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

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Dh?


Crimson

Recommended Posts

Crimson Rookie

I went to the hospital to have a swab taken. I hope they run the right tests. I have no idea what they'd test for. I asked specifically for a DH test. The Dr. didn't seem to get what DH actually is. I tried to explain it but I'm not sure I got my point across. Doctor's don't seem to like people who do their own research.

So, this turned up yesterday and started spreading down my hand.

0817091500a.webp

0817091501a.webp


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



Celiac.com Sponsor (A8-M):



ang1e0251 Contributor

Mine looked like that.

Crimson Rookie

I thought it looked like a less extreme version of the pics I've seen on the net. It is still spreading. And itchy. They tried to give me anti viral meds and steroids...ofcourse. Steroids for EVERYTHING. I've just been putting Benadryl Gel on them.

Were you tested? Do you know what to expect? The dermatologist that I made an appointment with for next Monday is supposed to have experience with DH. At least that's what the receptionist said.

I'm not trusting that the hospital is running the right tests. So, I went ahead and made the appointment instead of waiting for a referral of some kind.

I'm just very nervous about all this.

nasalady Contributor
I thought it looked like a less extreme version of the pics I've seen on the net. It is still spreading. And itchy. They tried to give me anti viral meds and steroids...ofcourse. Steroids for EVERYTHING. I've just been putting Benadryl Gel on them.

Were you tested? Do you know what to expect? The dermatologist that I made an appointment with for next Monday is supposed to have experience with DH. At least that's what the receptionist said.

I'm not trusting that the hospital is running the right tests. So, I went ahead and made the appointment instead of waiting for a referral of some kind.

I'm just very nervous about all this.

I'm sorry that you're going through this :(

My husband's DH looks like that. The dermatologist is supposed to biopsy the skin in a few places....not on the actual eruptions, but next to them, on clear skin. They will inject you with a local anesthetic before the biopsy.

The drug that treats DH is a pill called Dapsone. It has lots of bad side effects but my husband took it because he was desperate! DH is horrible!! The Dapsone did help with the itch and it helped it heal faster. He also uses a topical steroid cream.

Good luck with everything!

JoAnn

P.S. there is a old-fashioned test for DH that involves putting iodine on your skin (iodine soaked bandaid?) that some people in this forum have tried. I think you need a strong solution. If you leave it for several hours and you have DH, you'll develop a bandaid-shaped patch of DH there! Ouch. Here's the thread:

https://www.celiac.com/gluten-free/index.php?showtopic=57732

Crimson Rookie

Thank you for your replies. I'm sorry that your husband had to take the meds. I hope the best for him and that he gets much better!

So, here is a pic of what my arm looked like after the Dr. in the er took a swab and the blisters were busted.

0820090747a.webp

And here is the pic of the iodine patch test that I did. I used a solution of 2.4 % on a band aid and left it on for a couple of minutes before I moved the band aid and left it on for about an hour before I couldn't stand it anymore. It burned like mad!!! I took the band aid off and it left a stain that was one huge blister and one very bad small blister the next morning. The blister broke and the skin came off almost immediately. It's now *as you can see in the pic a nice square patch of raw skin*... icky, to say the least. I'm keeping it covered with antibiotic ointment and a bandage until I can see what this dermatologist says tomorrow morning. He's going to think I'm a nut case for doing this to myself!

Anyway... two days after iodine band aid debacle..... you can even see where I have a rough patch where I had the band aid before I moved it. It also scabbed over and the skin flaked off this morning.

0823091426a.webp

ChemistMama Contributor
So, here is a pic of what my arm looked like after the Dr. in the er took a swab and the blisters were busted.

A swab? You need a skin biopsy to properly diagnose DH. The doctor needs to biopsy near a blister, not the actual blister. However, your iodine experiment below pretty much cinches it...

I took the band aid off and it left a stain that was one huge blister and one very bad small blister the next morning. The blister broke and the skin came off almost immediately. It's now *as you can see in the pic a nice square patch of raw skin*... icky, to say the least. I'm keeping it covered with antibiotic ointment and a bandage until I can see what this dermatologist says tomorrow morning. He's going to think I'm a nut case for doing this to myself!

That is exactly what happened to me with the band-aid test. A huge blister, plus the other blisters nearby got bigger. My Dr. said "that's what I get for having a scientist as a patient, you're experimenting on yourself!!" :)

If you're still eating gluten, you should have a blood test to confirm celiac/DH, the University of Chicago has a great site to print so your Dr. knows which tests to run:

Open Original Shared Link

If you're itching, my doctor recommended Sarna lotion (the one that contains pramoxamine hydrochloride) to help with the itch and pain, it works rather well. nasalady below is correct, dapsone does work but the side effects are awful. Don't go gluten-free until you've had your blood tests and biopsy, then it's gluten free for you, m'dear! My condolences!! DH is awful.

Crimson Rookie

Thank you for the support. I really appreciate it! I will be checking that link as soon as I'm done here. TY!

Yea, I knew the Dr. at the ER had done it wrong.

But, I had said the last time that I broke out, I would go. So, I did. I did try to explain it to him. But, he had no clue what I was talking about. Again, I'm off to the dermatologist tomorrow morning. So, that's good.

I was gluten free for over a year. When this showed up, I started eating gluten again. The ball is rolling for me...I figure that I should because I would have to get more testing done. I will be making an appointment with a doctor that will take a month to get into see, so that should be enough time to get my IGA levels up enough to cause a positive blood test. Then I suppose it's off to the GI Doc...

I'm thinking instead of eating gluten foods that I may stay on my regular paleo type diet and just eat vital wheat gluten as kind of an additive to my food. I can't stand eating these foods. A few days of it and I feel like hell. Today I started taking wheat germ and swallowing down two table spoons of it with water after a meal. I'm not sure how much gluten is in that. So, tomorrow, I will be picking up the box of vital wheat gluten and doing the same with it. I just don't like glutenous foods. I should be able to keep the gluten reaction w/out having to eat the foods.

That should make it easier to switch back to gluten-free life. Just quit taking the vital wheat gluten.

I'm seriously curious if anyone has tried this on gluten challenge...


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



Celiac.com Sponsor (A8-M):



captaincrab55 Collaborator

Crimson, Just having that nasty rash, indicates that you came into contact with gluten. Do you know if you ate or handled something that contains gluten? I've met people that claim they can't even touch a slice of wheat bread without breaking out.

Crimson Rookie

haha Funny you should say that.... As stated, I had been gluten free for over a year. The only time I have trouble is when I come into contact with gluten. This one, as far as I can tell is because we had company over and had run out of paper plates to use for those who used buns *pretty much everyone but me* and used regular dishes. I washed the dishes and had the blisters the next day.

I know, should have known better.

*shrugs* live and learn, yes?

It's all good. I needed to do this.

Dan300 Newbie

Hi Crimson, your picture of the Iodine band aid patch test looks exactly like mine when I posted may 3rd, it would be nice to see if this is a valid test by trying the same thing with some one who dos'nt have DH , all I know is I started having skin problems 30+ years ago , been seeing doctors about this for 25+ years , in march with the help of this forum learned about DH and started going GFD in april . blood test in may were negative ( 5 weeks GFD ) and dermatologist at the VA biopsied the lesion instead of a DIF test next to it. they said the DIF was to expensive and would only do it if they really thought thats what I had !!! they blew off my Iodine test as they still had my diagnosis as nuerotic excorations , same as 3 years ago when I refused antibiotics again----- the doctor asked me if I thought I new more than him.... I got copies of my medical reports and at my june check up asked the doc about my biopsie , she agreed with my reading that it was negative for infection, I then asked her if that means if I then must have an autoimune problem, she said oh no it must be your nerves ?????? at least I got her to blood test me for nutrition vit ,minerals ect , about 10 different things. only B1 was a little low so I'm taking thiamin. also at that check up I was much improved and they still dismissed DH as it did'nt present like classic hives? symptoms . this is at Hines VA in Chicago with most of their Doctors coming over from Loyola so they should know what they're doing. now almost the end of August and I'm about 95% cleared up, last break out a couple of weeks ago and I can count the lesions I'm still dealing with on one hand , of course the purple marks take much longer to fade , this is the best I've been in along time and my friends have commented that I look better. I feel like I had to be my own Dr House to get my own self Diagnosis as they seemed to resent my research . Sorry about the long response just tired of 25 years of dealing with the medical system and since I'm almost all "Healed " up on a GFD then I must have DH & Celiac ?? thanks Dan

Crimson Rookie

Hi, Dan. Sorry that you've had such a hard time with diagnosis. Reading some of the stories here, I'm sure you realize that you are not alone in this. I was just sticking with the self diagnosis until this happened. Might as well go through with it.

About the patch test:

My husband actually agreed to put an iodine soaked band aid on his arm too. And his did stain and burn a bit, but did not blister up like mine did. He has an outline of where the adhesive from the band aid was touching him, but that is it. I will have to take a pic of it and post it here too! The difference is pretty obvious.

Ok, I visited the dermatologist today. And he looked at my arm and hands and said that it looked like eczema.... until I showed him the ones on my knee and on the backs of my ankles, the pics that I've posted here and my lab results from enterolab. Then he said that it was possible but rare. He dismissed the patch test and told me that all I did was create a chemical burn. I wish now that I HAD printed off the information on the iodine induced DH! <_< I'm none too thrilled about that.

He told me to come in when I have active lesions... I can call and come in when they appear then he will take a biopsy. I'm a bit unconvinced that he is the right dermatologist for me.

So. I find that my first day with a tbsp of vital wheat gluten is proving to really mess me up!

It seems to be aggravating my headache and joint pain *which is now NOT going away with pain medicine now* and making me feel even more sluggish and tired. I'll get through this.

Next step, try to get some blood tests done.

Anyone know a good Dr in the Eastern WV or Cumberland, MD area???

Just need one that will at least humor me.

Crimson Rookie

Sorry it took so long. So, this is my husband's arm. He put the iodine soaked band aid on for one hour. *same amount of time that I did* This is what his arm looked like two days later. There's a ring where the iodine had stained the skin but no blistering or other skin reaction. It looked similar to the area where I had the band aid on my arm for a few minutes before moving it to where I left it for an hour. But I did get a rash in that area.

There's still no skin reaction on my husband a week later.

0826090653a.webp

nasalady Contributor
About the patch test:

My husband actually agreed to put an iodine soaked band aid on his arm too. And his did stain and burn a bit, but did not blister up like mine did. He has an outline of where the adhesive from the band aid was touching him, but that is it. I will have to take a pic of it and post it here too! The difference is pretty obvious.

Ok, I visited the dermatologist today. And he looked at my arm and hands and said that it looked like eczema.... until I showed him the ones on my knee and on the backs of my ankles, the pics that I've posted here and my lab results from enterolab. Then he said that it was possible but rare. He dismissed the patch test and told me that all I did was create a chemical burn. I wish now that I HAD printed off the information on the iodine induced DH! <_< I'm none too thrilled about that.

He told me to come in when I have active lesions... I can call and come in when they appear then he will take a biopsy. I'm a bit unconvinced that he is the right dermatologist for me.

So. I find that my first day with a tbsp of vital wheat gluten is proving to really mess me up!

It seems to be aggravating my headache and joint pain *which is now NOT going away with pain medicine now* and making me feel even more sluggish and tired. I'll get through this.

Next step, try to get some blood tests done.

Anyone know a good Dr in the Eastern WV or Cumberland, MD area???

Just need one that will at least humor me.

Crimson, I really hope you find a good doctor/dermatologist! Preferably one who's had experience diagnosing DH!! I can't believe that doctor blew off the iodine patch test....that was the classic test for DH! :(

See the following article which shows a picture of the reaction of twin girls, one with DH the other with celiac disease but no DH, to the iodine patch test. Medical researchers use it, for crying out loud!!

Open Original Shared Link

Best wishes,

JoAnn

Crimson Rookie

Thank you, JoAnn. I have already printed the information on the iodine patch test and intend to take it to my next visit.

Yes, he blew it off. But he did agree to biopsy when I have fresh lesions.

So far, I've had small pimple like bumps that I end up scratching open either in my sleep or before I realize what they are. It took two weeks to really break out last time. So, I'm still on the gluten.

I put on a bit of weight at first *10 lbs in 4 days!* now it's falling off FAST. At this rate, I'm going to end up underweight again in no time. I got up to 125 and now it's dropping off at about two lbs a day. I'm about 5'4" and muscular because I instruct pilates and weight lift. I was able to build so much muscle during my gluten-free time...

Guess that's gone for now. I'm still strong, but I FEEL weak. Back to caffeine to make it through the day.

I intend to have blood tests run after another week or so of eating gluten.

I really should have done this all when I first got really really sick.... I just wasn't sure it was the issue until I went gluten-free. Once I did and felt so much better, I didn't want to go back.

Every day I say "I don't think I can do this again tomorrow" yet, every day, I make it.

It's bizarre to me.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      130,410
    • Most Online (within 30 mins)
      7,748

    Nicola mcculloch
    Newest Member
    Nicola mcculloch
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.3k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Pablohoyasaxa
      I feel your pain. Grain and gluten intolerant. Hang in there. This forum is very helpful
    • ElisaL
      IDK how common it is but it does happen. I'm celiac, allergic, and intolerant to the fiber in grains. (Fodmaps) So not only do I get sick from cross contamination, also gluten free wheat statch/fiber, and beauty products with wheat will get me. While I don't stop breathing the full body hives and short breath are not fun. Then once I make through that me and the bathroom become reacquaint. Sigh if I didn't feel so much better with the restrictions on my diet I'd feel sorry for myself. Least it makes for some good jokes about how the gremlin that lives in my gut really hates wheat. 
    • Wends
      Hi Dora77. “Questions I Need Help With” “1. Is it realistically safe to eat food my mom cooks…” YES - you wouldn’t be here if it wasn’t for your mother. Trust she still knows how to take the best care of you in her own way. Mishaps and cross contamination may happen - will happen on occasion, in fact - that’s life. But for the bulk of it as long as you’re aware of cc and try to avoid it for the most part, don’t sweat the small stuff! See the gluten free diet as a process. Own the process, Do Not let the process own you! “2. Do I need to worry about touching doorknobs, fridge handles, light switches, etc. that family members touched after eating gluten? What about public places like bus handles or school desks? Or like if i went to the gym, I would be touching stuff all the time, so there will be small amounts of gluten and those would get transferred on my phone if I touch my phone while in the gym. But I want to knos if it would be enough to do damage.” NO - this is OCD brain at its best! Hijacking your thoughts and justifying it because of the very real fear of gluten contamination. That’s OCD all over. Like a devil in the driving seat. Fears that are based on some kind of reality are hard to argue with. Boss it back! Recognise this for what it is. OCD using fear of gluten as its excuse to keep you entrapped. Own the OCD in this scenario, don’t let it own you. Normal cleanliness rules apply. Washing your hands before you handle food you’re putting in your mouth is fine. Washing after the gym is normal. Once daily cleansing wipe of your phone etc. Even if you did go rubbing your hands all over surfaces and licking them there might be a trace exposure to gluten possible. But I’m guessing you don’t usually do that sort of thing. Even if you inadvertently were to ingest trace gluten - it won’t be enough to do damage, no. It takes weeks to months of at least a few hundred milligrams of gliadin daily for the innate immune system followed by the adaptive immune system in coeliac disease to kick in and start producing antibodies and cause villous atrophy. “3. Is an endoscopy (without biopsy) enough to tell if my intestines are healed? I’d pay privately if it could help and if i dont get a refferal. Or do i need a biopsy?” Only biopsy, as the gold standard of diagnosis, can tell for certain if villi have recovered. Having said that video capsule etc. can give an indication of any inflammation. “4. Could my job (powder coating, sandblasting, etc.) expose me to gluten or damage my intestines through air/dust?” Assuming your employer provides all necessary PPE - appropriate mask and overalls etc. All you can do is take the precautions that are advised according to risk assessments and regulations of the relevant industry governing bodies? (I don’t know what this would be in the USA. Sorry. But there’s safety and governing regs in the UK for this sort of thing. Assuming it would be very similar over the pond in fairness). “5. Do I need certified gluten-free toothpaste, hand soap, shampoo, or moisturizer? (For example: Vaseline and Colgate don’t contain gluten ingredients but say they can’t guarantee it’s gluten-free.)” This comes down to personal threshold of gluten tolerance. People that are highly sensitive may need certified products. Especially those with dermatitis herpetiformis - the skin manifestation of gluten sensitivity. Listen to your body on this one. “6. Is spices like pepper with “may contain traces of gluten” safe if no gluten ingredients are listed? Or does everything need to be labeled gluten-free?” This one is easy - when following a strict gluten free diet, avoid products that say May contain traces of gluten. But it does not have to be labelled gluten free. There are many foods naturally gluten free. Having said that, there is nuance and personal tolerance threshold. If you’re super sensitive “may contain gluten” labelling is a godsend. But this kind of labelling is more aimed at informing customers with type 1 food hypersensitivity/ allergy reactions. The company is basically legally covering themselves, because there may be a risk of cross contamination. Not to be confused that it means there is cross contamination. In addition to products being labelled gluten free. Many products that are labelled can still contain gluten by the way - in fact any processed products labelled gluten free can still contain the allowable level of gluten (up to 20 parts per million according to Codex). A study was done not too long ago that showed gluten free processed products such as cereals, breads, flours etc. can and some are in fact contaminated and have above the legal allowable amount of gluten in them. While most gluten free products are fine for most celiac patients and tolerated, highly sensitive patients fail to heal fully if relying on processed gluten free products. The trace gluten exposure adds up for someone eating a typical western diet of gluten free cereal for breakfast, gluten free sandwich for lunch, gluten free pasta or pizza for dinner for example day after day, week after week. This is why, at least in the beginning after diagnosis, the gluten free diet should be one of whole real food - food that does not require a label. Meats, oily fish, eggs, beans, natural gluten free complex carbohydrates and vegetables according to custom and taste. Limit fruit as fructose worsens leaky gut and has been hypothetically linked to increased OCD and ADHD - Professor Richard Johnson published study on this recently. “7. Is continuing to only eat my own food the better choice, or could I eventually go back to eating what my mom cooks if she’s careful?” NO and YES. What you listed as your current, limited diet is nutrient poor. Correct it as soon as possible for your own sake and future health! Ditto what others have replied regarding vitamin and minerals that are lacking in malabsorption syndromes like celiacs and need replenishing. Gluten free products are not fortified. You were likely healthier, dare I say it, on a gluten containing diet for this reason. Your brain , and gut for healing and maintenance, needs lots of nourishment from omega 3s, B complex vitamins, folate, B12, iron, selenium etc. Meats, fish, natural fats that come with, do not fear - the brain is made of fat. Limit sugar, seed oils, and high glycemic cereals and fruit like bananas unfortunately as they can cause blood sugar highs and lows that can worsen anxiety in some people. Refined carbohydrates should be limited for the same reason. Fructose and simple sugars in excess feed the unhealthy gut bugs that wreak havoc with anxiety disorders like OCD. White potatoes can be problematic for some, also. It can take six weeks of elimination to see improvements. Note, consult your physician regards insulin adjustment if you reduce carbohydrates in the diet. Dr Bernstein diabetes protocol has worked for thousands. Ketogenic and low carbohydrate diets for mental and neurological conditions have shown improvements. Limited studies have and are being conducted under metabolic psychology and nutritional psychology. In a good proportion of anxiety disorders, mental, and neurological conditions including dementias, the brain is lacking nutrition and usable energy, not a drug. Similar in many autoimmune conditions, including celiacs, the prevailing hypothesis is that gut inflammation and resultant permeability allowing exposure to antigens begets triggering the genetically susceptible immune system response. Modern lifestyle exposure, one of the biggest being the food we choose to eat plays a huge role. Avoid ultra processed products, high in seed oils, refined grains, and sugar. Not just gluten can cause a leaky gut. Fructose, alcohol, egg white lysozyme, emulsifiers, added gums, the list goes on. “8. is cutlery from dishwasher safe if there are stains? Stuff like knives is used for cutting gluten bread or fork for noodles etc. I often see stains which i dont know if it’s gluten or something else but our dish washer doesnt seem to make it completely clean.” If in doubt have your own cutlery set, plate and dishes etc. for your sole use that you handwash yourself. Carry a camping fork/spoon set when out and about if needed. “9. I wash my hands multiple times while preparing food. Do i need to do the same when touching my phone. Like if i touch the fridge handle, I wash my hands then touch the phone. I dont eat while using my phone but i leave it on my bed and pillow and my face could come in contact with where it was.” That’s a classic OCD fear. Nothing to do with gluten as such. OCD brain is using gluten as the excuse here. I personally have the habit of using a cleansing wipe or dust cloth on my phone, nightly, that eases this sort of worry. For example a micro fibre dust cloth will do the trick, keep one on your nightstand? They are antibacterial as particles cling to the cloth. “10. Do i need to clean my phone or laptop if theyve been used by people who eat gluten? Even if no crumbs fall onto my keybaord, i mean because of invisible gluten on their fingers.”  NO. But again these OCD thoughts are hard to argue with. If in doubt, just a quick wipe with a cloth daily should suffice. Normal cleanliness practice. But if you don’t, or forget, don’t sweat the small stuff. “11. Does medication/supplements have to be strictly glutenfree? One company said they couldn‘t guarantee if their probiotics don’t contain traces of gluten.” Better if it is gluten free, yes. “12. I had bought supplements in the past, some of them say glutenfree and some of them dont(like the brand „NOW“ from iherb). I bought them and used them when i wasnt washing my hands so often, are they still safe? As I touched and opened them after touching door knobs, water taps etc. It was like a year ago when i bought those and even though i was eating gluten-free, I never worried about what i touch etc.” Still safe if do not explicitly contain gluten grains / derivatives AND if within the use by and use within dates. “I know this post is long. I’m just extremely overwhelmed. I’m trying to protect myself from long-term health damage, but the OCD is destroying my quality of life, and I honestly don’t know what’s a reasonable level of caution anymore.” Really hope these replies to your questions help. Just remember, in the midst of overwhelming thoughts and darkness under OCD clouded vision, the light and sunshine is always shining above. Take a moment or two when you are able in each day - even if it’s last thing at night - to meditate. Focus on something that you enjoy and appreciate. Or sit in a quiet space and try to relax and tune in to your higher self. Ask for guidance and soothing from your guardian angel. Over time it works but don’t worry if your brain is anxious. Eventually it will quieten down some. Try to focus on a real food, nutrient dense and naturally gluten free diet, this will help your anxiety and future health in the long run. Please eat real food - not cornflakes and sandwiches. Eat a steak, eggs or fish for example. Gluten exposures may happen, but don’t sweat it, dust yourself off so to speak, and carry on with a natural gluten free diet as best you can. Own your OCD don’t let it own you! Similarly, when it comes to a gluten free diet for celiac disease, own the process, don’t let it own you! You’re 18. That’s great. I’ve been managing OCD since childhood (in my 40s now. Many years of research, trial and error so to speak. Diet makes a difference. To quote Doc Brown to teenagers Marty and Jennifer, ‘ …your future hasn’t been written yet. No one’s has. It’s whatever you make it. So make it a good one.’
    • maryannlove
      Unfortunately not going to be able to let you know how Amneal is working because I still have almost 3 month supply of Mylan.  Had annual appointment with endocrinologist last week (though get scripts for blood work more often) and since was on my last refill, she sent new script to pharmacist.  Staying on my Mylan until it's gone.  (I tend to build up a supply because after trying a couple of endocrinologists for my Hashimotos, one finally got my thyroid regulated by my taking only six days a week instead of adjusting the strength which had me constantly up and down.  Will be forever grateful to her.  Apparently high percentage of folks with Celiac also have Hashimotos so all this relevant/helpful on Celiac.com.    
    • KimMS
      Thanks for sharing this! Have you started taking the Amneal? I'm curious how it's going for you. My pharmacy gave me the option of Accord, Macleod or Amneal. I didn't realize that Amneal was formerly Lannett, or I might have chosen that one. However, I did read some anecdotal reports that some people had side effects with Amneal, so I chose Accord. I have been taking it for 3-4 weeks and the past 10 days I have developed extreme fatigue/sluggishness, joint pain and some brain fog. I don't know if it is the new levo med, but nothing else has changed. Has anyone else taken Accord levo? Any issues? It seems to fall into the "no gluten ingredients, but we can't guarantee 100%, but it's likely safe category." I'm wondering if it is worth switching to Amneal or at least getting my thyroid levels checked. If the med is causing my symptoms, I'm guessing it's not because of gluten but maybe the potency is different from Mylan and I need different dosing. Accord was recalled for lower potency, but my pharmacist said the pills I have were not part of that lot.  
×
×
  • Create New...