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Omg...i Might Be On To Something


Rachel--24

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jerseyangel Proficient
for any of you looking for chicken to try, I recommend considering Kosher chicken...

I buy Empire Chicken from Wegman's--it's fabulous! Regular chicken always gives me problems, but this does not. It's lighter in color than the regular brands I see, and the taste is very clean.

Rachel-

thank you so much for the info. I have an appt (I set it up yesturday) for a new doctor who specializes in heavy metal toxicity and he has a partner he works with who specializes in lyme, they will perform any testing I need and I will bring in all my old tests for them to look at. these are the main things that came out of my doctors appt. yesturday. The doctor sounds pretty good I pm'd andrea alittle more detail on him I can do the same for you- Did you get my last Pm I forgot there was something else I wanted to add to it. Iw ill have to do that later.

Miamia--this is so good to hear! I'm excited for you. :)


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Rachel--24 Collaborator

Miamia....This is wonderful news!! I'm glad you are pushing forward...and I'm glad you are not upset with me. :)

I'm very proud of you and I'm looking forward to hearing how things go with the new Dr.'s. Hopefully your Dr. can move the appt. up for you...if not....its still great that you have something set up.

I'm mad at your Dr. too.....but there is something to look forward to now...and I have a good feeling about this. Hopefully once you start seeing the new Dr.'s you will be alot less confused about everything. :)

I look forward to reading your pm....I'd love to hear more about the new appts. you have set up...and yeah...still interested in whatever else you wanna add to the last pm. :)

Mtndog Collaborator

I want to find a kosher butcher! i was just saying that to my hubby the other night- for lots of reasons. The way the animals are treated is more humane and the meat is definitely better quality.

Mia- Sweetie :wub: :wub: :wub: I didn't know you weren't being treated (or should I say treated well?) You poor thing. Glad you have all these appts set up. If I'm at 32 on the celiac disease 57 and you're at 26, you must be feeling pretty bad from the Lyme. HUG! I think once you focus on this you will see results in other areas. You don't want to end up with celiac disease 57 of 0. I can't imagine how bad that would feel!

Jin- It's funny (not funny ha ha but funny ironic) that you actually said Lyme and fatal in the same sentence. I don't think people realize this. I didn't. Until saturday at my BIL's cookout TWO people said to me, "My God, if you've had it for four years you're lucky you didn't die." :ph34r: I'm too stubborn to do that.

But my friend, the MD, said that many Lyme patients commit suicide because doctors don't know what's wrong with them and they think they are doomed to a life of feeling sick. Or in neuro-Lyme they become so depressed that they commit suicide.

I told her that there were times that I thought about it but I was lucky in that I had two things going for me- a gut feeling that something systemic was going on and that I wasn't going to stop until I got an answer (I'm STUBBORN :P )

and that I had a lot of SUPPORT. I didn't go on to explain but you guys were first and foremost in my mind. If I didn't have you guys to laugh, cry, scientificate (new word?) and just generally hang with I seriously think I would have lost it long ago. :wub: :wub: :wub: :wub: :wub: :wub:

dlp252 Apprentice
the 2 brands I've eaten are Aarons and Empire chicken... I seem to react better to these chicken legs than the WF chicken I've eaten... I also prefer the Kosher lamb chops to the Wegmans organic lamb chops, and it's not even close though that probably depends on the butcher/store and where they get it from...

Ha, I didn't know they had kosher chicken! Glad to hear WF has some...I'll ask and maybe try some this week. I miss chicken!!!

I am so glad for this thread, it really encourages me to keep working on my health.

Ditto!!! Gosh, if it weren't for this thread, I would have NEVER found out about my lyme!!! I doubt I would have given serious consideration to metals either...would have spent the rest of my life thinking I had a candida issue only.

Mia, we do love you and are concerned about your health.

thank you so much for the info. I have an appt (I set it up yesturday) for a new doctor who specializes in heavy metal toxicity and he has a partner he works with who specializes in lyme, they will perform any testing I need and I will bring in all my old tests for them to look at. these are the main things that came out of my doctors appt. yesturday. The doctor sounds pretty good I pm'd andrea alittle more detail on him I can do the same for you- Did you get my last Pm I forgot there was something else I wanted to add to it. Iw ill have to do that later.

DITTO!!!!! I have been very worried about you and I'm glad you are moving forward with a new doctor. It took most of us a few tries before we found the right one. There are lots of ways they can treat the lyme...I'm on herbs and supplements now...the antibiotics will probably come later. The candida can be treated simultaneously if necessary.

yes money is an issue but my health is my top priority. I will find a way to pay I just need to figure out the irght treatment. I would give up anything, borrow money, be in debt, anything!!!, if i could be healthy again!!!

I love you guys-- Thank you so much for your support, concern, and pushing me in the right direction.

:wub: I think you can see that we love you back! :) This is how I feel too...I really can't afford the testing, but I've got to do it...I could feel my health really slipping badly in the last year...it just would have gotten worse and worse I think.

dlp252 Apprentice
Jin- It's funny (not funny ha ha but funny ironic) that you actually said Lyme and fatal in the same sentence. I don't think people realize this. I didn't. Until saturday at my BIL's cookout TWO people said to me, "My God, if you've had it for four years you're lucky you didn't die." :ph34r: I'm too stubborn to do that.

But my friend, the MD, said that many Lyme patients commit suicide because doctors don't know what's wrong with them and they think they are doomed to a life of feeling sick. Or in neuro-Lyme they become so depressed that they commit suicide.

I told her that there were times that I thought about it but I was lucky in that I had two things going for me- a gut feeling that something systemic was going on and that I wasn't going to stop until I got an answer (I'm STUBBORN :P )

and that I had a lot of SUPPORT. I didn't go on to explain but you guys were first and foremost in my mind. If I didn't have you guys to laugh, cry, scientificate (new word?) and just generally hang with I seriously think I would have lost it long ago. :wub: :wub: :wub: :wub: :wub: :wub:

I've been reading on lymenet about some of the people who have died from it...it's really very sad!

I'm pretty stubborn too, but in a lazy sort of way. :P Quite a few of my friends have now heard about this thread. :P I talk to them, but it's not quite the same because none of them really knows about any of the stuff we talk about...I was truly SHOCKED when one of my friends pushed me to get the lyme testing. She knows a little about it, but she's the only one.

And, definitely couldn't talk about scatology with them. :P

nikki-uk Enthusiast
AHA! Thx for clearing that up for me!

I think it was Ricky Gervais I saw on Leno joking that the Brit way of saying herb was right cuz "u can't ignore the H!".

Wish Jay had brought up heir. He also made fun of his own pronunciation of aluminum as aluminIum. Pretty weird to throw in an extra syllable, imo. Y'all don't mess w/ platinum that way do ya? I'll guess no.

Oh NO...don't get me started on the curiously different ways of (mis)pronouncing the English Language!! :lol:

HIDEOUSLY OFF TOPIC!!

:ph34r: I am wondering, Murph, if we should start a separate thread for parsing and such.....words and usages that drive us crazy (like our President (GDub, not Rachel :P ) saying NUKE-you-lar..... :lol:

DARE YOU to start that thread!!!!! :ph34r::)

CarlaB Enthusiast
Carla has mentioned mixing up abx to go after different forms of bacteria, I don't know if Mia's doctor has done that.

Yes, borrelia can change into three different forms. My LLMD believes in treating all three forms simultaneously, otherwise it will switch to the form you're not treating. All three forms require different meds. Then we're treating the babs at the same time, too.

Sorry about talking about you in front of you Mia. :ph34r:

Well, it certainly is better than talking about her behind her back! ;)

Looking at the whole picture....many positive bands on Western Blot, positive urine test (100% specific for Lyme), CD57 count 26, clinincal symptoms...there is really no doubt you need treatment....if he's not willing to treat then I would find a Dr. who will take this seriously....before the disease progresses.

Maybe he has a game plan...I hope he does...but if not I would seek better care. I know there must be some very knowledgable LLMD's in your area who will get you on the right track.

If your new doctor ends up not being an LLMD, my LLMD is about a two hour drive north of the city. He treats mercury, candida, Lyme, and everything else. His care is very comprehesive and I've never been this satisfied with a doctor in my life.

Let me know if you want his number, I'll PM it to you. His already booked till Sept., so if you want to see him, you might want to make the appt. sooner rather than later.

"My God, if you've had it for four years you're lucky you didn't die." :ph34r: I'm too stubborn to do that.

Yeah, you see these people, some of them very young, who get it and die. They also say that with babs it's even more dangerous. I think my immune system must be very strong! I've lived with this a long time and been relatively healthy most of that time. Lots of mystery illnesses and ER visits, but nothing like I'm suffering now.

I told her that there were times that I thought about it but I was lucky in that I had two things going for me- a gut feeling that something systemic was going on and that I wasn't going to stop until I got an answer (I'm STUBBORN :P )

Add to that the fact that I don't believe in it! I figure if it was my time, God would take me.

I certainly am no longer afraid of dying though.

Quite a few of my friends have now heard about this thread. :P I talk to them, but it's not quite the same because none of them really knows about any of the stuff we talk about

And, definitely couldn't talk about scatology with them. :P

My friends know about this thread, but they don't know where it is. ;):lol: We talk about personal stuff here, and with my "face-to-face" friends, I'd rather talk about it in person than have them reading it without my knowledge.

Scatology ... funny ... my nurse from the LLMD called me yesterday to tell me whether or not I had to go off the meds for this most recent test ... I was at Wild Oats ... her FIRST question was asking how my poop was! :lol:

Yesterday, I took two amoxy at lunch, and two at dinner, to try to up my dose. Today, I'm feeling rough. I only took one this morning, but I think I'll take two at lunch and dinner again ... I've got to get this bacterial load down!


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CarlaB Enthusiast
Oh NO...don't get me started on the curiously different ways of (mis)pronouncing the English Language!! :lol:

HIDEOUSLY OFF TOPIC!!

So, do you Brits say the "h" in "herb" or is it silent? Here the "h" is silent ... except when Adam says it. :lol:

nikki-uk Enthusiast
So, do you Brits say the "h" in "herb" or is it silent? Here the "h" is silent ... except when Adam says it. :lol:

IT'S HHHHERB!!!......NEVER SILENT!! :lol:

CarlaB Enthusiast
IT'S HHHHERB!!!......NEVER SILENT!! :lol:

Hmmm, maybe Adam's British and I just didn't know it! :lol::lol: The only reason you would get away with that pronunciation here is because of your accent. ;) People would think you were talking about a guy named "Herb."

AndreaB Contributor
I am very angry at my doctor right now actually and very confused but I do feel good that I have this new appt. set up unfortunatly it is not until July 3rd I am going to call my docs office today though and see if he can do anything about moveing it up - I think he owes me that.

You have a right to be angry, but you need to move on. Look forward to this new doctor and progress. I do hope they can move the appointment up but if not we'll be here to help pass the time. :):wub:

I told her that there were times that I thought about it but I was lucky in that I had two things going for me- a gut feeling that something systemic was going on and that I wasn't going to stop until I got an answer (I'm STUBBORN :P )

and that I had a lot of SUPPORT. I didn't go on to explain but you guys were first and foremost in my mind. If I didn't have you guys to laugh, cry, scientificate (new word?) and just generally hang with I seriously think I would have lost it long ago. :wub: :wub: :wub: :wub: :wub: :wub:

I'm glad you didn't and that you came back to us. Even though I'm not sick (hopefully the removal won't cause too many problems next year) I get a lot of support here too. :wub:

I was truly SHOCKED when one of my friends pushed me to get the lyme testing. She knows a little about it, but she's the only one.

I didn't know that. :)

Yeah, you see these people, some of them very young, who get it and die. They also say that with babs it's even more dangerous. I think my immune system must be very strong! I've lived with this a long time and been relatively healthy most of that time. Lots of mystery illnesses and ER visits, but nothing like I'm suffering now.

Add to that the fact that I don't believe in it! I figure if it was my time, God would take me.

I didn't realize people died so soon into the disease. :( I guess I thought the immune system could keep it in check for awhile like yours did.

I also agree with "when it's our time".

Scatology ... funny ... my nurse from the LLMD called me yesterday to tell me whether or not I had to go off the meds for this most recent test ... I was at Wild Oats ... her FIRST question was asking how my poop was! :lol:

:lol::lol::lol:

Yesterday, I took two amoxy at lunch, and two at dinner, to try to up my dose. Today, I'm feeling rough. I only took one this morning, but I think I'll take two at lunch and dinner again ... I've got to get this bacterial load down!

Boy! Sorry just upping it the one pill per meal brought you down again. :( Hope today goes better for you with dropping the breakfast dose. :)

AndreaB Contributor

Carla,

Any word on any of Chloe's tests yet? I figure you'd hear sometime between this week and next week.

tabasco32 Apprentice

hope everything goes good for you mia

hey rachel I was reading on the gluthione and since I am so toxic is it ok to take the whey protein. ALso what does castor oil packs do for you? should I be taking anything IV? My bloating has gotten worsse.

lisa

p.s.

Isn't a quart of water enyma a lot?

Murph Newbie
I knew fruit was not allowed on the Candida diet at all for those reasons. It is just the canned fruit seems to irritate it more. I think it is the corn syrup. I eat corn and I am fine, but the syrup is too much sugar, and is very bad for the stomach. Many people do not tolerate HFCS.

Yikes u eat THAT?!!

I've come to wonder if HFCS might be blamed in the future for the problems of many people. Read something about how our enzymes haven't evolved to digest it properly.

After a very long time sticking strictly to the anti-candida diet, I can have ONE fruit from a can. Pineapple in its own juice. Just the 2 ingred.

Charlie,

Certainly the Caprylic is good. Made me realize I left a lot out of my story regarding Candida. The Naturopath gave me all sorts of pills and powders. 2 powders & maybe 4 or 5 pills. Almost 2 yrs ago so I don't remember specifics. But I know some weren't available at stores.

I think my prev post may have made it sound like I got better on diet alone, and that would be wrong.

AndreaB Contributor
I've come to wonder if HFCS might be blamed in the future for the problems of many people.

I just read recently in my uswellness meats email that hfcs bypasses the mechanism in the body that says you are full......leading to overeating.......leading to overweight people. Seems to me I've read other stuff before that that stuff is NOT good to eat.

rinne Apprentice
NAC is a supplement, so you don't need a doctor for it. :)

:o:lol: Good.

...

Dear Rinne,

I wonder why the fruit irritates our system more? Perhaps it has more sugar than the chocolate. That is the only thing I can figure. Of course, the magnesium may have something to do with it. That is my take on it.

....

I have heard that honey is more easily tolerated than other sweeteners, it is interesting. I know fruit really causes my tongue to be much whiter. :huh::angry:

Jin.....fruit is LOADED with sugar and fungi/molds.

The riper the fruit...the more fungi/mold it contains.

When a fruit ripens....its actually fermenting....its basically rotting. Fungi and molds are always present in ripening fruit....yeasts are involved in the fermentation process.

Thee would be a higher content of fungi in ripe fruit than in chocolate. If someone has candida they would likely be very sensitive to molds and fungi in fruit. Fruit is not allowed on a candida diet.

Thank you Rachel, more bad news. :P:lol:

certain insurances cover the CD57 test... it's done through Labcorp so I think all Horizon insurances will cover the test... I don't know what the out of pocket cost would be..

I know a friend had it and she was dealing with Kaiser, though I am not positive that Kaiser did the test. Sorry, that is not so helpful.

Ok I keep premature posting so sorry if anything I says gets repetative. Rachel- I never think of you as butting in or anything like that I soooooo...... appreciate your opinion and advice- that goes for everyone here- It helps me to stay on track and push to get the right treatment. I am very angry at my doctor right now actually and very confused but I do feel good that I have this new appt. set up unfortunatly it is not until July 3rd I am going to call my docs office today though and see if he can do anything about moveing it up - I think he owes me that.

Miamia, I think you have every right to be angry with your doctor. I suspect that you are a very loyal person but perhaps now you can see that even well intentioned people can do harm if they are not paying attention.

It blows me away that you were the first one tested and had tested so strongly positive months before Rachel and I were tested. :angry::( I wish there was one emoticon for that feeling.

The important thing to do though is get the proper treatment, trust me bitterness does no good, :ph34r::lol: and I am so glad that you are doing that now. :wub:

.....

and that I had a lot of SUPPORT. I didn't go on to explain but you guys were first and foremost in my mind. If I didn't have you guys to laugh, cry, scientificate (new word?) and just generally hang with I seriously think I would have lost it long ago. :wub:

:wub:

Oh NO...don't get me started on the curiously different ways of (mis)pronouncing the English Language!! :lol:

HIDEOUSLY OFF TOPIC!!

DARE YOU to start that thread!!!!! :ph34r::)

HEINOUSLY SO! :lol:

Rachel--24 Collaborator
hope everything goes good for you mia

hey rachel I was reading on the gluthione and since I am so toxic is it ok to take the whey protein. ALso what does castor oil packs do for you? should I be taking anything IV? My bloating has gotten worsse.

lisa

p.s.

Isn't a quart of water enyma a lot?

Lisa...I do think you should take the whey....just not in the massive amounts that your Dr. suggested.

How much did you take when you got a reaction to it....was it alot??

Too much of anything at once is gonna be a shock to your system....especially something that promotes detox. Too much will make you feel worse.

I started out with about 1/3 of a scoop and then worked my way up...I'm at one scoop now. I havent had any problems with it at all....and I actually like the taste of it. Another good thing to take is minerals....multi-minerals.

The one I take is free of everything except the minerals....no vitamins....no other "extra stuff".

This is the one my Dr. sent to me...

Open Original Shared Link .com/Cardiovascular-Resea...s/dp/B00014GCWK

The reason she has me on this is to build up the minerals in my body because they are usually depleted during chelation. You need adequate amounts of minerals during the detox period and to replace what might get lost during chelation.

Seems like the minerals and amino acids in the whey go a long way in protecting our bodies from toxic metals. When we get better...its probably a good idea to keep taking this stuff for the added protection....too much of some minerals can be bad too but not enough definately leaves room for mercury to settle in.

After you get all your amalgams out you will probably want to be tested for vit/mineral deficiencies.

Castor oil packs:

The easiest way to use castor oil is to massage it into the body on the problem spot, along the spinal cord, the abdomen, or following the lymph drainage patterns. It can also be taken internally, but is a strong laxative and is used to treat constipation.

Despite being a simple procedure, the castor oil pack can produce good results. For the strongest effect, use a hot oil pack. Physiological effects of the castor oil pack include stimulating the liver, increasing eliminations, relieving pain, increasing lymphatic circulation, improving gastrointestinal function, increasing relaxation and reducing inflammation.

Heres some links for the castor oil packs.

Open Original Shared Link

Open Original Shared Link

I got everything I needed to make the pack at WF...they sell the wool cloth and oil. The heating pad came from Walgreens. Its kind of messy with the oil...you have to make sure you dont get it on anything because it'll stain. Other than that its pretty easy to do.

Conditions which have been responsive to castor oil applications include:

skin keratosis

ringworm

fungal and bacterial infections

wounds

abdominal stretch marks (prevention)

bursitis

sebaceous cysts

warts

Rachel--24 Collaborator
Isn't a quart of water enyma a lot?

Yeah...I fill up my enema bag with one quart water (or coffee) and just take as much as I can hold. I usually do two....so its not the full quart at once.

The second enema I can hold alot more....probably cuz any obstructions got flushed out or something.

The second one is always more comfortable for me and I can hold it a long time....its also more effective....probably cuz I'm retaining more (its reaching higher into the colon?) and I'm holding it longer...so its loosening up more toxins and waste.

It usually ends up that the first enema I use like 1/4 of the water....and the second one I'm using 3/4 (everything thats left). Its working pretty well for me so far.

Rachel--24 Collaborator
I know fruit really causes my tongue to be much whiter. :huh::angry:

Thank you Rachel, more bad news. :P:lol:

Sorry for the the bad news about the fruit....but yeah...its feeding the candida....hence the white tongue.

:P <------------This guy doesnt have candida...note the lack of white coating. :lol:

CarlaB Enthusiast

I had the BEST lunch! I was craving fresh berries, so maybe there was something in them that I needed. ;) So, I bought strawberries, raspberries, and frozen blueberries. I also made whipped cream from whipping cream (no sugar) ... it was heavenly and LOADED with calories because I was generous with the whipped cream! :P

Boy! Sorry just upping it the one pill per meal brought you down again. :( Hope today goes better for you with dropping the breakfast dose. :)

Thanks. I only took one at breakfast yesterday, too, then two at each of the other doses. So, I stayed with the same dosage today. I have to get used to this stuff and it's going to hurt every time I ramp up. I've talked with someone on Lymenet who takes a very large dose of it, and they said it hurt every single time they added some.

I'm doing better than last week though, but not as good as yesterday.

Carla,

Any word on any of Chloe's tests yet? I figure you'd hear sometime between this week and next week.

So far, everything that's come back has been normal. We're waiting on the IGeneX. I haven't been able to do the urine test with her for heavy metals, but we should be able to do that this week.

CarlaB Enthusiast
:P <------------This guy doesnt have candida...note the lack of white coating. :lol:

That's what my tongue looks like, too ... see? :P

Morgan had the same lunch as me .... when I told her the whipped cream had 50 calories per tbsp., she wasn't happy.

I'll have to start taking 2 or three tbsp. to Starbucks with me to increas the calories of my latte. Their whipped cream is the real stuff, but it has sugar. That sounds REALLY good. My latte is about the only calories I eat in a day that doesn't cause stomach upset ... the berries didn't either.

AndreaB Contributor
I'll have to start taking 2 or three tbsp. to Starbucks with me to increas the calories of my latte. Their whipped cream is the real stuff, but it has sugar. That sounds REALLY good. My latte is about the only calories I eat in a day that doesn't cause stomach upset ... the berries didn't either.

You've got to get your food and calories where you can. :P

DingoGirl Enthusiast
Oh NO...don't get me started on the curiously different ways of (mis)pronouncing the English Language!! :lol:

HIDEOUSLY OFF TOPIC!!

DARE YOU to start that thread!!!!! :ph34r::)

:ph34r::lol: no....won't...do...it.........staying OFF computer.......very busy, actually doing small paintings.....

must..............stay...........away............from.............

COMPUTER!!!!! :P

I had the BEST lunch! I was craving fresh berries, so maybe there was something in them that I needed. ;) So, I bought strawberries, raspberries, and frozen blueberries. I also made whipped cream from whipping cream (no sugar) ... it was heavenly and LOADED with calories because I was generous with the whipped cream! :P

OMG - - - this sounds like heaven.......I have to FIGHT to keep weight off, for the first time in my life....gained 25 pounds with gluten removal and oh, how I do miss being a size 2.... :( yeah, yeah, I know it wasn't healthy....but I did like that, all of my life......sometimes, I think I'll do a two-week gluten challenge just to lose a quick 10 pounds..... :ph34r:

help me......

Hi everybody! ;) just a drive-by - - - doing about one million things today, while I procrastinate in my job hunt. ;)

tabasco32 Apprentice

rachel is it ok for me to do the whey and chlorella now? I have no more insurance and money for my teeth. what do I do till then? I am scared to get more sick. My stomach burns and I feel pressure in my throat. Why is that? MY intestines hurt before a bowel movement. Maybe the whole flax seed I take is irritating it? DO you use an enyma everyday? I need milk of magnesia but I hate to use it. Dont know what else to do. I am goint to my naturopath on thursday for acupuncture.

CarlaB Enthusiast
sometimes, I think I'll do a two-week gluten challenge just to lose a quick 10 pounds..... :ph34r:

Just because it's gluten causing the diarrhea instead of a laxative, doesn't mean it's not bulimia. You don't want to go there. ;) You are probably at a healthier weight. I USED to have to watch my weight ... I'm sure when I'm healthy I will again.

My biggest problem now is everything I eat makes me sick. Drinking doesn't, so a latte every day is a good source of calories. With it making me sick, I have little appetite.

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    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
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