Відео

:( I tried to take naltrexone for alcoholism actually but the side effects were unbearable for me unfortunately

I was studying about how myalgic encephalitis is really a disfunction of the mitochondria, and generally from something like parasites, mold, Lyme and also toxins like heavy metals and such, etc. I’m working on all of these things, and it makes sense that a dysfunction of mitochondria is the root cause of the lack of energy, and that by healing our mitochondria, our energy reserves can often be restored, but it takes time. I always noticed a difference in energy when I use the infrared sauna followed by a freezing cold shower and do a coffee enema. God bless you with continued healing.

Way to go! Wholehearted. Have you ever been tested for chronic Lyme disease?

Thank you for the reminder to put one foot forward. Great video

Thank you Melissa for everything you have shared so far. It's incredible 😊 looking forward to be part of your next journey about pacing 😊❤ All the very best for the same ❤

Thanks Melissa you're doing a great job at spreading the awareness and congratulations on your books! I think it's adorable that your son narrates one of your books also! Anyone who deals with this condition and or CFS are warriors! 💜💙💜

Thank you 🙏❤️

Please can you list the supplements! Thank you 🙏🏽 x

Hi, please could you recommend the type and brand of product you were taking as I know there’s a wide range of recovery factor supplements! Thanks 😘

Tu. Long covud exacerbated everything🙏❤️

Melissa, a great interview and everything resonated with me in so many levels. I am a yoga teacher myself for over 16 years and 18 years with fibro. My personal practice are my life line and teaching yoga with compassion to others. I am not longer able to do headstand, arm balancing asanas etc, but who cares. My practice daily home practice is 20 minutes some day other days 5 mins. The breath is the center of my practice, and my teaching with guided meditation at the beginning and at the end. Do what you can, come as is and honour where you are that day. I have RA and hypermobiled hips too ☺️. Just started LDN 8 days ago and feel better with my pain already. It took me 2 years to convince my GP to prescribed and my RA doctor, just told me no 😔. Thank you so much Melissa for sharing your story, tips and the good and ugly of Fibromyalgia. Greetings from 🇨🇦 and 🇵🇦 💜🪷🙏🏽

Hi Melissa, just discovered your channel. Are you still going to the chiropractor?

Thanks Melissa! 💜

That’s wonderful to hear that you are transitioning to finding your own pace. Does that mean that your UA-cam channel will change its name? And if so, how do we go to that? I guess I feel the same way. My passions are creating my art, and my grandchildren. I would rather focus on finding what works for me so I can reduce my number and the strength of my crashes.😊😊

That’s wonderful to hear that you are transitioning to finding your own pace. Does that mean that your UA-cam channel will change its name? And if so, how do we go to that? I guess I feel the same way. My passions are creating my art, and my grandchildren. I would rather focus on finding what works for me so I can reduce my number and the strength of my crashes.

Thanks for sharing Melissa! I know this is a tricky topic but much needed 💜🙏💜

Thank you for sharing. ❤️ This made me feel much less alone.

Thanks Melissa and Deb! 💜🙏💜

Thanks for not making me feel as alone for having all these same symptoms x

So true about drs bit caring treatment earlier aftee 27 years ime sure fybromyalgia is a part of me

I understand this. I have had fibro since I was around 10, and I had issues with taking everything commonly prescribed. I started LDN and cut my dose twice, where it’s reset my digestion. Each change is a major decision. To even be on anything is a major decision.

Thanks Melissa 💜🪷🇨🇦🙏🏽

Thanks again for another video melissa!💜

Do you know at which lowest dose people can expect to start seeing benefits? Thank you.

Such a great video! This is extremely familiar to me. I really struggle to know my own limits. I have a friend who's quite bad with money, and we always joke that I spend energy like he spends money. As soon as I have a scrap of energy, I'm up, using it. I don't know how to just sit and rest. I'm working on nervous system retraining (through DNRS and Gupta) and it has helped so much! But as soon as I start feeling better, I burn myself out again😂😭😬 ooooops. Now I'm trying to develop the skill of Pacing. Gosh, it's so much harder than it sounds

hello. i have both m.e .and fibromaygia.mark

Hi Melissa, Is this program still running? I am much interested to join 'Working with Chronic Pain and Fatigue Series'.

Hi Melissa. My chiropractor advised that I wear sacriolic joint belt and I love it. It really helps with the pain.

Oh yeah the pain when someone touches or squeezes your upper arm, and having BP taken -ouch! 😮

Hi Melissa, thank you for sharing your experience with chronic pain. Having a horrible tonight with my pain!

Any sexual side effects in men that you’re aware of??

Thank you so much for speaking for us diagnosed with Fibromyalgia I’m in tears you couldn’t have explained it better.❤

👍

My pain doctor has me on 9 MG twice a day

Thanks again for spreading the awareness Melissa I can relate a lot to this video as well! I am proud of you too!💜

Thank you so much Melissa. Today, I don't feel so alone 🇨🇦🇵🇦💜🪷🙏🏽

Thank you so much for sharing your journey! There is nothing more powerful for the chronic illness community than hearing from another person who has LIVED it. The truth brings us all together and helps us ❤

Thank you. 🙏🏻 I just received my fibromyalgia diagnosis. After being super healthy and vibrant for most of my life, these changes in my body have been a challenge. As a yoga teacher, I appreciate the reminder to do yoga nidra-I need to do it more often! New sub here 💖

Thanks for making this video and spreading the awareness Melissa! You describe these conditions pretty well. I can relate to your step count goals as well(that's with pacing lol). Regarding insomnia, I take medication but also do meditations/yoga nidra,including listening to your yoga nidra videos (Which I love). Hope you're doing well and have a great week! 💜

Thank you, well said.

Thank you for sharing!

I talked to my GP about LDN this week. He will research it and got back to me in 2 weeks. I am desperate to find relieve from pain🪷💜🙏🏽

You must start with 0,1 mg! And than next week 0,2 mg and than 0,4, 0,8 and than finally 1,5 mg! Never start with high dose

That smile when you saw your masterpiece in that box.

Has anyone here for it from the NHS in the UK?

i love the vibe of the painting, you created that naturally, you are a natural in that way! ☀️✨️🌸⭐️🪷

Thank you!! I'm taking it for long covid and it seems to be helping.

I had some initial positive results, but it gave me insomnia, no matter when i took it. Adenosine Triphosphate helped some.