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

aprilh Apprentice
Hi April, how are the chiggers??

Hi Julie,

The Chigger bites are much better. I stripped my bed and had to wash EVERYTHING. I was worried that we set all our bags from being out of town on the bed and may have brought some in. They are so tiny you can see them. My little boy had about 15 bites!

Thanks for asking!


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



Celiac.com Sponsor (A8-M):



  • Replies 33.4k
  • Created
  • Last Reply
confusedks Enthusiast
I'll be hoping for the best Kassandra. If you have to go in maybe she'll surprise you and not bother you about the lyme.

Thank you! I hope it's okay too.

Oh no Kassandra! I hope Dr H calls you back in time. If not and you have to go just stand your ground, don't let them intimidate you, and just deal with the gyn issue you are there for.

But like Andrea said, maybe they won't make a big deal about it.

I REALLY hope Dr H calls back too! I've been taking my cell phone everywhere! :lol::):P

Kassandra I wish you could go see the gyno i saw a few weeks ago, she was the best! first real doctor who's ever actually LISTENED.

Well the good thing (or bad thing, lol) is that my uncle is really good friends with her, and he asked her if she's "Lyme friendly" and she said "Oh yea, I know all about it." So, we'll see. I hope it works out for the best. :)

mftnchn Explorer

Carla, just found out the Dr. E does have Enula and can test me for it with ART; not sure if she tested me last time for it, she did test some Nutrimedix stuff and I don't think anything came up as good for me.

Everyone, I am really feeling better. Yay for Vitamin D (and nattokinase, that maybe is helping too)!

Sherry

AndreaB Contributor
Everyone, I am really feeling better. Yay for Vitamin D (and nattokinase, that maybe is helping too)!

Yay!!!! :D :D :D

miamia Rookie

Hey all-

I finally caught up. There is too much to comment on an dI am really out of it. I have been ahving a rough time lately thats why I have not been posting much. M body is not happy. I have been being pretty abd with diet choices - its just that everything seems to be sitting bad so I feel like why not eat the wrong things but I know I am just making matters worse. I am going to try to be more disciplined.

I am in a bit of a waiting period becasue my doctors have to consult with eachother and one of them is away for the week. So hopefully they will talk at the begining of next week and I will know what my next step is . All I know is is I can not live the way I have been . Things are just so bad right now.

Sorry I missed out on the festivities of our 2000 page- very exciting!!!

I hope everyone is doing ok. I love you guys and I am going to try to start posting more.

Miamia

aprilh Apprentice
Carla, just found out the Dr. E does have Enula and can test me for it with ART; not sure if she tested me last time for it, she did test some Nutrimedix stuff and I don't think anything came up as good for me.

Everyone, I am really feeling better. Yay for Vitamin D (and nattokinase, that maybe is helping too)!

Sherry

That's great! What brand vit D are you taking?

confused Community Regular

yayyy sherry. Im glad you are feeling better.

I dont have much to say, but I have been reading along lol. Im still feeling pretty good since themold removal of the house Im just staying busy landscaping and painting my kitchen and all the kids activities. I know last year I could hardly force myself out of the house to even watch the kids play outside. Now on most days I am running circles around the kids and hubby lol.

paula


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



Celiac.com Sponsor (A8-M):



AndreaB Contributor
I am in a bit of a waiting period becasue my doctors have to consult with eachother and one of them is away for the week. So hopefully they will talk at the begining of next week and I will know what my next step is . All I know is is I can not live the way I have been . Things are just so bad right now.

Hope they can meet first thing of the new week.

Hugs Mia! :wub:

Paula,

Glad that removing the mold has made such a big difference in how you feel! :D

Nanjkay Apprentice
Here is the big list of symptoms:

Symptoms of Lyme Disease

The Tick Bite (fewer than 50% recall a tick bite or get/see the rash)

Rash at site of bite

Rashes on other parts of your body

Rash basically circular and spreading out (or generalized)

Raised rash, disappearing and recurring

Head, Face, Neck

Unexplained hair loss

Headache, mild or severe, Seizures

Pressure in Head, White Matter Lesions in Head (MRI)

Twitching of facial or other muscles

Facial paralysis (Bell's Palsy)

Tingling of nose, (tip of) tongue, cheek or facial flushing

Stiff or painful neck

Jaw pain or stiffness

Dental problems (unexplained)

Sore throat, clearing throat a lot, phlegm ( flem ), hoarseness, runny nose

Eyes/Vision

Double or blurry vision

Increased floating spots

Pain in eyes, or swelling around eyes

Oversensitivity to light

Flashing lights/Peripheral waves/phantom images in corner of eyes

Ears/Hearing

Decreased hearing in one or both ears, plugged ears

Buzzing in ears

Pain in ears, oversensitivity to sounds

Ringing in one or both ears

Digestive and Excretory Systems

Diarrhea

Constipation

Irritable bladder (trouble starting, stopping) or Interstitial cystitis

Upset stomach (nausea or pain) or GERD (gastroesophageal reflux disease)

Musculoskeletal System

Bone pain, joint pain or swelling, carpal tunnel syndrome

Stiffness of joints, back, neck, tennis elbow

Muscle pain or cramps, (Fibromyalgia)

Respiratory and Circulatory Systems

Shortness of breath, can't get full/satisfying breath, cough

Chest pain or rib soreness

Night sweats or unexplained chills

Heart palpitations or extra beats

Endocarditis, Heart blockage

Neurologic System

Tremors or unexplained shaking

Burning or stabbing sensations in the body

Fatigue, Chronic Fatigue Syndrome, Weakness, peripheral neuropathy or partial paralysis

Pressure in the head

Numbness in body, tingling, pinpricks

Poor balance, dizziness, difficulty walking

Increased motion sickness

Lightheadedness, wooziness

Psychological well-being

Mood swings, irritability, bi-polar disorder

Unusual depression

Disorientation (getting or feeling lost)

Feeling as if you are losing your mind

Over-emotional reactions, crying easily

Too much sleep, or insomnia

Difficulty falling or staying asleep

Narcolepsy, sleep apnea

Panic attacks, anxiety

Mental Capability

Memory loss (short or long term)

Confusion, difficulty in thinking

Difficulty with concentration or reading

Going to the wrong place

Speech difficulty (slurred or slow)

Stammering speech

Forgetting how to perform simple tasks

Reproduction and Sexuality

Loss of sex drive

Sexual dysfunction

Unexplained menstral pain, irregularity

Unexplained breast pain, discharge

Testicular or pelvic pain

General Well-being

Unexplained weight gain, loss

Extreme fatigue

Swollen glands/lymph nodes

Unexplained fevers (high or low grade)

Continual infections (sinus, kidney, eye, etc.)

Symptoms seem to change, come and go

Pain migrates (moves) to different body parts

Early on, experienced a "flu-like" illness, after which you have not since felt well.

Low body temperature

Allergies/Chemical sensitivities

Increased effect from alcohol and possible worse hangover

Donna-

I counted. I have 40 of these symptoms. I made an appointment with the LLMD who Carla recommended. He can't see me until the very end of August. I will try to to call occasionally for cancellations.

Thanks again for the help.

Nancy

CarlaB Enthusiast

Nancy, you might get in sooner with a PA. They are very good, and you still get to see the doc for about 30 min. of your first appt. When you work through a PA, you see/talk with them monthly and see the doc several times per year.

Of course, Aug. will be here before you know it. :)

aprilh Apprentice

Nancy,

that is great that you are looking into that.

EVERYONE!

I am going with my friend to take her son to an infectious disease specialist on Monday.

I posted about him before because I think he should be tested for lyme. He is 4 and been sick since birth. Been hospitalized 4 times, had ear tubes twice, tonsils out at age 3, constant immune system issues, allergic to everything under the sun, wierd hives and rashes sometimes, now he throws up every week for no reason - thats the short version. The GI doc and pediatrician don't know what else to check him for so they want him to go to this infectious disease specialist.

He has had an endoscopy to check for celiac - nothing.....many, many other tests.

She wants me to go so I can help ask questions and take notes for her.

I need help thinking of questions and testing that we might need the dr to look into. Anyone have any ideas????

AndreaB Contributor

Nancy,

I'm so glad you are seeing a LLMD! :)

April,

I don't know of questions, but I'm sure glad she's taking her son in for testing and that will be able to go with her. :)

Rachel--24 Collaborator

April,

Infectious Disease Specialists unfortunately are notorious for being very unhelpful (to put it nicely)....especially when it comes to Lyme Disease.

My worst experience EVER was with the IDS...hopefully you will have better luck but if he dismisses Lyme dont be too surprised and dont give up!

Let us know how it goes. There are a few tests that might be useful (in addition to Lyme testing) but I dont think it would be anything the IDS would be willing to sign off on.

I'm thinking it would be good to check for gut issues....yeast/bacteria. There are a couple good tests for this. My IDS didnt even believe in yeast overgrowth.....we had a big arguement about it and I was told that any positive results I'd had from diet changes was a placebo effect. :rolleyes:

This narrowminded type of thinking is common with IDS's but I think things are changing because of yeast being one of the more common problems found in autism.

dlp252 Apprentice
I counted. I have 40 of these symptoms. I made an appointment with the LLMD who Carla recommended. He can't see me until the very end of August. I will try to to call occasionally for cancellations.

Thanks again for the help.

You're welcome! I'm so happy you are going to see him! August really isn't all that far away, lol!

I need help thinking of questions and testing that we might need the dr to look into. Anyone have any ideas????

Yeah, what Rachel said...I'm hoping this one will be more up on things.

aprilh Apprentice
April,

Infectious Disease Specialists unfortunately are notorious for being very unhelpful (to put it nicely)....especially when it comes to Lyme Disease.

My worst experience EVER was with the IDS...hopefully you will have better luck but if he dismisses Lyme dont be too surprised and dont give up!

Let us know how it goes. There are a few tests that might be useful (in addition to Lyme testing) but I dont think it would be anything the IDS would be willing to sign off on.

I'm thinking it would be good to check for gut issues....yeast/bacteria. There are a couple good tests for this. My IDS didnt even believe in yeast overgrowth.....we had a big arguement about it and I was told that any positive results I'd had from diet changes was a placebo effect. :rolleyes:

This narrowminded type of thinking is common with IDS's but I think things are changing because of yeast being one of the more common problems found in autism.

I was afraid of this. If it were me, I would take him straight to the LLMD or something similar.

I am going to definately request lyme testing, but I am afraid she will not use the Igenex labs.

Thanks!

April

Green12 Enthusiast

April, glad the chiggers are better. Good luck with this IDS Dr, I hope he has an open mind and that it is a positive experience. I don't have anything to add about what to ask, I would think infections and yeast like Rachel said. Immunization complications? Not sure if an IDS deals with that.

Mia, (((HUGS)))

Sherry and Paula, glad you guys are feeling better.

Kassandra, that's good new the Gyn knows about lyme if you end up having to go to her.

Nancy, YAY, glad you made an appt. I agree that Aug will be here before you know it.

nora-n Rookie

I have posted about autism and vitamin D recently and the link to the front page for the vitamin D council is Open Original Shared Link and if you scroll down a little bit there is a link to the autism and vitamin D.

D increases Glutathione levels in short.

I wish someone started a blog just to keep the interesting links from this thread for reference. Some people on the thyroid forums have a personal blog for keeping their links. (congratulation with the 2000 pages, and with all the progress people have made)

nora

confusedks Enthusiast

Update on me: I had an "inner" pelvic ultrasound and guess what?! I am FULL of cysts. :( My ovaries are "textbook" for PCOS. The Dr didn't even ask me about Lyme, etc. and she was SO so sweet. She said that this is extrememly urgent.

She is sending me for a full evaluation with an endocrinologist. We are trying to get an emergency appt. next week. Unfortunately we have to have tests run before we stop the bleeding. All the endo's I have been reffered to are SO full! But I'm trying to use my connections. ;)

Basically, every time I have gotten my period, another cyst has formed in each ovary. Usually the ovaries make follicles and they're released and that's what causes your period, but mine don't know how to release. They need progesterone to do that, and I don't have any.

I'm trying to not stress, but she said that fertility will be a problem. :( What we are going to try to do after the endo evaluation is "pop" the cysts with really strong hormones. She is thinking about what she wants to put me on, and will let me know.

The endo is going to run "lots" of tests. Glucose tests, hormone tests, possible MRI of my brain. So all the testing will take a while, so we're waiting to find out if I can get in on Monday on an emergency basis and they can run all the tests in a day or two, then we'll be able to stop the bleeding.

But if I can't get in, we'll have to make an appt for about a month away from now, so we can stop the bleeding and then I'd go off the hormones and they will then run tests.

I want to get in right away, but the Dr said it will be a couple weeks worth of testing, so we might not be able to do that.

Ughhhhhhhh, so much to digest. Not to mention we weren't going to see the OB/GYN until Tuesday but the bleeding was so out of control they told us to get there immediately.

Quite a whirlwind day. :rolleyes:

AndreaB Contributor

Boy that sounds confusing Kassandra. :huh:

Hoping you can get seen real soon....

CarlaB Enthusiast

Sorry Kassandra. :( Keep us posted.

How much of a problem did they think fertility would be?

dlp252 Apprentice

Oh Kassandra, what a day!!!! Wow!

confusedks Enthusiast
Sorry Kassandra. :( Keep us posted.

How much of a problem did they think fertility would be?

She said that if I tried to get pregnant soon, it would never happen. We have to see if we can get all the cysts to "pop" so there is room in my ovaries for pregnancy. She kept using the words "severe" and "not good" and "bad case of PCOS." :( So I don't really know.

She is "very" concerned about fertility. :( Through all of this health stuff, I have hung on to the fact that one day I will have kids...that is what I have lived for. So this was very upsetting to me.

Over the next 3-6 months they will monitor me closely, and I will have to start BCP...but it has to be a really high dose, so we can hopefully get the cysts to stop forming.

The biggest concern is that my ovaries will get too full of cysts and they won't be able to take it anymore.

Oh Kassandra, what a day!!!! Wow!

Yes, a LONG day! LOL! And we're still trying to fight the clock to get an appt with an endocrinologist.

Rachel--24 Collaborator
Quite a whirlwind day. :rolleyes:

Kassandra...sorry you're having to deal with this now on top of everything but hopefully this will sort out the bleeding problems and hopefully they can get things figured out so that in the future you wont have the fertility problem.

Nanjkay Apprentice
Nancy,

that is great that you are looking into that.

EVERYONE!

I am going with my friend to take her son to an infectious disease specialist on Monday.

I posted about him before because I think he should be tested for lyme. He is 4 and been sick since birth. Been hospitalized 4 times, had ear tubes twice, tonsils out at age 3, constant immune system issues, allergic to everything under the sun, wierd hives and rashes sometimes, now he throws up every week for no reason - thats the short version. The GI doc and pediatrician don't know what else to check him for so they want him to go to this infectious disease specialist.

He has had an endoscopy to check for celiac - nothing.....many, many other tests.

She wants me to go so I can help ask questions and take notes for her.

I need help thinking of questions and testing that we might need the dr to look into. Anyone have any ideas????

Hi April-

Can't think of any questions but I thought of a story. My best friend's daughter Sarah has also been sick since birth. Severe allergies to everything also. About a year ago, she passed the 'wheat" challenge, she put Sarah on it, which means gluten. Six months later she was constipated, and reversed her potty training. Anyway, I asked my friend if Sarah was on ABX as a baby. She said she was at 3 days old because of her upper respiratory infection. She had to go on them or she would have died. Anyway, without any testing Sarah got off gluten. She has gained weight, she's gaining weight, her hair is thicker, the dark circles under her eyes are gone. To quote my friend, she told me today "By the way, Sarah is pooping like a champ!". She has only been off of gluten for 3 months max.

Anyway- when there are allergies like that, I believe the gluten has to come out of the diet, at least until the stomach can heal up a bit.

nancy

mftnchn Explorer
That's great! What brand vit D are you taking?

Vital Nutrients. I had ART testing on several samples, this is the only one that worked.

Sherry

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,556
    • Most Online (within 30 mins)
      7,748

    Rachel Wilson
    Newest Member
    Rachel Wilson
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
    • Scott Adams
      Navigating medication safety with Celiac disease can be incredibly stressful, especially when dealing with asthma and severe allergies on top of it. While I don't have personal experience with the HealthA2Z brand of cetirizine, your caution is absolutely warranted. The inactive ingredients in pills, known as excipients, are often where gluten can be hidden, and since the FDA does not require gluten-free labeling for prescription or over-the-counter drugs, the manufacturer's word is essential. The fact that you cannot get a clear answer from Allegiant Health is a significant red flag; a company that is confident its product is gluten-free will typically have a customer service protocol to answer that exact question. In situations like this, the safest course of action is to consider this product "guilty until proven innocent" and avoid it. A better alternative would be to ask your pharmacist or doctor to help you identify a major national brand of cetirizine (like Zyrtec) whose manufacturer has a verified, publicly stated gluten-free policy for that specific medication. It's not worth the risk to your health when reliable, verifiable options are almost certainly available to you. You can search this site for USA prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      What you're describing is indeed familiar to many in the Celiac community, especially in the early stages of healing. When the intestinal villi are damaged from Celiac disease, they struggle to properly digest and absorb fats, a condition known as bile acid malabsorption. This can cause exactly the kind of cramping and spasms you're seeing, as undigested fats can irritate the sensitive gut lining. It is highly plausible that her reactions to dairy and eggs are linked to their higher fat content rather than the proteins, especially since she tolerates lean chicken breast. The great news is that for many, this does improve with time. As her gut continues to heal on a strict gluten-free diet, her ability to produce the necessary enzymes and bile to break down fats should gradually return, allowing her to slowly tolerate a wider variety of foods. It's a slow process of healing, but your careful approach of focusing on low-fat, nutrient-dense foods like seeds and avocado is providing her system the best possible environment to recover. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: Thank you for sharing your story—it's a valuable insight for other parents navigating similar challenges.
    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
×
×
  • 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.