Eyelash/Eyebrow Loss

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Pirouette
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Date Joined Mar 2014
Total Posts : 6201
   Posted 11/4/2017 7:42 PM (GMT -7)   
OK - so you'll need to do what you can until you can move. You won't be able to make a lot of progress with the mold issues but you will probably be able to reduce the associated symptoms somewhat with the MCP. It will be a bit of a cyclic process since you'll still be breathing mold. But at least the mold you breathe won't be compounded day in, day out like it would if you did nothing.

Wearing a special mask for mold over your mouth and nose while you're home will help. I'm not sure of what the mold source is - air filtration units might help if the mold source is outside of your bedroom, for instance. So maybe you can at least control the environment in your room.

Dry air - being inside during the winter with the heated air always makes my nostrils dry and sometimes there is a little blood when I blow my nose so don't worry about that too much.

If you can't use a source like yelp.com to find out if a specialist has reviews, I think you should just try the naturopath or functional doctor who is closest to you are most affordable. The most important thing right now is to get some antifungals, and other support - finding the person with the best potential for a "long-term" relationship is less important right now.

And yes, they will likely want to test your adrenals - they always take a beating when we are very ill. It's very common for people struggling with Lyme to get much worse after steroids, which suppress immune function. Our immune systems are critical to maintain dominance over these infections.

Find the best quality MCO at the best price. PURE is best - make sure the product doesn't have any fillers and especially any sugars. Powder is best and usually cheaper. But if the capsules are cheaper you can always break open capsules and then it's the same as powder.

To start with I wouldn't use both charcoal and MCP. Keep the charcoal - after you make more progress with the detoxing and protocol, you can add in the charcoal - it won't help much with mold but in addition to MCP - will help remove other toxins from GI.

Yes, most of your symptoms should improve once you get the GI better healed and immune system stronger and get yeast/fungus and mold under control. It's very possible that you have very few remaining symptoms and treating Lyme & Co becomes pretty simple and quick.

Neuro Lyme usually indicates neurological symptoms from Lyme. Right now, I really think most of your issues are not due to the Lyme. But the only way to really know is to make a lot of progress with the y/f, mold and gut health. Only then will you know what is left and what it means.

Herxing is a form of sepsis that can occur when you kill pathogens and the debris creates toxins that can cause symptoms. The body knows how to detox and remove all this - but sometimes it doesn't do that very well and herxing can occur. Sometimes we treat too fast, too aggressively and the body just can't keep up and herxing occurs. Again - the yeast/fungal die off can be signficant as well as the reaction to binders - and this might cause herxing. That's why you go VERY slowly to begin with and slowly increase dose, frequency, intensity, etc.

It will be a slow process with a few steps forward and a few steps back but like you said - you will slowly make progress and your brain will eventually start working more reliably, and this will also ease your stress. When I started I was ALWAYS repeating steps - reading my notes over and over and over. I had post-it reminders EVERYWHERE. I even had reminders to look at my 'to-do' list and schedule. It got better but don't worry about redoing everything at first. Do whatever you need to do to establish a system and maintain it. It will get easier.

-p
LYME FORUM MODERATOR

Chronic late-stage lyme—likely infected in '98; Clinically dx Mar'14 w/ Babs, Fry Labs+ Bart-like, CDC+ Bb. First treated 4-5 viruses, GI/immune. Herbal antimicrobials in May; IV port-started Rocephin in Nov; added vancomycin Mar'16;
DETOX: Pinella/Burbur/Parsley/Milk thistle/Burdock/Red root; Samento/Banderol/Enula; JK/Turmeric; BFM-1; antifung; many supps; cholestyramine

Mergirl
Regular Member


Date Joined Oct 2017
Total Posts : 120
   Posted 11/6/2017 7:49 AM (GMT -7)   
Hi Girlie,


I'm sorry! I forgot to reply to your question from earlier about taking Thyroid medication.

No, I'm not currently on any. I suspect that has been one piece of everything making my symptoms worse though. I cannot get ONE endocrinologist here to diagnose and treat me. I'm about to see my 3rd the end of this month after waiting four months for the appt and they don't have the greatest rep. So far two of them say everything is in range but I know that it's not OPTIMAL. Why aren't they aware of this? It's completely ridiculous. I've read all about how this is just another thing that just keep getting undiagnosed over and over and that's what I'm experiencing.

Pirourette was kind enough to recommend I see a naturopath or functional med doc which I'm going to do some research and see if I can find a decent one here today and make an appt. I know I have other issues going on besides lyme, mold, thyroid, etc.

This is all really driving me crazy and making me feel so hopeless.

Mergirl
Regular Member


Date Joined Oct 2017
Total Posts : 120
   Posted 11/6/2017 8:21 AM (GMT -7)   
Hi Pirouette,

Thanks for your last reply and suggestions. I just have a few more questions.

Yesterday, again in the morning, I blew my nose and there was still a couple of light spots of blood that came out. This has happened over the summer too so I'm not sure if it's from dry air. Although I live on the upper floor of a two family house and it does get very dry and humid. Another reason why I suspect mold. I know that during the summer there was a direct source I was breathing the stuff in from, in and around an AC unit that I promptly got rid of. This actually delayed me going to a LLMD because I thought I was dealing with mold sickness. Although my symptoms go back to before I ever had that AC unit. Anyway, so the blood still comes out occasionally, usually the same nostril but might have switched around a couple times.

It's so disheartening because I know if there is mold here, there's not much I can do right now. Ordering a mask today, though I'm not sure what can would really help. I did order at least one hepa air filter so far yesterday that I'm going to try out in one room first and try to confine myself to that room with it as much as possible. If it seems to work out ok, then I'll probably buy another one. I have to be careful with what I'm spending too because I know the naturopath or func med doc will be more $$. I also ordered the MCP and coconut oil yesterday. So trying to follow your weekly protocol as best as I can.

I'm certain some kind of bacterial or fungal overgrowth is at play. I continue to find the white flakes around my eyes and my stomach is a mess! It's constantly grumbling and making noises and first thing in the morning it hurts. Yesterday I experienced ALOT of bowel movements. I don't know if this is a good thing or not, though it would happen sometimes before I ever started abx. Constipation has never been the issue for me. Also, and I'm so sorry for being gross but pretty sure I keep seeing what I think are parasites and or eggs. So incredibly disgusting. Would it make sense that those are coming out with taking abx or would they not have an effect? Also it appears I'm not fully digesting my food either. Again, this started happening months ago. But I've supposedly have had it for years. Never noticed that before this year.

I really would like to try the GI diet as soon as possible. I have read in other places where the bone broth fast would be beneficial for candida overgrowth and or leaky gut. I would like to try it and definitely willing to make the commitment for 3 or 4 weeks. I know it's easy to make but I'm honestly not up for doing much cooking lately. I've been trying to just mainly stick to whole , plant based foods. Already cut out sugar, gluten, dairy, etc a while back. It would actually be a relief to just drink broth day and night for a few weeks. I tried doing a little research online but do you ( or anyone reading this) Know of any I can have shipped to me? I know that most brands aren't great. Not organic, filled with sodium, etc. But there must be a couple that are pure, slow cooked bone broth. ( low sodium is important too for blood pressure and inflammation issues) Anyone recommend any? You can also email me if you don't want to post brand names on this site.

Also, a symptom I have been suffering from for months that I don't see mentioned much besides the occasional blood in the nose. ( Not a bloody nose tho) I've never had any drip or gush out. So it's hard to know if it's mold or just dry sinuses. Lyme also has seemed to give me some allergy issues when I never had them before either.


Thanks again for that protocol. Again, I'm going to try to follow it as close as I can. But yeah, I have to write everything down too or it goes out of my brain to never return or it will take days sometimes. I really wish I did have some help with this.

Oh, and herxing. Another question about that. Since a lot of my symptoms are brain and heart issues. Also burning red eyes but that comes and goes and horrible tinnitus. But for example for me, instead of increased pain and fatigue which I do get but not as prominent as the other things. Would a herx for me then be a worsening of the brain fog, memory problems, tinnitus, etc? Esp the brain fog. It's hard to know for sure but sometimes, it feels like it gets a little worse after I take my abx and supps. Just wondering.

I didn't want to get out of bed this morning at all. Most mornings. Do you have any suggestions for sleep as well or is that something that should improve once I get these other symptoms treated? I hope I can find someone here.

I know I'm asking a lot here and I do really appreciate your patience and time trying to help me with all of this. You guys are my lifeline right now. I hope someday in the near future, I'll be posting about how much better I'm doing. God, I hope.

Mergirl
Regular Member


Date Joined Oct 2017
Total Posts : 120
   Posted 11/6/2017 8:36 AM (GMT -7)   
One more question I forgot to ask,


Been getting this bleeding acne on my scalp for months now. They kind of hurt. Usually, one shows up, bleeds, scabs over then goes away and another will show up somewhere else on my scalp.

Anyone know if this is from lyme, bart or mold or perhaps a different co infection? So far all I have are clinical diagnosis of lyme and bart.

Cherry angiomas also showing up all over my body as well.

Thank you!

WalkingbyFaith
Veteran Member


Date Joined Aug 2017
Total Posts : 503
   Posted 11/6/2017 10:34 AM (GMT -7)   
Mergirl,

Until you get completely away from the mold, these are things you can do:

1. get an air purifier for the room you sleep in.
2. remove any contaminated possessions from the room you sleep in.
3. Spend as much time as possible in clean air, preferably outdoors or at least in a clean, mold-free, chemical-free environment. Pay attention to how you feel in different environments. Try to find a place where you feel safe and have less symptoms.
4. My doctor said sauna is one of the best ways to detox mold. See if a local YMCA or gym or spa has one that you can use.
5. Take MCP but beware that taking a lot of binders while still being exposed to mold can make you feel much worse. Pay attention to how you feel.

WalkingbyFaith
Veteran Member


Date Joined Aug 2017
Total Posts : 503
   Posted 11/6/2017 10:38 AM (GMT -7)   
Mergirl said...
One more question I forgot to ask,


Been getting this bleeding acne on my scalp for months now. They kind of hurt. Usually, one shows up, bleeds, scabs over then goes away and another will show up somewhere else on my scalp.

Anyone know if this is from lyme, bart or mold or perhaps a different co infection? So far all I have are clinical diagnosis of lyme and bart.

Cherry angiomas also showing up all over my body as well.

Thank you!


Can't say for sure as symptoms overlap, but considering your situation I would suspect mold over the others.

Be sure to discuss mold with the LLMD. The doctor should be aware of the connection between Lyme and mold.

Pirouette
Veteran Member


Date Joined Mar 2014
Total Posts : 6201
   Posted 11/6/2017 4:04 PM (GMT -7)   
Mergirl -

I am not sure about the parasites and abx - Be sure to mention what you're seeing in the stools at your appt. You might also take a photo - sometimes they are easier to identify by the eggs and carcasses left behind - and then it will be easier to know what to test for.

Doing the bone broth is excellent - I would be careful not to do the "cleanse" for too long - I think in your case 3 wks is way too long. With everything going on with you and your diarrhea and other GI issues, you're not getting enough nutrition as it is. Cleanses can be good for us but also demand a lot of resources from our body, which you don't have right now. Doing this too intensely or for too long can bring additional burden to your GI and immune system and make everything worse. Even in a healthy person a cleanse will make you weaker - and you can't afford that right now.

I would supplement a restricted liquid (soups, purees, juices) with bone broth - drink it like tea. I do this all the time. VERY helpful and nutritious. The brand probably doesn't matter as long as it is bone broth (not "chicken-flavored" broth) and organic/Non-GMO. Alternate between beef bone broth and chicken bone broth. The regular broths are now known to be full of toxic stuff, artifical hormones, antibiotics and other gunk (thanks to health ranger's lab testing). A great online source for a discounted product and really quick shipping is Vitacost dot com - they also have just about every other toiletry and supplement item you might need.

I'm not sure what you're asking about herxing but it is impossible to know what herxing you will experience before it happens - it is usually an increased intensity of your sx and sometimes new sx. Sometimes it's intense, sometimes it's almost unnoticeable. If you have intense herxing, it's best to increase detoxing and/or reduce treatment or slow it down. Significant herxing can be stressful on the body and generally not beneficial. Slow things down and slowly build up treatment again.

I'm not sure what sleeping issues you're experiencing but generally, sleep problems are due to adrenal imbalances. Your GI problems are also probably contributing. Your naturopath can help you figure this out.

I'm not sure what the open sores on your scalp are. You'll have to have the ND look at these too.

Cherry angiomas are common w/ bart and babs.

-p
LYME FORUM MODERATOR

Chronic late-stage lyme—likely infected in '98; Clinically dx Mar'14 w/ Babs, Fry Labs+ Bart-like, CDC+ Bb. First treated 4-5 viruses, GI/immune. Herbal antimicrobials in May; IV port-started Rocephin in Nov; added vancomycin Mar'16;
DETOX: Pinella/Burbur/Parsley/Milk thistle/Burdock/Red root; Samento/Banderol/Enula; JK/Turmeric; BFM-1; antifung; many supps; cholestyramine

Mergirl
Regular Member


Date Joined Oct 2017
Total Posts : 120
   Posted 11/7/2017 1:32 PM (GMT -7)   
WalkingbyFaith said...
Mergirl,

Until you get completely away from the mold, these are things you can do:

1. get an air purifier for the room you sleep in.
2. remove any contaminated possessions from the room you sleep in.
3. Spend as much time as possible in clean air, preferably outdoors or at least in a clean, mold-free, chemical-free environment. Pay attention to how you feel in different environments. Try to find a place where you feel safe and have less symptoms.
4. My doctor said sauna is one of the best ways to detox mold. See if a local YMCA or gym or spa has one that you can use.
5. Take MCP but beware that taking a lot of binders while still being exposed to mold can make you feel much worse. Pay attention to how you feel.



Thanks Walking.

Those are good suggestions. I did order an air purifier, just waiting for it to come. I'll try to remove what I can from my room but it's pretty bare bones as it is. I threw away some books and stuff a couple months ago when I found the moldy ac I was sleeping next to. Or trying to sleep. I'm still going crazy trying to figure all this out. I'll try to see if I can afford a membership to the Y or gym. Last I checked with the Y it was a little out of my current budget which is completely almost none existent. Not sure where I can go to try to avoid the mold, if it is here. I don't think there's ever been any water damage. It is an old house and can be quite dusty in areas. Lots of sheet rock and plywood boards and such. I've tried looking around but I don't see any. I know it doesn't mean it's not there. I'll try to spend more time outside but it's beginning to get quite cold here too.

I just wish I knew for certain what I'm dealing with here.

Still getting the blood spotting from nostrils, 3rd day in a row. I don't think it's ever happened this much before. My sinuses do feel pretty dry. An another complication, my regular docs office called the other day and said THEY received my Igenx test results. After I had been waiting for weeks. My doc said she doesn't know how to interpret the results. Has never seen or heard of the test before I requested it. According to her it doesn't state positive or negative. Now, this is all coming from her receptionist so I didn't get to speak to my doc directly. I don't understand why she couldn't get on the phone with me herself. I wanted the test results because I'm supposed to see my LLMD tomorrow and wanted to show him. But since I haven't been able to drive, I can't pick them up. They are going to mail me a copy but that will take a few more days. Hell, I already waited this long.

If some of this is mold or all of it. I'm not sure what I'm going to do. If I still had some money socked away it would give me some options at least but I don't. I did one of those cheap petri dish tests and some grew in it. I put it in an area where I suspect it. But to be fair, I also had the window open near by. Going to mail it in and see what comes back as far as what kind. Right now it seems that's all I can do.

Thanks again.

Mergirl
Regular Member


Date Joined Oct 2017
Total Posts : 120
   Posted 11/7/2017 2:10 PM (GMT -7)   
Hi Pirouette,


It looks like the protocol you laid out for me will be advanced a little bit. I called a naturpath yesterday, unfortunately, since there are few of those and FMDS in my area, yelp or online ratings weren't much help. None of them had very many ratings if any. So I kind of felt like I was closing my eyes and picking. But I tried my best. She had a cancellation for Thursday of this week. I don't know if it's a good sign or not. Just to walk in the door is going to be pretty expensive and I'm sure she will recommend I get some herbals or meds or something depending on whether or not she can sort through this mess. Less money I'll have to put away for an eventual move, if I survive all of this.

I also made a follow up appt with my allergist. I saw something online that they are familiar with mold issues. I kind of stopped seeing them when I got the lyme diagnosis. But I don't think I told them about the mold at the time either. Past or present (possible) exposure. Maybe there is something they can recommend or do to help. It's strange though, I've been here over 5 years and never got these kind of symptoms before. My symptoms were excruciating neurological pain. Head, neck, eyes, etc and pain and swelling in knees. Now it's brain, heart, eyes, ringing ears etc. Which makes me think it might have always been lyme and just progressed and changed over time.

I'm trying to separate my very long list of symptoms and read as much as I can to see which symptoms may be which but it all seems a little conflicting and confusing.

I wouldn't be surprised at all if one of my issues were adrenal in nature. I know I crashed completely after taking the steriods. Something keeps me from sleeping. For well over a year now.

I'll see if I can order some bone broth as well. Sorry, I think I misunderstood your instructions for the GI diet link you provided. I'll go back and recheck that since I already forgot what else was on there besides bone broth! I started using vitacost last month to order my supplements so I'll see what's available there.

I'm not sure what to tell the naturpath when I see her this week. I know it's a lot. Your list on separating the symptoms helps though. I'll use that.

My LLMD also thinks Cherry Angiomas and some of my other symptoms are Bart. Diagnosed me with that and Lyme. Yet here I am, still not 100% convinced. The proof is everywhere yet I'm still waiting to see positive blood tests. I did do a regular bart blood test and it came back negative, so did babs and ehrlichia aong with lyme, again. I know none of these tests are accurate but it doesn't make things any easier for me lately. I'm going to see about CIRS testing as well and if I can afford something like that. Will probably have to wait until at least next month though.

Also got the results of heavy metals. Nothing seems very high there either. But I still haven't seen the doc about those yet. Just got them yesterday.

I'll try to talk to him about the mold but my first appt , he wasn't really receptive to hearing about it. He just said something like everyone is exposed to mold everywhere and there's a doc around here somewhere I can see but I don't want to go down that rabbit hole. Or something to that effect. So, I didn't get a chance to tell him of my mold "injury" with the AC and how it correlated to some of my symptoms, or seemed to. I'll try again though.

Just so tired, overwhelmed and confused. I need my brain to work for all this and it's just not happening.

One more question. I see you had used cholestyramine. Was that for mold exposure or injury? Did it help? How did you find a doc willing to prescribe it? I think that would be challenging around here. Is the MCP similar to it in how it works for myotoxins?

Thanks again , P.

Georgia Hunter
Veteran Member


Date Joined May 2012
Total Posts : 2018
   Posted 11/8/2017 2:53 AM (GMT -7)   
My hypothesis on why we have cherry angiomas does not involve bartonella, it involves the translocation of GI bacteria to the periphery.

Mergirl
Regular Member


Date Joined Oct 2017
Total Posts : 120
   Posted 11/9/2017 2:32 PM (GMT -7)   
Hi Georgina,


Thanks for your response. Would you mind explaining a bit more what you mean by that?


Thanks smile

Georgia Hunter
Veteran Member


Date Joined May 2012
Total Posts : 2018
   Posted 11/10/2017 2:30 AM (GMT -7)   
Mergirl said...
Hi Georgina,
Thanks for your response. Would you mind explaining a bit more what you mean by that?
Thanks smile


The studies show that less than half of the people that have acquired the borrelia burgdorferi bacteria get Lyme Disease. This means that Lyme could occur from several possible etiologies and certain conditions contribute to the virulence of "Lyme Disease." When studying my condition which involves having Lyme and Babesiosis, I discovered literature that circumstantially supported Lyme Disease simply as a dysbiosis caused by borrelia. It formed a reasonable explanation for severe and persistent neurological Lyme and why treating is so difficult in many people. Yes, borrelia is present and most likely a causative agent, but the pH change in the GI tract altered microvascular blood flow which allowed translocation of normal bacteria from the GI tract into the periphery (synapses, joints, even CNS). The translocation, along with dietary eating patterns of high nitrogen intake, can contribute to dysbiosis and accumulation of too many gram negative anaerobes in the GI tract. In essence, borrelia is so difficult to treat because it makes our immune response fight everything else. It waters it down.

Gram positive bacteria in our GI tract produce bacteriocin and streptocins which are anti-bacterial proteins. This is why our GI tract acts as such a major component of our immune system. A translocation of these bacteria increases these proteins in our periphery and helps us reduce the amount of borrelia. These gram positive bacteria are beneficial in our GI tract but in our periphery, they come at a cost. Yes, they initially reduce oxidative stress, but they also cause complications.

Lactobacillus and other gram positive bacteria have been shown to increase growth in the presence of fatty acids, especially in the absence of riboflavin (Vitamin B2). They find plenty of fatty acids in the periphery. (Lineolic acid can suppress their growth and there are some interesting things there.) In the periphery, Lactobacillus can be considered a pathogen and alters lipids through lysosomal degradation. Lysosomal degradation comes from lysosomes and they are acidic organelles inside of our cells that have many functions including detoxifying our cells. Translocation could make detoxing very difficult for some no matter what their genetics show.

I could hypothesize that translocated bacteria can cause a form of temporal gangliosidosis. This needs more study.

astroman
Veteran Member


Date Joined Mar 2014
Total Posts : 4011
   Posted 11/10/2017 8:17 PM (GMT -7)   
Eyes-

I had something very similar, but being a guy, I dont count eyelashes LOL. The similar part was dandruff like skin flakes on my eyelids. It eventually got red, raw and slightly cracked. I think it was yeast or candida itself, my eyes burned too, and was hard to focus sometimes and lids were puffed up. I had systemic candida before per blood work antibodies, simple insurance covered test that average Drs dont know about., was from Quest or LabCorp. If its in your blood, its everywhere. I used coconut oil on my eyelids, its antibacterial, maybe anti-yeast, does not burn. I was on diflucan a couple times, but used it every day for about 1-1/2 months each time, it goes into your blood..Like ABX, its hard on the liver , so I got liver alt/ast tested just like on ABX. Oral Pill Nystain does not go beyond the gut, kinda worthless. Avoided sweets and carbs to rid candida too if thars what it is. The eye thing lasted two months for me.
Ended ABX for Lyme in 2015. Rebuilding / repairing / fine tuning since then. What an adventure this has been.

Mergirl
Regular Member


Date Joined Oct 2017
Total Posts : 120
   Posted 11/11/2017 5:14 PM (GMT -7)   
Hi Georgia,


Thanks for that explanation. It is clear and concise but I have to admit, my brain fog is so severe lately that I've read it several times now and still trying to grasp and retain it.

I'm sure my GI is part of the whole picture with me. I'm still getting IBS and malabsorbtion issues even today sad I feel like I have so much wrong with me between that, my eyes, adenals, mold, etc. And not even my llmd so far is helping with these issues. What you said makes sense too because if I've had Lyme and co for so long, why am I noticing more and more red spots show up just in the last year. Something just doesn't make sense here. That goes for a lot of my other symptoms too. Most are relatively recent.

Thanks again. I'm going to keep reading it until something sticks. This is so scary and frustrating.


Astroman,

You made me smile when you said you don't count eyelashes because you're a guy. Thanks for that and the info!

Candida or some kind of overgrowth makes sense. Unfortunately, I'm currently on Medicare because I haven't been able to work at all so I'm not sure they would cover the bloodtest for candida. If so I would def like to take it. I think I probably had it long before I started abx. But the eye stuff is still relatively new. Didn't notice anything until around 4 or 5 months ago. I usually don't notice losing eyelashes either or I didn't until I was finding several every single day. Some eyebrow hairs too but mostly lashes. Either on my face every time I looked in a mirror there was one or I would be writing on paper and one would fall out right in front of me. I collected them for a couple days and actually took a picture. There was a BUNCH.

My eyes are always bloodshot and glassy looking now. Little red lines in them. Never had this before. Occasionally they will burn a little of feel irritated. I started connecting it to the Lyme when I got diagnosed because a couple days after starting abx I think it was one of my herx symptoms. It got very very severe where I had to lay down with a cool cloth over my eyes.

But now there's always white flakes and gunk coming out of my eye or around or stuck in my lashes or brows. I'm trying the coconut oil treatment but just started and so far hasn't made much of a difference. This is just one thing that's driving me crazy lately. I feel like none of the docs of any kind around here are going to be able to sort through all of this.

My llmd said to call them and let them know if I get a yeast infection. Well, that hasn't happened but I certainly think I may have it inside and it may be coming out of my eyes. I have no idea anymore. So sick of seeing lashes on my face all the time. Like a lot of my sx it freaks me out. I think I'm going to call the llmd, tell them I do have a yeast infection and maybe they will give me some diflucan to try. Sounds like that's what a lot of people here to. I'm just surprised he doesn't seem all that concerned about candida. My gut has always been a problem and I read prednisone can cause or make it worse which I did unfortunately take earlier this year and that's when I really started the down slide with every single system in my body, including my stomach. I noticed the eyelash loss a couple months later.

Oh and I've def been avoiding sugar and carbs like the plague. Will continue that as well.

Thanks again smile
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