Makes perfect sense…actually a doctor that looks at the opinion and listens without prejudice …I'm so glad I found your channel..thank you for trying to make a very hard thing.. a little easier
Medical Marijuana stops my neuropathic pain so quickly!! The burning..it used to bring me to tears. It stops it!!! Also I hey severe muscle cramping in my head…on one side usually…and basically everywhere else…tho The head/face/neck cramp is the most severe….a couple of inhales of mm and it releases..I was shocked the first time this worked for me. It definitely relaxes me and helps me fall asleep but for some reason I dont stay asleep. I've been diagnosed since 1993 and have tried everything….cannabis wins for pain right now.
Question – I heard someone say the weight training reduces inflammation. Is the inflammation that it reduces, the inflammation that causes relapse/psuedo symptoms, and possibly new lesions? Recently diagnosed and so curious about so many things.
Tulsa Oklahoma
My spasms are getting stronger, pt does not help and major spasms affect my left side of my body. I am on the highest dose of the one med you recommend I cannot remember the name it begins with the letter b. Emily chicago
QUESTION: once remyelinating will be in, do you believe it will be possible to reverse at least some of the accumulated brain damage and restore previous level of function? Thank you
I am so interested in hearing about your thoughts on Lion's Mane also. I appreciate your help and simple explanations that even my young children understand.
How long does the effects of medical marijuana last?
Had some hair thinning and loss while on Ocrevus, but not so much that it was noticeable to others
Thank you for giving your patients the option of medical marijuana. I've had MS for 17 years and have been a medical marijuana patient in multiple states over the years. I Live with an increasing amount of pain over the years and I've been able to limit my use of medications including painkillers with the use of THC and CBD.
Thank you, thank you, thank you for becoming an official, certified, marijuana recommended. Have been doing it for 50 years. Would love to volunteer for clinical trials.
The guy with the fedora behind you looks like Bob Dylan. What's his story? Love all the work you do for us all. Peace, love, strength and balance to you, dear Dr B.
My family doctor in Washington, wrote an Rx for medical marijuana because of MS pain and for nausea.. She rewrites it every year. I’m glad that MM in Washington is not as confusing as Ohio.
Ketamine is horrible and did not help with pain. I say horrible because it brought on MS pain in my ear.
Sorry I missed your livestream yesterday! I would love to contribute toward any research regarding the use of cannabis and multiple sclerosis. I was diagnosed almost 4 years ago and the MRI that led to my diagnosis showed a plethora of lesions, both active and non; enough so that many of the doctors who reviewed my test results were surprised I had never experienced any symptoms. While the admitting doctor couldn’t professionally confirm that the use of marijuana could have aided in me not having any prior symptoms, she did firmly indicate that she had seen many patients that used cannabis and fared better when dealing with MS symptoms. Thank you, Dr. Boster, for speaking so openly on this topic and if you hear of any research studies being conducted on this, please think of me!
I lov e this man….he does fabulous work on MS!
Thank you for a great live stream yesterday Aaron. You answered a number of questions I had. I look forward to meeting you this year.
Hi Dr. B. I am a person with MS and living in Belgium. 2 weeks ago, I discovered your channel, and I already watched a lot of your video's. I must say, I already learned a lot about MS. Things that our neurologists here in Belgium do not explain to us. I have already started with a number of your tips about fighting spasticity like drinking more water, move around more. Now I will start to do the stretching as well. Thanks for all the interesting information that you share on your channel. Next time I will try to follow the live broadcast on the spot.
Thank you Dr. Boster for all your education on this platform. I’m 8 months on Tysabri and doing fabulous. Besides a few lingering symptoms, I feel like my pre MS self. My decision to choose Tysabri had a lot to do with what I learned from you. THANK YOU SOOOO MUCH!!!!
Just returned from (yearly) follow up with my provider. She's allowed 15 minutes per patient. Mentioned that she skipped the neurological exam, just replied that she sees enough by having spoken to me and having seen me walk, EDSS 7. About "down theres" – shipped me off to the gyneco-urologist and the gastro-entrologist (?). And about the flu vaccine, just clicked her tounge, nit. Admitted that I didn't need a neurologist to see that the MRI taken after the Ocravus was much improved, she agreed and that ended that discussion. Referral for yeary MRI and see you next year!!🤷♀️🙋♀️
Thank you for all of your participation today! #StrongerTogether
Makes perfect sense…actually a doctor that looks at the opinion and listens without prejudice …I'm so glad I found your channel..thank you for trying to make a very hard thing.. a little easier
Medical Marijuana stops my neuropathic pain so quickly!! The burning..it used to bring me to tears. It stops it!!! Also I hey severe muscle cramping in my head…on one side usually…and basically everywhere else…tho The head/face/neck cramp is the most severe….a couple of inhales of mm and it releases..I was shocked the first time this worked for me. It definitely relaxes me and helps me fall asleep but for some reason I dont stay asleep. I've been diagnosed since 1993 and have tried everything….cannabis wins for pain right now.
Question – I heard someone say the weight training reduces inflammation. Is the inflammation that it reduces, the inflammation that causes relapse/psuedo symptoms, and possibly new lesions?
Recently diagnosed and so curious about so many things.
Tulsa Oklahoma
My spasms are getting stronger, pt does not help and major spasms affect my left side of my body. I am on the highest dose of the one med you recommend I cannot remember the name it begins with the letter b. Emily chicago
QUESTION: once remyelinating will be in, do you believe it will be possible to reverse at least some of the accumulated brain damage and restore previous level of function? Thank you
I am so interested in hearing about your thoughts on Lion's Mane also. I appreciate your help and simple explanations that even my young children understand.
How long does the effects of medical marijuana last?
Had some hair thinning and loss while on Ocrevus, but not so much that it was noticeable to others
Thank you for giving your patients the option of medical marijuana. I've had MS for 17 years and have been a medical marijuana patient in multiple states over the years. I Live with an increasing amount of pain over the years and I've been able to limit my use of medications including painkillers with the use of THC and CBD.
Thank you, thank you, thank you for becoming an official, certified, marijuana recommended. Have been doing it for 50 years. Would love to volunteer for clinical trials.
The guy with the fedora behind you looks like Bob Dylan. What's his story? Love all the work you do for us all. Peace, love, strength and balance to you, dear Dr B.
My family doctor in Washington, wrote an Rx for medical marijuana because of MS pain and for nausea.. She rewrites it every year. I’m glad that MM in Washington is not as confusing as Ohio.
Ketamine is horrible and did not help with pain. I say horrible because it brought on MS pain in my ear.
Sorry I missed your livestream yesterday! I would love to contribute toward any research regarding the use of cannabis and multiple sclerosis. I was diagnosed almost 4 years ago and the MRI that led to my diagnosis showed a plethora of lesions, both active and non; enough so that many of the doctors who reviewed my test results were surprised I had never experienced any symptoms. While the admitting doctor couldn’t professionally confirm that the use of marijuana could have aided in me not having any prior symptoms, she did firmly indicate that she had seen many patients that used cannabis and fared better when dealing with MS symptoms. Thank you, Dr. Boster, for speaking so openly on this topic and if you hear of any research studies being conducted on this, please think of me!
I lov e this man….he does fabulous work on MS!
Thank you for a great live stream yesterday Aaron. You answered a number of questions I had. I look forward to meeting you this year.
Hi Dr. B. I am a person with MS and living in Belgium. 2 weeks ago, I discovered your channel, and I already watched a lot of your video's. I must say, I already learned a lot about MS. Things that our neurologists here in Belgium do not explain to us. I have already started with a number of your tips about fighting spasticity like drinking more water, move around more. Now I will start to do the stretching as well. Thanks for all the interesting information that you share on your channel. Next time I will try to follow the live broadcast on the spot.
Thank you Dr. Boster for all your education on this platform. I’m 8 months on Tysabri and doing fabulous. Besides a few lingering symptoms, I feel like my pre MS self. My decision to choose Tysabri had a lot to do with what I learned from you. THANK YOU SOOOO MUCH!!!!
Just returned from (yearly) follow up with my provider. She's allowed 15 minutes per patient. Mentioned that she skipped the neurological exam, just replied that she sees enough by having spoken to me and having seen me walk, EDSS 7. About "down theres" – shipped me off to the gyneco-urologist and the gastro-entrologist (?). And about the flu vaccine, just clicked her tounge, nit. Admitted that I didn't need a neurologist to see that the MRI taken after the Ocravus was much improved, she agreed and that ended that discussion. Referral for yeary MRI and see you next year!!🤷♀️🙋♀️