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

Dry Face Skin


mcdoncj

Recommended Posts

mcdoncj Newbie

Does anyone have dry facial skin. Seems to be dry skin & flaky especially around my hairline & sides of my face. I have just gotten this. I have had celiac for years & have it very much under control, but, this latest thing is awful. If anyone has this problem please answer this & what you did for it. Thank You so much!!!


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



Celiac.com Sponsor (A8-M):



MySuicidalTurtle Enthusiast

I have the flakeness around my forehead and nose so bad. I used to be in the pool year round (swimming, polo, and synchro) and had some flakeyness but never as bas as when I went gluten-free. It drives me mad.

Canadian Karen Community Regular

I have the exact same thing also.... around my nose and in the centre of my forehead just above my eyebrows... Also, this time of year, I also get extremely dry scalp that drives me bananas.... Haven't found anything to relieve it yet....

If anyone finds a solution, let me know!!!!

Karen

darlindeb25 Collaborator
;) try to find a good peppermint lotion--i found the best one i have ever had from a store in michigan called, "World Market" but they have since quit making it :( and it is excellent--i have used it on sunburn--takes the sting out--if i have a headache i put it on my face and it helps with the pain--the scent alone is so cooling--my mom says to put peppermint oil under your eyes--it may just work for dry spots too--i do know my lotion is great for itching--i love it :D deb
jboom Newbie

I get the same thing on my forhead and sides of my nose. I use a scrub and lotion, it doesn't seem to matter what lotion they all work the same. It usually just keeps it from getting any worse not really any better.

Do you think its Celiac related or do we just have dry skin?

MySuicidalTurtle Enthusiast

I am not sure but I never had it likes this before going gluten-free. . .just a little but now it's bad.

Connie R-E Apprentice

One of those serious scrubby pads (for the skin) will take it away, but I think it is a skin reaction from a food allergy. I'm allergy to soy, and if I eat it, I get the flaky forehead skin, too. If I don't eat soy, I don't get it. Get it? ;)

Everyone has their own unique allergies! It probabily won't even be soy for you--but, it's as good as any to start with!

Good luck narrowing it down!

Connie

gluten-free since 1-'98


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



Celiac.com Sponsor (A8-M):



MySuicidalTurtle Enthusiast

What exactly are the scrubby things?

Connie R-E Apprentice

:P I'm not exactly a frou-frou girl, so I don't know technically what they are called, but the look kinda like a fiberous synthetic loofa... (or the center of a floor buffing pad)! :wacko: And, they come with a sponge on the other side... ..mine is pink...

LOL!!

Does that help any? :lol:

Connie

MySuicidalTurtle Enthusiast

Hmm, not really. . .where did you buy yours? I am sure that if I take that discription I would find the product at some bath store!

Pegster Apprentice

Ask for a facial loofah. THey have them at the grocery store in the face products department. You could get one at Walmart or kMart.

plantime Contributor

You might try adding omega-3 oil to your diet. I use ground flax every day, when I don't, the dry flaky skin comes back. My herbal remedies book says that celiacs have problems getting nutrients from fats (as if we didn't know that!), and to consume fish oil supplements. I'm not saying it will work for everyone, it just works for me!

Carriefaith Enthusiast

I have very dry skin. When my face gets really dry and flacky, I use a lotion/cream. Maybe try lotions/creams that are designed for the face. They are usually less harsh.

Carriefaith Enthusiast

also... drink lots and lots of water and take vitamin E supplements. This may help some.

pixiegirl Enthusiast

My favorite scrubby thing is the Buff Puff I use the one for sensitive skin, its not quite as scrubby. People that have very dry skin should only exfoliate about once a week. Drink lots of water, most people don't drink enough. I've had very very dry skin for years, the flakey kind and I discovered La Mer products about 3 years ago. The are the only product for me that keeps the flakies away all day. However, once you see the price of them you will drop over dead, expensive is an understatement.

I've had people tell me that I'm being ripped off by these products but I firmly believe that everyone is different and what works for me may not work for you. People have told me to try Aquaphore (makes me shiney and break outs), eucrine, Oil of Olay, clinic, I've tried them all but still the La Mer is the only one that keeps me flake free. I only use the lotion (not the cream which is way too emolient for even me) and I only use it in the cold months of the year because its too much for me in the summer. And I only need a little bit, so its not as costly for me as it seems.

Susan

flagbabyds Collaborator

Make sure that all your lotions and all your champoos are gluten-free because that can cause dry skin

minibabe Contributor

I have recently been diagnosed and do you have to use gluten-free produts on your skin. And yes I have never had a problem with my skin unitl I went gluten-free. I have it around my hair line and above my eye brows. It is really frustrating b/c I have never had this problem before. Is this directly related to Celiac diease? and if anyone has any ideas please help :(

  • 7 months later...
BabySnooks Rookie
I get the same thing on my forhead and sides of my nose. I use a scrub and lotion, it doesn't seem to matter what lotion they all work the same. It usually just keeps it from getting any worse not really any better.

Do you think its Celiac related or do we just have dry skin?

<{POST_SNAPBACK}>

I also just started getting flaking and redness (when I scratch it) on the side of my nose and just above eyebrow. I have psoraisis and thought it was an outbreak, but who knows....it could be something else.

  • 3 weeks later...
Connie37 Newbie
I have recently been diagnosed and do you have to use gluten-free produts on your skin.  And yes I have never had a problem with my skin unitl I went gluten-free.  I have it around my hair line and above my eye brows.  It is really frustrating b/c I have never had this problem before.  Is this directly related to Celiac diease? and if anyone has any ideas please help  :(

<{POST_SNAPBACK}>

Connie37 Newbie

Sorry, I am new at this posting stuff. I have had lots of problems with dry skin. when I quit eating what I was allergic to, it went away. The cod liver oil or Omega 3 may be part of it too. It is in baby food and in animal food to enhance hair and skin and much more.

I do take a cinnamon capsule with it to mask the taste.

I really agree with the ones who said to check for gluten in your products, to cut out all allergy foods and to take the essential oils.

I never believed my skin would look normal again. I also bought a pumice stone by dr scholls and I used a long white paddle Dr scholls makes for feet. My skin is still a little bit of a problem.

The thing is, I was moisturizing over the dry flakes. It never reached my skin. I had to exfoliate first.

There are some skin forums out there. That's where I learned alot. I think its and eczema forum. Sorry I can't remember the exact type of eczema.

God Bless You

Connie

carrielynn Apprentice

My son also has flaky skin. I don't know if this is a result of going gluten-free or not... he may have had flaky skin before hand. But he definitely has it now, especially on his face.

I was reading Dr. Whitaker's Health and Healing newsletter for this month and there was an item about supplementing with silicon in your diet. It says:

"Although you get silicon in your diet, especially from whole grains, absorption diminishes with age. The first signs of silicon deficiency are brittle hair and nails and loss of skin elasticity. That's why supplementing with the most bioavailable form of silicon, stabilized orthosilic acid, is a great way to improve your skin, hair and nails. In a recent study of 40-65 year old women with prematurely aged or sun-damaged skin, this supplement was shown to improve skin elasticity, reduce wrinkle depth, and ameliorate brittleness in nails and hair. A good brand is BioSil from Jarrow Formulas, available in health food stores..."

What caught my eye is that you get silicon from whole grains. If you're not eating whole wheat anymore, then it seems you're not getting the silicon you used to be getting and maybe that affects skin moisture. I don't know, it just seemed that there could be a connection in my mind.

The PhD nutritionist who diagnosed my son with celiac disease (although he has not been "formally" dx with DH, we just think that's what he has) "prescribed" Biosil for him, so he's been taking that for about a month or so. The PhD said it takes 3 months to notice results, so we're being patient.

I'd be interested in hearing other people's experiences with BioSil (or equivalent).

Carrie

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,188
    • Most Online (within 30 mins)
      7,748

    Leeila
    Newest Member
    Leeila
    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

    • Ginger38
      So I recently had allergy testing for IGE antibodies in response to foods. My test results came back positive to corn, white potatoes, egg whites. Tomatoes, almonds and peanuts to name a few.  I have had obvious reactions to a few of these - particularly tomatoes and corn- both GI issues. I don’t really understand all this allergy versus celiac stuff. If the food allergies are mild do I have to avoid these foods entirely? I don’t know what I will eat if I can’t  have corn based gluten free products 
    • Kris2093u4
      Geography makes a difference.  I'm in the West and Trader Joe's gluten-free bread tastes great and is a better price than most gluten-free breads sold elsewhere in my area.  
    • JForman
      We have four children (7-14 yo), and our 7 year old was diagnosed with NCGS (though all Celiac labs were positive, her scope at 4 years old was negative so docs in the US won't call it celiac). We have started her on a Gluten Free diet after 3 years of major digestive issues and ruling out just about everything under the sun. Our home and kitchen and myself are all gluten-free. But I have not asked my husband/her dad or her other siblings to go completely gluten-free with us. They are at home, but not out of the home. This has led to situations when we are eating out where she has to consistently see others eating things she can't have and she has begun to say "Well, I can't have <fill in the blank>...stupid gluten."  How have you supported your gluten-free kiddos in the mental health space of this journey, especially young ones like her. I know it's hard for me as an adult sometimes to miss out, so I can't imagine being 7 and dealing with it! Any tips or ideas to help with this? 
    • Jane878
      By the time I was 5 I had my first auto0immune disorder, Migraine headaches, with auras to blind me, and vomiting, sensitivity to light and sound. I was 5 years old, and my stepfather would have pizza night, milling his own flour, making thick cheesy gluten pizza, that I would eat and the next day, I would have serious migraines, and my mother & stepfather did nothing about my medical problems. When I was 17 in my first year at college, I was diagnosed with my 2nd known auto-immune disorder, Meniere's disease. I was a elite athlete, a swimmer, and soccer player. And once again my parents didn't think anything of understanding why I had a disorder only older people get. Now after my mother passed from Alzheimer's disease she also suffered with living with gluten. She had a rash for 30 years that nobody could diagnose. She was itchy for 45 years total. My brother had a encapsulated virus explodes in his spleen and when this happened his entire intestines were covered with adhesions, scar tissue and he almost lost his life. He has 5 daughters, and when I finally was diagnosed after being pregnant and my body went into a cytokine storm, I lost my chance to have children, I ended up having Hashimoto's disease, Degenerative Disc disease, and my body started to shut down during my first trimester. I am 6ft tall and got down to 119lbs. My husband and I went to a special immunologist in Terrace, California. They took 17 vials of blood as we flew there for a day and returned home that evening. In 3 weeks, we had the answer, I have Celiac disease. Once this was known, only my father and husband made efforts to change their way of feeding me. At the family cabin, my stepfather & mother were more worried that I would ruin Thanksgiving Dinner. It wasn't until one of my cousins was diagnosed with Celiac disease. They finally looked into getting Gluten Free flour and taking measures to limit "gluten" in meals. He did nothing but ask for me to pay for my own food and wi-fi when I came to the cabin to stay after our house burned down. When he informed my mother, they proceeding to get into a physical fight and she ended up with a black eye. The is just more trauma for me. Sam had no interest in telling the truth about what he wanted. He lied to my mother that he had asked my husband if I could pay for "food" when he asked Geoffrey if I had money to pay for my wi-fi. My mother hates when he spends so much time on the computer so he lied and said I could pay for my own food. I will remind you I weighed 119lbs at this time. (At 6ft) that is a very sick looking person. Neither parent was worried about my weight, they just fought about how cheap my stepfather was. As my mother was diagnosed with Alzheimer's disease in 2014. He had her sign over the will to a trust and added his children. He had no testimonial capacity at the time, so she signed without proper papers. Making this Trust null and void. When I gave my brother my childhood home, my mother stated I would be getting an equal part of inheritance to the house on Race. It currently worth 2.0 million $. I got nothing, and my stepfather has since disowned me b/c of my claim and he knows that my mother would never have left it uneven between my biological brother and myself. She sat me and my husband down, as we lived at the Race Street house and treated and took care of it as our own. My brother took over b/c he was going through a horrific divorce and needed a home so he could get a better custody deal with his soon to be ex-wife who was a Assist DA for Denver. She used the girls against him, and he & I were the primary caregivers. We, Judd and I spent the most time with them pre the divorce. Once Judd moved into the house, he threw all of my mother, grandmother and my family heirlooms out to the Goodwill. Nobody told my mother about this as she was going through cancer treatment and had Alzheimer's disease in her mother and her sister. My stepfather and biological brother took advantage of this matter, as I called a "family council" that my brother just never could make it to at the last moment. All of the furnishing, kitchen ware, everything was in the house my brother just moved into. He had had 2 weddings, I chose to elope b/c my stepfather ruined my brother's first wedding by talking about his relationship with my brother in front of my dad and his entire family, insulting him and having my grandfather leave the ceremony. It was a disaster. My stepfather just plays dumb and blames my father for the slight. I was the only child not to have a wedding. So, my mother and stepfather never had to pay for a thing. My mother had had an agreement with my father he'd pay for college and all medical issues with their kids, myself and Judd. So truly my mother never had to pay for anything big for me in her entire life. I am looking for anyone that has had a similar story, where they grew up in a household that had a baker that regularly milled flour and ate gluten. What happened to you? DId you suffer from different auto-immune diseases b/c of living with a baker using "gluten" Please let me know. I have been looking into legal ways to get my stepfather to give me what my mother had promised, and he erased. Thank you for listening to my story. Jane Donnelly  
    • trents
      Possibly gluten withdrawal. Lot's of info on the internet about it. Somewhat controversial but apparently gluten plugs into the same neuro sensors as opiates do and some people get a similar type withdrawal as they do when quitting opiates. Another issue is that gluten-free facsimile flours are not fortified with vitamins and minerals as is wheat flour (in the U.S. at least) so when the switch is made to gluten-free facsimile foods, especially if a lot of processed gluten-free foods are being used as substitutes, vitamin and mineral deficiencies can result. There is also the possibility that she has picked up a virus or some but that is totally unrelated to going gluten-free.
×
×
  • Create New...