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

Are We There Yet?


WendyLee

Recommended Posts

WendyLee Rookie

I am newly diagnosed Coeliac by blood work and an Endoscopy. No known history in the family. I have always been a 'well' person. Would go to the Doctor only twice a year for my HRT script.

At the end of the year I turned 60 it all started. I neglected to go to the physio for a sore shoulder and ended up, all through 2008 with an extremely painful Frozen Shoulder (Adhesive Encapulitis). That same year my lovely father-in-law died with bowel cancer he had neglected to tell us about and our youngest dau's marriage was in severe meltdown.

We have two girls, both living over 2000klm away in Queensland. At that time both were married to soldiers based up there who were doing deployments to Afghanistan.

By Christmas Eve 2008 I went into a nosedive with major anxiety I believe brought on by the extreme pain and stress of the last year. Was prescribed Citalopram and after about 10 days of adjustment, it kicked in and was my new best friend until Nov 2010. When I had a very big 'blip' and crashed. I came back up again and thought nothing more of it.

We had had another horrific year with the eldest dau. Youngest dau's marriage was in healing mode and that was good but eldest's husband got to Afganistan on his 5th deployment and decided he didn't want to be married anymore to his wife of 18 years, he wanted the younger girl in Admin and so started a campaign of terror when he came home. I was up north helping her to pack up house and move. She has two boys. Just a note here that even after all this time he is still terrorizing her.

The 'blip' in my antidepressant treatment at the end of Nov 2010 happened on a weekend when ex son in law took the youngest boy of 4 years for a 3 hour visit and didn't bring him back. We had no idea where they were. The custody papers that my dau thought were all in order, weren't, he had never signed them so the Police were powerless. Eventually after 3 days he bought his son back to my other dau's place. But the damage had been done. Post Traumatic Stress was burnt into all of us.

What has all this to do with my coeliac problem, most of it I believe. All the stress "turned it on".

I flew up to Queensland in May of 2011 for 2 months to help. Had a couple more 'blips' but then when I came home, I had a slight one on Friday night 6th Aug watching telly and I have been sick ever since.

My former doctor of 10 years kept upping my Citalopram until I couldn't function. I was feeling 'unwell', fatigued all the time. Off my food. Another doctor in the same practice kept changing me from one AD to another until a couple of months back I changed to a Doctor who practices Integrated Medicine. He listened quietly to my story and straight off order the blood work for Coeliac....had the biopsy 2 weeks ago and here I am.

The only symptoms I have had is chronic fatigue and just not feeling well. The bloods showed a deficiency in Vit D but my iron and essentials are normal.

Gliadin IgA - 86 (< 20); Gliadin IgG - 100 (< 20); Transglutaminase IgA Ab - 27 (< 4); Biopsy has shown a shortening and flattening of the villi.

I've started the GFD as of Saturday 17th March 2012. That is written in red in my diary :P:)

I've had a wretched 2 weeks. I began taking another AD some months ago before I knew about the celiac disease, it's called Mirtazapine. Now I was unsure if it wasn't being totally nice to me. Mirt. can have a side effect of making you anxious (go figure)....I didn't know which symptoms were celiac disease or the drug so last week (with doc's approval I decided to cross fade from Mirt. to Citalopram because I knew what to expect from the Cit. BIG mistake, only started Cit. on 10mg and I was SO sick for 4 days that I stopped it. Now I'm not on anything.

I hate the mornings, mainly. I wake with my stomach filled with ferrets all running about and hot and sweating. I usually cry (big sook). Work up the courage to have breakfast. Use to have a cuppa tea first up but find that makes me worse. As the day goes on I can feel a tad better but I'm usually a bundle of misery.

Yesterday I took an Ativan 1mg that I just happened to have and within 45 minutes I felt a calm wave over me and for the rest of the day I could actually function. I've taken another one at 10 am this morning because I have an acupuncture appt. at 2pm and I think I really need it (the acupuncture that is). Still had a weep sitting in the sun.

My so lovely husband says I'm being too hard on myself and I should go back onto the Mirtazapine if it will help.......I JUST DON'T KNOW ANY MORE! I don't know what to expect.

The glossy Coeliac mags are all full of bright ppl having great lives, traveling the world and recipes, but what was their life like before the GFD kicked in......and I can barely face food.

I don't pretend that the diagnoses was a blessing, I am a person who has not been seriously ill in her life, never had an operation, never broken anything and now, not only do I feel so wretched, my freedom of choice for the rest of my life has gone and I have to get use to it, no fish n chips from the corner shop, no Smarties at the kid's parties. I know there's substitutes but it's not the same. I will get use to it but at the moment it sucks.

I've been put on a Health Care Plan of dieticians, bone density tests, follow ups etc so that's all good but it's the day to day grind of getting from one day to the next. I just Praise The Lord I don't work and my husband is a caring and capable man.

And so endeth my testimonial. I apologies for the length and if I've put it in the wrong spot, so sorry. You are all great folk out there.

Wendy Lavender - Australia


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



Celiac.com Sponsor (A8-M):



pricklypear1971 Community Regular

First, I'm sorry to hear about your family troubles. I hope it settles soon for the sake of all.

Second, I don't know a thing about antidepressants and how they affect your body going into the gluten-free diet.

Third, if Smarties are the little round candies made of sugar and coloring they are completely gluten-free and have as many as you want.

Most people go through a period of withdrawal. Yours may be worse than normal and is causing some of your depression issues. Also, many of us are unsure about what to eat and have very incomplete diets in the beginning. You need to eat healthy, whole foods as much as possible.

I hope others chime in here, since I'm out of my depth regarding your meds and dealing with depression and Celiac.

mushroom Proficient

Oh my, I am so sorry you are having such a tough time of it, Wendy :( But things eventually do get better. Believe it or not, some of the way you are feeling could be a withdrawal from gluten, as it acts as an opioid in the body and withdrawing from it is similar to the withdrawal from nicotine or other addictive substances. Hang in there until you get over the hump. Be kind to yourself, and I am glad you have a kind and caring husband. I hope your daughter has all her custody issues in order and you can start relaxing a bit on that score. These things are all very distressing. And grams to the rescue on her white steed :P

You may find as you get further into the diet that your depression (which is probably attributable to celiac) will lessen, and you may need less and less of the medication. I hope you are supplementing with plenty of Vit.D and that your bone scan turns out well.

Are you making sure that all your medications are gluten free? Including all your OTC supplements, all your toiletries and personal care products. You will also need to decontaminate your kitchen, get yourself a new toaster for gluten free only, new colander/strainer, new wooden/plastic cutting boards and utensils, new non-stick frypan (the old one is probably scratched and gluten can contaminate your food). You will also have to train your husband to clean up all his gluten crumbs, assign him an area of the counter than can have gluten on it, and try to get him to agree to eat gluten-free at home if he will go along with it. It will make your life a lot easier. :) You will need to go through your pantry and fridge and have a total reorganization, either getting rid of the gluten or putting it in places where it cannot contaminate your food. You will need your own containers of butter, jam, peanut butter, and have a rule that anything shared is to be taken out with a clean spoon.

Do keep us informed of how you are progressing and ask any questions that pop up. If you google around the forum, put your feet up and do some reading, you will find a lot of interesting information. :)

Darn210 Enthusiast

Welcome to the board Wendy. It will get better!!!

My former doctor of 10 years kept upping my Citalopram until I couldn't function. I was feeling 'unwell', fatigued all the time. Off my food. Another doctor in the same practice kept changing me from one AD to another until a couple of months back I changed to a Doctor who practices Integrated Medicine.

When the intestines are damaged, not only are you not absorbing all your nutrients, you also aren't absorbing all your medication. As you start to heal, you may find that you don't need as much AD medication since you are now absorbing it properly. You may not need it at all as depression can be a Celiac symptom, but time will tell on that one.

In the beginning, the diet can sound overwhelming, but you'll be surprised how quickly you adjust. Get yourself a few safe meals (for us it was tacos, (rice) pasta dishes, grilled meat & veggies) and then build and experiment from there.

So that you don't feel deprived, a good place to start is your favorite comfort food. What do you like? We can help you convert it to gluten free . . . we've got a lot of experience on this board converting recipes.

Third, if Smarties are the little round candies made of sugar and coloring they are completely gluten-free and have as many as you want.

What we call Smarties in the US are gluten free. I know that in at least one other country (was it Canada?) they are not. You need to check the ingredients of Smarties in Australia.

butterfl8 Rookie

I know sometimes with depression it's hard to get out of the pit. Here are some of our more hopeful stories. Your story is amazing. All of that trama, stress, and pain, but now you have a way to feel better! I'm not trying to trivialize your pain, just to give you some hope. This diagnosis may be just what you need to feel amazing.

Give the diet some time. If YOU feel that you needs meds to help you over the rough patch, then by all means find something helpful. But know that after a while, you may not need them. Get yourself on a diet with NO gluten, including your toiletries. We're all here to help--you can feel better.

-Daisy

Victoria6102 Contributor

In America, Smarties are powdery sugary colored candies. In Canada, Smarties are chocolate candies similar to our M &ms. And that kind, the Smarties like the ones in Canada, are not gluten free. What we call smarties, they call rockets.

pricklypear1971 Community Regular

Sorry to cause all the confusion. These are the smarties I was talking about.

Open Original Shared Link


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



Celiac.com Sponsor (A8-M):



Takala Enthusiast

Celiac causes malnutrition, which then affects hormones and moods - anti depressants also will effect gut function, because the bulk of the body's serotonin is in the gut, not the brain, and your gut being in an uproar from the effect of the anti depressants will further effect your mood.

You are going into the autumn season down there, so your days are getting shorter, while ours are getting longer here in North America, and this also has an effect on mood for some people.

The classical ways of getting a grip on depression are to make yourself exercise whether you feel like it or not, every day, even if it is for just a short period, and to take a multivitamin, a B vitamin complex, and some mineral supplements, and to "eat well." If you cannot bear the thought of getting outside, I recommend getting a pet that will insist you go outside with it several times a day, or it jumps on you.

Some of us were so sick before being diagnosed or figuring this out (be thankful you at least live in a civilized country with healthcare instead of hit and miss) that we are grateful and see it as a method of regaining some control over our lives, instead of the feeling of losing it.

The glossy Coeliac mags are all full of bright ppl having great lives, travelling the world and recipes, but what was their life like before the GFD kicked in......and I can barely face food.

Yeah, and most of them are younger than you and I, aren't they ? <_<:huh: It's like People magazine is full of celebrity women who just had a baby 6 weeks ago, and they're now back to being a size 4 and jet setting off to exotic locales, photographed in bikinis, with the nannies tending the children after completing their latest business project. B) And they're never sleep deprived. It's idealized, but it's not quite reality.

WendyLee Rookie

First, I'm sorry to hear about your family troubles. I hope it settles soon for the sake of all.

Second, I don't know a thing about antidepressants and how they affect your body going into the gluten-free diet.

Third, if Smarties are the little round candies made of sugar and coloring they are completely gluten-free and have as many as you want.

Most people go through a period of withdrawal. Yours may be worse than normal and is causing some of your depression issues. Also, many of us are unsure about what to eat and have very incomplete diets in the beginning. You need to eat healthy, whole foods as much as possible.

I hope others chime in here, since I'm out of my depth regarding your meds and dealing with depression and Celiac.

Phew :rolleyes: so pleased Smarties are gluten free. I was told that there was gluten in the covering of them. Thank you for your support. In a ideal world I'd be eating how I usually eat with a full apetite with lots of good food but at the moment meal times are a pain. My husband has suffered Chronic Fatigue Syndrome for years so we have already been around the labels with that one but I never thought I'd be just as ill as he is. I was suppose to stay the healthy one.

Cheers

Wendy

WendyLee Rookie

Oh my, I am so sorry you are having such a tough time of it, Wendy :( But things eventually do get better. Believe it or not, some of the way you are feeling could be a withdrawal from gluten, as it acts as an opioid in the body and withdrawing from it is similar to the withdrawal from nicotine or other addictive substances. Hang in there until you get over the hump. Be kind to yourself, and I am glad you have a kind and caring husband. I hope your daughter has all her custody issues in order and you can start relaxing a bit on that score. These things are all very distressing. And grams to the rescue on her white steed :P

You may find as you get further into the diet that your depression (which is probably attributable to celiac) will lessen, and you may need less and less of the medication. I hope you are supplementing with plenty of Vit.D and that your bone scan turns out well.

Are you making sure that all your medications are gluten free? Including all your OTC supplements, all your toiletries and personal care products. You will also need to decontaminate your kitchen, get yourself a new toaster for gluten free only, new colander/strainer, new wooden/plastic cutting boards and utensils, new non-stick frypan (the old one is probably scratched and gluten can contaminate your food). You will also have to train your husband to clean up all his gluten crumbs, assign him an area of the counter than can have gluten on it, and try to get him to agree to eat gluten-free at home if he will go along with it. It will make your life a lot easier. :) You will need to go through your pantry and fridge and have a total reorganization, either getting rid of the gluten or putting it in places where it cannot contaminate your food. You will need your own containers of butter, jam, peanut butter, and have a rule that anything shared is to be taken out with a clean spoon.

Do keep us informed of how you are progressing and ask any questions that pop up. If you google around the forum, put your feet up and do some reading, you will find a lot of interesting information. :)

I hadn't though of detoxing from the gluten. I had talked about 'grief' with the counselor but 'withdrawal' from gluten makes sense. Thank you for pointing that out.

I've hit the cupboards and now my neighbours have all my gluten stuff, I was amazed at how little there was. I've been toasting under the grill in the range while Husband still uses the toaster, it does a better job of the gluten bread, anyway. Our meals have been very simple as his diet, being CFS, is sparce so it's not such an effort but he will need to clean up his crumbs. My butter is separate and he doesn't eat jams. I have discovered that my favourite Green Tomato Pickles is gluten free and that's a plus. :P

I called the pharmacy to ask about meds and they are all clear.

My Doctor was very vague about me starting back on meds so I guess I stay off them and hope his Esoteric Acupuncture this afternoon will work magic.

Cheers WendyL

WendyLee Rookie

I know sometimes with depression it's hard to get out of the pit. Here are some of our more hopeful stories. Your story is amazing. All of that trama, stress, and pain, but now you have a way to feel better! I'm not trying to trivialize your pain, just to give you some hope. This diagnosis may be just what you need to feel amazing.

Give the diet some time. If YOU feel that you needs meds to help you over the rough patch, then by all means find something helpful. But know that after a while, you may not need them. Get yourself on a diet with NO gluten, including your toiletries. We're all here to help--you can feel better.

-Daisy

Thank you for the link, I will read them all.

My children will verify that I like things to happen yesterday :lol: so for me to hurry up and wait and give the diet time is so hard. I have read how patient some ppl are, they have been battling unknown ill health for years before being diagnosed, for me it's only been 8 months so I do see that I am so lucky to be diagnosed so soon.

WendyLee Rookie

Celiac causes malnutrition, which then affects hormones and moods - anti depressants also will effect gut function, because the bulk of the body's serotonin is in the gut, not the brain, and your gut being in an uproar from the effect of the anti depressants will further effect your mood.

You are going into the autumn season down there, so your days are getting shorter, while ours are getting longer here in North America, and this also has an effect on mood for some people.

The classical ways of getting a grip on depression are to make yourself exercise whether you feel like it or not, every day, even if it is for just a short period, and to take a multivitamin, a B vitamin complex, and some mineral supplements, and to "eat well." If you cannot bear the thought of getting outside, I recommend getting a pet that will insist you go outside with it several times a day, or it jumps on you.

Some of us were so sick before being diagnosed or figuring this out (be thankful you at least live in a civilized country with healthcare instead of hit and miss) that we are grateful and see it as a method of regaining some control over our lives, instead of the feeling of losing it.

Yeah, and most of them are younger than you and I, aren't they ? <_<:huh: It's like People magazine is full of celebrity women who just had a baby 6 weeks ago, and they're now back to being a size 4 and jet setting off to exotic locales, photographed in bikinis, with the nannies tending the children after completing their latest business project. B) And they're never sleep deprived. It's idealized, but it's not quite reality.

It must of been extremely difficult for ppl with Coeliac, not that long ago, right across the board, Doctors attitudes, ignorance, lack of support, lack of gluten free food. I am most grateful that I have this network, yes, even the glossy mags

Wendy

AVR1962 Collaborator

Wendy, sorry to hear you have been thru so much. Reading your intro I could see how stress could play a big role leading to your diagnosis. I too have been on that same stress path and I do beleive that is what triggered me as well. What I can assure you about your daughter, which she hopefully realizes now, is that the guy was a crumb in the first place to be able to do what he did and she is better without him. My first husband did the same and while it is hard on the kids because they love both parents, I realize my life was spared from what I would have endured had we stayed together. He had to make it look like my fault and made up all kinds of lies to our kids which was a continual stresser for many years but they are adults now and they ahve to make their choices....it is not easy.

I am 49 and was diagnosed this past Sept. For me it was like waking up in someone else's body and I had no clue what just happened to me.

There a wonderful amoujnt of knowledge here and you will learn more here than you will from docs as this still seems to be way over their heads as far as conprehension and how everything relates. At least that is what I have found.

Be patient with yourself and feel very fotunate that you have the diagnosis. Take one day at a time. I have felt like an old dog trying to learn a new trick and my adult daughters get laughingly frustrated (great girls and very supportive, they both are on gluten-free diets) and tell me all I am doing wrong but I am learning......it's a process.

Annette

pricklypear1971 Community Regular

Phew :rolleyes: so pleased Smarties are gluten free. I was told that there was gluten in the covering of them. Thank you for your support. In a ideal world I'd be eating how I usually eat with a full apetite with lots of good food but at the moment meal times are a pain. My husband has suffered Chronic Fatigue Syndrome for years so we have already been around the labels with that one but I never thought I'd be just as ill as he is. I was suppose to stay the healthy one.

Cheers

Wendy

Please make sure we are talking about the same Smartie. This is the one we have in the US and it is gluten-free. Open Original Shared Link

WendyLee Rookie

Wendy, sorry to hear you have been thru so much. Reading your intro I could see how stress could play a big role leading to your diagnosis. I too have been on that same stress path and I do beleive that is what triggered me as well. What I can assure you about your daughter, which she hopefully realizes now, is that the guy was a crumb in the first place to be able to do what he did and she is better without him. My first husband did the same and while it is hard on the kids because they love both parents, I realize my life was spared from what I would have endured had we stayed together. He had to make it look like my fault and made up all kinds of lies to our kids which was a continual stresser for many years but they are adults now and they ahve to make their choices....it is not easy.

I am 49 and was diagnosed this past Sept. For me it was like waking up in someone else's body and I had no clue what just happened to me.

There a wonderful amoujnt of knowledge here and you will learn more here than you will from docs as this still seems to be way over their heads as far as conprehension and how everything relates. At least that is what I have found.

Be patient with yourself and feel very fotunate that you have the diagnosis. Take one day at a time. I have felt like an old dog trying to learn a new trick and my adult daughters get laughingly frustrated (great girls and very supportive, they both are on gluten-free diets) and tell me all I am doing wrong but I am learning......it's a process.

Annette

Thx Annette for your encouragement. Yes, as time goes by, eldest realises that some parts of her life are less complicated without the third "child's" ego to cope with.

I think you're right about the Doctors, mine was rather pleased with himself to be able to make the diagnosis and pass me onto other staff members for Health Care Programs but when I tried to ask him about the 'anxiety' which I knew was being triggered by my bowel but could going back on an antidepressant stop that, he was most dismissive and not at all helpful and they get annoyed when we self-administer! :blink:

I have been trying to go back to family history research as a distraction, so here's hoping that will work.

Wendy

WendyLee Rookie

Please make sure we are talking about the same Smartie. This is the one we have in the US and it is gluten-free. Open Original Shared Link

I will check our Aussie Smarties to see if they're gluten-free before I start scoffing them. :D

cavernio Enthusiast

Might I suggest you go visit a depression forum and going off antidepressants? Because what you're talking about seems like classic 'discontinuation' symptoms from many anti-depressants. (discontinuation in quotes because that's the official term for it...pharmaceutical companies felt that calling it withdrawal was too close to making them seem addictive)

While I don't have any personal experience going off of a tricylic antidepressant, I had a pretty terrible time going off an SSRI, effexor. When I complained about getting sudden dizzy spells and snaps in my brain if I was an hour late with a dose, they switched me to a slow release version of the same thing.

Well, when I eventually went off of that version, I still felt terrible, and crying uncontrollably was one of the symptoms. The slightest thing would set me off. In fact, many people take the withdrawal to actually mean that without the drug, their depression immediately comes back terribly, and so will not quit the drug.

Even tapering off the drugs can still cause the awful withdrawal.

I'm very anti anti-depressants myself, (anti pretty much any drug due to the underhandedness of the industry...when I was on antidepressants they didn't even HAVE discontinuation symptoms listed, despite that they HAD to know about them if they had done proper studies...) and I hope you remain anti-depressant free as there are recent studies that show anti-depressants seem to increase the likelihood of becoming depressed again.

Also, I find that many of the users on this forum find that they get depression symptoms (can't be called full-blown depression unless it lasts for a long time, but its all the same really) if they accidentally have gluten after being gluten-free for awhile. There's hope that maybe going gluten-free will make you feel a lot better just by itself :-)

Also, with all the terrible things that have happened in your life, at least anxiety and depression is a natural reaction. I mean, its terrible and all, but at least it makes sense.

WendyLee Rookie

One thing I didn't know about or was 'selectively deaf' to as DH (Dear Husband) pointed out, was gluten withdrawal. It would explain why in the weeks before going gluten-free I wasn't feeling too bad. I had been eating enough gluten up until the endoscopy so the result would be true. But then when I stopped, somehow I thought I would feel better not feel like I'd been hit by a bus!

It's a case of 'stupid woman'. I always research stuff so I know what I'm dealing with but this time around the desire to reseach celiac disease to any degree hasn't been there. Head in sand perhaps? :blink:

WendyLee Rookie

I'm feeling heaps better than yesterday and a lot of that is due to you lovely ppl giving me information about gluten withdrawal. It's helping me deal with it. Also the father-in-law of our youngest dau has given me a family history project and that has been keeping my mind busy.

As my girls are always telling me "it's all good!!!"

Wendy

gilly31 Newbie

Hi Wendy,

I was so struck by how similar your story is to mine. We also share the same gluten free date!!! I also started the diet on March 17th, 2012. My anxiety/celiac was triggered by my parents very messy divorce (Dad cheated on my Mom with her best friend) and my Mom's subsequent depression. I entered full blown anxiety/insomnia when my Mom became suicidal and I felt like my #1 job in the world was keeping her alive. A year and half later, I realized that there was something more than just anxiety when I started having all the GI symptoms and REALLY bad heartburn all the time. I was also very lucky to get the diagnosis quite quickly.

Anyway, what I wanted to share with you is that:

#1--you're definitely not alone in your struggles and I completely understand how hard it is.

#2--I went through 3 counsellors/psychologists before I found one that really helped. We used cognitive-behavioural acceptance and commitment therapy, which is different from cognitive behaviour therapy (which is a more common technique). It might be something to look into. It really was a godsend for me. Finally something clicked and things started to change for me.

#3-- my first two weeks on the diet have been pretty awful as well. I think I have definitely been experiencing some gluten withdrawal. I do feel like I'm starting to see the light at the end of the tunnel though and things are starting to look up, so I really hope the same is happening for you!

Your post really moved me and I know that you will get the relief that you so clearly deserve!!

WendyLee Rookie

Might I suggest you go visit a depression forum and going off antidepressants? Because what you're talking about seems like classic 'discontinuation' symptoms from many anti-depressants. (discontinuation in quotes because that's the official term for it...pharmaceutical companies felt that calling it withdrawal was too close to making them seem addictive)

While I don't have any personal experience going off of a tricylic antidepressant, I had a pretty terrible time going off an SSRI, effexor. When I complained about getting sudden dizzy spells and snaps in my brain if I was an hour late with a dose, they switched me to a slow release version of the same thing.

Well, when I eventually went off of that version, I still felt terrible, and crying uncontrollably was one of the symptoms. The slightest thing would set me off. In fact, many people take the withdrawal to actually mean that without the drug, their depression immediately comes back terribly, and so will not quit the drug.

Even tapering off the drugs can still cause the awful withdrawal.

I'm very anti anti-depressants myself, (anti pretty much any drug due to the underhandedness of the industry...when I was on antidepressants they didn't even HAVE discontinuation symptoms listed, despite that they HAD to know about them if they had done proper studies...) and I hope you remain anti-depressant free as there are recent studies that show anti-depressants seem to increase the likelihood of becoming depressed again.

Also, I find that many of the users on this forum find that they get depression symptoms (can't be called full-blown depression unless it lasts for a long time, but its all the same really) if they accidentally have gluten after being gluten-free for awhile. There's hope that maybe going gluten-free will make you feel a lot better just by itself :-)

Also, with all the terrible things that have happened in your life, at least anxiety and depression is a natural reaction. I mean, its terrible and all, but at least it makes sense.

Thx for the suggestion. I've been a regular lurking in NoMorePanic for some time and there is a wealth of info in there that doctors either don't know or won't tell you. I've been able to kick the rotten habit of AD's as of 19 March, not long :wacko: but thankfully they are Mirtazapine and a lot easier to come off than most of the others. Now I know what is causing this anxiety I can weather it a bit easier.

I'm disgusted and concerned that once you have been prescribed AD's and been on them for a while, the doctors don't look passed them when you keep going back feeling unwell. They are only too happy to increase the dose or start you on the AD merry-go-round. And as far as I'm concerned and a lot of other folk out there, they ARE addictive! It can months to get off the darn things.

You are also so right about "making sense". When you can find an explanation for why you are all just "wrong", it goes a long way to starting the road to becoming "right".

many cheers

Wendy

WendyLee Rookie

Hi Wendy,

I was so struck by how similar your story is to mine. We also share the same gluten free date!!! I also started the diet on March 17th, 2012. My anxiety/celiac was triggered by my parents very messy divorce (Dad cheated on my Mom with her best friend) and my Mom's subsequent depression. I entered full blown anxiety/insomnia when my Mom became suicidal and I felt like my #1 job in the world was keeping her alive. A year and half later, I realized that there was something more than just anxiety when I started having all the GI symptoms and REALLY bad heartburn all the time. I was also very lucky to get the diagnosis quite quickly.

Anyway, what I wanted to share with you is that:

#1--you're definitely not alone in your struggles and I completely understand how hard it is.

#2--I went through 3 counsellors/psychologists before I found one that really helped. We used cognitive-behavioural acceptance and commitment therapy, which is different from cognitive behaviour therapy (which is a more common technique). It might be something to look into. It really was a godsend for me. Finally something clicked and things started to change for me.

#3-- my first two weeks on the diet have been pretty awful as well. I think I have definitely been experiencing some gluten withdrawal. I do feel like I'm starting to see the light at the end of the tunnel though and things are starting to look up, so I really hope the same is happening for you!

Your post really moved me and I know that you will get the relief that you so clearly deserve!!

What an absolutely terrible and shocking thing to happen to both your Mum and you! I can really understand to state that you both would of been in after watching my dau. It should never happen to any individual, it's like having a death in the family but with the added trauma of lies and betrayal. I can quite understand how you got to where you are, the stress would of triggered the celiac disease just as mine did so we were both lucky to be diagnosed early rather than later like so many others. Oh I hope your Mum is recovering, it's the anger and the feeling of being powerless that eats you up. My eldest has learnt to swear most badly since.

I've started seeing a physiologist that I saw last year for the depression. She's a lovely older lady and loves Blues. She just lets me talk (I'm good at that) and throws in suggestions. Her last suggestion to me was that is was normal for me to feel "grief" over the diagnosis.... I hadn't seen it like that....even though I was pleased to find out why I was so ill, I felt "let down" somehow and then I'd get cross with myself for feeling ungrateful and selfish. My husband has suffered from Chronic Fatigue Syndrome since the late 70's, so our lives have been somewhat dictated by his lack of ability to do most things....I've been the "doer" in the family, running all over the place and now I've been stopped in my tracks.

You've been feeling like a wet rag too, have you? Yesterday and today have been better for me. I started drinking more as well. I put a little raspberry and apple cordial in a 600ml bottle and keep it handy. I found I hadn't been drinking much at all. Read some place that it could help to flush the system and that made sense.

So we both started on the 17th March 2012, a Red Letter Day for us both and here's the best of luck to both of us. Hope you start to feel better real soon.

Cheers

Wendy

WendyLee Rookie

Today was ok. I managed to drag out all my winter clothes, scarfs and pashminas and do a big wash.....well several big washes. The clothes line was most colourful. Everything smelt musty from the wet summer.

Mornings are still a drag. Waking is a bit like Phillipe and Isabeau in the movie "Ladyhawke" were for just once second I feel fabulous.

Wendy

GFinDC Veteran

HI Wendy,

Is it getting kind of breezy in here? Sorry dumb joke. :)

Good job on the washing, I will have to try that sometime.

Here's an article on gluten ataxia for your reading amusement. There are also lots of things out there about the link between gluten and pschizophrenia, which is one the hardest wurdsz to spiel I thunk.

If you do searches on gluten and opioid you will get lots of hits too.

Open Original Shared Link

I think this Ask a Patient site is good for getting info on drug side affects. Stuff doctors don't tell you.

Open Original Shared Link

Something I am trying is Rhodiola and it seems to have a nice effect.

I am not sure if you've had your thyroid checked yet? It is a good thing to do since thyroid problems can go along with celiac sometimes. And low thyroid can cause lots of symptoms. Just a thot.

Gluten withdrawal can be rough. But after a while your gut heals or at least recovers some and you can start absorbing nutrients better. Staying away from dairy, sugar and soy are helpful when starting the gluten-free diet. Whole foods are a good way to go. Meds, vitamins, shared condiments etc can all be problems. Also watch out for teas and coffees that are flavored, and seasoning blends.

Like most things it gets easier after you have done it a while. The adjustment period may not be fun but probiotics and digestive enzymes can help.

WendyLee Rookie

HI Wendy,

Is it getting kind of breezy in here? Sorry dumb joke. :)

Good job on the washing, I will have to try that sometime.

Here's an article on gluten ataxia for your reading amusement. There are also lots of things out there about the link between gluten and pschizophrenia, which is one the hardest wurdsz to spiel I thunk.

If you do searches on gluten and opioid you will get lots of hits too.

Open Original Shared Link

I think this Ask a Patient site is good for getting info on drug side affects. Stuff doctors don't tell you.

Open Original Shared Link

Something I am trying is Rhodiola and it seems to have a nice effect.

I am not sure if you've had your thyroid checked yet? It is a good thing to do since thyroid problems can go along with celiac sometimes. And low thyroid can cause lots of symptoms. Just a thot.

Gluten withdrawal can be rough. But after a while your gut heals or at least recovers some and you can start absorbing nutrients better. Staying away from dairy, sugar and soy are helpful when starting the gluten-free diet. Whole foods are a good way to go. Meds, vitamins, shared condiments etc can all be problems. Also watch out for teas and coffees that are flavored, and seasoning blends.

Like most things it gets easier after you have done it a while. The adjustment period may not be fun but probiotics and digestive enzymes can help.

Dumb jokes accepted B)

The Doc checked my thyroid and all seems ok there, PTL. I think it's just plain old gluten withdrawal and the mornings are the worse...get better as the day progresses, then I start all over again. Having lactose free milk but I did have some yoghurt last night with live culture but suspect I'm paying for it. Was taking some supplements but I think my body is telling me to hold off for a while so not taking anything except my HRT of a night. Not much sugar in my diet and no soy, never been a soy fan. I think my normal type tea could be an issue at the moment. Have cut back to two a day now that would be a tragedy if I can't have my tea :(

For two days over the weekend I ground up 10 Schuessler Tissue Salts (General Tonic), put them in a bottle of water and sipped it over a few hours, didn't do it yesterday. I think that helped somewhat so having another go to see if it was just a fluke.

Will have to get some probiotics and leave the yoghurt alone for a while and look at the digestive enzymes. At least I feel better than last week :P Next week is a new chapter as well.

Thx muchly

Wendy

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,950
    • Most Online (within 30 mins)
      7,748

    stichael
    Newest Member
    stichael
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
    • DebJ14
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.