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Omg...i Might Be On To Something


Rachel--24

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happygirl Collaborator

I would just like to add that I still don't believe that Susie is 45. I just don't buy it!!!!!!!!!!!


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CarlaB Enthusiast

Okay, I'm going to try to remember all the questions, but if I forget, I'll only be able to check the last ten posts while I'm posting!

Charlie, I've checked all the meds I've taken before I took them for their gluten-free status, but I forgot to for the minocycline. I'm taking it now. I don't worry about the other stuff, but if you're really concerned, you could go to a compounding pharmacy.

Susan, yeah, Laura and I seem to herx about the same time. I don't know if we'll continue that way, but mine are every 24 days.

And, you know, I have receding gums, too. I don't know why ... I follow all the "rules" of taking care of my teeth. Adams' are perfect, but my gums recede. Dentists always tell me I brush too hard with too hard of a toothbrush ... but I don't. When I get the braces off, I want to get them fixed ... don't know how, but I'm going to talk to a cosmetic dentist. After the braces, I want them to look GREAT! :D

Bev -- WOW! :o Now I wonder what mine was ... I'll need to put it on my list of questions for the doctor.

dlp252 Apprentice

Charlie - I don't take any prescriptions at the moment except for the ocassional Zyrtec for allergy symptoms, so I haven't had to worry about fillers and such.

I know Rachel was having some of her stuff done at a compounding pharmacy...I think her thyroid stuff, but I'm not sure she's on any other prescription stuff either yet.

I buy most of my supplements at Whole Foods or my doctors' offices, so those are pretty allergen free.

Lately I've been taking the capsules apart too...figure it's just one less burden on my body. :P

AndreaB Contributor

Donna,

Just noticed your new avatar and I'm sure you'll be telling us about it when you get back over here. :P

Another cute one btw.

AndreaB Contributor

Susan,

I love all the photos of you and the girls (or girl :P )

Have to agree with Laura.......you don't look 45!

jerseyangel Proficient
Donna,

Just noticed your new avatar and I'm sure you'll be telling us about it when you get back over here. :P

Another cute one btw.

Susan,

I love all the photos of you and the girls (or girl :P )

Have to agree with Laura.......you don't look 45!

Double ditto :lol:

dlp252 Apprentice
Donna,

Just noticed your new avatar and I'm sure you'll be telling us about it when you get back over here. :P

Another cute one btw.

Not sure on the details of this one...like why I would be so dressed up. These were the sons of one of my mom's good friends. I think we lived very close by and I used to play with these guys all the time. Can't even remember their names, lol. My mom liked to dress me up, but generally only dresses when we went visiting, lol. I'll have to ask her more about this. :lol:

You can't make it out, but I'm holding a cat... not my cat either I don't think, lol.


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AndreaB Contributor
You can't make it out, but I'm holding a cat... not my cat either I don't think, lol.

I wouldn't have known if you hadn't told me. I think I can make it out now that I know what it is. :P

DingoGirl Enthusiast
I would just like to add that I still don't believe that Susie is 45. I just don't buy it!!!!!!!!!!!

bless you, dear girl. But, if you saw me up close :ph34r: you could see it - fine lines and such.

A few weeks ago, I was out with my young and gorgeous nieces at a pub. The CUTEST "boy" (man child) kept staring, and I thought he was interested in my nieces. So, finally he comes over, says, can I sit here? my friends are being mean to me. And guess who he was interested in? :o that's right. So, he is adorable, and he sees my jewelry and says, "are you a Christian? so am I? :wub: (my love for him deepens), and we are flirting, and he tells me he is 30 (dang). And he thinks I am 36. HAH!! So I let him think that for the next half hour, and then made the MOST EGREGIOUS ERROR of telling him my real age. :blink: And within five minutes, he left our table. HARRUMPH! He revisited again later, but he had lost that lovin' feeling.

AND THAT IS THE LAST TIME I REVEAL MY AGE TO ANYONE!!!!!

:angry::lol:

Okay, now, WHY do I have energy today? It was like three weeks of pure heinosity, and today - - I am cleaning - no choice - like a tornado, my niece has been here for a couple of days, and her boyfriend is coming to stay also either today or tomorrow......and I am furiously preparing. Cleaning out closets, drawers, sterilizing everything - it smells fabulous in here. WHERE did this energy come from? Maybe all of the sleep? I don't know. But I will tell you something, I feel almost elated at how much I"m getting done - after letting these things go for so long - and how organized everything is becoming.

You know something, I think part of the depression is about feeling so overwhelmed by my house and environment at times. Things pile up when you're exhausted, and you get more and more overwhelmed, and then more depressed, and then it all just seems impossible to do, so you let it go....and then it gets WORSE - and then it's like climbing Everest without supplemental oxygen, so you just bail and go back to basecamp :lol: .......it's a vicious cycle to which I"m sure we can all relate!

BTW niece's boyfriend John is quite strong (a very ardent climber) and handy - he's goign to be helping me with some stuff here. :) I am ecstatic!

okay......back to work.

jerseyangel Proficient

I see the cat--very cute :D

AndreaB Contributor
Okay, now, WHY do I have energy today?

But I will tell you something, I feel almost elated at how much I"m getting done - after letting these things go for so long - and how organized everything is becoming.

You know something, I think part of the depression is about feeling so overwhelmed by my house and environment at times. Things pile up when you're exhausted, and you get more and more overwhelmed, and then more depressed, and then it all just seems impossible to do, so you let it go....and then it gets WORSE - and then it's like climbing Everest without supplemental oxygen, so you just bail and go back to basecamp :lol: .......it's a vicious cycle to which I"m sure we can all relate!

BTW niece's boyfriend John is quite strong (a very ardent climber) and handy - he's goign to be helping me with some stuff here. :) I am ecstatic!

okay......back to work.

I can definately relate.

School......we haven't finished and Seth is down for a nap. I don't like doing school during nap time so I guess we'll wait. She can do her paperwork but I've got to go over the book part.

Mtndog Collaborator

Hello loves- gotta make this another quickie as we are having major thunderstorms and the internet keeps going in and out :angry:

Susie- I don't give a rat's patootie.....even if you have fine lines you look 35 and gorgeous. You MAY NOT disagree, you may simply and HENCEFORTH accept all compliments with a thank you :P

So, uhm, I DO have Lyme, right? I mean the C*D* 57 only tests for those killer cells that are impacted by Lyme so I guess I'm a Lymie. It was pretty funny...I was sipping barium while talking to my LLMD's nurse who's a hoot. She was cracking up!

I just want to say thank you ALL (every last one of you) for all the support you have given me. I know I had to step away for a bit and really think about it and listen to my own body and I'm glad i did, but I'm glad to be back.

CarlaB Enthusiast

We're glad to have you back. :rolleyes:

I hope the barium tastes good!

I don't know whether the C D 57 proves Lyme ... seems like a sure thing for you at this point ... it's a clinical diagnosis, and the sickest tend to have negative blood tests ... so your blood tests could be negative and your LLMD might still determine you have it.

Oh, and Susan, we've earned these fine lines and wrinkles! ;)

AndreaB Contributor
I just want to say thank you ALL (every last one of you) for all the support you have given me. I know I had to step away for a bit and really think about it and listen to my own body and I'm glad i did, but I'm glad to be back.

We are glad you're back as well. :D

I think the CD57 is pretty specific for lyme. It's used as an indicator of how the lyme infection is doing. Rachel and Charlie would probably be able to say more about it.......maybe Donna too. :)

Rachel--24 Collaborator

Well....I think I'm locked out of page 1051. :rolleyes:

I read the page but cant recall what I wanted to respond to except Miamia was saying something about rice cakes feeding candida??

I did wanna say that lots of other things you're eating will also feed candida...like those chicken nuggets. If you get a particularly strong reaction to a certain food....like the rice cakes...its more likely you are reacting to something in the food. Yes...it would still feed candida but I doubt thats why you reacted.

Its mostly white starches (i.e. white rice, potatoes) that rapidly turn to sugar. My candida situation is pretty bad but I still ate potatoes, and dont forget the ice cream (with actual cane sugar and milk sugar), plus apples and popcorn. I was feeding the candida plenty but I did not get reactions to these foods because apparantly they were pretty safe as far as molds and chemicals.

However, a single bite of a rice cake and I'm reacting pretty noticeably...half of a rice cake has me pretty messed up for at least 2 days. :angry:

Its like this with alot of foods. The more I ate the ice cream and fed the candida...the more sensitive I became to molds and chemicals. I've come to learn that the reactions are not actually from "feeding" the candida. If candida is consistently causing a problem...its not going to cause dramatic symptoms after one meal or snack. Those reactions are occurring because having the candida means you get alot of sensitivities to various things.

You especially become sensitive to yeast and molds. If you eat something with vinegar...or drink wine (which is loaded with yeast).....you will react quite strongly and most likely feel bad for days.

I dont think the candida got especially happy with the rice cakes...I think its more likely you are sensitive to them.

I'm pretty sure my candida was feeling pretty darn good having 1-2 pints of chocolate ice cream everyday....I dont think my problems with rice and rice cakes comes from the candida consuming sugar. If that was the case I'd have been pretty miserable those 8 months I ate ice cream everyday. :blink:

If you can eat homemade pizza, chicken nuggets and other foods and be ok....then theres something about the rice cakes. If it had to do with feeding candida you would have the same problem with these other foods....because they feed candida as well.

Thats my guess. :)

I dont eat ice cream, popcorn or apples anymore....(yeah..I know....it about time I got smart about this :rolleyes: ) but I still do eat some potatoes and oatmeal...which are very starchy. I also had yams. :ph34r:

Anna told me to never eat the starches like potatoes by themselves...this is when they will rapidly turn to sugar. She said to always eat them with protein...which slows it down and allows less sugar for the yeast. There must be truth in it because if I eat the potato by itself...I get more head "fullness". If I eat it with meat...I barely notice anything after eating. :)

This would not work for me with rice cakes because I'm actually reacting to the rice cake itself....its nothing to do with it turning to sugar. Plus I always ate brown rice cakes...never white.

Rachel--24 Collaborator
I think the CD57 is pretty specific for lyme. It's used as an indicator of how the lyme infection is doing. Rachel and Charlie would probably be able to say more about it.......maybe Donna too. :)

There is no scientific evidence proving that low CD57 can *only* be caused by Lyme. They do not know this for sure. All that is really known is that people with Lyme do tend to have low CD57....which then goes up with treatment.

However....this is not always the case. For some people the CD57 is right on target with how they're feeling....and it stays on target...showing gains when symptoms improve and showing a decline when they are feeling bad.

Other times the numbers dont sem to correlate. They dont know all that can affect the CD57 cells but also those whos numbers dont correlate....may have symptoms which are unrelated to Lyme....most likely co-infections or mercury.

I'm sure if I treated Lyme very aggresively my numbers might increase indicating well being...but I can pretty much guarantee I'd still feel like crap because Lyme isnt the main reason for my symptoms to begin with.

Rachel--24 Collaborator
Rachel - - I can totally identify with this. When I moved in here, into Stepford, two years ago, I think my neighbors were waiting for a mattress or refrigerator to show up on my front lawn. :ph34r:

:lol::lol:

Yeah....my neighbors are probably totally confused by my inconsistency with maintaining the yard. :ph34r:

At times I was out there everyday...meticulously grooming, cutting and making evrything perfect....then I just let it all go. :huh:

Sometimes one of my neighbors will mow my lawn for me.....I'll come home and its been mowed. He probably just doesnt know what to expect from me anymore. :P

He only mows half the lawn though...I have two lawns in the front so one will be neat and tidy (the one on his side) and the other....well...not so neat and tidy. :P

I would just like to add that I still don't believe that Susie is 45. I just don't buy it!!!!!!!!!!!

Yeah....I'm not buying it either!! <_<

I know Rachel was having some of her stuff done at a compounding pharmacy...I think her thyroid stuff, but I'm not sure she's on any other prescription stuff either yet.

My only rx's are my thyroid meds and Nystatin. I dont use the compounding pharmacy anymore....I only did that when I was tring to see if corn was causing all this. Obviously it wasnt corn...so I dont worry about it anymore.

The Nystatin is the same exact stuff whether I get it from the compounding pharmacy or not...only thing is that they put it in capsules and I have to pay $50 instead of $10. :unsure:

My co-pay for compounded stuff is $40 more...so I dont see the point.

Its hard to get the *right* Nystatin from a regular pharmacy...they never get orders for it....have no idea what it is...and I always have to inform the pharmacist on how to get it, how to store it, and how its taken. :blink:

Charlie....if you take Nystatin do not take those little orange tablets and definately do not take suspension (liquid). The suspension has sugar in it...kinda defeats the purpose. :rolleyes:

The tablets arent effective. I use oral powder...one time they tried to give me "topical" powder....like for athletes foot fungal issues :blink: .....the pharmacists arent familiar with the oral powder at all.

Its very bitter tasting but way more effective than the other stuff. It has to be refridgerated. I get the stuff which is actually used for compounding...so its not in capsules yet. I measure it myself. Even my Dr. didnt know I could get it from a regular pharmacy this way. Its safer than Diflucin which is hard on the liver and you need liver testing while on it.

Nystatin can be taken long term and is known to be safe.

You know something, I think part of the depression is about feeling so overwhelmed by my house and environment at times. Things pile up when you're exhausted, and you get more and more overwhelmed, and then more depressed, and then it all just seems impossible to do, so you let it go....and then it gets WORSE

Yup...thats exactly what happens to me..whether its home, work, bills, the yard, etc. I cant allow myself to get overwhelmed in any way or my health declines...along with my mood. :(

My mom helps me out with the bills now since that was one of the most overwhelming things for me.

I hope the barium tastes good!

I loved the stuff I had to drink for my last barium.

I would drink it everyday. :P

CarlaB Enthusiast
if you take Nystatin do not take those little orange tablets

I take the tablets ... why are they ineffective?

dlp252 Apprentice

Fun and games at the clinic today, lol.

So I have my PT/chiro/prolotherapy session today. I give copies of all my tests results to Nancy who gives them to Dr. Carrie. Dr. Carrie looks them over and says, oh good, your lyme test was negative. :lol: So eventually I say, well I DID have past infection show up as positive. In fairness, she only glanced quickly at them and showed them to Dr. Rick. They were both concerned about the mold results though. :(

Then, I'm getting my prolotherapy injections and she's doing my elbow area, and hits a nerve. Shot shooting pain down my entire arm into my fingers. After that my arm went numb and I couldn't open my hand! I could close my fist, but I couldn't open my hand past just barely open and I had no strength in my arm. She walked me back to the PT area and told the guy who would work on me about it and gave him some special instructions. It was quite scarey because I couldn't pick anything up...like my purse, lol. Anyway, while I was getting adjusted my fingers opened up a bit more and after the PT guy worked on me I was able to open and close my hand like normal...my arm just felt weak. It feels pretty normal now though.

I also soaked in a nice hot bathtub with some epsom salts...Had my own little sauna going. :P

AND THAT IS THE LAST TIME I REVEAL MY AGE TO ANYONE!!!!!

Yep, I always feel the need for full disclosure and I'm always sorry afterwards. :P

You know something, I think part of the depression is about feeling so overwhelmed by my house and environment at times. Things pile up when you're exhausted, and you get more and more overwhelmed, and then more depressed, and then it all just seems impossible to do, so you let it go....and then it gets WORSE - and then it's like climbing Everest without supplemental oxygen, so you just bail and go back to basecamp .......it's a vicious cycle to which I"m sure we can all relate!

This is actually very true! I've heard it from a number of sources. It's exactly what's happening to me...the place is so bad here that it's absolutely overwhelming. Basecamp wasn't enough...I've had to go back to the village. :P

So, uhm, I DO have Lyme, right? I mean the C*D* 57 only tests for those killer cells that are impacted by Lyme so I guess I'm a Lymie. It was pretty funny...I was sipping barium while talking to my LLMD's nurse who's a hoot. She was cracking up!

I just want to say thank you ALL (every last one of you) for all the support you have given me. I know I had to step away for a bit and really think about it and listen to my own body and I'm glad i did, but I'm glad to be back.

You're welcome! I don't know if the killer cells are ONLY impacted by lyme, but from what I read, they are more specific to lyme than the other types of cells. I don't think my LLMD would have made a lyme diagnosis based on that alone, but he's using it together with the other test results and my symptoms and my energy level.

We are glad you're back as well.

Ditto!

Its like this with alot of foods. The more I ate the ice cream and fed the candida...the more sensitive I became to molds and chemicals. I've come to learn that the reactions are not actually from "feeding" the candida. If candida is consistently causing a problem...its not going to cause dramatic symptoms after one meal or snack. Those reactions are occurring because having the candida means you get alot of sensitivities to various things.

Oh for pete's sake, lol. It's like my eyes have just been opened... :lol: I'm thinking my candida isn't a big problem because I've had no die off, cuz Scott said it didn't look bad in ART and because I haven't had any big reactions. DUH, Donna, what the heck are you thinking. :P This is exactly what is happening to me. Where's the head banging icon when you need it! :P

Rachel--24 Collaborator
I take the tablets ... why are they ineffective?

I'm pretty sure they're mostly for oral candida...and not infection of the GI tract. I had first read about the oral powder (and instructions on how to take it) in one of my Candida books "The Yeast Syndrome). The book recommends only taking the oral powder as it is far more effective.

I asked my Kaiser Dr. for Nystatin and ended up getting the little orange tablets. The ones you suck on right?? I got those and they didnt do anything. My Dr. wasnt familiar with Nystatin...let alone the powder stuff...it wasnt listed in his little rx book. :rolleyes:

I showed him what it said in my candida book and eventually he was able to figure it out and get me the script. It works....I used it while I was doing my anti-candida stuff 2 years ago. That guy Groovy2 from LN would often post on the candida board about using only oral powder and about how strong it was in comparison. Thats been my experience with it as well.

He was the one that mentioned that it must be kept cold or it will lose some of its strength. It says it right on the bottle but my pharmacy had never kept it refridgerated. :angry:

Now I always make sure to let the pharmacist know how it should be stored. In the past there have been times I forgot to put it back in the fridge and yeah....I could tell it wasnt as strong anymore. I've ruined many bottles this way. :(

Most people who are familiar with Nystatin would definately tell you to use the oral powder for GI infection. My LLMD prescribed the oral stuff...but he was under the impression it only came from compounding pharmacies....which isnt the case....you can get it....but apparantly not many people do cuz the pharmacies are pretty dumb about it. :rolleyes:

dlp252 Apprentice

My ENT (now retired) prescribed Nystatin for me during the midst of my sinus infection cycle thing and I think I had white tablets...I didn't suck on them. I wonder if they would still work the same though. Good to know that when Dr. S prescribes (and he did say he might down the line) antifungals that it will be the good stuff.

CarlaB Enthusiast
The ones you suck on right??

No, you swallow these.

AndreaB Contributor

Boy Donna! You're appointment sounded scary. I would have been scared too.

I had an incident when Talitha was a baby (I think it was her and not Micah) where I couldn't move my hands, couldn't make a fist. Scared me to death. I think it lasted around 20 minutes. I called the doctor but they were no help. :angry:

Rachel--24 Collaborator
No, you swallow these.

Hmmm...

I only know of 3 kinds of Nystatin.

Pure Nystatin Oral powder....mix with water.

Oral liquid suspension...tastes sweet cuz of sugar.

Tablets which you suck on.

Are you sure you're directions said to swallow them?? I never heard of a nystatin pill that you swallow....will have to look that one up.

I was trying to find out more about the powder stuff and found this post from that guy who emailed me....telling me I may have Lyme. I had to laugh. :lol:

When I had candida at its worst-

every thing would bother me--

smells-perfume gasoline- cleaning

products--

Things I would eat--any thing with

yeast or mold in it--

You have to do the No carb diet

--If you cheat you will pay- I did-

Nystatin powder by far worked the

best the best for me--Must be

kept cold.

Take probiotics and yogert

Go to Yeast Connection .org

it is a good site for candida

--Also notice how many

of the people on this site sound

like they have Lyme.

Candida was one of my early lyme

symptoms

Yup...this post was written in June 2005.....thats when I was on the Yeast Connection.....and thats also when he emailed me. :lol:

I should let him know he was right. :P

AndreaB Contributor
I should let him know he was right. :P

Wouldn't be a bad idea. :)

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      @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.  
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