The money I would pay for someone like him to read my MRI !!! At 10:49 he mentions something that has given me hope about my presumptive diagnosis of MRI. My MRI shows bilateral "lesions" around the zones of terminal myelination and based on his comments, this is a naturally hypertensive area and should not be confused with MS lesions. Oh lord, I hope I am right!!! Seeing a Neurologist this coming Friday, fingers crossed!!
My late husband was a “case study” at the Cleveland clinic in the early 80’s. He had one of the first MRIs done in the country there. He had MS AND neurofibromatosis as well. I forget the neurologists name that saw him, but he went through a round of cyclophosphamide for about a week there. It didn’t help. He never had a remission and died in 1993 at the age of 37. He had cognitive impairment, was blind, had a urinary catheter, feeding tube, colostomy and was on oxygen in a hospital bed in our living room. I cared for him all those years. It will be 30 years this May that he died.
I realize that the actual intention for this video is to perhaps help physicians better understand how M.S. presents on a MRI...but I have to say that I am SO grateful I came across it. I am a 45 year old woman who was diagnosed with M.S. at 43 and, until now after watching this video, I have not fully understood what I was seeing on my scans. So thank you so much Dr. Stephen Jones for this amazingly informative video! Side note: I have been on Tysabri for a little over 2 years now and test JC positive, so the information on how PML might present itself is also very appreciated, as this is a pretty big fear of mine. Thanks again! D.D.
I have just been diagnosed with MS. For years I have been diagnosed with Chronic Fatique Syndrome, then Fibromyalgia and with five Lumbar Surgeries and surgery on my Spinal cord in my Neck
Thea Hess- My goodness I am so sorry. It's unimaginable and heartbreaking so many go year's without a proper diagnosis. I'd like to know some time how your diagnosis finally was figured out? I'd seen your comment is from 6 year's ago hope you're doing better these days, hope to hear of your follow up. Much hugs and light to you.
10:33 He mentions certain areas of the brain that will Flair Hyperintensity and for it not to be confused with MS lesions. Wow.... This language is all so interesting but so foreign to understand but I try. I admire this man, he's really brilliant and most importantly is compassionate, wish he could read my MRI. I thank him for all that he does.
just had my MRI feel sick after ,hopefully I dont have MS I already feel like shit I am 39 always been active but a year ago I started to feel muscle weakness my right eye is blurry I cant go to the gym or be active like before doctor said I have to be careful I don't fracture my bones imagine that who would have thought this was gonna be my life 😔
Can you r doctor know for sure if you have MS with a brain scan? I cant get the doctor or neurologist to give me a brain scan .I believe i have it bc i have all the symptoms for years but cant find the right doctor for help being in the medical card.
The money I would pay for someone like him to read my MRI !!! At 10:49 he mentions something that has given me hope about my presumptive diagnosis of MRI. My MRI shows bilateral "lesions" around the zones of terminal myelination and based on his comments, this is a naturally hypertensive area and should not be confused with MS lesions. Oh lord, I hope I am right!!! Seeing a Neurologist this coming Friday, fingers crossed!!
How are you doing today? Hope you're doing better. Any updates?
My late husband was a “case study” at the Cleveland clinic in the early 80’s. He had one of the first MRIs done in the country there. He had MS AND neurofibromatosis as well. I forget the neurologists name that saw him, but he went through a round of cyclophosphamide for about a week there. It didn’t help. He never had a remission and died in 1993 at the age of 37. He had cognitive impairment, was blind, had a urinary catheter, feeding tube, colostomy and was on oxygen in a hospital bed in our living room. I cared for him all those years. It will be 30 years this May that he died.
fantastic!!! thanks for the indepth explanation of the images. I've never had anyone fully explain any of this to me.
I realize that the actual intention for this video is to perhaps help physicians better understand how M.S. presents on a MRI...but I have to say that I am SO grateful I came across it. I am a 45 year old woman who was diagnosed with M.S. at 43 and, until now after watching this video, I have not fully understood what I was seeing on my scans. So thank you so much Dr. Stephen Jones for this amazingly informative video! Side note: I have been on Tysabri for a little over 2 years now and test JC positive, so the information on how PML might present itself is also very appreciated, as this is a pretty big fear of mine. Thanks again! D.D.
amen
Did you ever end up switching off tysabri? Start ty myself next week
I have just been diagnosed with MS. For years I have been diagnosed with Chronic Fatique Syndrome, then Fibromyalgia and with five Lumbar Surgeries and surgery on my Spinal cord in my Neck
Thea Hess arachnoiditis
Sorry it took so long to diagnose. I was lucky and diagnosed quickly in the Navy 26 years ago
Thea Hess- My goodness I am so sorry. It's unimaginable and heartbreaking so many go year's without a proper diagnosis. I'd like to know some time how your diagnosis finally was figured out? I'd seen your comment is from 6 year's ago hope you're doing better these days, hope to hear of your follow up. Much hugs and light to you.
10:33 He mentions certain areas of the brain that will Flair Hyperintensity and for it not to be confused with MS lesions. Wow....
This language is all so interesting but so foreign to understand but I try.
I admire this man, he's really brilliant and most importantly is compassionate, wish he could read my MRI. I thank him for all that he does.
Contact doctor Akhigbe for your MS cure with his herbal medication
Message him on Whats App
✝️ 2348140126449🇳🇬🇳🇬⏭️⏭️❤️❤️❤️
I'm in the car right on my way to get an MRI wish me luck
i had infected sinuses
happy to hear everything is ok with you.
voltaspeeder17
thx
I just left after getting mine done
Good luck
Excellent! Thank you.
This was so fascinating. I am not a radiologist, but I enjoyed this video thoroughly. No wonder people go into radiology. Wow!
Agreed
just had my MRI feel sick after ,hopefully I dont have MS I already feel like shit I am 39 always been active but a year ago I started to feel muscle weakness my right eye is blurry I cant go to the gym or be active like before doctor said I have to be careful I don't fracture my bones imagine that who would have thought this was gonna be my life 😔
What was the outcome ?
Can we have ms with normal brain and spine mri?
wonderful lecture..great job !
Contact doctor Akhigbe for your MS cure with his herbal medication
Message him on Whats App
✝️ 2348140126449🇳🇬🇳🇬⏭️⏭️❤️❤️❤️
Thanks for this informative lecture
Dr.hussain khaleel consultant neurologist Iraq
I have MS. I'm not a doctor but I love this stuff.
Are you cured? Can you see everything?
@@lordzmusic8461 it cant be cured
Thank you
Can you have MS if you have MANY MS symptoms,butMRI Scans do not show lesions?
Can you r doctor know for sure if you have MS with a brain scan? I cant get the doctor or neurologist to give me a brain scan .I believe i have it bc i have all the symptoms for years but cant find the right doctor for help being in the medical card.
Ceraneller atrophy and degeneration and moderate is my diagnosis and what's a good treatment..
When I had my mri in the spring my Nero said I had numerous new white areas but contributed it to age I’m 63
i need soneone to read my mri
ok where you mri
Not on histogram or facebook or any Twitter accounts need to knowledge about histomstatic legal in relation to atrophy,with atrophy and.
Any information about calcium in the brain?Fahr's disease?