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

Hair Loss - Help


nvsmom

Recommended Posts

nvsmom Community Regular

I thought I posted on this yesterday but I guess it got lost with the forum changes. Anyway...

I'm about 4 months into the gluten-free diet. At 2 months, I noticed that I was getting some new growth, which was very welcome because my hair has been steadily thinning for over a decade. Unfortunately at around that same time, I had some sort of autoimmune attack, possibly from my undertreated Hashimotos or another autoimmune problem (lupus suspected) that is yet undiagnosed, and my hair loss increased dramatically; I'm talking a dozen hair balls in the shower alone. My hair thinned noticeably at the front and I have some very thin spots at the back of my head which I can luckily mostly cover with longer hair. The AI attack is mostly subsiding so my hair loss has slowed again, and I do still have the short spikes of regrowth sticking out of my head... Attractive. LOL My husband gave me some looks of sympathy when I asked him to check it for me. :(

My question is: Does anyone have tips or ideas to encourage hair regrowth, and to prevent or slow those periods when my body wants to ... shed?

I currently take biotin on top of B12 (my B levels are good). I also supplement with omega 3 fish oil, cod liver oil and evening primrose oil 2 to 3 times a day. As far as I know, only my D levels are a bit low and they are just on the low side of normal, the rest of my blood levels are really good for a celiac... or even a non-celiac. I take a lot of other vits and supplements but these are the only ones I know of related to hair.

I don't use any special lotions or shampoos but I'm willing to try some... I'm willing to try almost anything. My hair is getting very thin; my pony tail is smaller than a dime. If I was a guy, and it got much thinner, I would be thinking about shaving it off just so I wouldn't have to deal with it.... my husband wouldn't appreciate that look and to be honest, I'm to vain to do that.

Any help would be appreciated. :)


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



Celiac.com Sponsor (A8-M):



Findin my way Rookie

Hi Nicole,

You could try a good b complex vitamin. I think it's b6 that's needed for hair growth. Get one that has methylcobalmin (b12) and 5-MTHF (folate). AOR is a respected brand in Canada and their b complex is pretty good.

I'm so sorry to hear about the possible Lupus. Hopefully it's not Lupus, but something more treatable. Thinking about you.

nvsmom Community Regular

Hi Nicole,

You could try a good b complex vitamin. I think it's b6 that's needed for hair growth. Get one that has methylcobalmin (b12) and 5-MTHF (folate). AOR is a respected brand in Canada and their b complex is pretty good.

I'm so sorry to hear about the possible Lupus. Hopefully it's not Lupus, but something more treatable. Thinking about you.

Thanks for the advice... I don't take a B6 so I'll add that to my grocery list.

I'm not sure about the lupus, it could be something else (like MCTD or UCTD) or just residual celiac or hashimoto problems, or nothing autoimmune related (doubt that one). I'm waiting to see a rheumatologist but apparently there is a doctor shortage since I haven't heard back from anyone after being refered to a rheumatology triage a month ago. I sooo wish I could wash my hands of the whole medical community... I consider them to be a necessary evil! LOL

Linda422 Newbie

I thought I posted on this yesterday but I guess it got lost with the forum changes. Anyway...

I'm about 4 months into the gluten-free diet. At 2 months, I noticed that I was getting some new growth, which was very welcome because my hair has been steadily thinning for over a decade. Unfortunately at around that same time, I had some sort of autoimmune attack, possibly from my undertreated Hashimotos or another autoimmune problem (lupus suspected) that is yet undiagnosed, and my hair loss increased dramatically; I'm talking a dozen hair balls in the shower alone. My hair thinned noticeably at the front and I have some very thin spots at the back of my head which I can luckily mostly cover with longer hair. The AI attack is mostly subsiding so my hair loss has slowed again, and I do still have the short spikes of regrowth sticking out of my head... Attractive. LOL My husband gave me some looks of sympathy when I asked him to check it for me. :(

My question is: Does anyone have tips or ideas to encourage hair regrowth, and to prevent or slow those periods when my body wants to ... shed?

I currently take biotin on top of B12 (my B levels are good). I also supplement with omega 3 fish oil, cod liver oil and evening primrose oil 2 to 3 times a day. As far as I know, only my D levels are a bit low and they are just on the low side of normal, the rest of my blood levels are really good for a celiac... or even a non-celiac. I take a lot of other vits and supplements but these are the only ones I know of related to hair.

I don't use any special lotions or shampoos but I'm willing to try some... I'm willing to try almost anything. My hair is getting very thin; my pony tail is smaller than a dime. If I was a guy, and it got much thinner, I would be thinking about shaving it off just so I wouldn't have to deal with it.... my husband wouldn't appreciate that look and to be honest, I'm to vain to do that.

Any help would be appreciated. :)

Know just what you mean I had a big bald spot right on top of my head and two big sore that wouldn't heal on my arm, I was told it was cause of the lupus and the sun. But now that I have gone gluten free my hair is coming back and my sore are all gone. I also have a flat top. At least now when I comb my hair I am not picking it up from all the place.

I went gluten free May 16 so it may just take some time.

rosetapper23 Explorer

What I've used in the past after a glutening or Hashimoto's flareup (with resultant hair loss) are the following products with much success: BioSil, NeoCell Super Collagen, and chelated zinc. For a number of us here, BioSil has been the most effective.

nvsmom Community Regular

Know just what you mean I had a big bald spot right on top of my head and two big sore that wouldn't heal on my arm, I was told it was cause of the lupus and the sun. But now that I have gone gluten free my hair is coming back and my sore are all gone. I also have a flat top. At least now when I comb my hair I am not picking it up from all the place.

I went gluten free May 16 so it may just take some time.

Thanks Linda. My hair was coming in quite nicely on the gluten-free diet but then something flared up and it fell out worse. I'm hoping being gluten-free will help it grow in again... like before.

What I've used in the past after a glutening or Hashimoto's flareup (with resultant hair loss) are the following products with much success: BioSil, NeoCell Super Collagen, and chelated zinc. For a number of us here, BioSil has been the most effective.

Thanks Rosetapper. I'm hoping it was just a hashi's flareup since I had just started on synthroid a week or two before the "shedding" occurred. I'll look into The Biosil and NeoCell. Thanks. :)

rosetapper23 Explorer

Good luck! With these products, you should start seeing little "fluffies" around your hairline in about three weeks.


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



Celiac.com Sponsor (A8-M):



flowerqueen Community Regular

Hi Nicole, has anyone tested your TSH levels recently, like you said it could be under treated Hashimotos. I had under active thyroid diagnosed many years before Coeliacs disease and I lost 50% of my hair. Fortunately I had very thick hair then, and lots of it, prior to losing it. I did notice more hair loss when my Coeliacs symptoms were at their worst. (2 yrs ago) but I had extremely low ferritin levels (have you been checked for anaemia?) and I had to have high doses of iron for it. I also had very low vitamin D levels, so perhaps these levels need checking too.

Hope this is helpful to you.

nvsmom Community Regular

Good luck! With these products, you should start seeing little "fluffies" around your hairline in about three weeks.

Fluffies are good! LOL To bad this isn't the 80's, I could tease my hair back into sky high knots and curls. LOL

nvsmom Community Regular

Hi Nicole, has anyone tested your TSH levels recently, like you said it could be under treated Hashimotos. I had under active thyroid diagnosed many years before Coeliacs disease and I lost 50% of my hair. Fortunately I had very thick hair then, and lots of it, prior to losing it. I did notice more hair loss when my Coeliacs symptoms were at their worst. (2 yrs ago) but I had extremely low ferritin levels (have you been checked for anaemia?) and I had to have high doses of iron for it. I also had very low vitamin D levels, so perhaps these levels need checking too.

Hope this is helpful to you.

I did have thick hair when I was a teenager. Back in the 80's (decade of shoulder pads and big hair) I had a perm and my hair looked so thick it's width was almost past my shoulders...and I've got wide shoulders. It's been thinning for so long, and mostly very slowly (except for a few periods like a month ago and postpartum) that it snuck up on me. I can't ignore it much anymore. :rolleyes:

My last TSH was a 7 something or other, with a range of 0.2-6.0. This is down from a couple of months ago when it was in the teens. I'm fairly new to being diagnosed with Hashi's but have had symptoms and marginally elevated TSH tests for about 15 years. I've only been treated (synthetic T4) for about 2 months. My doctor is very slow in increasing my doses so my symptoms are not changing, nor are my free T4 or total T3 levels. At this rate, I doubt my Hashi's will be under control until some time in the new year... and from what I've heard, when the med levels are changing, that can cause more hypo symptoms. :wacko:

I'm not anemic, or at least I wasn't in the summer when it was last checked. My D was near the lower end of the normal range, but since that lab result (in summer) I have quadrupled my (sublingual) D intake so I imagine it will start improving. I will request that my labs be rechecked around the New Year (for a 6-7 month check on how I'm doing on the gluten-free diet).

Thanks for the advice. I appreciate it. :)

rosetapper23 Explorer

Good grief! Your doctor is killing you! Is there any way you can changes doctors (like PDQ?)? A level of 7 is unacceptable! You should try to get as close as possible to 2. Also, sometimes the synthetic stuff simply doesn't work--if your body is unable to make T3 from T4, you'll never get better....and so what you'd need is Armour Thyroid, which provides both T3 and T4. Are you really stuck with this doctor? Some doctors are extremely weird when it comes to increasing the dose, Yes, too much thyroid medication CAN kill a person, but, generally, you can "up" the dosage by a safe amount without worrying that. With Armour Thyroid, their site said that I could increase the dose safely by 1/2 tablet...so I did when it became obvious that my thyroid level was too high. You might check out the website of your particular medication to see what they recommend for increasing the dose safely. You can then present that evidence to your doctor and demand a higher increase in dose.

nvsmom Community Regular

Good grief! Your doctor is killing you! Is there any way you can changes doctors (like PDQ?)? A level of 7 is unacceptable! You should try to get as close as possible to 2. Also, sometimes the synthetic stuff simply doesn't work--if your body is unable to make T3 from T4, you'll never get better....and so what you'd need is Armour Thyroid, which provides both T3 and T4. Are you really stuck with this doctor? Some doctors are extremely weird when it comes to increasing the dose, Yes, too much thyroid medication CAN kill a person, but, generally, you can "up" the dosage by a safe amount without worrying that. With Armour Thyroid, their site said that I could increase the dose safely by 1/2 tablet...so I did when it became obvious that my thyroid level was too high. You might check out the website of your particular medication to see what they recommend for increasing the dose safely. You can then present that evidence to your doctor and demand a higher increase in dose.

He's still in the process of bringing my TSH down, I'm just impatient with the process. He started me at 50mcg synthroid for 7 weeks and now I'm on 75mcg and will be checked again in about a month. He has said that he is aiming for a TSH below a 6 (top of the lab range) and I'm pretty sure that I'll have to fight him to treat my symptoms rather than the labs. I feel no different now (at about a 7) than I did when my TSH was above 14... I just wish the thyroid ranges weren't so broad; for patients who have doctors that live and die by lab results, it's a bit daunting.

And I am sort of stuck with my doctor for now. There is a shortage of doctors in my city so it's very tough to find a good one who is accepting new patients.

I would like to try armour, but I thought it might be easier to get him to switch if I could get my TSH closer to a 2 or 1 first... I'll see.

And thanks again. :)

Chiana Apprentice

I've been on the diet for almost two years now, and I didn't realise how bad my hair loss was (I'm in my early 20s) until I stopped losing it a few months ago. I woke up one morning, got in the shower and thought about how strange it was that there wasn't any hair in the drain...or in my hair-brush...or all over my clothes. It just took almost two years to get to this point. I try to eat a high-fat, whole-grain diet. If you can get a doctor to prescribe it, the b-complex shots (it contains all the b vitamins - not just b12) are good for hair/nails, but if your digestive tract heals and you eat a healthy diet, you won't need them.

AVR1962 Collaborator

I used BioSil drops and zinc tablets.

frieze Community Regular

He's still in the process of bringing my TSH down, I'm just impatient with the process. He started me at 50mcg synthroid for 7 weeks and now I'm on 75mcg and will be checked again in about a month. He has said that he is aiming for a TSH below a 6 (top of the lab range) and I'm pretty sure that I'll have to fight him to treat my symptoms rather than the labs. I feel no different now (at about a 7) than I did when my TSH was above 14... I just wish the thyroid ranges weren't so broad; for patients who have doctors that live and die by lab results, it's a bit daunting.

And I am sort of stuck with my doctor for now. There is a shortage of doctors in my city so it's very tough to find a good one who is accepting new patients.

I would like to try armour, but I thought it might be easier to get him to switch if I could get my TSH closer to a 2 or 1 first... I'll see.

And thanks again. :)

The upper limit on TSH is really about 3....per the endocrinology congress from about 6-8 years ago!!!!!! I am not aware of the time needed between med adjustments, so can't help you there....

Just went hunting....lol. Per the european endo journal, 4 weeks is the accepted interval, down from 8 apparently.

nvsmom Community Regular

I've been on the diet for almost two years now, and I didn't realise how bad my hair loss was (I'm in my early 20s) until I stopped losing it a few months ago. I woke up one morning, got in the shower and thought about how strange it was that there wasn't any hair in the drain...or in my hair-brush...or all over my clothes. It just took almost two years to get to this point. I try to eat a high-fat, whole-grain diet. If you can get a doctor to prescribe it, the b-complex shots (it contains all the b vitamins - not just b12) are good for hair/nails, but if your digestive tract heals and you eat a healthy diet, you won't need them.

Two years? Sigh. LOL I'm glad to hear it thickened up for you. :)

nvsmom Community Regular

I used BioSil drops and zinc tablets.

Thanks. I'm now taking them both. :)

nvsmom Community Regular

The upper limit on TSH is really about 3....per the endocrinology congress from about 6-8 years ago!!!!!! I am not aware of the time needed between med adjustments, so can't help you there....

Just went hunting....lol. Per the european endo journal, 4 weeks is the accepted interval, down from 8 apparently.

I've quotoed that number to my doctor, and my son's doctor (his TSH was almost a 5), but they keep saying that our labs are different, ergo the different ranges, but they won't tell me how. I think they avoid American standards even if they are right... just my personal opinion though.

6-8 weeks is the accepted waiting period up here and I'm not pushing that. As a newly healing celiac (4 months) I doubt my gut is picking up the hormones as well as it should so I'm willing to give it time, although I complain about the waiting. LOL ;)

Lady Eowyn Apprentice

Hi

Just thought I would add one of my seemingly random posts.

I would say that you will not feel well with a TSH that high, but would like to add that it's important not to just rely on TSH results alone. IMHO they are unreliable and variable and unlikely to reflect how you feel. There are other thyroid tests that should be part of the picture too - not to mention symptoms - good luck with getting a doctor to listen to those!!!

I have had Hashi's for 36 years - took thyroxine for the first 30 years - was never well but in hindsight, I think this was because of celiac - which I also suspect was the cause of the Hashi's. Now take ERFA Thyroid (Canadian) which is brilliant.

A couple of other points spring to mind:

To test for iron you need to have Ferritin Serum (iron storage) tested not the general test for anemia. Low ferritin gives problems with taking thyroid meds.

I can't take Cod Liver or Fish Liver oil because it makes me hypo within 36 hours even with meds. Luckily eating fish seems ok.

This is my own view - gluten also seems to block the meds and makes me hypery as does low ferritin. Have no idea why this should be but then again gluten has loads of horrible effects.

My hairloss comes and goes (sorry to keep banging the same drum) - it is directly related to gluten and I think, soy.

Excellent website re Hashi's and thyroid in general is Stop the Thyroid Madness.

nvsmom Community Regular

Hi

Just thought I would add one of my seemingly random posts.

I would say that you will not feel well with a TSH that high, but would like to add that it's important not to just rely on TSH results alone. IMHO they are unreliable and variable and unlikely to reflect how you feel. There are other thyroid tests that should be part of the picture too - not to mention symptoms - good luck with getting a doctor to listen to those!!!

I have had Hashi's for 36 years - took thyroxine for the first 30 years - was never well but in hindsight, I think this was because of celiac - which I also suspect was the cause of the Hashi's. Now take ERFA Thyroid (Canadian) which is brilliant.

A couple of other points spring to mind:

To test for iron you need to have Ferritin Serum (iron storage) tested not the general test for anemia. Low ferritin gives problems with taking thyroid meds.

I can't take Cod Liver or Fish Liver oil because it makes me hypo within 36 hours even with meds. Luckily eating fish seems ok.

This is my own view - gluten also seems to block the meds and makes me hypery as does low ferritin. Have no idea why this should be but then again gluten has loads of horrible effects.

My hairloss comes and goes (sorry to keep banging the same drum) - it is directly related to gluten and I think, soy.

Excellent website re Hashi's and thyroid in general is Stop the Thyroid Madness.

Thanks Lady Eowyn. :) I think you are right on a bunch of things:

I don't feel well with a TSH of 7 something. I think I have a doc who loves the TSH so getting him to treat me once I get in the accepted range (a 6) if I still have hypo symtpoms will be a challenge. I have had the TPO Ab done and I was at the very high edge of normal, free T4 was near the bottom range of normal, and I've had total T3 done (also low end of normal) but I'm not sure why he bothered with that one instead of free T3. :rolleyes:

I think I've had hashi's for 10-15 years... at least. It was back then that I started requesting tests but my TSH was always a high normal or just a bit high and my doctors said that was fine... I trusted them... dumb on me, eh? LOL I've only been on synthroid for a couple of months so I'm still waiting to get my TSH down. At the moment he has me on 75mcg a day which I'm guessing won't be enough if I have had hashi's that long, and because I'm about 165lbs... not petite by a long shot. It's hard to wait though...

I'll go back and check my ferritin levels, or if that test was done. Thanks for the tip.

And fish oil, eh? I take a tonne of that stuff: 6 or so capsules a day. Huh. :blink: I hope it doesn't keep me hypo.

I have NEVER been hyper. Ever. Last time I remember having too much energy was about age 9. LOL No symptoms of it at all, and from what I've heard, hyper symptoms are memorable! LOL

I had some hair regrowth with the gluten-free diet but I still get (got) a period of massive shedding. Something else definitely caused it. I'm guessing hypothyroidism or some connective tissue problem. Hard to say... I just hope it doesn't shed again for a few months, my hair is not laying nicely on my head anymore... it's not good. :unsure:

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Wheatwacked replied to Jmartes71's topic in Coping with Celiac Disease
      8

      Related issues

    2. - NanceK replied to Jmartes71's topic in Related Issues & Disorders
      7

      My only proof

    3. - Wheatwacked replied to Scatterbrain's topic in Sports and Fitness
      4

      Feel like I’m starting over

    4. - Scott Adams replied to Kirita's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      Recovery from gluten challenge

    5. - Scatterbrain replied to Scatterbrain's topic in Sports and Fitness
      4

      Feel like I’m starting over


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,288
    • Most Online (within 30 mins)
      7,748

    Greg R.
    Newest Member
    Greg R.
    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

    • Wheatwacked
      Your goal is not to be a good puppet, there is no gain in that. You might want to restart the ones that helped.  It sounds more like you are suffering from malnutrition.  Gluten free foods are not fortified with things like Thiamine (B1), vitamin D, Iodine, B1,2,3,5,6 and 12 as non-gluten free products are required to be. There is a Catch-22 here.  Malnutrition can cause SIBO, and SIBO can worsen malnutrition. Another possibility is side effects from any medication that are taking.  I was on Metformin 3 months before it turned me into a zombi.  I had crippling side effects from most of the BP meds tried on me, and Losartan has many of the side effects on me from my pre gluten free days. Because you have been gluten free, you can test and talk until you are blue in the face but all of your tests will be negative.  Without gluten, you will not create the antigen against gluten, no antigens to gluten, so no small intestine damage from the antigens.  You will need to do a gluten challange to test positive if you need an official diagnosis, and even then, no guaranty: 10 g of gluten per day for 6 weeks! Then a full panel of Celiac tests and biopsy. At a minimum consider vitamin D, Liquid Iodine (unless you have dermatitis herpetiformis and iodine exasperates the rash), and Liquid Geritol. Push for vitamin D testing and a consult with a nutritionist experienced with Celiack Disease.  Most blood tests don't indicate nutritional deficiencies.  Your thyroid tests can be perfect, yet not indicate iodine deficiency for example.  Thiamine   test fine, but not pick up on beriberi.  Vegans are often B12 deficient because meat, fish, poultry, eggs, and dairy are the primary souces of B12. Here is what I take daily.  10,000 IU vitamin D3 750 mg g a b a [   ] 200 mg CoQ10 [   ] 100 mg DHEA [   ] 250 mg thiamine B1 [   ] 100 mg of B2 [   ] 500 mg B5 pantothenic acid [   ] 100 mg B6 [   ] 1000 micrograms B12 n [   ] 500 mg vitamin c [   ] 500 mg taurine [   ] 200 mg selenium   
    • NanceK
      Hi…Just a note that if you have an allergy to sulfa it’s best not to take Benfotiamine. I bought a bottle and tried one without looking into it first and didn’t feel well.  I checked with my pharmacist and he said not to take it with a known sulfa allergy. I was really bummed because I thought it would help my energy level, but I was thankful I was given this info before taking more of it. 
    • Wheatwacked
      Hello @Scatterbrain, Are you getting enough vitamins and minerals.  Gluten free food is not fortified so you may be starting to run low on B vitamins and vitamin D.   By the way you should get your mom checked for celiac disease.  You got it from your mom or dad.  Some studies show that following a gluten-free diet can stabilize or improve symptoms of dementia.  I know that for the 63 years I was eating gluten I got dumber and dumber until I started GFD and vitamin replenishment and it began to reverse.  Thiamine can get used up in a week or two.  Symptoms can come and go with daily diet.  Symptoms of beriberi due to Thiamine deficiency.   Difficulty walking. Loss of feeling (sensation) in hands and feet. Loss of muscle function or paralysis of the lower legs. Mental confusion. Pain. Speech difficulties. Strange eye movements (nystagmus) Tingling. Any change in medications? Last March I had corotid artery surgery (90 % blockage), and I started taking Losartan for blood pressure, added to the Clonidine I was taking already.  I was not recovering well and many of my pre gluten free symptoms were back  I was getting worse.  At first I thought it was caused a reaction to the anesthesia from the surgery, but that should have improved after two weeks.  Doctor thought I was just being a wimp. After three months I talked to my doctor about a break from the Losartan to see if it was causing it. It had not made any difference in my bp.  Except for clonindine, all of the previous bp meds tried had not worked to lower bp and had crippling side effects. One, I could not stand up straight; one wobbly knees, another spayed feet.  Inguinal hernia from the Lisinopril cough.  Had I contiued on those, I was destined for a wheelchair or walker. She said the symptoms were not from Losartan so I continued taking it.  Two weeks later I did not have the strength in hips and thighs to get up from sitting on the floor (Help, I can't get up😨).  I stopped AMA (not recommended).  Without the Losartan, a) bp did not change, after the 72 hour withdrawal from Losartanon, on clonidine only and b) symptoms started going away.  Improvement started in 72 hours.  After six weeks they were gone and I am getting better.  
    • Scott Adams
      Hopefully the food she eats away from home, especially at school, is 100% gluten-free. If you haven't checked in with the school directly about this, it might be worth a planned visit with their staff to make sure her food is safe.
    • Scatterbrain
      Thanks to those who have replied.  To Cristina, my symptoms are as follows: Dizziness, lightheaded, headaches (mostly sinus), jaw/neck pain, severe tinnitus, joint stiffness, fatigue, irregular heart rate, post exercise muscle fatigue and soreness, brain fog, insomnia.  Generally feeling unwell. To Trents, We didn’t do any of the construction but did visit the job site quite often.  While getting the old house ready we stirred up a lot of dust and I’m sure mold but haven’t been back there for over a month.
×
×
  • 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.