Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Very Sick Four One Year


marielynn22

Recommended Posts

marielynn22 Newbie

Hi my name is marie, i am 22! one year ago i got really really sick..started with diahrea and gas/ bloating...but within a month or two i got really sick, splitting neck/head pain.., numb hands, wierd moodiness, and confusion, also dizzyness, lighheadness, my vision dims like a car light and then back up again, i have been constipated for months, i have twitches all over my body sometimes the last for days and then come back a week later...I guess what im asking is does this sound like a case of lymes to you, i saw the lymes specialist in bc..and he said yes..but my doctor says no, and i cant afford to go on antibiotics unless its going to help because i am already very weak and sick..i basically ache all over, and my heart throbs threw my body, and i am very bad in hot weather. I saw that you have lymes, and was wondering if you have any advice, i have been tested and it was negative but where i am from the specialist said that is it less than 25% accurate here.

well thanks for hearing me out!

marie


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



Celiac.com Sponsor (A8-M):



dlp252 Apprentice

Your symptoms do fit with lyme, but also many other conditions could cause it. Did the lyme specialist do the testing? If not, it probably wasn't very accurate because they probably didn't use the best lab for the tests...the tests are not that accurate anyway, but even less so by labs that do not specialize in lyme.

Your regular doctor most likely will NEVER say you have lyme...they are very reluctant to diagnose it.

Do you still see the lyme specialist? There are some supplements and herbs that he can try first...but it's really a good idea to do that with some supervision.

I'm being tested now for lyme, metals toxicity, mold exposure and a bunch of other stuff...should get my results next week.

Rachel--24 Collaborator

It does sound like Lyme....and you could also have Celiac as well (if you are genetically susceptible).

Alot of Dr.'s know even less about Lyme than they know about Celiac...I would definately see a Dr. who specializes in Lyme and not a regular Dr.....and not an infectious disease specialist (surprisingly they know nothing about Lyme).

Its true that the tests are not sensitive at all so you could very well have Lyme as the tests are often false negative. See a knowledgeable Dr. who uses Igenix for Lyme testing. Its the best lab....with the most sensitive tests. Igenix picks up Lyme when most other labs miss it.

Igenix can also be false negative....there is still no test which is 100% accurate but this lab has the MOST reliable testing available at this time.

AndreaB Contributor

Igenex's website is Open Original Shared Link

Also, I'm assuming you're in Canada. You can check out canlyme at Open Original Shared Link I'm not sure if they have a message board or not but they could point you to a LLMD.

From what others have said a good LLMD will test for many things. So many symptoms overlap with other illnesses so it's a good idea to have checked out with someone who will test for different things it could be.

CarlaB Enthusiast

I sent you a PM, please let me know if you don't get it.

marielynn22 Newbie

Hi, thanks so much for the replys. I have seen the ONLY Lymes specialist in BC..but i have to say i wasnt convinced with our meeting. He basically asked me a few questions, and yes i had multiple symptoms matching up, but i also never had a rash..and my sickness started in my stomach. I have been tested for lymes twice. I showed up positive for ricksettia but a very low posistive and even lower the second time. Today i ordered the test kit from IgeneX for lymes so thankyou for that information, i was very surporised they could send it to bc. Does anyone know if it can really affect you mentally, i have been very irritable, but the past two days, i feel very spaced out, and very overwhelmed like im numb in my brain, mentally i feel very confused.

Also i've been off gluten for a week now, does anyone know if you begin to feel better very soon after or does it take months? also can you feel worse at first? im just really confused with the way i feel in my head, such a scary feeling.

thanks

CarlaB Enthusiast

YES! Lyme can affect you mentally! I get such brain fog that it's better described as disorientation and mental confusion. I also get "Lyme rage" where I'll get upset over stupid things that normally don't bother me.

I also get digestive symptoms. gluten-free helps tremendously, but not completely.

I also never had the rash ... 50% of Lyme patients never see a rash.

You can feel worse when you first go gluten-free. I did. It varies on when a person sees improvement after going gluten-free ... some feel better right away, others take some time to see a difference.


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



Celiac.com Sponsor (A8-M):



marielynn22 Newbie

Hey, do any of you with lyme's have troubles in hot weather, i mean i just feel weak beyond belief and exhausted..very grumpy too..i was wondering if this is a symptom of lymes. Im stuck in abit of a rut, because the only lyme specialist in my province is actually in abit of trouble for misdiagnosis i have heard. so other than order the IgeneX tests and wait, i dont know how to follow through with a doctor..Yikes. I am really starting to think its lymes though specially the way i have so many twitches and they keep getting worse and worse and the pain in my neck and head is just insaine...i am worried i will not be able to get better because it has gotten so bad...well thanks for the helP!

dlp252 Apprentice

I'm still waiting for my results, but I also never had the rash...still I have about 47 of the 75 symptoms I've seen associated with lyme.

I often get foggy headed and spacey, and I also have the rage that Carla spoke of...lots of digestive issues too which didn't clear up with a gluten/casein free diet. The gluten/casein DID clear up most of my sinus troubles though, so that was very good. And, if this DOES turn out to be lyme, staying away from those two biggies and suger will help a great deal.

I also have the pain in my neck which never goes away and hasn't been helped by chiropractic, physical therapy or other traditional pain management therapies.

The heat issue...yep, I have trouble in the hot weather. Not so much sun related, but definitely heat related. It definitely makes me feel lethargic and weak.

CarlaB Enthusiast

I get heat exhaustion very easily.

Don't be discouraged, just try to find out where you can get proper treatment. I'm making progress and I went undiagnosed for 35 years. You do need to proceed with finding treatment because some of the neuro symptoms can become a permanent problem. Don't let that scare you, just let it motivate you.

A lot of Lyme docs have to fight to keep their medical license. It's more convenient for the medical profession and insurance companies if chronic Lyme doesn't exist. That's why I have to fly on and airplane to get to my doctor.

  • 2 weeks later...
Clark Bent as Stupor-Man Contributor
Hi, thanks so much for the replys. I have seen the ONLY Lymes specialist in BC..but i have to say i wasnt convinced with our meeting. He basically asked me a few questions, and yes i had multiple symptoms matching up, but i also never had a rash..and my sickness started in my stomach. I have been tested for lymes twice. I showed up positive for ricksettia but a very low posistive and even lower the second time. Today i ordered the test kit from IgeneX for lymes so thankyou for that information, i was very surporised they could send it to bc. Does anyone know if it can really affect you mentally, i have been very irritable, but the past two days, i feel very spaced out, and very overwhelmed like im numb in my brain, mentally i feel very confused.

Also i've been off gluten for a week now, does anyone know if you begin to feel better very soon after or does it take months? also can you feel worse at first? im just really confused with the way i feel in my head, such a scary feeling.

thanks

I never had a rash either, don't even remember getting bit by a tick (aside from 15 years ago when I was a kid)... I was tested for lyme with the standard ELISA screening test in both 2002 and 2006 and both tests came back negative... I tested positive on the IGM WB from Igenex last month and have likely had lyme for years...

lyme can cause a lot of neurological symptoms, which are primarily my symptoms as I don't really have the joint pain/arthritic type symptoms... I've had daily headaches and neck pain/tightness, visual problems (floaters, sensitivity to lights), and the brain fog, confusion symptoms for years, which I feel are all largely tied to lyme...

I also have a lot of trouble with heat in general nowadays... I have a fan at my desk at work on 24-7 and get hot much more easily than nearly everybody else in typical settings... this has become more magnified over the past year or so...

if you can't get an appt with the one specialist to get your blood drawn for the Igenex test, it's possible though unlikely you could do it with a non-lyme specialist doctor if you have one you have a good rapport with... otherwise, I'd try and find the closest LLMD to you and set up an appt with them for the Igenex test...

and don't worry about how you'll recover and whatnot... just focus on what you can control... first off, you might be pinpointing what's going on relatively soon as many people go undiagnosed for much of their lives... I've had headaches every day for 5+ years and have been able to improve a lot of my symptoms even prior to my lyme diagnosis through dieting, supplements, and physical activity... I'm now optimistic that some symptoms that have persisted to a greater extent than others will decrease as I go through my treatment for lyme... you seem to be taking a pro-active approach in figuring out what's going on and that gives you an edge right there...

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      130,383
    • Most Online (within 30 mins)
      7,748

    runfucamg
    Newest Member
    runfucamg
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Mrs Wolfe
      Thank you.  I’ll be sure to look into those. 
    • Katerific
      I was diagnosed with microscopic colitis and celiac a couple of years ago.  The GI doctor prescribed a course of budesonide, which moderately helped until I tapered off.    After a lot of ups and downs over the course of 2 years, I am finally in microscopic colitis remission.  Since I am also diabetic, I was started on metformin and Jardiance.  Metformin by itself helped moderately.  I added Jardiance and I was much better.  I stopped the metformin and relapsed and when I added it back, I regained remission.  I think metformin and Jardiance helped my colitis because they reduce inflammation in the gut.  Metformin is known to favorably modulate the gut microbiome and reduce inflammatory cytokines.  Similarly, emerging evidence supports the anti-inflammatory properties of SGLT2 inhibitors like Jardiance.  Once I was on both, the diarrhea stopped completely, even though nothing else ever worked long-term.  There is a Facebook group that can be very informative and helpful.  Look for "Microscopic Colitis and Lymphocytic Colitis Support Group.  You will find that members of the Facebook group identify other pathways to remission of microscopic colitis.
    • knitty kitty
      Hello, @Mrs Wolfe, I crushed three vertebrae moving a chest of drawers.  I take a combination of Thiamine Vitamin B1, Vitamin B12, and Pyridoxine B6.  Together these vitamins have an analgesic effect.  I think it works better than OTC pain relievers.   I also like  "Takeda ALINAMIN EX Plus Vitamin B1 B6 B12 Health Supplementary from Japan 120 Tablets" .   It's all three vitamins together in one pill.  Works wonderfully!
    • knitty kitty
      It's the Potassium Iodide in the HRT pills that is triggering Dermatitis Herpetiformis and the increased IGG levels.   The thyroid is stimulated by the Potassium Iodide, which stimulates immune cells to make more IGG antibodies.   Thiamine Vitamin B1 helps the thyroid function.  I like Benfotiamine and TTFD Thiamax.  
    • Mettedkny
      @Scott Adams Xiromed is one of the generic manufacturers of Progesterone pills.
×
×
  • Create New...