i so appreciate Lilian's multi-faceted perspective, and share in seeing what she sees from my own lens. This is not a quick and easy read - it's worthy of contemplation, as we all hold so many pearls to string on the thread of Truth and healing the brain/nervous system. Bravo
Weird one I came across a while back and I don't recall the source but it was about reducing stress by looking left and right horizontally. Neurological manipulation of dopamine or something. I'll try and find it
Thanks for the article! Along with MS, Parkinson's has been categorized as an autoimmune disease, which includes psoriasis and a number of others. After a family member contracted a rare type of psoriasis (hands and feet) which caused the extremities to build up callouses resulting in cracking painful cuts on her hands and feet, a dermatologist prescribed the usual meds you see advertised on tv without success. A friend and former nurse who had experienced pain from a back injury recommended seeing her health coach about using medical cannibas oil (not CBD). In fact, the dermatologist said some of her patients that used CBD got a rash.
We still decided to give it a try and as predicted, got a rash, so the decision was made to consult the health coach. After speaking to the coach about the psoriasis, we decided to begin using the oil, which was a combination of sativa and indica (60%/40%). Within a week, the callouses reduced to normal growth resulting in the cuts healing. Daily use of the oil in a capsule form has kept the symptoms away for six years.
I asked the health coach if he had any clients with MS and he said he did, but since there are different types of MS, the results were mixed.. For some, there was no improvement; for others, it keeps the symptoms at bay.
As a result of our experience, I decided if I ever was unfortunate enough to get an autoimmune disease I would begin using cannibas oil rather than prescriptions by pharmaceutical companies. It's your health, you decide.
First of all, a great big THANK YOU to Gary Sharpe for sharing your work. May I ask how long your therapy sessions are? You mentioned in begining, you had long sessions. I find 1 hour is not adequate for clients. I am curious also, what modality did you use w the individual w the Veteran w PTSD? I have a young client who is a delivery room Nurse. Her hands shake and always have as far as she can remember. I’d love to learn more from you on what therapy modalities are most effective. Thank you kindly from Vancouver BC 🇨🇦. 1 more question, is the FB group helpful to all that live w stress? 🙏🏽❤️
Thank you.
i so appreciate Lilian's multi-faceted perspective, and share in seeing what she sees from my own lens. This is not a quick and easy read - it's worthy of contemplation, as we all hold so many pearls to string on the thread of Truth and healing the brain/nervous system. Bravo
Weird one I came across a while back and I don't recall the source but it was about reducing stress by looking left and right horizontally. Neurological manipulation of dopamine or something. I'll try and find it
Thanks for the article! Along with MS, Parkinson's has been categorized as an autoimmune disease, which includes psoriasis and a number of others. After a family member contracted a rare type of psoriasis (hands and feet) which caused the extremities to build up callouses resulting in cracking painful cuts on her hands and feet, a dermatologist prescribed the usual meds you see advertised on tv without success. A friend and former nurse who had experienced pain from a back injury recommended seeing her health coach about using medical cannibas oil (not CBD). In fact, the dermatologist said some of her patients that used CBD got a rash.
We still decided to give it a try and as predicted, got a rash, so the decision was made to consult the health coach. After speaking to the coach about the psoriasis, we decided to begin using the oil, which was a combination of sativa and indica (60%/40%). Within a week, the callouses reduced to normal growth resulting in the cuts healing. Daily use of the oil in a capsule form has kept the symptoms away for six years.
I asked the health coach if he had any clients with MS and he said he did, but since there are different types of MS, the results were mixed.. For some, there was no improvement; for others, it keeps the symptoms at bay.
As a result of our experience, I decided if I ever was unfortunate enough to get an autoimmune disease I would begin using cannibas oil rather than prescriptions by pharmaceutical companies. It's your health, you decide.
First of all, a great big THANK YOU to Gary Sharpe for sharing your work. May I ask how long your therapy sessions are? You mentioned in begining, you had long sessions. I find 1 hour is not adequate for clients. I am curious also, what modality did you use w the individual w the Veteran w PTSD? I have a young client who is a delivery room Nurse. Her hands shake and always have as far as she can remember. I’d love to learn more from you on what therapy modalities are most effective. Thank you kindly from Vancouver BC 🇨🇦. 1 more question, is the FB group helpful to all that live w stress? 🙏🏽❤️