O oh dear lovely Emma - I wept (ofc) reading your elegantly clear eyed analysis of the way this fucking monster gnaws at our very soul but leaves us looking ( to the casual observer) just fine.
I’ve been trying to understand what chronic pain is doing to a few of the people I love. I’m reading this slowly because it’s something I have to take in bit by bit, it’s too difficult to read all in one.
Thanks Neena. Yes blue light depletes dopamine, especially artificial light.
If PD is a condition where more dopamine is needed, it follows that supporting natural dopamine secretion can be attained by getting red/infrared and full spectrum sunlight, which regenerates the nervous system.
I’m sorry but what are you on? Do you have Parkinson’s? Do you really think it is helpful to dump a piece of techno dross like that in response to Emma’s writing..? FFS..
Thanks Nick for your kind comment. My family member has it. I can send you research if you're interested. Check out Gary Sharpe on Substack as well.
Btw this will be the last time I leave a comment here. I don't need to be disrespected and told the insights offered are rubbish. The wise only need to hear a word, and understand the message. I hope you can hear mine.
I am sorry you feel this way, Roman. As you are aware many people feel it is appropriate to offer us ‘advice’ on our illnesses, and sometimes it makes us ultra sensitive. I think you will understand that it is an incredibly frustrating disease and there is nothing more we’d like than solutions. Your research and insights are, of course, valid and worthy to be listened to. Many people come to my writing as an escape from the solution based approach and are seeking an emotional expression. I value your presence on my pages and do hope that you will stay. With love Emma xxx
Well. Yes. But what then? It's still our one precious life and l want to make the most of it, even though it is bloody hard sometimes. I hardly ever think about who l was, what l could once do. Because it makes me sad. So nowadays l just get on with it. I'm trying to become a saint because they suck it all up and simply smile in a calm, saintly manner. Must be my Catholic roots poking out. Anyway, sending lots of love to the Emma you have become. You're wonderful if if you don't feel it 🥰
Brilliant and pithy as always. I was about to highlight the pithiest take-aways then realized the piece is one huge takeaway. Thank you wise Emma for so elegantly and eloquently capturing the realities of this life we never asked for but somehow manage to soldier through.
O oh dear lovely Emma - I wept (ofc) reading your elegantly clear eyed analysis of the way this fucking monster gnaws at our very soul but leaves us looking ( to the casual observer) just fine.
😘😘
I’ve been trying to understand what chronic pain is doing to a few of the people I love. I’m reading this slowly because it’s something I have to take in bit by bit, it’s too difficult to read all in one.
Love to you and your loved ones xxx
Emma, this is perfect.
Although I so wish you didn’t know your subject so intimately xxx
Thank you and it could be a lot worse....I have you guys to keep me smiling 😘
Do you try to avoid blue light at night? Artificial blue light is a huge driver of neurological disease.
Thank you Roman, I have read your posts and Gary Sharpe’s I think we have spoken on this topic before.
Thanks Emma.
I didn’t know this, Roman. 😔
Thanks Neena. Yes blue light depletes dopamine, especially artificial light.
If PD is a condition where more dopamine is needed, it follows that supporting natural dopamine secretion can be attained by getting red/infrared and full spectrum sunlight, which regenerates the nervous system.
Here's some more info:
https://romanshapoval.substack.com/p/why-parkinsons-begins-in-the-eye
Thank you, Roman. I will read this now.
I’m sorry but what are you on? Do you have Parkinson’s? Do you really think it is helpful to dump a piece of techno dross like that in response to Emma’s writing..? FFS..
Thank you, Nick for your championing and support.
Thanks Nick for your kind comment. My family member has it. I can send you research if you're interested. Check out Gary Sharpe on Substack as well.
Btw this will be the last time I leave a comment here. I don't need to be disrespected and told the insights offered are rubbish. The wise only need to hear a word, and understand the message. I hope you can hear mine.
If you want the research, you can send me a message to info@thepowercouple.ca
Take care.
I am sorry you feel this way, Roman. As you are aware many people feel it is appropriate to offer us ‘advice’ on our illnesses, and sometimes it makes us ultra sensitive. I think you will understand that it is an incredibly frustrating disease and there is nothing more we’d like than solutions. Your research and insights are, of course, valid and worthy to be listened to. Many people come to my writing as an escape from the solution based approach and are seeking an emotional expression. I value your presence on my pages and do hope that you will stay. With love Emma xxx
Thank you very much Emma for your kind comment.
...wonderful even if you don't feel it! 😘
Hi dear Emma
Well. Yes. But what then? It's still our one precious life and l want to make the most of it, even though it is bloody hard sometimes. I hardly ever think about who l was, what l could once do. Because it makes me sad. So nowadays l just get on with it. I'm trying to become a saint because they suck it all up and simply smile in a calm, saintly manner. Must be my Catholic roots poking out. Anyway, sending lots of love to the Emma you have become. You're wonderful if if you don't feel it 🥰
Thank you, lovely Sarah xxx
Brilliant and pithy as always. I was about to highlight the pithiest take-aways then realized the piece is one huge takeaway. Thank you wise Emma for so elegantly and eloquently capturing the realities of this life we never asked for but somehow manage to soldier through.
Thank you, Andi xxx