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

Chronic Fatigue, Any Suggestions?


txplowgirl

Recommended Posts

txplowgirl Enthusiast

Ok, I've been gluten free now for 8 months. Everything has either improved or disappeared. The one remaining problem is with chronic fatigue. My Dr says that I do not have Chronic Fatigue Syndrome but It sure feels like it to me. There are days I am just so tired I can't hardly move with no reasonable explanation for it. Slept good the night before, nothing strenuous. etc.

Maybe just a part of my fibro and i'll have to live with it but I would like to feel better in this area. I take good doses of Vit B-12, Vit D, DHEA, Vit C, Magnesium.

I've cut out the gluten, dairy, soy, msg, aspertame, lowered my sugar intake, nightshades, etc.

Does anyone have any other ideas or sugestions?


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



Celiac.com Sponsor (A8-M):



YoloGx Rookie

Feeling tired all the time is indeed no fun. Unfortunatley many of us here have had those kinds of problems.

I highly suggest taking olive leaf extract and/or tea regularly. It really works against things that cause chronic fatigue of whatever sort. It kills underlying bacterial, viral and yeast/fungal infections as well as a variety of microbes. You could also add neem leaf to be certain in case you think the cause might be parasitical on a microbial level.

Parasites are another thing to check into. Have you??

Maybe start with the olive leaf and neem first and then do more if needed.

I also suggest eating whole natural foods rather than pre-prepared things to eat.

Other things that help are certain supplements that speed up the mitochondria--like R-Lipoic acid and N-acytlcystein (NAC). These two are wonderful anti oxidants and make your other antioxidants work better. Esp. good as one ages.

L-glutamine can also help you feel more energy. Don't take it if you have kidney or diabetic issues. It gives extra energy plus soothes the intestines. Its also a great thing to take if you have been glutened or suspect that you might be, like in cases where you eat out.

Another thing I have found to help is to blend fresh vegetables and have that every day. Very energizing.

Ditto with fresh ground flax seed (1 tblsp) with a little marshmallow root powder (1 tsp) added and apple pectin (1/4 tsp.) ground in a small dedicated coffee or seed grinder. Mix in a large glass of water. Gives you much needed Omega 3's, helps with elimination and soothes/heals the intestines.

Bea

Roda Rising Star

Have you had your thyroid, iron and ferritin checked?

txplowgirl Enthusiast

Have you had your thyroid, iron and ferritin checked?

Hi Roda, Yes, I have, according to the Dr, my Iron is ok. He told me I was no longer anemic after nearly 38 years. Ferritin levels are ok too. Thyroid is normal also. But I do know that he just checked the TSH not the T3 or 4 because when I asked, he told me I didn't need those. Kind of irritated me but he refused to run them. Thyroid problems run in the family. So, i'm kind of suspicious there. My mom has been on different thyroid meds for nearly 40 years now. I've been half tempted to ask her for few pills and cut them down a little and try them.

Hi Yolo,

Parasites are another thing to check into. Have you?? No, I haven't, I just can't quite grasp the thought of parasites in my body. :( But, I will look into the olive and neem leaves. As for flax seed, it causes me to bloat and get really gassy, so that is really out. B) I'll also give the L-glutamine a try see if that helps any.

Thank you both for your help.

Roda Rising Star
Have you had your thyroid, iron and ferritin checked?

Hi Roda, Yes, I have, according to the Dr, my Iron is ok. He told me I was no longer anemic after nearly 38 years. Ferritin levels are ok too. Thyroid is normal also. But I do know that he just checked the TSH not the T3 or 4 because when I asked, he told me I didn't need those. Kind of irritated me but he refused to run them. Thyroid problems run in the family. So, i'm kind of suspicious there. My mom has been on different thyroid meds for nearly 40 years now. I've been half tempted to ask her for few pills and cut them down a little and try them.

Your doctor was wrong in telling you that you don't need the other tests. For a full thyroid work up you should have a TSH, Free T3, Free T4 and thyroid antibodies. My endocrinologist and I have found that I function the best with a slightly elevated Free T3 and Free T4 in the upper normal range. It does keep my TSH on the low normal side. I supplement with levothyroxine(T4) and liothyronine(T3). This combo works well for me.

wschmucks Contributor

Diddo on the Thyroid. Go back and insist (tell him you know he doesnt think it would be necessary, but you really need to do it, just to east your mind). My TSH has always been very normal, but if you test my Free T3-- its low, so I am hypo. If you dont test the Free T3 my results look perfectly normal...like every Dr told me for years. I would google: "stop the thyroid madness", its a good source for making sure you get an accurate diagnosis. American Drs have been screwing this up for years.

Yolo is right about the parasites and olive leaf. It seems with Chronic fatigue there are multiple problems, usually: hormones, immune system, viruses/ parasites and nutrition. I would do a few rounds of Parashield (herbal supplement to help kill parasites), add the immune boosters and check out your thyroid and sex hormones to make sure everything is where its suppose to be. Dont push yourself too much when youre tired, but try to get in some walking and such. Good luck, i hope you feel better soon.

Billygean Apprentice

Time... it took years for me, but I got there


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



Celiac.com Sponsor (A8-M):



txplowgirl Enthusiast

Thank you guys for your support, really means alot to me.

Roda, I have a question, Can you find levothyroxine and liothyronine at a health store or are those prescription meds? I've never asked my mom what she takes, she just refers to them as her thyroid meds. I guess I need to ask don't I. ;)

Jean'sBrainonGluten Newbie

They are prescription meds and the dose needs to be verified by repeat thyroid blood tests.

Roda Rising Star
Thank you guys for your support, really means alot to me.

Roda, I have a question, Can you find levothyroxine and liothyronine at a health store or are those prescription meds? I've never asked my mom what she takes, she just refers to them as her thyroid meds. I guess I need to ask don't I. ;)

Both of those medicications are Rx meds. I see my endocrinologist every 4 months with follow up blood work. Levothyroxine is generic synthroid. Liothyronine is generic cytomel. There are other rx thyroid medications out there but these are the only two I have taken. Alot of people just take a t4 drug like synthroid. Others like me take a combo of t4 and t3 separately. There is a rx medicine called Armour that is a t4/t3 combination pill. Some people swear by it, but my doctor likes the two separate pills because she feels it is easier to adjust the t3 dosage better. T3 is much more potent than t4 and it's effect is days not weeks so if you were to get too much/little, dose can be adjusted pretty easily. Just ask for the full pannel and if something looks "off" then find a good endocrinologist. Alot of doctors are still hesitant to prescribe t3. I know my regular doctors I see alot of the time don't even know what it is and I know that the endocrinologist I see does not have all her patients on it. That said, I do well on it, but as with anything I'm sure it is not necessary for everyone. A good endocrinologist will tailor your meds according to your needs. My doctor's reasoning for putting me on it was despite the t4 supplementation my Free T3 labs test was still low and I was symptomatic that was even with a normal TSH!

lcarter Contributor

If you are finding the doctor you go to is frequently refusing to run tests you feel are necessary or not listening to you fully, it might be a good idea to change [primary care] doctors. It is a little known fact that doctors are rewarded by insurance companies for not ordering too many labs or other procedures for their patients. Some doctors are more influenced by this than others, which can cause a conflict of interests as far as you are concerned. Or, it could be that your doctor is not as up-to-date as he/she could be in a particular area. Also, in many parts of the US, specialists will not see you without a primary care doctor's referral. So, if your doctor refuses to refer you..that is another occasion which should ring the alarm that it might be time to seek out a new primary care doctor. For whatever reason, if you feel you are not getting what you are paying for...ask and look around... there are lots of other choices out there. Request a doctor recommendation from the local celiac and/or thyroid group in your area for someone knowledgeable and sympathetic.

wschmucks Contributor

I actually just found a clinic started by one of Dr Oz's colleagues, who personally battled chronic fatigue syndrome to the point of being homeless. Its the Fibromyalgia and Fatigue Clinic (u can google it)-- there are about 10 nationwide. Im going to check it out cause ive been battling this for the past few years and have been bed ridden for 4 months. Might be worth looking into.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,945
    • Most Online (within 30 mins)
      7,748

    Miyasato
    Newest Member
    Miyasato
    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.