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

Mtndog Collaborator

Thanks Sherry! appreciate the sharing!


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



Celiac.com Sponsor (A8-M):



  • Replies 33.4k
  • Created
  • Last Reply
Rachel--24 Collaborator
We had two people (used to work in my department) who were out on disability for over a year each...they finally were terminated, but I think my employer had to wait that long.

Yeah...you can only be on disability for 1 year exactly and after that you can be terminated. I went off and on diasability 3 x and then the last time I stayed off for one full year and I knew that after 12 months I'd have to go back to work.

It turned out that you need to be back at work for 3 months straight in order to start a "new" claim and then get a full year. I only worked two months in between the last claims and so my "year" was up sooner than I'd thought it would be. All of a sudden I got no more checks and I had no insurance. :huh:

I didnt even know that my last two claims were actually considered one claim and as soon as the months added up to one year...that was it. It was scary...thank God at that time I had been on the Candida diet a couple months and was able to go back to work.

If it werent for the diet I dont think I could have made it through 3 months of working before I could go back on disability. Fortunately I never got that bad again and I've been back at work almost 2 years now. :)

I didnt have insurance either since I had to work 2 full months until it got reinstated. I had to pay out of pocket for those months that I wasnt covered.

Rachel--24 Collaborator
Tomorrow is my endocopy- I think my biggest fear is that they will find refractory sprue (or just that my villi ain't looking so hot) or Crohn's and want to put me on steroids.

Bev,

I seriously dont think they are going to find Refractory Sprue...and I highly doubt Crohns as well. I think they arent going to find anything...which is good considering the choices. ;)

Even with all I've got going on....all this craziness in my gut and not being able to eat anything...having lost 25 lbs. at one time and having all my food coming out undigested...very high malabsorption score with Enterolab...even with all that GI stuff I had a "text book" perfect biopsy. Villi were standing tall and proud. :D

Also my colonoscopy looked totally clean and perfect...although he couldnt get around one turn to complete it. From what he saw everything was totally normal...same with the baruim tests I took. So even though it *feels* like there must be something totally serious going on (I thought for sure I had a brain tumor) that is often not the case.

Of course mercury and Lyme are totally serious too but they are also very treatable. :)

AndreaB Contributor
Hi Andrea and everyone,

Hi Sherry! :D Glad you joined us. I just noticed you hail from the same part of the country (even though you're not here now). We are 1/2 North of the Oregon/Washington border.

Mtndog Collaborator
Bev,

I seriously dont think they are going to find Refractory Sprue...and I highly doubt Crohns as well. I think they arent going to find anything...which is good considering the choices. ;)

Even with all I've got going on....all this craziness in my gut and not being able to eat anything...having lost 25 lbs. at one time and having all my food coming out undigested...very high malabsorption score with Enterolab...even with all that GI stuff I had a "text book" perfect biopsy. Villi were standing tall and proud. :D

Also my colonoscopy looked totally clean and perfect...although he couldnt get around one turn to complete it. From what he saw everything was totally normal...same with the baruim tests I took. So even though it *feels* like there must be something totally serious going on (I thought for sure I had a brain tumor) that is often not the case.

Of course mercury and Lyme are totally serious too but they are also very treatable. :)

Rachel- YOU ROCK! I think I just need to hear this because I'm getting anxious since the hubby is away! Here's to villi standing tall and proud :rolleyes:

Rachel--24 Collaborator
Crying is always part of a herx for me ... I don't know if it's just my brain needing the detox or if I'm really this upset ... or maybe a little of both.

Tears are another way the body detoxifies. I have always said that when I get a really bad reaction my body literally forces me to cry. Lots of times my tears would be "sticky"...or they would burn...other times the tears are wet and normal. It didnt matter that I wasnt upset about anything....I would cry involuntarily and also a HUGE amount of mucus will be excreted through my nose while I'm crying.

Its just normal "wet runny nose" that you get when you cry but its in massive amounts. :huh:

After the crying episodes would subside I would feel a 1000 x better. I think I've learned that crying eliminates toxins and makes me feel alot better. There have been many times that I've felt really toxic but my body wasnt making me cry....so I would sit down and try to think of the saddest stuff ever...and try to get the tears flowing.

I swear that its helped me feel better every single time. :)

dlp252 Apprentice

My dial up connection sucks, lol. :lol: I can't get to the previous page....I can get to the page before that.

I can see that we have a new poster, but I can't read the post, lol. Hi Sherry! Welcome...I'll have to read what you wrote tomorrow from work. :P


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



Celiac.com Sponsor (A8-M):



Rachel--24 Collaborator
The thing that helped the very most was coffee enemas. My doctor gave me an instruction sheet on this--otherwise I certainly would have never tried it!

(I just discovered about celiac, and I have always had constipation mostly as symptoms, so this helped in that area too).

What the explanation sheet said is that the coffee stimulates the release of bile, so helps cleanse the liver I guess which is doing all the detoxing for us.

Hi Sherry,

Thanks for sharing your very encouraging story. :)

Coffee enemas really are good for detox. Even though I dont mention it here....cuz its not really something I wanna advertise :ph34r: ....I have done these. I have different recipes I've tried and I didnt start out with coffee enemas...I just did warm water for awhile then "graduated" to coffee.

I used to be really really constipated so it was really helpful for that too. This was 2 years ago when I was focusing on Candida. I havent done anything since then because I got side tracked thinking I could just eliminate gluten and all would be fine. Obviously it wasnt the case but I had yet to be diagnosed with Lyme and mercury issues as well as candida.

I've been wanting to get back to coffee enemas for a few weeks now except I keep forgetting to buy the coffee everytime I'm at the store. :rolleyes:

Enemas arent too much fun but hey....anything that helps me feel better is worth it! ;)

happygirl Collaborator

just got home...and i think i'm in a flare (started last night...slowly)

but, wanted to offer my words of encouragement to

BEV for her endoscopy tomorrow...i'll be thinking of you

CARLA for her herx

PATTI for the glutening....

love to you all...off to bed. xoxo

Rachel--24 Collaborator
but, wanted to offer my words of encouragement to

BEV for her endoscopy tomorrow...i'll be thinking of you

CARLA for her herx

PATTI for the glutening....

Ditto to that....

and to add to it....

Laura for her "flare"

Hope everyone feels better...and Bev...we're all rooting for you!! :wub:

mftnchn Explorer
Hi Sherry,

Thanks for sharing your very encouraging story. :)

Coffee enemas really are good for detox. Even though I dont mention it here....cuz its not really something I wanna advertise :ph34r:

Hi Rachel,

LOL re advertise...for sure, I don't mention this to too many people! This forum has been a safe place tho to talk about the unmentionable things. I thought it might help somebody. Glad to know I am not the only one who has found this helpful!

Sherry

AndreaB Contributor
Ditto to that....

and to add to it....

Laura for her "flare"

Hope everyone feels better...and Bev...we're all rooting for you!! :wub:

Agreed.

Don't forget Patti has her appointment tomorrow as well.

Rachel--24 Collaborator
This forum has been a safe place tho to talk about the unmentionable things.

Yeah...except I dont know how "safe" I feel with a big smiling picture of me right next to my post talking about how great coffee enemas are. :rolleyes:

CarlaB Enthusiast
Ditto to that....

and to add to it....

Laura for her "flare"

Hope everyone feels better...and Bev...we're all rooting for you!! :wub:

Thanks, Laura, hope you're feeling better soon, too.

AndreaB Contributor
Yeah...except I dont know how "safe" I feel with a big smiling picture of me right next to my post talking about how great coffee enemas are. :rolleyes:

:lol::lol::lol::lol:

I needed that......thanks. :)

Rachel--24 Collaborator

Hey Donna.....Are you taking the same Transfer Factor that I'm on??

Is it the Transfer Factor LymPlus??

I havent started it....you cant take it around food...and I'm kind of always eating....so there is just no opportunity for me to take it yet. :rolleyes:

I gotta "factor" it in somehow. :lol:

Oh...and I'm also still a little fearful of the yeast. :ph34r:

Anna actually didnt test me for it so when I went to check out with Amy there was the one homeopathic that Anna talked to me about and tested me for....but also this Transfer Factor. Amy handed it to me and I was like "Is that mine??" :unsure:

I was freaking out inside and just kept saying that it has yeast. :o

I told her I didnt know what it was for because Anna didnt talk to me about it. She went and asked Anna....then said it was for my gut.

If I was afraid to take it there was one other thing I could take instead (cant remember the name) but it had alot of herbs in it.....I saw alot of ingredients and got even more freaked out. :rolleyes:

So Amy went and talked to Denise and said if I wanna hang out a minute she'll test me for both of them. I tested better for the second one....Denise said my body really liked that one alot. Anna came in and Denise told her I'm ok for both but especially the second one.

Anna still wanted me on the Transfer Factor right now....and not the other one. Hopefully the brewers yeast thing wont be a problem. :unsure:

Stupid yeast. :angry:

AndreaB Contributor
So Amy went and talked to Denise and said if I wanna hang out a minute she'll test me for both of them. I tested better for the second one....Denise said my body really liked that one alot. Anna came in and Denise told her I'm ok for both but especially the second one.

Anna still wanted me on the Transfer Factor right now....and not the other one. Hopefully the brewers yeast thing wont be a problem. :unsure:

I hope it's not a problem. Anna must have her reasons for wanting you on this one. :unsure:

Rachel--24 Collaborator
I hope it's not a problem. Anna must have her reasons for wanting you on this one. :unsure:

Yeah...and she was saying why she wanted me on the Transfer Factor instead....but I was too busy stressing over the yeast so cant rememeber what she said. :rolleyes:

Rachel--24 Collaborator

Whole Foods was out of organic potatoes...so instead I bought two yams. :o

I will eat my yams with protein.....same as Anna said to do with potatoes.....and then I will pray. :lol:

I'll pray that I dont get stupified by the yams....like what happened last year when I went into my "sweet potato haze". :rolleyes:

NoGluGirl Contributor

Dear Bev,

I am keeping my fingers crossed for your endo tomorrow! I had one done about six years ago. I do not think they found anything. We are all pulling for you in Rachelville! We will be anxious to hear your results.

Dear Rachel,

I think I have had trouble with malabsorption in the past. Once, I ate granola, and three days later, it came out looking a lot like it did when it went it! :blink: That was odd. My stomach cramped something terrible that day, too. The GI doc I had up at IU said it was impossible to poop food out whole! :rolleyes: Yeah, apparently NOT! Hopefully, you will have better luck with oats than I did!

Dear Carla,

The problems with Lyme never seem to end, do they? :( I hope you recover soon. Those herxes you describe sound like how I feel everyday with the fatigue. It is like you were run over by a train. What sucks is I am so tired, and have so much work to do.

I am behind on my school work, have study group meeting Saturday, and have not read the material for this week yet. Plus, I have to get stuff ready for a yard sale I am participating in for Saturday. I have to have the stuff ready tomorrow, though. My Aunt Chris is picking it up to take to the sale site. Wish me luck! I am hoping to get enough for some new cookware that cannot be glutened! This time, I am putting it in an airtight Rubbermaid or other container so no one has any excuse to gluten my stuff! :angry:

Dear Sherry,

I am so glad you shared your story about Lyme. I could have it, too. I am upset though, because I have no insurance. :( I am too ill to work a regular job, and am trying to get my own company going. I have some questions for you. Did the Lyme make you nauseous, and make you feel strange all over? I have Candida, and know that can add to it. Rachel and Carla think I have Babesia as well as Lyme. They have reported similar symptoms. There are days doing the dishes is barely possible.

Sincerely,

NoGluGirl

mftnchn Explorer

Hi Rachel,

I need to check my bottle of transfer factor, not sure there is yeast in mine. I am currently not taking it because I am supposed to be off milk, so I am more worried about the milk content. Its on my list to discuss with my allergist. Transfer factor seemed to be helpful for me. It gives you a way to fight the lyme...(just like babies get protection from some illnesses through being breastfed.)

Hi NoGlueGirl,

I had a lot of weird symptoms with lyme, however, I was probably also gluten sensitive at the time but didn't know that. My primary symptom was joint muscle pain. The pain would hit in one area then travel to another area in the space of a few hours. (Like a swollen painful ankle I couldn't put weight on, a few hours later it was fine and I had a shoulder pain). Would get worse at night typically, I could wake up in the middle of the night and feel like my upper back was on fire. Would also get worse with exercise or exertion. I could swim a very mild workout in the morning and be fine afterward, but have a bad flare that night. Fatigue, fogginess were also biggies. Felt like I had the flu a lot. Creepy crawly sensations on my face--which seems to be related to chemical sensitivity. Allergies initially went WAY out of wack. I tested for 7 weeks one summer and they never found anything I wasn't allergic to. I didn't experience nausea until the last 1.5 years, apparently from h pylori infection. The compounding pharmacy I have used told me that a lot of the patients they see that have lyme disease end up with gastritis (usually caused by h pylori).

I think I got lyme disease in about 1982-1983 when I had a tick bite, as the symptoms started not long after that. I hit a low in about 1985, where I could hardly get out of bed about 5 days a week. My allergist helped me a lot, and gradually I improved to some degree but not the joint symptoms which worsened.

I don't want to make this post too long but feel free to ask anything else.

One more thing, I plateaued eventually on antibiotics, but every time I tried to taper them off, I would flare again. What finally got me over the hump was using Cat's Claw tincture. I started out working right up from 1 drop a day to 10 because it didn't seem to bother me. WOW, did I ever have a major herx after about 1 month!!! After that, I dropped way back on the Cat's Claw, and then increased it really gradually. Eventually I took 20 drops a day (10 each am and pm) for a number of months. After that I was able to start successfully cutting back on antibiotics and finished all of them in Feb 2007. Except I am still taking Lamisil for candida, have to take it at least 6 more months, but can taper off gradually.

No insurance is a real challenge. I was able to buy most of my antibiotics over the counter here in China, that was a big help. Supplements really cost, but I needed them to protect my body from the antibiotics. Cat's Claw is herbal, about $36-40 a bottle but it lasts a month or two depending on how much you are taking.

Sherry

Rachel--24 Collaborator

Sherry,

Great info. I'm currently taking Cats Claw (Prima una de Gato). I havent herxed from it yet...I'm at about 7 drops twice a day. My LLMD wants me getting up to at least 18 drops.

I have not been on antibiotics at all because of heavy metals/candida/chemical sensitivites, etc. My Dr.'s want the toxic burden lowered first. I have alot of mercury and other metals to deal with...this is actually what caused me to get sick in the first place....and then found out about Lyme.

I guess the Lyme and Babesia were causing impaired detoxification but I didnt get sick until I got hit with a large amount of mercury and then the yeast pretty much exploded after that and a couple short rounds of antibiotics.

I dont know if I'll ever be on antibiotics for Lyme. I'm doing more alternative stuff...Klinghardt/Derksen methods of detox and healing. I have two LLMDS....one is ND and the other M.D.. Neither one is talking about antibiotics at this stage.

Its really great to hear that Cats Claw helped you so much. :)

The biggest causitive factor for symptoms in my case is the candida. Its caused alot of food/chemical/environmental sensitivities and a whole lot of symptoms. Right now I'm trying to get that under control and hopefully start detoxing better. The yeast is pretty severe and probably overloading my liver and detox pathways so that I havent been too successful with taking any of the necessary supplements for detox.

I get that same creepy crawly feeling on my face...but also my arms and back. Its from chemicals for me too....but I get it even moreso from mold.

I took Transfer Factor last year (before I was diagnosed) and I do think it was helping me...it was a totally different TF from what I'm going to be taking now.

I was also in bed most of the time and having really scary symptoms, weight loss, severe depression, memory loss, eye problems, numbness/tingling,etc.

I was off work for two years but what pulled me out of it was going on the candida diet, eliminating chemicals, eating organic...just avoiding alot of toxins.....in less than 2 weeks there was dramatic improvement and I've been functioning and back at work for 2 years now. :)

I'm still really toxic though...whats inside has mostly stayed inside....I just try not to add to it. Hopefully I'm headed in the right direction and will soon start detoxing alot of what I've been holding onto.

rinne Apprentice
Oh sorry....yucky. If what I'm experiencing is a herx, it is nasty. I passed out so hard yesterday after noon and I feel like every CELL in my body aches. How long do these things last, if indeed that is what it is? I want to cry but I'm literally too tired and miserable.

Sending hugs, for me they generally lasted about two days with headache, extreme irritablity - mood swings, crawling skin sensations, body aches and overall feeling of exhastion. I haven't herxed in quite a while and mostly did so when I was taking the salt/c in the beginning. I moved on to Samento and Noni for about three months and most recently have been taking chlorella, probiotics and candidastop. I am so much better and though I know the candida is really a problem I am still eating my treats. :ph34r:

I think the most important thing though is that I have really begun to have some feeling of confidence that I will be well again, when I think back a year ago and how ill I was, at once point I had a lot of blood with bowel movements and it went on for three days. I didn't tell anyone about it or about other scary stuff. :ph34r: I remember what it was like to feel as if all my organs were swollen and in pain and then I would pull the skin away from my body and know that the pain was in the tissue and not inside but given that my digestion wasn't working I tormented myself with fear of the worst things.

I am stubborn and I really trust that our bodies given the ability to heal will heal, I think it has been the detoxing that has been most helpful.

Rachel, I have the same thing you do with stress causing immediate physical symptoms

Andrea suggested that I jump in here even though I don't have time to read this whole thread! Whew!

Sherry

Hi Sherry and welcome, but what? You didn't read the past 1000 pages? :lol:

Many of my symptoms over a period of years sounded like yours.

Tears are another way the body detoxifies.

Me too, I look for sad movies.

just got home...and i think i'm in a flare (started last night...slowly)

but, wanted to offer my words of encouragement to

BEV for her endoscopy tomorrow...i'll be thinking of you

CARLA for her herx

PATTI for the glutening....

love to you all...off to bed. xoxo

Yes, and encouragement for you too. :)

Yeah...except I dont know how "safe" I feel with a big smiling picture of me right next to my post talking about how great coffee enemas are. :rolleyes:

Clearly you are our fearless President. :P:lol:

mftnchn Explorer

Wow, Rachel. You have really been through it. Thanks for bringing me up to speed on all of that. Glad you are stable enough to work, and hope that the treatment for candida rapidly makes some progress. I suppose you are on a really low carb regimen?

I've been asking myself whether this whole thing is like the question, what comes first, the chicken or the egg? Like what came first, allergies, candida, lyme, celiac, etc. etc.?

I also have high mercury levels, which haven't really gone down yet. One day when I was in my doctor's office, one of the staff commented that it seemed like a lot of the patients with lyme disease had elevated mercury levels.

I live with the candida to some degree too, but was taking two antifungals throughout the antibiotic treatment, and probiotics that have helped.

I'm not sure about what the Klinghardt/Dirkson approach is, is there a website for it?

BTW, I didn't have the Igenix testing, but I need to wait until I am home from my trip to look up the name of the lab. This lab actually took pictures of the lyme in the blood via florescence of some kind. It is quite sensitive to small amounts of lyme. My doctor told me he had never had a person who tested positive, test negative after treatment. Until he started using Cat's Claw. I don't know if I will test negative, haven't done one in awhile.

Wow, its so amazing to find a group of people with similar histories!

AndreaB Contributor
Wow, its so amazing to find a group of people with similar histories!

I'm glad you joined us. :D

I don't have lyme (let's just say it's not very likely), but I believe that I have some problems with mercury as I have a lot of amalgams. My oldest daughter and my youngest son also have a lot of intolerances so I'm thinking they have problems with mercury as well.

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - cristiana replied to Scatterbrain's topic in Sports and Fitness
      5

      Feel like I’m starting over

    2. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      8

      My only proof

    3. - Wheatwacked replied to Jmartes71's topic in Coping with Celiac Disease
      8

      Related issues

    4. - NanceK replied to Jmartes71's topic in Related Issues & Disorders
      8

      My only proof

    5. - Wheatwacked replied to Scatterbrain's topic in Sports and Fitness
      5

      Feel like I’m starting over


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,294
    • Most Online (within 30 mins)
      7,748

    laurallee
    Newest Member
    laurallee
    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

    • cristiana
      Hi @Scatterbrain Thank you for your reply.   Some of these things could be weaknesses, also triggered by stress, which perhaps have come about as the result of long-term deficiencies which can take a long time to correct.   Some could be completely unrelated. If it is of help, I'll tell you some of the things that started in the first year or two, following my diagnosis - I pinned everything on coeliac disease, but it turns out I wasn't always right!  Dizziness, lightheaded - I was eventually diagnosed with cervical dizziness (worth googling, could be your issue too, also if you have neck pain?)  A few months after diagnosis I put my neck out slightly carrying my seven-year-old above my head, and never assigned any relevance to it as the pain at the time was severe but so short-lived that I'd forgotten the connection. Jaw pain - stress. Tinnitus - I think stress, but perhaps exacerbated by iron/vitamin deficiencies. Painful ribs and sacroiliac joints - no idea, bloating made the pain worse. It got really bad but then got better. Irregular heart rate - could be a coincidence but my sister (not a coeliac) and I both developed this temporarily after our second Astra Zeneca covid jabs.   Subsequent Pfizer jabs didn't affect us. Brain fog - a big thing for people with certain autoimmune issues but in my case I think possibly worse when my iron or B12 are low, but I have no proof of this. Insomnia - stress, menopause. So basically, it isn't always gluten.  It might be worth having your vitamins and mineral levels checked, and if you have deficiencies speak to your Dr about how better to address them?    
    • knitty kitty
      @NanceK, I do have Hypersensitivity Type Four reaction to Sulfa drugs, a sulfa allergy.  Benfotiamine and other forms of Thiamine do not bother me at all.  There's sulfur in all kinds of Thiamine, yet our bodies must have it as an essential nutrient to make life sustaining enzymes.  The sulfur in thiamine is in a ring which does not trigger sulfa allergy like sulfites in a chain found in pharmaceuticals.  Doctors are not given sufficient education in nutrition (nor chemistry in this case).  I studied Nutrition before earning a degree in Microbiology.  I wanted to know what vitamins were doing inside the body.   Thiamine is safe and nontoxic even in high doses.   Not feeling well after starting Benfotiamine is normal.  It's called the "thiamine paradox" and is equivalent to an engine backfiring if it's not been cranked up for a while.  Mine went away in about three days.  I took a B Complex, magnesium and added molybdenum for a few weeks. It's important to add a B Complex with all eight essential B vitamins. Supplementing just one B vitamin can cause lows in some of the others and result in feeling worse, too.  Celiac Disease causes malabsorption of all the B vitamins, not just thiamine.  You need all eight.  Thiamine forms including Benfotiamine interact with each of the other B vitamins in some way.  It's important to add a magnesium glycinate or chelate supplement as well.  Forms of Thiamine including Benfotiamine need magnesium to make those life sustaining enzymes.  (Don't use magnesium oxide.  It's not absorbed well.  It pulls water into the intestines and is used to relieve constipation.)   Molybdenum is a trace mineral that helps the body utilize forms of Thiamine.   Molybdenum supplements are available over the counter.  It's not unusual to be low in molybdenum if low in thiamine.   I do hope you will add the necessary supplements and try Benfotiamine again. Science-y Explanation of Thiamine Paradox: https://hormonesmatter.com/paradoxical-reactions-with-ttfd-the-glutathione-connection/#google_vignette
    • Wheatwacked
      Your goal is not to be a good puppet, there is no gain in that. You might want to restart the ones that helped.  It sounds more like you are suffering from malnutrition.  Gluten free foods are not fortified with things like Thiamine (B1), vitamin D, Iodine, B1,2,3,5,6 and 12 as non-gluten free products are required to be. There is a Catch-22 here.  Malnutrition can cause SIBO, and SIBO can worsen malnutrition. Another possibility is side effects from any medication that are taking.  I was on Metformin 3 months before it turned me into a zombi.  I had crippling side effects from most of the BP meds tried on me, and Losartan has many of the side effects on me from my pre gluten free days. Because you have been gluten free, you can test and talk until you are blue in the face but all of your tests will be negative.  Without gluten, you will not create the antigen against gluten, no antigens to gluten, so no small intestine damage from the antigens.  You will need to do a gluten challange to test positive if you need an official diagnosis, and even then, no guaranty: 10 g of gluten per day for 6 weeks! Then a full panel of Celiac tests and biopsy. At a minimum consider vitamin D, Liquid Iodine (unless you have dermatitis herpetiformis and iodine exasperates the rash), and Liquid Geritol. Push for vitamin D testing and a consult with a nutritionist experienced with Celiack Disease.  Most blood tests don't indicate nutritional deficiencies.  Your thyroid tests can be perfect, yet not indicate iodine deficiency for example.  Thiamine   test fine, but not pick up on beriberi.  Vegans are often B12 deficient because meat, fish, poultry, eggs, and dairy are the primary souces of B12. Here is what I take daily.  10,000 IU vitamin D3 750 mg g a b a [   ] 200 mg CoQ10 [   ] 100 mg DHEA [   ] 250 mg thiamine B1 [   ] 100 mg of B2 [   ] 500 mg B5 pantothenic acid [   ] 100 mg B6 [   ] 1000 micrograms B12 n [   ] 500 mg vitamin c [   ] 500 mg taurine [   ] 200 mg selenium   
    • NanceK
      Hi…Just a note that if you have an allergy to sulfa it’s best not to take Benfotiamine. I bought a bottle and tried one without looking into it first and didn’t feel well.  I checked with my pharmacist and he said not to take it with a known sulfa allergy. I was really bummed because I thought it would help my energy level, but I was thankful I was given this info before taking more of it. 
    • Wheatwacked
      Hello @Scatterbrain, Are you getting enough vitamins and minerals.  Gluten free food is not fortified so you may be starting to run low on B vitamins and vitamin D.   By the way you should get your mom checked for celiac disease.  You got it from your mom or dad.  Some studies show that following a gluten-free diet can stabilize or improve symptoms of dementia.  I know that for the 63 years I was eating gluten I got dumber and dumber until I started GFD and vitamin replenishment and it began to reverse.  Thiamine can get used up in a week or two.  Symptoms can come and go with daily diet.  Symptoms of beriberi due to Thiamine deficiency.   Difficulty walking. Loss of feeling (sensation) in hands and feet. Loss of muscle function or paralysis of the lower legs. Mental confusion. Pain. Speech difficulties. Strange eye movements (nystagmus) Tingling. Any change in medications? Last March I had corotid artery surgery (90 % blockage), and I started taking Losartan for blood pressure, added to the Clonidine I was taking already.  I was not recovering well and many of my pre gluten free symptoms were back  I was getting worse.  At first I thought it was caused a reaction to the anesthesia from the surgery, but that should have improved after two weeks.  Doctor thought I was just being a wimp. After three months I talked to my doctor about a break from the Losartan to see if it was causing it. It had not made any difference in my bp.  Except for clonindine, all of the previous bp meds tried had not worked to lower bp and had crippling side effects. One, I could not stand up straight; one wobbly knees, another spayed feet.  Inguinal hernia from the Lisinopril cough.  Had I contiued on those, I was destined for a wheelchair or walker. She said the symptoms were not from Losartan so I continued taking it.  Two weeks later I did not have the strength in hips and thighs to get up from sitting on the floor (Help, I can't get up😨).  I stopped AMA (not recommended).  Without the Losartan, a) bp did not change, after the 72 hour withdrawal from Losartanon, on clonidine only and b) symptoms started going away.  Improvement started in 72 hours.  After six weeks they were gone and I am getting better.  
×
×
  • 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.