Australian Tea Tree Oil Review #teatreeoil

Australian Tea Tree Oil Review #teatreeoil

Australian Tea Tree Oil Review #teatreeoil

I have never used Tea Tree Oil before so when I saw that I could get a free bottle to review I knew I had to jump at the chance.  I have always heard so many great things about this product that I was excited to receive it and use some of it.  I have to say that Australian Tea Tree Oil I received in order to review was a much bigger bottle than I thought I would be.  The shipping was also super quick for me because it was shipped out of Salt Lake City and that is where I live so it was almost overnight.

I also love that this came with a ebook on 53 ways to use Tea Tree Oil which was great for me because I am new to using oils so this was super helpful.  I also loved that it gave me great ideas on how to use it in bath water and different oils to mix with it.  I did use this on my Psoriasis and it did make a few places heal but not all of it.  I had hoped that I would help it all go away but it figures I wouldn’t get that lucky.  I know that this bottle will last me over a year because of how little you have to use of the product.  I am now hooked on this product and I will always make sure that I have a bottle of it handy.

Buy Yourself A Bottle!

More Information About This Product

One of the most versatile essential oils. Naturally fight Acne, Toenail Fungus, Lice, Yeast Infections, Skin Tags, Cold Sores, Dandruff, Ringworm, Fleas, Warts, Psoriasis, and More.
Use to make your own Shampoo, Lotion, Soap, Face Cleaner, Body Wash, and Toothpaste.

Stop polluting your home and make all natural Household Cleaners, Detergents, Shower Sprays, Bathroom Disinfectants, and Kitchen Sprays.

Every large 4 ounce bottle comes with a FREE 100 PAGE GUIDE. We provide you with all the ways to use tea tree oil to improve your life, and replace harmful cleaners around the house.

Many essential oils are diluted to cut costs. We insist on the absolute best quality. We Have the Tests to Prove Our Tea Tree Oil’s Purity and Potency.

FTC:I received free product in exchange for my honest review.  I received no other compensation for this review.
I received one or more of the products mentioned above for free using Regardless, I only recommend products or services I use personally and believe will be good for my readers.

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Multiple Sclerosis Tuesday-My Current Thoughts & An Update


I thought I would so another Multiple Sclerosis Tuesday post this week.  Instead of talking about anything in particular I would just write down some thoughts I have been having about MS and a little update on what is going on with me right now.

Lately I have hated the fact that diseases like MS even exist.  I have gotten to know so many people that have auto-immune diseases and it just piss’s me off to know that god lets people suffer like we do.  That being said I know it is in his plan for all of us and that he gave us these things because he knows we can handle them.  I know that it is true but I often wonder if at times we aren’t given more than we can handle anyway that isn’t the point of this post.

I also have been wishing that people would stop judging those of us who have MS and think we are lazy because we can’t really do much.  Now that being said I for the most part can keep up with anyone and if I don’t tell you I have MS right now you can’t tell.  Even my own family thinks I am lazy because when I get home from work all I want to do it take my bath and go to bed.  People don’t take the time to ask or even realize how much energy it takes for me to just make it through my work day.

As for an update on me nothing much has changed since my last update.  I am back to getting my headaches almost every day again but I thinking that is just a part of the MS for me.  Also my Psoriasis is back with a vengeance which totally sucks.  It isn’t really the fact that it itch it find I am more embarrassed but it than anything else.  I mean it does hurt if I find myself scratching it but other than that I can ignore it.  I am glad that I wear a jacket all the time at work because it just makes me feel self conscious about myself.

That is all for this post.  If there is anything at MS that you would like to know more about please let me know in the comments below and I will make sure I get it written for you.

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I swear if it isn’t one thing it is another thing.  There always seems to be something wrong withme.  I have been doing really well whenit comes to the MS and now I have a new issue. I would much rather deal with the MS that what I have going on now but Iguess I don’t get a choice in all of it.  I think I have psoriasis (I haven’t gone to a doctor for it yet buteverything I have researched leads me to believe that I have it.) Psoriasis isa chronic condition in which the immune systems sends out faulty signals thatmakes the skin cells reproduce faster than they should.  What gets to me is that this is another thingthat my immune system does wrong!!!!  Iam starting to think that they should get rid of my immune system because it iscausing more problems that it is worth. There are several different types of psoriasis and I the one I have iscalled inverse psoriasis.  This type isfound in folds of skin like your armpits, genitals and under breasts.  They say that this type is aggravated mysweat and friction.  Well what in theheck am I supposed to do now???  I guessI can use this as an excuse when doctors tell me I need to exercise.   For me personally the spots that I have areitchy and painful to say the least. Right now I have it under both arms. They are ok on days that I don’t sweat and have my jacket on.  I am glad that work is always cold because Ican wear my jacket and not look like a freak.  They also say that there isprobably a genetic link but as far as I know I am the only one in the familythat has it but we all know that I am always the odd ball.  I think I developed it because of the Tysabrithat I take for MS because of how the drug works it messes with the immunesystem.  I will probably never know forsure what is causing it and it will never go away.  It makes me sad to know that I now have todeal with this disease everyday for the rest of my life.  It embarrasses me to say the least.  I can only imagine what people think if theysee it.  They look like big bug bitesmost of the time except when they get the “scales” looking tops on them.  It is the weirdest thing I have ever seen andonce they start to peel it gets caught on things and hurts then it starts toitch.
Here a few pictures of what it looks like.  I am not posting any pictures of me becauseit is too hard to take pictures of mine because of where they are at.

Sources: Registered & Protected

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