Your favorite resources: Would anyone care... - My MSAA Community

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Your favorite resources

greaterexp profile image
11 Replies

Would anyone care to post links to resources you rely on for credible information related to MS in some way? There is a wealth of information out there, but not all of it is based in fact and can actually be dangerous. Some sites I like deal more with the emotional or even humorous side of dealing with MS.

I'm most fond of MSAA for obvious reasons - you all! But I also appreciate:

multiplesclerosisnewstoday....

Positive Living With MS on Facebook

YouTube videos with Dr. Aaron Boster

I have a long list of bookmarks, but wondered what you all would share. Please share blogs and books you find relevant. I am nibbling at a book called "People with MS with the Courage to Give." (I'm sorry I don't know how to underline the title correctly.)

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greaterexp profile image
greaterexp
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11 Replies
carolek572 profile image
carolek572CommunityAmbassador

Good post, greaterexp I love the ones that you have mentioned, and may I add

multiplesclerosisnewstoday....

Also, you do not need a Facebook presence to enjoy 'Positive Living with MS', you can simply sign up to receive the newsletters, just like I do.

Keep Smiling,

Carole :-D

RoyceNewton profile image
RoyceNewton

good idea, I like health unlocked, resilience article, 10 tips to build a stronger you. Also on a general health not, something always good to know. Bill Bryson "The Body"

Midgey_Midge06 profile image
Midgey_Midge06

My favs r multiple sclerosis news today and positive living with ms. Most of my posts on my facebook r reposting those blogs cuz they r so great.

rjoneslaw profile image
rjoneslaw

thanks for doing this

Jesmcd2 profile image
Jesmcd2CommunityAmbassador

Love the post greaterexp ! Of course there is mymsaa.org 😊😂 but I do ck out msfocus.org also! Can't forget National.. 🤗💕🌠

Cutefreckles72 profile image
Cutefreckles72

Thank you for the resources. I will continue to read and learn more. Excellent post.

CraigS profile image
CraigS

Having PPMS, doesn’t leave a lot of resources to confide in. There’s no real research being done since it affects such a small populous. So, having said that, I look to y’all for insight and comfort.

Thanks for being there.

Craig

carolek572 profile image
carolek572CommunityAmbassador in reply toCraigS

Yes, you do have PPms, as do I, but that doesn't prevent me from managing this 'ms' with other approaches that involve my diet, sleep, and my attitude. I rely on my neuro, for a lot of my healthcare. She is the best! As is my PCP. I hope that you have a great healthcare team that you can rely on as well, CraigS

greaterexp profile image
greaterexp in reply toCraigS

multiplesclerosis.net/livin...

I hope that changes soon.

greaterexp profile image
greaterexp

multiplesclerosis.net/commu...

This fellow has a great way of putting into words what I'd like to say.

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