If you are a loyal follower; you would have seen a while back that Ive posted some of the weird and wonderful DM’s I receive from followers. Most the time these are from the arb guys. The “passer by’s” I’d like to call them 😂
Note that I don’t always disclose their names as I really dislike “naming and shaming”. A lot of you disagree with this; however I do not feel good/satisfied/better/empowered in embarrassing someone else; and certainly not out there to “teach lessons”. This is good comical fun though…
I’m often asked how I even deal with it or cope with it. Very easily. 1. They have no idea who I am, 2. They were raised not respecting women 3. They have problems with their sexual lives 4. They are trollers
U no pretty anyway!!!!!
Sugar Daddy Proposal
Wanting to get spoilt rotten with good money, afford luxury clothes, shoes and good lifestyle with a weekly allowance? Am a sugar daddy looking for a loyal and honest sugar Baby to take care of, kindly HMU if interested.
I’m still waiting 😎
Dude: Hey kan u send naked video pvt
Me: You first
Dude: Ai jis do video call
Me: No, just send me a video of you
Dude: No do not hafe video of me
Me: Send me a video of you
Me: Send me a video of you
Me: A naked one
Me: Dude – seriously? Let’s think about this. Really carefully
Me: You really think I will send “naked pictures or videos” of me? To you? Who are you even? If you want naked videos or pictures go look on pornsites. Bye
Me: BTW send me your parents details – I need to congratulate them on teaching you manners and respect
Dude: Hiiiiiiiii sexy
Dude: You are so gorgeous, and have an incredible delicious body. Tell me, would a fine women like you be taken? Let’s hook up sometime and I can show you a few things *insert an unusual amount of arb emoji’s*
Dude: I guess the cat caught your tongue *insert double of the above amount of emoji’s*
Me: Hey there, thank you. No – however you did appear to message me at 3am. And in all fairness I was catching up on some much needed beauty sleep. No kitties in sight! That leads me to my next answer. I have never gone anywhere against my will, therefor not “taken”. I am however married 🙂
Dude: Aaaaaaaah sorry. Just delete this message. Thanks. I didn’t mean any of it anyway
Me: WHAT? Are you telling me I’m ugly?
Dude: That is not what I meant.
Me: Oh, so I’m not gorgeous, nor fine?
Dude: No, you are very beautiful
Me: Oh you’re assuming that I won’t be lost anymore since I’m “taken” therefor you won’t need to show me “a few things”?
Me: Out of curiosity; what exactly were you going to show me (considering you appear to be 19 and I am 39)
USER NOT FOUND
Too Easy 2
Dude: Can I ask you something?
Me: (think: here we go….) Typing: Sure 😊
Dude: When you pose, do you get horny. Or do you turn the photographer on?
Me: No, and no. This is a job. Do you get turned on at work?
Me: Well I don’t
Dude: Can I send you a picture?
Me: No thank you
Dude: Have a nice evening
Dude: If you change your mind……
Dude: Thnx 4 da follow love ur gallery wow
Me: Thank you
Dude: Pleasure do you mind sharing some pictures or videos mwa
Me: You may find all my images on artbyam.com
Dude: Was hoping u would make it more special by sending it 4 me Swt *insert roses and hearts and kisses and hearts and roses*
Me: Thanks. I’m a professional model. I don’t swap images. All my images are “special”
Dude: Im totally aware of that but u caught my attention and I find u so attractive its also my dream and vision to become a pro bodybuilder
Me: I suggest you do your research prior to addressing any lady and disrespecting her. I am not a porn star. One of the lessons I suggest you learn (on your way to get your Pro card and being a prominent figure within the industry) is respect and being humble. NOT asking to swap nude videos.
Me: Have a nice life
Dude: Hey! hgd?
Dude: halo sexy; wmj?
Me: what does that even mean?
Dude: jmr mooi dang. js bja mooi!
Dude: Jys rrg bja mooi
Whilst I do try and engage as much as I can with my followers on IG, I limit my time on Facebook. I also found that the people on Facebook are – in general and not everyone – a little more rude and crude. Perhaps I have just started loosing interest due to the very strict rules and restrictions. Regardless, I value each person who follows me, respects me and takes the time to appreciate what I do. Whatever their thoughts, assumptions or intentions are!
Version 3 will most likely be posted soon! Hope you had a little giggle 😜
I usually drift off during my lash appointments. It’s the small matter of having to lie still and not being able to open your eyes for at least an hour and a half. Sometimes two hours. Unfortunately for Sammy, I’m a fiddler and struggle to keep still. So, the only other alternative is to catch a snooze. You’d think that sounds like bliss – to me catching a nap during the day is something familiar but unwanted.
It’s quite a laugh really. Sammy has confirmed that I
twitch a lot. I know this of course, as I often jerk myself awake!
However, during my last appointment Sammy asked me out
the blue; what is Lupus?
You see; I’ve probably mentioned this a few times to
people (I certainly do not hide it) that I have Lupus. Or rather I was
diagnosed with said disease.
Rewind to when I was a little girl, and forever ill with
something. Later on, in life I realised that it worried my mum quite a bit
since we had access to an incredible medical team (I was raised in a military
house and so we had always gone to 1 Military Hospital which was during the
80’s and 90’s one of the best), however the specialists were unable to
distinguish what was wrong with me. I have vivid memories of the halls and
rooms, the smells and sounds that I absorbed whilst mostly feeling out of it or
hardly conscious due to high fevers.
One of my worst memories was when the team decided that
my fever was so high and my body so sore, I had to be tested for meningitis. I
was tiny and didn’t quite understand why my mum couldn’t be with me, nor why
they rushed me into some strange room or required 4 staff members to pin me
down after forcing my body into foetal position only to stick the thickest
needle (which at the time seemed to me as big as a milkshake straw) into my
It must have sounded like I was being cut open alive,
second before I passed out. It was to my knowledge the most excruciating pain.
When I regained consciousness, I was still there. Minutes later my mum was
allowed to see me and hold me. Anyway, it turned out that it wasn’t meningitis.
As always; they sent us home with those medium sized
pharmacy packets filled with syrups telling my mum it’s a “virus infection”.
This carried on for years. During high school I seem to
fall ill every time during exams. I’m talking about fevers that made me
hallucinate. And I actually loved school (I’m not kidding). I used to play hockey
and run long distance and cross country at school. However soon realised that
my knees were acting up. At that point my mum was a single parent and due to
the financial strain on the family I really tried not to fall ill or create any
attention regarding my health or any injuries. So of course, I hid that as long
Are you really sick though?
Years later, living in Britain I was ill more often than not. A common feeling/assumption/observation for an outsider is that a Lupus sufferer is a hypochondriac. Always feeling like poop but no one can determine what is wrong. The thing is that you feel so awful however you look fine. You seem fine. And eventually a brave face and pretend everything is okay, because it has to be right?
I spent so much time at different institutions to be tested that in hindsight I am relieved that we were there and the NHS looked after me so well. Till today we joke in our household that everyone with a health issue should get checked by me “the doctor” since I’ve been around that environment so much!
At some point I was so ill that my husband considered bringing the family back to South Africa in case something goes wrong – I’d then at least be close to my family.
During 2007 I finally started feeling excited and
hopeful. Why? Because I was diagnosed with PCOS (polycystic ovary syndrome),
Liver Cirrhosis, Rheumatoid Arthritis, Costochondritis, Hypermobility Syndrome,
Alopecia and circulation issues to name a few. Now this sounds disastrous,
however to me I finally had a diagnosis! That would mean that I could start
treating it. Within days my ANA test returned positive for SLE (Systemic Lupus
What is that? SLE or Lupus is a systemic auto immune disease.
It occurs when your body’s immune system attacks your body’s tissues and
organs. The cause for this to happen is unknown. This disease can not be cured,
and can be fatal.
Whilst I was excited, my family was in shock and
petrified. The specialists wanted to start treating the lesions on my liver as
a matter of urgency. I needed to go for various blood tests as my blood
platelets were abnormal. The first round of chemo was suggested as well as a
well-planned programme to start treatments and medication.
I was severely anaemic, and as a result of the cysts on
my ovaries I seemed to be on my monthly cycle most the month – every
month. My body rejected several
treatments and to be honest I was in bed more often than not.
My children will tell you that they recall playing in the
hospital halls whilst waiting for me to be scanned/tested/prodded/poked.
The day the specialist told me that I will start chemo
the following day; the penny dropped. What if my body is not happy with all the
years’ meds, stresses etc.
I met with Cindy the following day instead – a naturopath
we met through our business who said that she will help me at least start
feeling more human. We sat for hours and talked about my medical history and
whatever I’ve done in the past. EVERYTHING.
She worked out the most laughable programme (especially
compared to the modern medicine world that I knew) and I agreed to give it a
That was the day I gave up red meat, anything with gluten and diary. I started my green juice habit that day too. Till today I drink a “green juice” and swear that it is one of the single best add-ons to ANY diet. There were also strange treatments like liver packing, urine washing and enemas.
Back to recovery
Within days I could stay awake for longer, and within weeks I started feeling better. My hair started growing back and my joint swelling started subsiding.
I would never ever suggest to anyone to ignore their
specialists or not to go seek medical attention if and when they are ill or
have been diagnosed with any ailment, illness or disease. In fact; when I have a migraine – pass me a
migraine cocktail please! When my hips pop out or my back spasms so much that I
have to be carried to bed – pass me the Tramacet!
Personally? I believe whole heartedly to listen to your
body. I get teased and I get mocked for my health habits, my routines and my beliefs
– its okay though. Against my medical team’s beliefs in London – I’m better
than I’ve ever been!! I’m fit, I’m healthy
and in shape.
Weight training has been an incredible saving grace.
Oddly, weight training is phenomenal for arthritis. And purified water….an
I live a healthy life and only now and then have little
setbacks. Stress and “over doing” things would encourage a flare (a flare is
when I become ill).
Please feel free to ask me anything with regards to this.
Should you wish to make a difference – please support the chosen foundation in
your country. In South Africa it’s http://www.lupusfoundation.co.za/