Your favorite resources

[greaterexp]

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.)

[carolek572 CommunityAmbassador]

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

[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]

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]

thanks for doing this

[Jesmcd2 CommunityAmbassador]

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

[Cutefreckles72]

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

[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 CommunityAmbassador in reply to CraigS]

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 in reply to CraigS]

multiplesclerosis.net/livin...

I hope that changes soon.

[greaterexp]

multiplesclerosis.net/commu...

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

[sashaming1]

nationalmssociety.org

msconnection.org