Відео

Education = Empowerment

My favorite is, “You don’t look sick.”

Thanks Aaron 💪🏾 Feels good hearing this

Sounds like my mother 😂😂😂 are you ok now???!! Dear Lord, thank you for giving me the tools to be strong, and stay strong ❤

Midnight CBD healed my panic attacks. #midnightcbd

I know this is off topic from this video but have you seen rash or skin discoloration with ms?? About 15 years ago I got this odd rash or spots on my legs about the same time I started experiencing ms symptoms. No doctor has ever been able to tell me what it is. It's always there but sometimes more faded, sometimes darker and more noticeable. I'm dying to know what's caused it...

I really need to come see you. You’re passionate about it and to be frank, my neurologist isn’t. I’m 23 and was diagnosed when I was 15. I deal with many things from ms and you seem to be speaking to me directly to me with most of your videos. Keep up the good work and I’ll be reaching out!

Could BPC-157 and TB-500 be good options for this protocol?

I go to UCSF. Haven't had an MRI in at least 3-4 years, maybe 5. I'm in my 30s. Even though this is considered a top notch medical center, my doctor sucks. They never order MRIs. When they do order them or order blood tests, nobody EVER follows up with results or anything. My doctor doesnt care or listen. He asks me yes or no questions while staring at his computer and a quick exam and that's it. The care at UCSF is awful.

My brain scans show MS lesions, but spinal tap was normal and they said no MS because there was no significant event that i could tell them about. I'm so frustrated. I feel weak, I'm in pain and the Cog Fog is crazy. Where do I go from here?

I make insane dreams in the good way!!!

How about this? My father has had Gillian Barre Syndrome for 44 yrs. I was diagnosed RRMS in Feb 2022. My sister coddles him while being disgusted by my inability to work.

So true, it's so great to hear a ms specialist understand how it makes us feel!

I have one friend and she’s been my friend for 30 years and I can’t tell you how hurt I was when she recently said to me My disease had changed me and she didn’t know how to respond to me anymore. I’m not sure what she means by that I just don’t move as well but I’m the same person.

People don’t know how devastating and destructive Multiple Sclerosis is until they get it or have someone close to them that does :| ✌️ ♥️

The heat is kicking my butt

OMG your entire post happens to me as well. Ppl always compares their "tired" feelings whenever I say I'm extremely fatigued. I had a person tell me that her sister has lupus so she understands what I'm going through bc its the same as MS 😮 I got defensive and told her no its not the same. The nerve of her and everyone else 😢

I get oh what's wrong? Is your medication not working? 😡 It's so frustrating yesterday was a good day, today when you see me is a crap day. I'm fed up with the dumb questions

I’m scared because I’m jvc positive and neuro recommends Briumvi ,PML risk?

Thank you for spreading awareness, I dont see MS mentioned much at all and this kind of surprised me. My Dad started showing symptoms in the 80's, but not much was known about MS back then. He was in a near fatal motorcycle accident in the early 90s and all of his symptoms were attributed to that. It wasn't until 2017, when his legs couldn't support him and he fell from his semi truck that doctors discovered that he had MS. It has progressed significantly since. He is 100% wheelchair bound now and struggles to transfer himself from chair to wheelchair to car, etc. He does Ocrevus infusions every 6 months, but that just slows the progression. There is definitely no cure. It had been a devastating disease and I am so glad that medical professionals and researchers are learning more and there are things that can be done to slow the progression. It just came a little too late for my father.

This is second to hearing people tell you, about other people they know with MS and how poorly they ended up. Then you tell them there are different types of MS and it affects people different. They look at you, like you're lying to yourself. Don't get me started on explaining chronic fatigue. 9/10 the other person (thinking, they're being helpful) say "I get really tired too"

So very true. None of my family understands nor do they want to be educated. Frustrating is an understatement!

So true! Been living with MS for 23yrs and now starting to have a lot of changes with walking.

Generally I really like your videos, but this one has an unpleasant cliffhanger for those of us with many lesions!

I have never had mono.

I have MS, and also a family history of cancer. My Mother passed at 32 of Ovarian cancer. So my doctors will not put me on hormone replacement therapy. I know I would probably feel better, but I also am grateful they understand the risk for me.’

Thank you Aaron.

Im starting kesimpta soon. My lovely UK neurologist gave me the option of Ocrevus or Kesimpta, but said his preference is kesimpta because i can inject at home, and its slightly more preservative of the immune system. I feel very blessed to have such amazing experts to support me, here in london - and all for free - on the NHS. Also Dr.Boster you are so positive, clear and proactive that you lift my spirits, as well as educate me, thanks from the bottom of my ❤

What are you option on kesimpta thank you

Hi Dr Booster. When I was first diagnosed they found 11 lesions in my brain, 1 on my spine. This was long ago and I’m now 72 and haven’t had an MRI for 10 years till now and had stopped doctoring. I have many long term symptoms such as eye problems, PBA, weakness and brain fog and fatigue after being in heat. Over past 5 years I have lost most ability to walk but no real acute issues. Recent MRI doesn’t show those 11 lesions anymore! Is this normal? Could I have smoldering MS and all my continued issues be from lesions that have disappeared?

I learn a lot from Dr. Boster!

I have always wondered, what amount is considered "many lesions?" Or, when MS became a reality in the medical community, was a scale published for a "standard," as new patients were being diagnosed? A scale showing the disease's progress, according to the amount of lesions during this 5-10 year range your talking about Dr. Boster? Thank you, I hope this made sense, lol.

So if I get new spots 20+ years after dx, I don’t need to be as concerned?

Thank u Dr B

My uncle killed himself because he had MS. I had no idea how bad it was. I wish I could’ve done something

Sorry, but I found this just confusing and maybe that’s the whole point to make me wanna know more and it did work. I’m looking at your other videos, but you know a little bit more about this would’ve been great.

Thank-you Dr Aaron, wish I had known this 10 years ago.

This doctor is amazing! Great person , changing the way people look and treat MS, transforming lives and making people more confident toward a neurological condition that now has good treatments- ‘ thanks to Science and to the effort of amazing specialists like Dr. Aaron Boster!’ I learn a lot with your videos! Thanks a lot! Love from Rio.

This explains misdiagnosed MRI's

I take Aubagio, does anybody else take this and do you feel it’s working??

@AaronBosterMD thank you for confirming what I’ve known all along, but Nuerologists don’t want to admit! I’d rather know and be prepaired, then kept in the dark!

I’m all for being a “ stable mable” in all areas concerning MS, until they find a fix- Tho I’m always up for improvement!

What happens when I have to go to a cookout or party with family and friends who don’t care about their diets? No one I know seems to care. I have a fast metabolism and have a BMI of 19.5. People don’t understand why I care what I’m eating and I worry they think I’m a little nuts.

For 15 years, my MRI reports have stated “too many lesions to count”. That , in and of itself, makes me hopeless.

@Aaron Boster I have a burning sensation on the skin of my lumbar/sacral and cervical spine. The cervical spine is also sore around the C7 spinous process. I have a big list more. I seem to be having more problems since the insurance forced me to use generic Gilenya. Do you have any suggestions for me to talk to my neuro? I wish I lived in your area.

I discovered I was misdiagnosed as having MS. I have Leukodystrophy. I am not sure which type I have, I’m too old to have the most common types. I next see my neurologist in August. I see Dr. Pace in Owasso, Michigan.

What are your thoughts on Briumvi ? PML risk? 1:40

I get something that feels like the worst gas pain of your life under my ribcage and it radiates around to my back. It brings me to my knees and I can’t breathe for several minutes. MS hug?

Dr. Boster’s UA-cam channel is great for learning about all things MS. R.I.P. River 😢