MUA Undress Me Too swatches!

Hello ickle pickles!

Wait no more, here are the swatches from the fantastic MUA Undress Me Too palette, which is a dupe for the Urban Decay Naked 2 palette.

There are 10 fantastic colours, one which is great in the flesh but doesn't show up because it's a perfect match for my skin (Naked) and one which is abysmal (Lavish) - at least in my palette. I think I got a dodgy one. The bottom row are sublime, there's an amazing taupe in there (Exposed) which should suit absolutely everyone.

Without further ado:

Naked blends in so well you can't see it and Lavish is crap.



What do you think? Which one is your favourite? 

Thanks for reading!

You can buy the Undress Me Too palette for £4 here. MUA ship worldwide so get in! I like this more than the first Undressed palette. I can see myself getting through this beauty in no time at all.


MUA Undress Me Too palette - Urban Decay Naked 2 dupe!

Hello loves!

When I saw MUA were releasing a new palette last week I was in there with both feet, especially as it's a dupe for the Urban Decay Naked 2 palette.

Click on photos to enlarge.


Because I'm a shit I'll keep you waiting until tomorrow for the swatches! Rest assured, 11 of them are absolutely stunning.

Meanwhile, it's £4 and you can get it here.

To nick a phrase from Gandalf, fly you fools, FLY!
(You're not fools, of course, but go get this baby. You will not regret it!)

A bitchin' breakfast and a super-supplement

Hello lovebirds!

I decided to show you what I normally have for breakfast. It's a super healthy start to the day and I wanted to share! 

I use:

About 200ml unsweetened soya milk
A banana
A tablespoon of virgin coconut oil
About half a tablespoon of agave nectar
A huge handful of kale
A level teaspoon of proto-col Green Magic (see end of post.)

Click photos to enlarge.

First I pour in the milk, as the blender needs liquid in the bottom to get all blendy with. Then I throw in the kale, chop a banana (or two) and sometimes I chuck in grapes, strawberries or blueberries too. I put in a tablespoon of coconut oil and a bit of agave nectar to sweeten the smoothie. 



Normally I would put the Green Magic in the blender but this morning I forgot because I was busy taking photos. As I forgot I just stirred it in with the finished smoothie. I blend for about 30 seconds on low power and 30 seconds on high power. This will make you just over a pint of delicious smoothie. I can't taste the kale at all. All I can taste is banana and coconut. You can also throw seeds in the mix. They add a beautiful nutty crunch to it. I use chia seeds or sesame seeds. You can also pop a small amount of porridge in if you're really hungry, but add more liquid or the smoothie will be more of a lumpy! ;)


Why the kale? I tend to be on the anaemic side most of the time so I have kale for iron. I hate red meat.
Why the coconut oil? It's really good for your skin, hair and nails and is a good fat.
Why the agave nectar? It's low GI and a lot better for me than sugar or sweeteners.
Why the banana? For taste and for potassium.
Why the Green Magic? It's touted as an energy fix and as I have CFS I need all the help I can get. A friend of a friend of a friend went from being bed ridden with CFS to getting a part time job after a few months on it and a friend of a friend (who wasn't ill) has seen her energy levels rise considerably.

I'm wary of 'miracle cures' but even if it gives me enough energy to be able to cope with the housework better than I can now I'll be happy, and any more than that is a bonus. You're supposed to be able to tell a difference after 6-8 weeks and I've been taking it for a week, so it's far too early to tell. I hope it works. It's £28 for a 2 month supply from Amazon. Other sellers charge more.

200g = 2 month supply


proto-col green magic is a revolutionary blend of 16 of the worlds best super food nutrients including Spirulina and Chlorella. Naturally rich in protein, essential fatty acids, enzymes, sea minerals, amino acids, vitamins and antioxidants.


proto-col green magic is an enzyme rich array of organically grown terrestial plants skilfully blended with micro-aquatic plants forms, Royal Jelly and a mixed culture of lactose-free intestinal flora.


proto-col green magic delivers vast amounts of nutrition in little mass, with no harmful fats, sugar, artificial flavours or colours.


Dosage: Adults. Take 1 teaspoon 1 to 3 times daily, depending on your nutritional needs. Can be mixed with your favourite juice or purified water.


Ingredients - Hawaiian Spirulina, Broken Cell Wall Chinese Chlorella, Soya Lecithin, Barley Grass Juice, Wheat Grass Juice, Kamut, Rice Kernel Membrance Powder, High Pectin Apple Fibre, Icelandic Kelp, Wheat Sprouts, Nova Scotia Dulce, co Enzyme Q10, SOD w/catalase, Royal Jelly, Jerusalem Artichoke Powder, Lactobacillus Acidophilus and Bifidus Bacterium (Lactose free).

Lactose free, gluten free, dairy free.
Suitable for vegetarians - product does contain Royal Jelly

Do not exceed stated recommended amounts.

It's dark green, smells like fish food (that'll probably be the sea minerals) and tastes as you'd expect something that smells of fish food to taste - a little bit funky! As well as my morning level teaspoon, I have two others mixed up in apple juice or soy milk throughout the day. It's certainly not unpleasant when mixed with liquid. It doesn't make me gag at all, and I have a super-sensitive nose, so many things do make me gag. You do have to stir it very well, or else it'll clump. I normally stir, have a mouthful (snigger), stir again and so on until it's gone.

I will report back in about two weeks with my findings!

What do you normally have for breakfast? 

Although I love my smoothies, once a week you can't beat a bacon sarnie for breakie!

Thanks for reading. Keep your eyes peeled for my catch up blog The Sunday Sandwich later, which will have some photos from the week as well.


OPI 'If You Moust You Moust' NOTD

Hello dolls!

Here's my latest mani using OPI If You Moust You Moust, a lovely pink shade, and a purple shatter from OPI.


I bought these from the Lena White website.

Keep your eyes peeled later for The Thursday Fap!

What's on your nails?

Thanks for reading!

Wednesday Waffle - Walks

Hello lovelies!

I want to talk about walks. I've always loved walking.


When I was a child and I needed to think something through, I'd take myself off walking on my own - often barefoot - because I've always been a bit of a free spirit. You might think 'What would a child have to worry about?' but I've always been an old soul, and my mum and dad split up when I was really young so I was often troubled.

There was this one place I used to gravitate to. It's a small burial ground in my home town. It's not a graveyard as it's not attached to a church, but there used to be one there hundreds of years ago. The gravestones are all placed along the walls of the burial ground. It has a spectacular view across the town as it's high up on a hill and I used to stand there for ages trying to work out my problems. I've always felt at peace among the dead.

When I started going to senior school I got plenty of exercise as I lived about 2 miles away from my school and walked there and back every day up hill and down dale as we didn't have a car. Going into my teens I still walked to process my thoughts, but mostly out of necessity. Anywhere local I wanted to go, I had to walk to. I'd always prefer to walk rather than getting on a train or bus. When you're on foot the world's your oyster - you're not crammed in a moving lump of metal with lots of other people, being forced to listen to their noise. I walked miles and miles every week. When I started my first job, again I walked. I had a 2 mile walk each way initially, and once I'd moved house it was a 3 mile walk each way. Any time I was pissed off about anything, I'd stomp around until I'd worked it out of my system.

I was still walking everywhere when I met hubby. It wouldn't be unusual for us to walk 8 or 10 miles in a day on the weekends. We walked on holidays, we walked at home, we walked round London when we'd been to see his parents - you get the picture. 

It was on a holiday in 2007 that my illness first came to light. I'd been feeling quite off for a while, but we had decided to book a caravan holiday in Torquay 3.5 miles away from the town centre so we'd be forced to cram loads of walking in every day. The first day or two I was suffering and thought 'Oh, you've only just finished work, you'll have a couple of days of good sleep and then you'll be fine.' But it didn't get better, it got worse. There were a few times on that holiday where I'd be walking along crying as I didn't feel like I could put another foot in front of the other without collapsing. Plans of our walking holiday were abandoned and we walked part way to town every day and got buses or cabs the rest of the way. Being the optimistic fool I am I just brushed it all off and it wasn't until April 2008 when things really went to pot physically that I knew the future was full of question marks.

I've documented very recently (last week) how things with my health have affected me, but I've never really spoken about how I've had to give up on my love of long walks. I'll talk at the end about the way I've adapted walks to suit me so I can get some exercise when the pain allows it.

When I was first ill, say for the first 3 years, I railed against it hard. I'd try to do the things I liked to do, like walking a long way, until it got to the point where my body was screaming at me to stop. If I had a good day, I thought I was cured. I'd do everything at once and end up feeling awful for days. It's called 'boom and bust' and I've gradually learned not to do it. The big wake up call was when we moved about 4 years ago. Obviously packing up a home is a hard job on its own, but when it came to moving day, I carried just 3 boxes down from our top floor flat one at a time, put them in the van then went back upstairs. After the 3rd box my friend took one look at me and ordered me to sit down. I did feel tired and breathless but I didn't know what she meant until I looked in the bathroom mirror. My whole face and neck was purple. I looked like I was going to have a heart attack. I busied myself with cleaning up and ordering people about as required, but didn't do any lifting from then on. At the new flat I was putting things in the right rooms, and doing some light unpacking (the kettle, oh how lovely to see you again my friend!) but again not really doing any heavy lifting. The aftermath of the move meant I was sleeping for about 14 hours a day (or more) for almost a month. I'd literally get up, have something to eat, fall back to sleep, wake up at teatime, be awake for a few hours then have to go back to bed. Rinse and repeat, do not pass go. Lesson learned.

So after that I curtailed my activities further - I wasn't working, but I still tried to have a pretence of a social life once in a blue moon. As we lived fairly near to town, I'd have little excursions into town and got some exercise that way, but if I took the opportunity to capitalise on a sunny day and have a longer walk, I'd overdo it and have to get to bed as soon as I got in. With Fibro you have a delayed pain reaction, so one minute I'd be fine and the next I'd be in tears of pain and exhaustion. I would literally get in the front door, crawl up the stairs on my hands and knees to our top floor flat (yes another one, what a prat!) get into bed fully clothed (as I didn't even have the energy to take my clothes off!) and be out like a light.

Soon after this point walking to town became too much as walking on concrete for any length of time started to jolt my joints. When we moved again 2 and a half years ago (I did NO lifting or carrying at all this time, ha!) from a place right near town to somewhere about 3 miles out of town I would occasionally still try to walk the whole way. It wasn't pretty. As time went on. I'd walk less than halfway and book a cab for the rest of the journey, and then as I got worse I'd get a cab there and back. So every time I go to town without hubby now, I go there by cab and back. By bitter experience I know if I were stupid enough to try to walk to town tomorrow I'd be in pain for several days afterwards. I have to pick my battles. Some things are just not worth the pain.

We'd worked out that walking around towns was bad news for me a couple of years ago, so we tried forest or country walks, and that summer that was grand up to a point. We'd drive to somewhere where I could walk without hurting myself. I could rest when needed as woodland tends to have lots of benches or logs to sit on and the softer ground was sympathetic to the cries of my joints. As is often my way, when something goes well I want more, more, moaaaaar. After a second walk over this particular weekend we were about to go back to the car when I looked down to close a farmer's gate and BOOM! The next thing I knew I was laying down. As I turned to the left to roll over and get up, I saw asphalt - my head was in the road. At first I thought I just fell, but hubby said I just tipped over backwards suddenly. More to the point there was no sense of falling. None. One second I was latching the gate, the next my head was about to be road pizza. For the second time since I'd had Fibromyalgia and CFS, I'd passed out from overexertion. (The first time it happened I was hoovering. I woke up with a big headache and a lump on my forehead where I'd conked out and bashed my head on the radiator.)

So then I realised this CFS business was a serious bugger and I'd better rethink this walking malarkey. So the walks got shorter, and then other problems appeared. Walking in woods in the summer is fine - the ground is usually dry, but once it starts to rain, there's lots of mud for me to slip in. My legs went east and west respectively while I was trying to climb up an almost vertical slope one time and I almost pulled hubby down with me when he offered me a hand ;) Then CFS made my balance worse, and I started tripping a lot. There are no end of tree branches and holes in the ground in woodland, so hubby found himself having to walk in front of me pointing out every inch of terrain in case I had a fall. It was a massive pain in the tits for both of us. I was scared of falling and hurting myself, and he was probably scared I'd fall on him and flatten him, hahahaa!

For a while it looked like I'd have to give up on walks altogether, but the dead came to save me! I love photography and history, and if I can put them together then all the better. We started driving to old churches with parking nearby. There are always LOADS of benches in graveyards and as they're places of solitude no one minds if you sit on a bench for half an hour. I can walk around taking photos of old gravestones, sit down for a breather if I need one, even eat a spot of lunch if we brought some. When I've had enough we go back to the car to go home.

Another thing I worked out was I can walk a bit further if there are no stupid hills to contend with. I'm not the sharpest knife in the drawer at times! I have a very gammy knee and it really doesn't like hills. It tends to get a bit irate and start wobbling about dangerously if it has to contend with hills, so another thing we can do now we have the car is drive to somewhere where it's all flat and have a little perambulate. I live in a town which is up and down like no one's business but there is one very flat bit - the sea front. Genius - what do seafronts always have? Loads of friggin' benches, that's what! Why do you think old people love the seaside so much? Benches, mo'fuggers!

So, although I can no longer go on bloody great yomps through town and country, I can adapt walks to my health sitch and still get a little bit of time out in the fresh air, which is what really invigorates me. On the days where I'm really not up to a walk, hubby will sometimes indulge me by taking me on a drive, as just getting out of the house can be a tonic.

In my roundabout, not-at-all-articulate way this is positive, or it's supposed to be. No matter what changes ill health may bring you, it is possible to adapt and still do something that makes your heart sing, just perhaps in a slightly more gentle way than you used to do it.

Thanks for reading!

Vanity

Hi lovelies!

Here's something I wrote on Tumblr a while ago. I thought I'd share it here too.

I’ve been thinking a lot about vanity, and specifically if vanity can exist without narcissism, or within an acceptable level of narcissism. I think so.

I believe in vanity as self-care and as a part of self-love. I think glorifying yourself to a certain extent is a great thing. For me, as a person with depression, it’s important for me to remind myself that I look good sometimes, and I take pleasure from it. My way of reinforcing that is to make myself up and take a tonne of photos. Those photos exist in stark contrast to the woman I see in the mirror - often washed out, sad, sometimes anaemic, listless. They exist to say ‘THIS is you, not the woman in the mirror.’ I think I probably need to feel ‘cheered up’ by looking good a lot more now than I did when I was well. It’s literally one of the only things keeping me sane.

Because I’m British, because we’re so good at being humble, I used to feel guilty for posting a lot of photos of myself in case people thought I was ‘up’ myself or self-obsessed. Now I don’t give a monkey's. I won’t apologise for doing something which helps me to feel a little more human. We all have our struggles. We all nurse the pain somehow, be it drugs, booze, food, sex, etc. In my case I pile on make up and pull faces in front of a camera.

When you see my face, know it’s therapy for me. I’m probably having a really shit day and need to make myself feel better. I don’t actually need validation from anyone else, although likes and comments are always appreciated. Just having a representation of me out there where I look like me but better is enough for me.

Be vain. Glorify yourself. Who cares what everyone else thinks. We’re only on this blue and green blob once.

Are you vain? Good for you if you are! Vain=good.

Thanks for reading.


Saturday INvisible Health Spotlight #02

Hello lovelies,

In today's spotlight we will be talking about Rheumatoid Arthritis. Today is Rheumatoid Arthritis Awareness Day.

Rachel is 39.

Here is what she has to say:

It's 2am and I'm awake.  Wide awake.  I cannot move my right arm or lie on my right side due to pain in my shoulder, my knees are both hurting, my leg muscles spasming.  My ankles and feet are considering joining my pain party.  I've already taken pain killers two hours ago and resorted to deep heat, none of it is working.  I eventually drift off to sleep at around 5am.  The alarm goes off, its 6am.  Now I can't move.  My hands are stuck in a claw like grip, my whole body feels stiff.  I'm struggling to open up my hands.  My ankles, knees, hips and shoulder all hurt.  I feel like an 80 year old.  I manage to get myself up, run my hands under the hot tap and get in the shower.  I've got to go to work.  In a zombie like state, I get myself ready for work, have some breakfast and take my medication.  I'm so tired. 

I have a 15 minute walk to the bus stop, some days I can work normally other days every step is painful.  I then have to sit on a sometimes freezing cold bus for up to an hour to get to work.  I used to own a car, but due to my illness I decided to cut my hours and couldn't afford to run the car.  I work as a PA, four days per week, working 30 hours per week from 9:00 am - 5:00 pm.  Throughout the day, my pain levels dip and peak.  I also have waves of nausea due to my medication.  I struggle to concentrate and just want to sleep.  Simple tasks can be an effort, holding a phone (my elbows will lock), gripping a pen to write, typing.  These can all cause me problems.

I usually arrive home from work at around 6:00 pm.  Some nights I cook dinner at other times my partner will.  By now its an effort to even stand up.  After eating I take more meds.  My evening consists of sitting on the sofa with my heat pad trying to control the pain levels that are increasing after rushing around all day. I can't take my painkillers too early as I will need them to help me get through the night. If I can't get my pain under control I know I'll be in for another bad night.  Usually after a hot bath or shower I am too tired to stay up and end up going to bed around 9:30 pm - 10:00 pm.  It's the only way I can manage to get through my working week.  By this point I will have taken 8 prescription strength co-codamals.  I can't afford to give up work yet and I push myself to keep up with everything as I don't want to let people down.  This description of my day is quite normal for me.  I have not had a day without pain in three years.

At the age of 38 I was diagnosed with Rheumatoid Arthritis.  Oh I hear you say, my Nan, Dad, Aunt, Uncle has Arthritis.  I have Rheumatoid Arthritis it is an auto-immune disease and different from the arthritis that affects many elderly people.  My immune system mistakenly thinks its under attack.  It then tries to fight this attack by producing too many anti-bodies which can then attack the joints, muscles and if you are really unlucky your internal organs.  The result of this is inflammation, stiffness, pain, fatigue, deformity and mobility problems.  The fatigue itself can be so debilitating and I would describe it as trying to wade through water.  Rheumatoid Arthritis can affect anyone of any age and does not discriminate.  It is an aggressive disease which has to be treated aggressively.  Treatment usually takes the form of highly toxic medications including chemotherapy which can result in other complications.  These medications work to suppress the immune system to try and slow down its attack on the body. This also makes you susceptible to infection and you can become very sick very quickly. Can you imagine having to take a low dose of chemo for the rest of your life? Side effects include, hair loss, stomach upsets, nausea, mouth ulcers etc.  Chemotherapy can also affect the patients fertility making their chances of having a family particularly difficult.  Sometimes remission can be achieved but for most patients this does not happen.

The only visible sign of my RA is my fingers are showing signs of deformity.  They are no longer straight.  Please remember that not all disabilities are visible.  The next time someone is fumbling for change in the supermarket queue or using a disabled parking space yet look able bodied - they may not be. 

There is no cure at this time for RA.  It is a chronic, progressive disease.  I am currently waiting to start another treatment called Anti TNF.  Whilst this can be very effective it also carries risks.  Personally, I try not to think about the future, its a scary place.  This illness has taught me to be more aware of disability and those around me, to appreciate the little things and I'm thankful for the love and support I get from my friends and family.  I will continue to take each day as it comes as no two days are ever the same. I would not normally write about my condition to this extent but today is Rheumatoid Disease Awareness Day.  I don't want to be treated any differently and I have accepted my condition.  What I struggle to deal with is peoples lack of empathy and patience.  But, generally unless something affects someone directly they won't understand.  This could happen to anyone.  I have Rheumatoid Arthritis - but its just arthritis right?

 
------------------

I'm sure we'll all agree that Rachel is fighting a terrible battle to continue a normal life. Again, it just goes to prove that you can never tell someone's struggle just by looking at them. Often the sick and disabled have a fight on their hands to be believed - it's hard to be believed by friends who have problems accepting the changes in us. It's hard to be believed by loved ones who see the tasks we do every day out of necessity but don't realise the toll it takes on us. It's even more of a battle to be believed by the the judging arseholes who write articles calling the sick and disabled 'work shy' 'scrounging' and 'lazy'.

If you want to share YOUR story of illness or disability with us, you can email me at leahjdm @ gmail.co.uk (Just remove the space either side of the @ symbol, I'm trying to keep spammers at bay.)

Thanks for reading.


Frugal February

Hello lovelies!

I decided to sign up to Frugal February recently. You can read more about it on Gemma's blog here. Basically you can buy basics like deodorant and toothpaste but not makeup, clothes, music, books, magazines, etc.

My spending definitely got out of control over Christmas and in the January sales and I've known for a long time I've had a real issue with spending. I'm a little worried about what I'm going to do instead of spending, because I spend to cheer myself up when I'm down, and I'm down quite a lot.

I'm hoping not buying will give me time to dredge up lovely things from the depths of my wardrobe and my make up stash, and perhaps lead to me making things out of my craft stash as well.

There's also a bigger implication. Things are possibly going to get very financially difficult for us in the near future, so this is a test to see if I can hack not just a frugal month but a frugal life. Also, I really need to address why it is I overcompensate with spending to cheer myself up. I've spoken about this at length before but I still haven't learned to break the habit.

How do I envisage the month will go? Slowly, ha! Thank God it's the shortest month! :)

On a serious note, I will be deleting any emails that come in with discount codes immediately. As Oscar Wilde said I can resist anything except temptation!  Even reading blogs will probably be very triggering for me. I might turn the want to spend into a positive and post wishlist blogs along the lines of 'What I would've bought this week.'

Whatever happens, I'm sure it'll be an interesting experience!

Are you doing Frugal Feb or have you done something similar in the past? Any thrifty tips you want to share?

Thanks for reading!