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

Can Ssris Stop Celiac Symptoms


Gutbomb

Recommended Posts

Gutbomb Rookie

I am in the process of being tested for celiac but have been supposedly diagnosed with ulcerative colitis by one Doctor and IBS by another. For the past 5 years I have been taking lexapro and have had very few symptoms. I know that lexapro and other SSRIs can significantly help people suffering IBS but is that true for celiac too? From what I have read only going gluten-free will stop symptoms.

Amanda


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



Celiac.com Sponsor (A8-M):



home-based-mom Contributor
I am in the process of being tested for celiac but have been supposedly diagnosed with ulcerative colitis by one Doctor and IBS by another. For the past 5 years I have been taking lexapro and have had very few symptoms. I know that lexapro and other SSRIs can significantly help people suffering IBS but is that true for celiac too? From what I have read only going gluten-free will stop symptoms.

Amanda

Only gluten free stops the damage being done to your body, whether you have ever had any symptoms or not. The symptoms you may or may not have are not good indicators of how much damage is being done internally. Your goal should be to stop both symptoms and damage. ;)

Gutbomb Rookie
Only gluten free stops the damage being done to your body, whether you have ever had any symptoms or not. The symptoms you may or may not have are not good indicators of how much damage is being done internally. Your goal should be to stop both symptoms and damage. ;)

I am just trying to figure out why I would stop having symptoms for years at a time if it were Celiacs and not IBS. Just trying to make sense of my crazy GI mess.

curlyfries Contributor

My daughter was diagnosed with spastic colon when she was little. The symptoms went away during her teen years, but are now back. I hear that is not uncommon. Of course now we realize that it was probobly celiac all along.

tom Contributor
I know that lexapro and other SSRIs can significantly help people suffering IBS but is that true for celiac too? From what I have read only going gluten-free will stop symptoms.

IBS *is* a symptom, not a causative diagnosis.

So if SSRIs reduce IBS symptoms, they may be in reality reducing intestinal celiac symptoms.

Unclezack Newbie
I am just trying to figure out why I would stop having symptoms for years at a time if it were Celiacs and not IBS. Just trying to make sense of my crazy GI mess.

Over the many years before I went gluten free, I had good days and bad days. There were times I would go six months to a year with no symptoms. Eventually, I had nothing but bad days and the older I got, the worse the symptoms got until I quit eating gluten. I was diagnosed with IBS. I can't tell you why, but it happened to me too.

Judyin Philly Enthusiast

HI

I was dx'd years ago with IBS when in reality it was undx'd celiac all those years.

Because of Fibro i started on just 25 mgs of zoloft a day maybe 10 years ago. I'm still on it.

I have found swimming as a great stress and muscle relaxer too. dong that about 15 years when i'm healthy enough to do it weekly

so.......IMO for me.....the SSRI's help my pain and help me stay FOCUSED SO I can be totally compliant with my eating gluten-free, sf, cf, df, nightshades and low oxalates diet. whew........ ;) Yes it's a list.

IMO the SSRI might help you relax and cope with the the gluten-free living life style. To me after being undx'd for so long and many damages b/c of this........I'd say 'gluten free' the rest of you life is the answer.

Good luck

Judy


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



Celiac.com Sponsor (A8-M):



veggienft Rookie
I am in the process of being tested for celiac but have been supposedly diagnosed with ulcerative colitis by one Doctor and IBS by another. For the past 5 years I have been taking lexapro and have had very few symptoms. I know that lexapro and other SSRIs can significantly help people suffering IBS but is that true for celiac too? From what I have read only going gluten-free will stop symptoms.

Amanda

I've been waiting for someone to post on this board that selective serotonin reuptake inhibitors (SSRI's) were inhibiting their celiac symptoms. The following studies showed that SSRI's are reasonably strong anti-fungal drugs. One would have to speculate that SSRIs' only ability to combat depression lies in its anti-fungal action:

Open Original Shared Link

----------------------------------------------------------------

In two recent publications, Lass-Fl

Judyin Philly Enthusiast

Vegienft

Currently candidiasis can't be gotten rid of. It can only be controlled ......like with SSRI's ......or a sugar-free diet.

Gee, don't use sugar and pretty much eat a diet to fight the candidiasis...........but you think even on the diet it never goes away........is just controled?

Hummmmmm?

thanks for the info

Judy

veggienft Rookie
Vegienft

Currently candidiasis can't be gotten rid of. It can only be controlled ......like with SSRI's ......or a sugar-free diet.

Gee, don't use sugar and pretty much eat a diet to fight the candidiasis...........but you think even on the diet it never goes away........is just controled?

Hummmmmm?

thanks for the info

Judy

.....last I checked it was true. I've read doctors advising people to get antifungal drugs for their canididiasis. But I've also read followup from lots of people complaining that the candidiasis always comes back. If you have new info, I'm all ears.

Here's a site which tends to under-represent how many men get candidiasis, but it's a pretty good explanation of the disease:

Open Original Shared Link

and a couple more good candida sites:

Open Original Shared Link

Open Original Shared Link

Probiotics help. And abstaining from chlorine does too.

Your swimming therapy in Philly probably means indoor swimming ......recurrent breathing of chlorine gas. A British study of children who did that found elevated childhood asthma, which other studies associate with celiac and candidiasis. I wonder what other symptoms get elevated by breathing indoor pool chlorine.

Open Original Shared Link

Judyin Philly Enthusiast
.....last I checked it was true. I've read doctors advising people to get antifungal drugs for their canididiasis. But I've also read followup from lots of people complaining that the candidiasis always comes back. If you have new info, I'm all ears.

Here's a site which tends to under-represent how many men get candidiasis, but it's a pretty good explanation of the disease:

Open Original Shared Link

and a couple more good candida sites:

Open Original Shared Link

Open Original Shared Link

Probiotics help. And abstaining from chlorine does too.

Your swimming therapy in Philly probably means indoor swimming ......recurrent breathing of chlorine gas. A British study of children who did that found elevated childhood asthma, which other studies associate with celiac and candidiasis. I wonder what other symptoms get elevated by breathing indoor pool chlorine.

Open Original Shared Link

tHANKS SO MUCH FOR THE LINKS

I'LL READ THOSE.

YOU KNOW YOU AMAZE ME..........THE SWIMMING POOL...........MY FIBO WAS SO BAD FOR 10 YEARS SWIMMING IN CHLORINE POOLS.

Sorry just noticed the caps.......... ;)

then i had a hip replacement and went to a new therapy pool and they use bromine. (?) and i was so much better as was my breathing.

we have a brand new beautiful YMCA but just walking into the pool area.....i couldn't go in.

Will read and get back to you

thanks again.

judy

i read 3 of the 4 ........will finish but didn't want to forget

i have been using a great porbotic for years

I avoid abx at all costs but have celluitis again so am on clindomycian (?) and really upping the probotics now.

thanks again.

judy

veggienft Rookie

Open Original Shared Link

......It requires moderate plumbing skill and an hour or two to install. I think this one has the G.E. RO membrane. If you can find a system or just a replacement membrane that's made by Dow Chemical (I think "Thin Film"), they're about three times as effective.

Change out all the pre- and post- filter cartridges once a year.

..

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,857
    • Most Online (within 30 mins)
      7,748

    LowellFrancis
    Newest Member
    LowellFrancis
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Rogol72
      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • 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    
×
×
  • 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.