Stop Genocide Now!
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“Never say that you can't do something, or that something seems impossible, or that something can't be done, no matter how discouraging or harrowing it may be; human beings are limited only by what we allow ourselves to be limited by: our own minds. We are each the masters of our own reality; when we become self-aware to this: absolutely anything in the world is possible.
Master yourself, and become king of the world around you. Let no odds, chastisement, exile, doubt, fear, or ANY mental virii prevent you from accomplishing your dreams. Never be a victim of life; be it's conqueror.”
― Mike Norton
Blog Post
www.facebook.com/SuicidePreventionAwarenes/?rc=p
Every person on this earth is beautiful, talented and amazing.
Thank you for your kind visit. Have a wonderful and beautiful day! xo❤️ ❤️ ❤️
Breast cancer death rates declined 40% from 1989
to 2019 among women. The progress is attributed
to improvements in early detection.
This picture is dedicated to all women in Flickr please auto explore and you can save your life!
Am I out of my head?
Am I out of my mind?
If you only knew the bad things I like
Don't think that I can explain it
What can I say, it's complicated
May 12 is ME/CFS/Fibromyalgia International Awareness Day, a day to bring attention to how ME/CFS/Fibromyalgia affects those suffering from the illness.
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a serious, long-term illness that affects many body systems. Often, people with ME/CFS may not be able to do their usual activities. People with ME/CFS have severe fatigue and sleep problems. ME/CFS may get worse after people with the illness try to do as much as they want or need to do. This symptom is known as post-exertional malaise (PEM). Other symptoms can include problems with thinking and concentrating, pain, and dizziness.
Fibromyalgia (FM) is a medical condition characterised by chronic widespread pain and a heightened pain response to pressure. Other symptoms include tiredness to a degree that normal activities are affected, sleep problems and troubles with memory. Some people also report restless legs syndrome, bowel or bladder problems, numbness and tingling and sensitivity to noise, lights or temperature. Fibromyalgia is frequently associated with depression, anxiety and posttraumatic stress disorder. Other types of chronic pain are also frequently present.
Thanks for viewing 💙💜💙
Wishing all my Flickr Friends a Very Merry Christmas, may it be a peaceful and happy one. To all those who do not celebrate Christmas I wish you happy holidays and much joy! And I send love to you all!!! :-)
Please be aware that I shall be off Flickr mostly for a while, I will try to come and check out your works. Keep all the good work coming, wet your creative juices and enjoy yourselves my friends!
Until the next time.
Right now we are all aware of whats happening in our RL but here in SL we still want people to be aware of the dangers and ~Mikki From ~Bold Llama~ has come up with this tee for us...
Yes we can't get it here in SL but its still affecting us all in some way or another... Just be safe everyone and have some fun here in SL with the ~Stupid Cupid Hunt~ to keep your mind off everything else..
The Hunt runs from the 3rd of February until the 28th.
The Bold Llama Company Love Is In The Air Tee
7 Deadly Skin Sweetheart Apricot
Magika Hair December
Maitreya Body Tweaked by me
Lelutka Head Lilly
Props
DIVIA's Designs Christmas Village
Shot at
Background:
"Forget ME not" was created to raise awareness about M.E (Myalgic Encephalomyelitis) - an extremely debilitating, life changing, complex chronic disease that has received shamefully low attention and fundings for research for decades. Patients are being disbelieved, misunderstood and dismissed. There is no treatment and no cure.
Over 20 million people across the globe are affected and in the aftermaths of COVID this number is quickly rising (many Long Covid patients end up being diagnosed with M.E).
During our events in May we will create awareness, break the stigma and fundraise for the "Open Medicine Foundation" who conduct research into M.E, Long Covid, Fibromyalgia and related chronic conditions. They are a registered, US based non-profit organization that has been around for over 10 years.
You can also support by wearing this blue ribbon exclusively made by Enewa, when you click the information box at the Forget ME Not sim.
Get it here in-world: Forget ME Not events place and exhibit 💙
To know more about the event and how you can raise awareness and support the cause to research and find cure for ME/CFS, link here: Facebook: forgetMEnotSL 💙Flickr group: forget ME not SL
💙 Website and donation page: Forget ME Not SL site
The 10th Annual Drive for the cure Canada (to raise Prostate Cancer awareness) held its annual car show at the Brampton Powerade Centre. there was a bevy of beautiful classic cars; so many wonderful automotive designs from years gone by and all in one place. there were well over four hundred cars on display. .
I have always loved sports cars, that is probably why I love this classic 1957 convertible Porsche 356 speedster in jet black, it was lovingly restored and maintained by the fifth owner who spent nine years rebuilding and repairing this lovely small classic..
Thank you for visiting for marking my photo as a favourite and for the kind comments,
Please do not copy my image or use it on websites, blogs or other media without my express permission.
© NICK MUNROE (MUNROE PHOTOGRAPHY)
You can contact me
by email @
karenick23@yahoo.ca
munroephotographic@gmail.com
munroedesignsphotography@gmail.com
or on Facebook @
www.facebook.com/MunroePhotography/
On Instagram
Smile on Saturday - Made by Me
😊 😊 😍
A Statement Against Pollution
This was a sculpture I did for an exhibition done in collaboration with the Moving Ethos Modern Dancer Company called Purity & Pollution. It was floating in the pool during the exhibition. It is entirely made out of garbage (rubbish) and is mostly made of plastics, although glass and cans (tins) are included and the surfboard of course. I am trying to encourage people to throw their garbage (rubbish) in the appropriate places, not just throw it anywhere thereby destroying, land, birds, animals, the ocean, and other waterways.
Thank you for your kind visit. Have a wonderful and beautiful day! ❤️ ❤️ ❤️
I have been debating recently whether to post about this. Its a bit of a tussle between me being reluctant to go into my health publicy vs a strong desire to raise awareness to my like minded friends about something a bit nasty that I think landscape photographers, hikers, campers (really anyone that loves the outdoors) should be really careful of.
My health was great until the summer of 2019 when I was suddenly knocked off balance by a range of weird symptoms. I was put on beta blockers for a racing heart. My speech went all weird. I was pretty scared. Finally this summer I was diagnosed with Lyme Disease (aka the Great Imitator) as it copies other illnesses and can be misdiagnosed. I had to be tested to rule out MS etc... Even after the correct antibiotics I am left with speech fatigue (I just sound a bit drunk all the time), brain fog and constant nerve tingling. This is the reason why I had to take redundancy from my job.
However I am lucky. I have a reasonable quality of life. For a start I still have enough energy to get up for sunrises. Some sufferers are in a lot of pain, fatigued and bedridden. I know of someone who partly lost his eyesight.
I may have to seek private treatment in the New Year from a Lyme specialist clinic despite having no job. This is the reality for a lot of LD sufferers.
Because ordinary mosquitoes love me (I'm always getting bitten) I don't remember my tick bite and this proved costly and made diagnosis harder, I spent months blaming the meno.
Please look out for ticks all year round. If you do get a bulls eye rash go to the doctor without delay and get antibiotics. Don't wear shorts on summer shoots. Carry a tick removal kit.
There is loads of information on the Lyme Disease UK website and their support group has been invaluable to me.
Thank you to my friends on here for being supportive. Sorry for the long post x