrated place right now, I just wanted to make sure I didn't upset you. ;)

Kassandra

melmak5 Contributor
I agree. She thinks I am going to go on the abx and feel better. For all we know, I was put on ones similar to these when I was a kid and I reacted. There are so many unkonwns it is crazy. The hydrogen breath test sounds grueling...you btreathe into a bag every 15 minutes for anywhere from 90 minutes to 3 hours!!!!! YUCK! They give you this sugary solution you have to drink before you breathe into the bag. Also, I have to fast...

Okay, I am glad you didn't read into that the wrong way. I am in such a frustrated place right now, I just wanted to make sure I didn't upset you. ;)

Kassandra

I did this, its not bad at all.

Its just more of a bother. No pain, no poking, just drinking some sugar-water and breathing heavily once in a while.

Bring a magazine or two... and a gluten-free snack. The nurse tried to give me COOKIES after the test was over, with my chart in their hands!

mftnchn Explorer
IV might actually make a difference for you since its much more effective....also bypasses the gut. Of course more effective means more risk if you're not excreting well. Definitely need to check into that first. Its also a good idea to start with a low dose rather than the max.

I'm avoiding orals until late in my treatment because of my leaky gut/yeast situation. I'll switch to DMSA later on.

I had thought you'd been on IV all this time.

I was originally on the creme version which he preferred for me, but it wasn't stable long enough for me to take with me. I think he didn't want me to do IV DMPS on my own over here. I think he was also concerned with overwhelming my system that tends to be sensitive.

Yes, all of this needs to be reviewed and perhaps a different approach when I get to the USA.

I haven't ever had problems with the IV challenge for the orange jug except last winter I thought I did. It turned out I was reacting to bismuth--at least that is my conclusion.

CarlaB Enthusiast

I did a three day random stool collection. They could name the specific bacteria that was there.

I understand your frustration ... I personally think you should get the IGeneX testing, then go to the LLMD .... I just don't think these other docs are going to fix anything. You need the iron, but other than that, I don't think they can help you .... you had the bullseye rash .... they'll treat the symptoms forever but never get to the underlying problem.

confusedks Enthusiast

Carla, I totally agree with you! The thing is my mom doesn't quite get that it's almost 100% Lyme related. She keeps saying, "what if it's not Lyme, then we will have gone to an LLMD for nothing!" I get what she's saying, but I am positive it's Lyme related stuff.

Then I talked to a cousin of mine who is 30 years old and she had the nerve to tell me that I need to lose sight of the root problem! :(:huh::angry::o I don't get that at all...she is the one who has had fibro, CFS, etc. Can you talk about Lyme!? And, her mom has had health problems her entire life pretty much and was diagnosed with Lyme, but they never treated it!! :o

I am so glad this forum is here...otherwise I;d be pretty lonely these days...lol! I am glad you all believe in me!

Now, if only I could get my mom on board. <_<

Kassandra

mftnchn Explorer

Kassandra, I guess what is puzzling is that you can say the same thing about this GI, what if it doesn't pan out as helpful? How can your mom decide not to go to the LLMD based on that possibility but see other docs and not consider that question?

I agree with Carla about what you need to do, and am not impressed with your GI, or the "tug of war" between your GI and hematologist, although the latter sounds better.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,951
    • Most Online (within 30 mins)
      7,748

    SY8
    Newest Member
    SY8
    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

    • 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
    • DebJ14
×
×
  • 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.