Wednesday, November 17, 2021

Farewell For Now

Farewell For Now ...

It’s the end of an era for me! For a decade my Blog has been the place where I shared my life’s stories in detail - my inspirations, my artworks and the meanings behind them, my exhibitions and publications, my successes, my travels, my struggles, and my thoughts. But for the past three years I haven’t written a word ... I haven’t even visited. It’s become increasingly obvious that societally our attention span has shortened significantly and there are very few left who enjoy spending a chunk of their day reading the musings of an artist. On social media we are constantly entertained and over the years I’ve watched posts and video clips get shorter and shorter because folks get frustrated and bored; they want that gratification quickly. When I first joined the online world as a professional we were advised to keep videos and posts under 15 mins, then years later it was 4 mins, then a few years ago it became 1 min, and now it’s within 15 seconds. There just doesn’t seem to be a place for Blogs like this anymore. I’ll be continuing my journey as a chronically ill neurodivergent Artist and Mineral enthusiast on my other platforms. I would be so honoured if you’d join me there! Thank you so much for your support! ❤️


Tuesday, February 19, 2019

Artist Guest Speaker at TAIE International Institute

Artist Guest Speaker
Secondary School Presentation
TAIE International Institute

Remember that time I did a presentation for a Secondary School class? I don't blame you! I barely spoke of it! I was still trying to pull myself out of a depression and come to terms with my newly (and finally!) diagnosed disease but when the opportunity arose to speak to this art class I jumped at the chance. Since seeing success as a full-time artist I had wanted to do presentations for students. I'm an Ontario Certified Teacher (just renewed the other day! You?) but I haven't taught in many years ... almost seven now ... and I was really looking forward to a little taste of the classroom again. I do miss having students and shaping young lives. I can only hope I'm making some small impact with my art and online presence. But more than missing teaching, I wanted to spread the word that it IS possible to be a successful artist, something no one, even in my own arts specialized secondary school, ever promoted or encouraged. I will never make it sound easy, it sure as heck isn't, but it is possible. I have been shaped by the ups and downs of life and I feel I have so much I can share that might benefit the generations to come. This was a beautiful moment and I am so glad I was able to rise to the occasion and achieve something I had always wanted to do. As always, many blessings! :) 

Friday, September 14, 2018

My Disease Does Not Define Me ... How I Perceive It & Combat It, Does

YOU are not your disease. Don’t be afraid to tell people you have a disease. For years I tried to hold it in because I didn’t want people to pity me and I didn’t want to elicit negative emotions. I pride myself on being a positive person who inspires others to be positive too. So telling people I had a disease or even talking about it seemed contrary to my very being. But when it comes down to it I’m more than just a positive person, I am REAL with my followers. I think that’s way more important than false positivity. And I learned the hard way that false positivity can cause major mental issues. I needed to accept the negative as part of a real whole life but instead I shut down. As I slowly came out of the dark, implemented new habits into my health regime, and began to improve, I realized that not being open and honest about what I was going through was one of my biggest mistakes. I told myself that because I was sick I would forever more be this walking pile of negativity to others. Right? Am I alone in feeling that way? I thought, “How could anyone be happy around a sick person”. But I know how now. You accept there will always be negativity in your life. You accept that some people won’t want to hold that, even the small moments of it might turn them off. But those people weren’t worthy of all the other amazing parts of you, if they are so willing to leave. And I’m not saying it’s OK to continuously publicly wallow in self pity, I’m saying just telling someone you’re not feeling well today is enough for them to be like “ugh, too negative”. And that’s alright. They’ve got there own stuff weighing on them, or they’re buying into the idea that life is only good when it’s positive positive positive all the time. That’s not true.

Life is tastier when bad things happen. Now I know that’s a fucked up thing to say, and I certainly don’t wish ill on any person, but once you’ve got “it” (whatever negative shit “it” is for you), you’ve got it, so you might as well get as much “good” out it as you can. Who knows what the future will bring, you might be cured, you might get worse, no one knows. All you know is that today is however today is. And if it’s possible, try to get as much “good” from your illness as you can. Some days you just can’t and that’s normal. “What the heck does she mean by “good”? What could possibly be good about having a debilitating disease?”. Let me level you with, having a disease is 95% the worst, but it does allow for 5% of learned perspective that I think is really powerfully positive.

For instance, every time I include a new thing to my health regime and it pays off, I feel very accomplished, intelligent, more healthier over all, now and in the long run, because this is something that will be a permanent part of my routine. I’m not doing anything fast and drastic, just slow steady improvements. I once said to my very sad Papa, “You have to try to think of the positive. Because I’m sick I will now be forced to live my healthiest life and that will pay off in the long run when I’m older”. I believe that. I know that. If I hadn’t gotten sick I would not have been pushed to do all the wonderful things my body thanks me for now.

Another is, I’m tough as nails! I get procedures done frequently enough and they are inevitably painful and uncomfortable, meh, I don’t even notice anymore. I had to get a large needle a couple weeks ago and was told this one would really hurt, it literally felt like a mosquito. Both the doctor and nurse were shocked. LOL I get the same reaction from medical professionals doing tests, all the time. It’s a weird thing to be proud of, but why not?! I’m a weakling physically but man I can accept and conquer pain. I’ve had years to accept it and get used to it. I know if you’re in the real heat of it, that sounds crazy, but trust me, it will eventually happen.

I’m also proud of how intelligently and determinedly I dealt to improve my disease. Every medical practitioner I’ve seen in the past couple years calls me one of a kind. Most recently, my Physiotherapy appointments for my damaged shoulder were supposed to last 7 weeks, but only lasted 3. They were so impressed and when I asked, “Why has this never happened before (at their office).” They replied, “Because people want a magical quick fix, they don’t do the work”. Oh. That’s not even something I can imagine, I do the work and I do it all day long, not just twice a day. LOL So that kind of determination, I think, is something to be proud of.

I feel liked I’ve learned so much more about myself and life, and those types of big learning moments unfortunately tend to happen during and after bouts of great suffering. I’m learning to accept that that is life. On the worst days I just can’t, but for the most part I’m able to welcome that. The past week has been a bad one with my usual symptoms flaring up and some new fun ones to add to the mix, but it won’t affect me now like it used to. I just believe so strongly that I’m going to push myself to do all the things I deeply want to do no matter what, so let whatever come, I’ll do everything I can to be healthy and continue to learn, that’s all I can do. And there’s my honest story. It’s both negative and positive because that’s life and I think that’s more inspiring than just positive platitudes. When you start telling people you have a disease, ya you might get pity and sadness, but once you show them your strength they will admire you all the more. Trust me. The key to a completely healthy life is honesty and self love. You’re a real full person, worthy of sharing your truth even if it makes some uncomfortable. Those who truly connect with you on a soul level will stick around and I have no doubt that some who were scared off will come back.

We are not innately negative people because we have a disease (physical or mental), that is only one part of us and even it can have some positive impact on who we are. Be honest, be true, this is your life’s journey, you can’t control every part of it, you can’t run from it, so don’t hide it. You are a multifaceted spirit, complicated and unique, you can’t allow one aspect to be your whole. The true you is not the person you were before you were sick, your true you is NOW. Life has a way of changing us, for good or bad, I believe that’s its purpose. I may be experiencing something bad but it will change me for the good. I decide. And so can you.

Wednesday, April 11, 2018

The Natural Things I Do to Maintain my Autoimmune Rheumatoid Disease

Here I am, after years of suffering, feeling beautiful and whimsical and more free in my body than I have been in ages. Someone who hasn't battled what I battled might not understand how beautiful this photo truly is. Imagine being in so much pain your brain refuses to think. Imagine your joints being so stiff you literally cannot move your neck, arms, or waist/hips. Imagine you can't brush your own hair. Imagine you can barely bathe yourself because you can't reach behind you. Imagine you can't eat. Imagine having chest pains and dizziness and heart palpitations. Imagine you're living through all of that, and MORE, and yet no one can tell you what is going on. Not your family doctor, not the ER doctors, not the DOZENS of specialists you saw, not even the "Dr. House" type doctor, the one who is supposed to figure out mystery illnesses, all he could tell you is that your vitamins are low. Imagine this goes on FOR YEARS. I thought I was dying, I was living through hell, but I never gave up hope. My life truly began to change the day I received a diagnosis. Ankylosing Axial Spondyloarthropathy. An autoimmune disease that most often hits men over 40. Some people might think a diagnosis of a serious disease is depressing, for me it was what began to lift my depression. Not knowing, being treated by health care professionals like you're just crazy and stressed, is absolutely the worst. I needed to know I wasn't going to die. I was reassured that if I took care of myself I would not die from THIS disease, although having it leaves me open to others. Challenge accepted! Whatever comes my way, comes. After all, this isn't the first time I've been diagnosed with something. I was diagnosed with a small brain tumor at 22 so it seems battling health issues will be my burden. I'm determined to take that burden and turn it into something that can help and inspire others. In this modern day of widespread illness, I need to be strong so I can show others how to be strong too. 

I plan to build on this blog post slowly over time so that I can share what I do to help myself live happily with this very painful and limiting disease. Let me make this very clear, I AM NOT A DOCTOR. I am simply a person with a sick body who has turned her life and disease around for the better. I am not going to provide hard scientific facts, it doesn't interest me nor do I have the time for that. Please, if you're interested in trying something but want to know the science behind it, do your own research. That's how I found all of this out. Google is your friend. But also keep in mind that for every article saying "This is beneficial" there will be another saying "This doesn't work". Science is a lot more fickle than we like to think. Ultimately, if it's not dangerous, it's up to you to decide if it's worth a try. I'm creating the list of everything I do; it's up to you to decided to take and leave what you will. 

What type of symptoms did I have BEFORE I started these natural remedies and practises? 
2) Inflammation - EVERYWHERE
3) Blurry Vision
4) Dizziness
5) Full Head Feeling (Likely inflammation of the skull)
6) Unable to think or focus
7) Seeing spots/Loosing vision
8) Numbness in my arms and legs
9) Tingling in my arms and legs
10) Heart Palpitations
11) Incredible Pain in Chest
12) Unable to move Neck
13) Unable to lift arms
14) Unable to twist at the hips
15) Unable to bend down
16) Headaches
17) Difficulty breathing
18) Clogged Sinuses
19) Constant choking on flem
20) Constant Nausea
21) Constant Acid Reflux
22) Terrible continuous Nightmares
23) Anxiety/Depression
24) Loss of all emotion
25) Swollen ankles/knees
26) Major stomach pains
27) Vaginal Pain/Intercourse Pain
28) Unable to eat
29) Loss of Weight (about 20 pounds over a few weeks)
30) Growths due to excessive inflammation on my lungs and in my abdomen
31) Breast Pain and lumps
32) Possibly more but this is what I can come up with for now 

What type of symptoms do I experience NOW
1) Pain - but not as intense as before. My body tends to focus on one or two places now rather than everywhere at once
2) Inflammation - same as pain 
3) Occasional Dizziness but it is rare
4) Full Head Feeling - I only get this a few times a month at the most
5) Unable to think or focus - this only happens when I get the full head feeling
6) Heart Palpitations on occasion 
7) Incredible pain in the chest - still something I am working on. I do get this often.
8) Unable to lift ARM - My right shoulder has damage so I have a hard time lifting it above my head 
9) Headaches - 2-3 a week
10) Swollen Ankles/Knees - On a rare occasion
11) Stomach Pains - Occasionally 
12) Possibly a couple of other rare things but generally this is what I deal with. 

As you can see a lot of the symptoms have subsided. The "now" list still appears long and arduous but it is much more manageable. Most of my daily symptoms revolve around pain and inflammation and while I can't always control it with natural remedies, I have learned to live with it and still be a happy person ready to take on life! I make highly detailed art with my damaged joints. I travel all over the world, sometimes even SOLO. I exercise and I walk. I have friends that I actually see! I have hobbies and interests! My mind is excited and passionate again! If you've been where I've been you'll understand how amazing that is. :) 

I've achieved this without the use of pharmaceutical drugs, for the most part. The only non-natural medication I have used throughout this entire ordeal is single dose extra strength Advil. I use it anywhere from 0-4 times a week only when the pain and symptoms are beyond what I can bare. Most weeks I do not use Advil. But during a bad flare up, after I have tried everything I can think of, I will resort to it. 

This probably sounds like I am against pharmaceutical drugs and that is not the case. It was my personal choice to try to stay away from them as much as possible (based on a variety of scientific reasons) but I had the ability to do so. I was reassured that I wasn't dying. I was getting permanent damage but that was something I was willing to risk. I understand that not everyone feels that is the right path for them and I wholeheartedly respect that. I'm going to pass along what I've learned and seen success with because I truly believe it will benefit anyone, regardless of what choice they've made concerning pharmaceuticals. I am NOT here to judge. We sick people get enough of that in our daily lives. Just keep in mind that I support you in your journey, you may not have chosen the same path as me, but that does not mean it is a "wrong" path. I learned a long time ago that life is not made up of "rights" and "wrongs" .... but rather individual journeys. It's my hope to be a positive influence on your journey. :) 

I've decided I'm going to try to list these things starting with what was MOST EFFECTIVE for me. Please keep in mind that our bodies are different and what works amazingly well for me may not for you. It's all a matter of trial and error, but do try to give things a good shot.


I decided to start with this one because it really had a HUGE impact on my pain and inflammation and it's so easy and cost effective. When I first felt the results I cried to everyone I knew how much of a miracle it was. A beautiful gift from the Earth! Try it, please, it doesn't hurt! :) 

Here's how it works. 

Apple Cider Vinegar is the only vinegar that becomes Alkaline once inside the body. Back in the 1950s a nurse who was working in a Rheumatoid Clinic discovered that this could cut a major amount of pain from the lives of her patients. The reasons we experience so much pain and damage to our joints is because there is constant inflammation sitting there which eventually leads to a build up of acid and it's that acid that deteriorates our joints. The inflammation, the acid, and the deterioration ALL come together to cause us our incredible amounts of pain. The apple cider vinegar actually NEUTRALIZES the acid build up and helps take down inflammation. It sounds too good to be true, trust me I know, but it WORKS! 

ON TOP OF THAT, when you consume Apple Cider Vinegar WITH THE MOTHER you are actually helping your digestive system too! "With the mother" means that the vinegar hasn't been pasteurized so all of the original GOOD bacteria remain in it. You can actually see them! Drink that seemingly gross stuff up because it helps! These good bacteria act as a natural probiotic. You're effectively putting good bacteria in your gut which will attack and get rid of the bad bacteria. I'll be doing a whole other point on gut health (stay tuned) but this is part of it. Not only that, but I have tried Apple Cider Vinegar without the mother and while it still helped it did not cut nearly as much pain as "with the mother" did. 

What happened? 

Some people who have tried this said it only took 3-4 days to help! I was a little bummed when that wasn't the case for me. It took me 3.5 weeks for it to kick in! So, like I said, give it a real go! Don't give up if you don't see results immediately. Within that first month my pain and inflammation was down a whole THIRD of what I had been experiencing. That's A LOT of pain reduction. A lot, a lot. 

What did happen within days was a much happier digestive system. WAY less stomach pains. NO indigestion. Normal bowel movements. Honestly, it's worth it just for this benefit but the pain management makes it pretty miraculous in my eyes. 

I started with TWO TABLE SPOONS in a glass of water 6-8 times a day. Make sure you shake your bottle of vinegar every time to get all those bacteria flowing and not just sitting at the bottom. Once I felt I had reached the maximum amount of pain relief I would get, I started to slowly take less of the vinegar and found that my pain relief stayed the same. It has been 1.5 YEARS since starting this regime and it still works. I now only take 1 TABLE SPOON in a glass of water 3-4 times a day. Some people may need more, some less. You'll have to gauge that for yourself. I have tried not taking it, while travelling for instance, and the pain does return after a while. So I know it's still working and that I still have to take it. I've tried Apple Cider Vinegar capsules while travelling and they certainly help but they are not even remotely as effective as the real thing. 

My Favourite - Braggs With the Mother. I have tried many others, this is the most effective for pain management and tastes the least strong. Get it on Amazon HERE.
Water - Always include your vinegar in at least a full cup of water.
Straw - I recommend always using a straw and trying to make sure it doesn't hit your teeth. The acid can hurt your enamel over time. Some people use it to whiten teeth but I've also heard of it turning teeth yellow, so I am always careful about my teeth. I recommend a metal straw so as not to hurt our ocean life. Get a set on Amazon HERE.
Before Eating - I take my first glass as soon as I get up in the morning with cold water. It shoots me right awake and it kicks in really fast. My mornings are the best! Throughout the day I will take my vinegar with room temperature water about a half hour before a snack or meal. Remember, it helps digest your food!

It seems like such a simple solution that can't possibly be true, but it is! After using it for a few months I had my specialist appointment with my Rheumatologist. She doesn't seem to care much for my natural way of doing things and is always trying to convince me to take immunosuppressants but she respects the fact that I've researched everything and have a solid plan in place. A plan that is working according to the tests she regularly runs on me. The interesting thing is that she actually trains new rheumatoid doctors and when I told one young male about the vinegar he was very excited. I expressed how annoyed I was that no one had told me about this simple natural miracle and he said that it is something they are aware of but because there isn't enough modern scientific studies done on it they are LEGALLY NOT ALLOWED to tell us about it! That's the kind of nonsense that really bothers me about modern medicine. But, I am here to share! Give it a try! I'd love to hear how it goes. :) 


Coming soon ..... 

Wednesday, February 21, 2018

Malinda Prudhomme Art HAND JEWELED PRINTS Now Available!


I am SO excited to OFFICIALLY release my collection of HAND JEWELED 8" x 10" Beauty Art Prints! Now everyone can afford a sparkling piece of art! :) 

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Malinda Prud'homme's paintings that include real acrylic gems are among her fans favourite pieces. She receives frequent inquiries about prices but for many the cost of these time consuming and expensive paintings is beyond their budget. This is why Malinda decided to offer hand jeweled prints! So that those who really love that radiant sparkle paired with beauty portraiture can enjoy a piece of their own at a fraction of the cost. :)

SIZE: 8"x10" paper with a white border for easy framing/matting. It will easily slide into a standard 8 x 10" frame or matte.

SPECIFICS: These prints are reproduced from original paintings by Mixed Media Artist Malinda Prud’homme. They are printed in-studio on Supreme Satin photo paper which has a lovely weight, a flawless velvety smooth surface, is tear resistant, curl resistant, and fade resistant. The artist will adhere real acrylic gems to the print by hand. She will choose in the moment what gems to apply as the print is not completely covered. While she will NOT be copying the gem patterns exactly as seen in these images, she will stay true to the amount of gems portrayed. Prices will vary based on the amount and colour of gems. Every portrait comes with either the colours shown in the photos, all crystals, or crystals and aurora borealis (multicoloured shimmer - AB) crystals. You can make your selections using the drop down lists. 

All prints are signed by the artist at the bottom of the print.

SHIPPING: The print will be sent in a 100% recycled hard cardboard Mailer. 

Please remember that this image is copyrighted & not to be reproduced for any purposes without permission from Malinda Prud’homme. Purchase of this print does not transfer any image rights.

For more images and information please visit