WHAT ARE GLIAL CELLS?

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What are 'Glial cells' and what do they have to do with CRPS? In this video, I will discuss what happens with your glial cells after you get CRPS and how this can affect your pain levels.
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Disclaimer: All content found on The CRPS Network, including: videos, images, audio, or links were created for informational purposes only. The content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health providers with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have watched or read on this channel.
Reliance on any information provided by Jennifer Katherine, The CRPS Network, or medical professionals presenting content for this channel is solely at your own risk.

Опубликовано:

7 май 2019

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Комментарии : 13

@CRPSRSD 5 лет назад

I have wrote a thesis on these cells and I found out they can be affected by cannabis and can help slow them down which can help to reduce pain great video keep up the good work 👏👏👏👏👏👏👏

@TheCRPSNetwork 4 года назад

WOW! YOU WROTE A THESIS ON GLIAL CELSS?!?! AWESOME! I did not know that about mmj, but just another reason why cannabis is amazing!

@kristabowers6725 4 года назад

Medical Cannabis has been helping me tremendously. I use a 1:1 ratio of THC to CBD, about an hour before bedtime.

@creativegirl9710 2 года назад

@@kristabowers6725 Same here! It's not "medical." They are ginger chewies with the THC/CBD ratio. They help with sleep. And after my last ketamine infusion I felt a wave of nauseous at home. So the ginger chewy helped.

@TheJustonemore 5 лет назад

I alway called them glee-al. That’s another great video

@staceyshaffer180 5 лет назад

Thank you for yet another very informative video. Can I get a shirt like yours? I’d like to wear it to all my doctor appointments. 💕

@TheCRPSNetwork 5 лет назад

Thanks! I got it online from teespring.

@juliep3180 5 лет назад

Thank you for the information! I'm looking forward to finding out more about the medication you spoke about. 💕

@fromfranceswithlove8084 2 года назад

Súper informative, thanks! I love your dog though! Looks like a Coton de Tulear ❤️

@creativegirl9710 2 года назад

I've been on LDN for a couple years now. I read and read everything I could on it since it was a drug. I expected more relief from it because it seemed like a miracle for all the video stories I watched. It took me months to titrate up to 4.5mg. It was a rough couple months. It effects your sleep while trying to dose up and my body felt like I'd been hit by a bus. Finally after getting to 4.5mg it seemed like my brain was functioning better. Like it got turned on. I kept waiting for more symptom relief like my nerve pain, histamine issues, arthritis but didn't get any. Anyway I have stayed on it since it gave me a little help. Better then nothing.

@TheCRPSNetwork 2 года назад

LDN helps me. It’s difficult to find that magic pill that will help 100% but if you can get 10% relief from it, 10% of relief from something else and so on...you can get a considerable amount of relief. I use LDN, PEMF therapy (most effective by far), essential oils, avoid inflammatory foods, mmj, meditation to calm my nervous system. It’s definitely a cumulative approach.

@creativegirl9710 2 года назад

@@TheCRPSNetwork I've done all of those too. Paleo diet since 2013. I bought a PEMF mat but it does not relieve my nerve pain. It's good for an afternoon nap, Lol. I love EO and learned about them many years ago about when I changed my diet. I have a diffuser by my bed. I usually take a ginger chewy CBC/THC at night. Listened to a meditation tape every night for years. Did laughing yoga, tried a neuroplasticity program, acupuncture, foot massage, etc. I've been seeing NDs pretty much since my mysterious pain issues starting slowing me down--since 2011? And it's just gotten worse each year.