Dr. Hauser is the Robert A. Fishman Distinguished Professor and Chair of the Department of Neurology at the University of California, San Francisco.
Statistics on Reels: Determination of Sample Size for Phase II Clinical Trials in Multiple Sclerosis
I created this video with the YouTube Video Editor (//www.youtube.com/editor)
Sunlight and Multiple Sclerosis - Dr. Marc Sorenson
Dr. Marc Sorenson discusses the link between the lack of sunlight and increased incidence of Multiple sclerosis (MS).
CIGNA Partners with EMD Serono for Multiple Sclerosis Medication
CIGNA (CI) announced today that it has entered into the nation's first outcomes-based contract with EMD Serono to develop a specialty medication aimed at ...
Statistics on Reels: Statistical Learning Approaches to Construct IPWs in MSM Cox
The Performance of Statistical Learning Approaches to Construct Inverse Probability Weights in Marginal Structural Cox Models: A Simulation-based ...
Multiple Sclerosis - My Story Part 1 - 18/5/11
How MS bit me on the arse - Part 1 2010 was a really crappy year, it all started for me back in May...
Hi there wow now thanks to your videos I'm understanding so Much more your
inspirational I'm not yet diagnosed but my symptoms are similar, two MRIs
have multiple lesions on my brain and cervical I have chronic fatigue and
really bad balance I feel I can't sit on a chair without the feeling of I'm
going to fall off I have numbness in my arms and a creapy crawly feeling in
my scalp and legs its really hard to figure this all out oh well I'm off to
the neurologist again next week
Cheers
Hi my name is joel. I also was diagnosed in 2010. And also went through a
break up also that year. Depression and stress made it even worse cause i
really didn't understand what was going on with me. But i thank god that im
still alive & yes it gets hard for me cause i can't do the things that i
used to. I have RRMS. It gets tough at times but i don't let it get the
best of me. We have to fight this disease in a positive way. And pray that
1 day they'll be a cure.
I was just diagnosed January 23rd this year broke up with my exs cause he only want sex and I am Christian and is against sex before marriage never was really into it
+ray cabello I like how she tells her story with all the details, emotions and psychological introspection. It's like listening to a friend telling a personal story that I can relate to (I was also diagnosed with MS).
Hi. I have had some weird symptoms for a few years now and it started with
a tingling in my nose. That was some years ago since that started and since
then I have had many symptoms that sent my to a neurologist. he examined me
and found that I had no reflexes in my feet. so I had an MRI witch was back
in 2007 and it was clear. I am now 41 years old and I am having new
symptoms like loss of balance,numbness, and panic attacks. every morning I
wake up my fingers are numb. I have had blood tests,heart monitor blood
pressure monitors and all was ok.
my new symptoms are scary and I find it hard to walk down the street trying
to keep my balance without looking like ive had a few drinks.
my doctor tells me im ok but I know something is wrong. can you give me
some advice please because I am at my wits end?
Thank you.
Regarding your numb fingers, you should look into whether you might have carpal tunnel syndrome. I used to have it as I do a lot of power lifting/weightlifting which can stress the wrists, and there are various ways to get it sorted.
Wow, Lucie. What a lack of compassion and absolute cold heart you have. And very sorry for you, there's no medication for YOUR condition of being a MEAN B***CH! I have every hope for you that you will somehow have a life changing event that will put you back in touch with your HEART, if you even have one.
From someone who's uploaded a video highlighting the positive virtues of "reflection and happiness"... Very callous given she has very little choice in the matter.
Lady are you kidding me? Please....knees hurting, arthritis & all your
other symptoms scream LYME disease.
Do a search for "LYME BORRELIOSIS AND MULTIPLE SCLEROSIS: ANY CONNECTION?"
Do you see how many people tested positive for Lyme....a SIGNIFICANT
NUMBER. Even with flawed testing this was the case. There are many
different species of spirochete (Lyme) causing bacteria, not all of them
are being tested for in their tests. That is why the tests are so bad and
flawed!
The CDC this year admits they were wrong. They reported that only
30,000/yr new cases exist, but that the number is 10x more, so 300,000/yr.
Well, they are wrong again! Do a search for "one million lyme germany" and
you will get a hint for what the numbers might be in the US. If all these
people are going around with symptoms, but never find the root cause
imagine how big those numbers are.
You can watch a free documentary on hulu called "Under Our Skin" or see
clips of it on youtube. You can see how many people who were diagnosed
with MS tested positive for Lyme. It is a growing epidemic & the CDC is
not doing squat about it. There are doctors out there that are giving
their life to promote awareness, but if you don't know what you are
afflicted with you don't even know where to look.
You didn't just call it Lymes? It's Lyme. and there is very much accurate testing labs. Band 23 is ONLY indicative for LD antibodies and nothing else. So there is NO false positive when band 23 comes up
I have two lesions and all your symptoms.. Neuro said not MS, but lyme. I've been on medication forever.... Question.. My eyes hurt 24/7!!!! I wanna poke them out!!! I haven't found this with others and MS??
Lymes was one of the first things they tested me for prior to diagnosis along with Diabetes due to my symptoms. Both are normally considered before MS and usually tested for before testing for MS.
Thanks so much, I had begun to ask questions about Lyme but discovered how difficult it can be to detect... Knees not been sore since the beginning but it is worth re investigation. Thank you.
Multiple Sclerosis & Me Ep.3
Multiple Sclerosis & Me Ep.3 In this Vlog about MS & Me I talk about caregivers and the benefits of being your own caregiver. Thank You for watching! Please ...
Thanks Jane. I do not have MS. I do have ITP (rare platelet disorder).
chronic stage 4 kidney disease, liver disease, diabetes and high blood
pressure. I've had a total hip replacement and fused back. I say all this
to express how when you have these big issues come up it is so easy to let
someone else take the reins and drive the horse. I did and in the end it
wasn't helpful just like you said. Now I am trying to take control again
and it is hard. My husband is my caregiver and he is great. Problem with
that is that he wants to do EVERYTHING for me. That is no life for him or
me. So I am working on this. Please keep sharing. Humor has been my best
medicine.
+Mr619jose619 She and Sound did one on the collab channel. Cheers to you post-dispensary-visit. Some pretty long lines today. One dispensary was giving out free T-Shirts to customers.
Bob Marley said "The simple truth is that everybody will hurt you at some
point in life. The secret is to surround yourself with people you are
willing to sacrifice for". This comes a lot of pain because we care about
these people more than strangers but not as willing to forgive them as we
do with strangers.
+1997wolverine I call them my tribe. And they are absolutely every bit as much a part of your family, as they are your real family. I've had friends that have saved me from myself at low points in my life. I will never forget that.
Jane, I do not have MS. I do have 11 herniated and 3 ruptured disks. I got
robbed and fought back in 2010. I was supposed to have surgery, found out
two weeks before, I was pregnant. I had my beautiful daughter who just
turned nine. I am in pain 24 hours a day. I have stenosis, fibromyalgia,
and osteoporosis in my spine. I have been on so many different patches and
pills, all it did was made me sleep and still be in pain. After a year of
PT and 30 trigger and cortizone shots, I felt strong and mentally prepared
for what life was going to be. I went cold turkey off the pills and began
using weed as my meds. I was able to maintain.
I got robbed at 30 years old, it changed who I was and what I could become!
It made me find my true strengths and weaknesses. I do not know your pain
Jane, any pain to me is too much.
Now on the topic of caregiver, I make all of my decisions because only I
live with my pain! I am the one that knows one day I will not be able to
walk, my solution for that is I am going to have a horn and a loud speaker
so I can honk and yell crap just when I am driving my car!! I do have a
supportive and loving husband who went through watching his wife cry while
trying to sit in a chair after getting a neck injection along with 4
trigger shots in between her neck and her sholders. He does not like me
smoking but definitely likes his wife now instead of drugged. My mom also
lives with us and she too has back issues. She also has seen what I have
gone through and hands down she supports me using weed.
Jane my heart, prayers, and tons of good Karma is getting sent to you!!
Watching your videos keeps things in perspective for me. You keep me strong
when I am feeling weak. You have made me laugh when I had been crying. Keep
your head up! I look forward to more videos!!
I'm a 26 year old stay at home dad. I've been diagnosed with PTSD and
generalized anxiety disorder with agoraphobia. Six years ago i met the love
of my life and we;re still together today. I will tell you that over the
past six years of her and i being together that i lost control of
everything. I could barely leave my home and ultimately my doctor
considered me disabled and here i sit. Not until 2 years ago when my son
was born did i start to push myself back into wanting to be a part of
society and start to become myself again. Over the past two years i've
managed to be able to start driving on my own again and many other small
things that "normal" people do. I'm proud of myself for that.
+IIR3C01LII I have also had anxiety, I'm doing better now, but just wanted to tell you, I know how you feel and I'm sorry you are dealing with that. It's great you have found the strength to keep pushing through, I'm pushing through mine too - so we are not alone. Sending good vibes your way. ((hugs))