Lauren,
I just wanted to let you know that I have been watching your videos as well as some of the other youtube videos for ms that are on here for the past few months or so. You really have been inspiring to me. I too am from Detroit Michigan but moved away several years ago to another state. I was recently diagnosed with ms. I have learned from so many of the ms videos on here as well as your videos about MS and I hope to learn more too.

Hey Lauren!

I wish to thank you for your videos! I have learned a lot more by watching your videos then from my neurologist. This is very good what you are doing, keep up the good work :-D and Thanks :-D

Regards from the Faroe Islands :-D

Hallur

I love how brave you are. I just found out on Nov 17, that I also have MS. Ive been crying my eyes out trying to deal with this news, my family cant deal with it so they stay away. My husband left about 6 months ago so I'm dealing with a lot of issues at once. Seeing you gives me hope....I dont have to give up or stop laughing! :) Thanks for being a light for others.

I sent you a video as a " response" on one of your uploads. I just wanted to say how much I appeciated oyur channel. Hugs from Astrid, Norway.

Ciao Lauren! I thought of coming by to say hi! :)
I hope you are doing well and I hope that the postcard I sent you will get to you very soon!
Ciao!
baci
Angela

I was wondering if I missed it or if you'd do a video on ms and pain. So many people and docs think ms isnt painful...we know different! I mean a video sharing your experiences and such. And maybe what ms freq' sxs you still have? Its just a request and none of my business LOL . Hey take care :O)

hey lauren..you are an amazing girl darling! stay strong.. my cousin is also fighting this disease and seeing you trying to over come this bring her hope and joy.

PS ; Youre a blessing! (to soooo many girl !) Seeing your experience and honesty in hospital makes me just a little less affraid and your experiences in general. Oh I love your teddy bear...I have several LOL and yes theyve been in hospital w/ me too (past issues not ms).

Lauren: I had to say thank you for your work here at you tube! I send ((hugs)) of thanks. I wasnt going to comment as you have so many but when I watched your video of your exacerbation before tysabri I just had to say thank you.
I have tremor sxs that affect me that look pretty much like you did (my voice too). As you know it comes and goes with severity. Several neuros at the beginning of my dx said dont worry about the tremor Lady Hepburn had tremor and shes a starlet! I laughed but at that point it just didnt help, now I use that comment LOL.
Thank you for making yourself humble and vulnerable by showing the face of ms to us, Id not seen anyone with my trembly tremor walk head voice etc...Im sorry I came to know you in this way but am so grateful you shared your experience! (inc'd the fact you came out of the exasp too) More hugs and sincere prayers.....slothofms.

I just wanted to Thank you for all these video's. You are an amazing lady. My name is Zelma, I am 28yrs old. I have had MS since 2000, took them 7yrs to diagnose, Feb 07 is when I was finally diagnosed. I was on Rebif for 15 months and it made me so ill. They switched me to Copaxone, I was on that for 10 months and was having severe relapses. I was lucky to have a good day every 2 weeks. I'm a stay at home mom with 2 small children so it has been very tough. I had an mri recently which showed that I have a good dozen lesions and that I have been getting worse. So now I'm in my cleasing month to get the copaxone out of my system and beginning of november I'll be starting the Tysabri. Again Thank you so much.