My palette didn't come with any names attached and this bothers me a bit .
There has to be names for these Gorgeous Eye Shadows?
So I went on the Hunt I was browsing the Internet on a mission and out of sheer luck I stumble on a picture of this palette and all the names . Holy Crow !
(all due to my settings for web search being set to images and not web )
It seems that a clear sleeve comes in the palette with the names printed on it.
Mine didn't it was just the clear sleeve.
But I wonder if this is because I purchased mine from Ulta ?
If you buy them off Makeup Revolutions Web-site do you get the sleeve with the names on it ?
Now I am curious, If you know anything about this Please comment Below.
Any way back to the names.
Without further delay .
Left to right
1st - Forever, Bay , Myth, Song , Mermaids, Fishtail, Treasure, Imagine
2nd- Seashell, Creature, Magic, Urchin, Sea, Land, Kingdom, Harmony
3rd - Enchant, Starfish, Pretty, Princess, Waves,Turtle, Mineral, Prince
4th - Future, Ariel, Pinksea, Ocean, Splash, Undersea, Seabed, Whale
I knew they had to have names . My task for the day is Complete . LOL
No Really It was driving me Crazy....
Now On to my thoughts for today .
My Lupus has been in a holy hell of a flare for weeks I am just so darn exhausted all the time and sleep a lot.
I can't seem to get my body adjusted to a pattern of normal sleep and it sucks.
I can say is it is too cold outside and my body hurts .EVERYWHERE.
Which does not help at all.
My daughter has been super sick and I can't be around her.
I already have a low Immune System on top of Lupus .
When I get sick I am sick for weeks and usually end up in the Er .
This has sucked, all I want to do is hold her, and take away all her pain but I can't . My husband took her to Insta-Care and they loaded her up on Medication so hopefully she will start to feel better soon .
Praying that none of my other 4 kids get it......
I am so tired of people saying things to me about this disease . They have NO IDEA what I am going through and don't want to ask .They just assume that it's not that bad and I am blowing it all out of proportion?
Because it's not the same for them. WTheck
I just want To scream at the top of my lungs but that isn't me I choose to ignore them, but that doesn't mean it doesn't bother me ....
Ever Feel like That?
I know every one has different symptom and that no two diagnoses are ever the same.
I see my struggle and other Lupus Fighters struggles and it boggles my mind.
How someone can say they have this disease and not see a Dr. or take any medications ? If I didn't have my Dr. or my medications I would be curled up on the floor crying or worse probably dead .
(That is just based on my symptoms and how I handle things )
I am not one to judge people but when we are talking Lupus This is a sensitive subject for me that I am trying to Understand . Any one else have any Insight to this ?
I know you can be in Remission for some time And people have different ways to treat it .
If you can treat this all holistically I would like to hear more .
My treatment is part holistic and western medicine if it relieves the pain I feel and I can live a normal life to a point I will do anything .
The other question I am always asked? Would you take Medical Marijuana ?
I consider myself to be LDS but I am not the person who makes it to church every sunday.
Honestly I have never been good enough like the other LDS people I know and baptism's and things have caused huge fights and fall out's because of who was invited ,who wasn't, etc.. That is when it all stopped for me
My thoughts of Medical Marijuana to help ease the pain?
I am not against that at all. Yes I said that !
I just couldn't smoke it .. Gross , Yuck , Or I wouldn't use it to Get high .
If it was in candy or a oil form Then Yes I am all for It. If it can help me live a fuller life. (Well one that I can Manage .) And better than I am Now Sign me Up I believe that they both can help.
I hate to admit this but lately I have been super Depressed. I know it's the Winter Blues but I can't help feeling like I am All Alone ! Even though I know I am Not. It's so hard to fight the urge to be happy
I try to go places, I really do. But I walk outside, Can't handle the cold and I am back inside Trying to warm Up for hours .
I haven't felt like doing anything .
(Not even to go see what new Makeup is out, watch a movie ,eat dinner etc.
And Yes my husband has tried a few times to get me out . No Luck
I missed my Monthly get together for us Lupies here In SLC . I haven't been to one yet.
But I really want to go . I just keep forgetting. So I have signed up to receive a reminder a few days in advance and hopefully this will remind me .
Thank you Noelle From The Lupus Utah Chapter for doing this .
As Far as today I at least got up and did some makeup but only enough to cover my rash. It was just mild , Red Nothing drastic But enough to bother me .
Remember how I said I was reaching out to companies for samples and stuff ?
I have heard back from some of the companies I contacted for PR products They have said Right Now it's not something they can do, But they will keep me in mind for the future. I get it, I don't have a huge following and No YouTube channel with subscribers so why would they send anything to me. This will not stop me I will continue to keep on trying . If you know of anyone that can help me in this dept I would love for you to contact them or let me know .
Ipsy Bags will be coming Soon for myself and my daughter so I will have that review up when I get them.
On another note.
I registered for the -Walk to end Lupus Now
This will take place in May the info can be found here https://www.firstgiving.com/utahlupus
This is a goal I am doing for myself . I know that this is going to be very hard for me but I am doing it. I am always exhausted , and being out in the sun sucks for me .. This is going to be a task.. My family will also be there with me .
If you are interested in walking with me you can sign up and Join my Team Here or just click the widget on the side bar.
Bbloggerfightinlupus team https://www.firstgiving.com/team/315249
If you can't walk with me I am looking for sponsors to donate to help me reach my goal ! Anything you can give is appreciated .
Well Now that it is 4 a.m and I am actually tired . Thank you for reading
As Always
Stay Strong and Keep Fighting
Love ya all,
Misty
Don'tHideEmbraceIt
Lupus Fighter and Warrior
There has to be names for these Gorgeous Eye Shadows?
So I went on the Hunt I was browsing the Internet on a mission and out of sheer luck I stumble on a picture of this palette and all the names . Holy Crow !
(all due to my settings for web search being set to images and not web )
It seems that a clear sleeve comes in the palette with the names printed on it.
Mine didn't it was just the clear sleeve.
But I wonder if this is because I purchased mine from Ulta ?
If you buy them off Makeup Revolutions Web-site do you get the sleeve with the names on it ?
Now I am curious, If you know anything about this Please comment Below.
Any way back to the names.
Without further delay .
1st - Forever, Bay , Myth, Song , Mermaids, Fishtail, Treasure, Imagine
2nd- Seashell, Creature, Magic, Urchin, Sea, Land, Kingdom, Harmony
3rd - Enchant, Starfish, Pretty, Princess, Waves,Turtle, Mineral, Prince
4th - Future, Ariel, Pinksea, Ocean, Splash, Undersea, Seabed, Whale
I knew they had to have names . My task for the day is Complete . LOL
No Really It was driving me Crazy....
Now On to my thoughts for today .
My Lupus has been in a holy hell of a flare for weeks I am just so darn exhausted all the time and sleep a lot.
I can't seem to get my body adjusted to a pattern of normal sleep and it sucks.
I can say is it is too cold outside and my body hurts .EVERYWHERE.
Which does not help at all.
My daughter has been super sick and I can't be around her.
I already have a low Immune System on top of Lupus .
When I get sick I am sick for weeks and usually end up in the Er .
This has sucked, all I want to do is hold her, and take away all her pain but I can't . My husband took her to Insta-Care and they loaded her up on Medication so hopefully she will start to feel better soon .
Praying that none of my other 4 kids get it......
I am so tired of people saying things to me about this disease . They have NO IDEA what I am going through and don't want to ask .They just assume that it's not that bad and I am blowing it all out of proportion?
Because it's not the same for them. WTheck
I just want To scream at the top of my lungs but that isn't me I choose to ignore them, but that doesn't mean it doesn't bother me ....
Ever Feel like That?
I know every one has different symptom and that no two diagnoses are ever the same.
I see my struggle and other Lupus Fighters struggles and it boggles my mind.
How someone can say they have this disease and not see a Dr. or take any medications ? If I didn't have my Dr. or my medications I would be curled up on the floor crying or worse probably dead .
(That is just based on my symptoms and how I handle things )
I am not one to judge people but when we are talking Lupus This is a sensitive subject for me that I am trying to Understand . Any one else have any Insight to this ?
I know you can be in Remission for some time And people have different ways to treat it .
If you can treat this all holistically I would like to hear more .
My treatment is part holistic and western medicine if it relieves the pain I feel and I can live a normal life to a point I will do anything .
The other question I am always asked? Would you take Medical Marijuana ?
I consider myself to be LDS but I am not the person who makes it to church every sunday.
Honestly I have never been good enough like the other LDS people I know and baptism's and things have caused huge fights and fall out's because of who was invited ,who wasn't, etc.. That is when it all stopped for me
My thoughts of Medical Marijuana to help ease the pain?
I am not against that at all. Yes I said that !
I just couldn't smoke it .. Gross , Yuck , Or I wouldn't use it to Get high .
If it was in candy or a oil form Then Yes I am all for It. If it can help me live a fuller life. (Well one that I can Manage .) And better than I am Now Sign me Up I believe that they both can help.
I hate to admit this but lately I have been super Depressed. I know it's the Winter Blues but I can't help feeling like I am All Alone ! Even though I know I am Not. It's so hard to fight the urge to be happy
I try to go places, I really do. But I walk outside, Can't handle the cold and I am back inside Trying to warm Up for hours .
I haven't felt like doing anything .
(Not even to go see what new Makeup is out, watch a movie ,eat dinner etc.
And Yes my husband has tried a few times to get me out . No Luck
I missed my Monthly get together for us Lupies here In SLC . I haven't been to one yet.
But I really want to go . I just keep forgetting. So I have signed up to receive a reminder a few days in advance and hopefully this will remind me .
Thank you Noelle From The Lupus Utah Chapter for doing this .
As Far as today I at least got up and did some makeup but only enough to cover my rash. It was just mild , Red Nothing drastic But enough to bother me .
Remember how I said I was reaching out to companies for samples and stuff ?
I have heard back from some of the companies I contacted for PR products They have said Right Now it's not something they can do, But they will keep me in mind for the future. I get it, I don't have a huge following and No YouTube channel with subscribers so why would they send anything to me. This will not stop me I will continue to keep on trying . If you know of anyone that can help me in this dept I would love for you to contact them or let me know .
Ipsy Bags will be coming Soon for myself and my daughter so I will have that review up when I get them.
On another note.
I registered for the -Walk to end Lupus Now
This will take place in May the info can be found here https://www.firstgiving.com/utahlupus
This is a goal I am doing for myself . I know that this is going to be very hard for me but I am doing it. I am always exhausted , and being out in the sun sucks for me .. This is going to be a task.. My family will also be there with me .
If you are interested in walking with me you can sign up and Join my Team Here or just click the widget on the side bar.
Bbloggerfightinlupus team https://www.firstgiving.com/team/315249
If you can't walk with me I am looking for sponsors to donate to help me reach my goal ! Anything you can give is appreciated .
Well Now that it is 4 a.m and I am actually tired . Thank you for reading
As Always
Stay Strong and Keep Fighting
Love ya all,
Misty
Don'tHideEmbraceIt
Lupus Fighter and Warrior
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