New to this site - Hello everyone! - My MSAA Community

My MSAA Community

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New to this site - Hello everyone!

Baltoric profile image
16 Replies

I am new here. I saw this site described in the latest MSAA Motivator magazine. I am trying to connect with others with MS. I am a 47 yr. old married gwm just trying to navigate my way the best way I can with MS, and all its surprises, along for the ride.

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Baltoric profile image
Baltoric
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16 Replies
greaterexp profile image
greaterexp

Welcome to a great site filled with lovely, helpful people. It’s wonderful to connect with people who really understand what life with MS is truly like. This is where many of us ask questions, vent, and get encouragement.

We look forward to getting to know you better.

Royjr profile image
Royjr

Welcome Baltoric and I know you’ll enjoy this group of fantastic people. I know I have

Midgey_Midge06 profile image
Midgey_Midge06

Welcome! This is a great place to connect w others struggling w the rollercoaster of MS

Kenu profile image
Kenu

Welcome to our crazy group of MSers😜. What a great place to vent and find out lots of information on MS from people who care 👍. I was diagnosed twenty three years ago and have been on seven different DMT’s through the years. Currently on Aubagio for sixteen months and doing great 👍 No side effects and last MRI stable and no relapses 🙏. Lot of great people here 👍😉🐾 Ken

ssdw1958 profile image
ssdw1958

Glad you could make it but I wish you didn’t have to. I was diagnosed 2004. This is the right place to be find out what’s going on. But I have to tell you we are all learning together because this disease is a day to day. Meaning new medicines come out all the time. But this a good place to learn about MS and it is a good place to vent wether it’s good or bad.

Ssdw1958

SueAB profile image
SueAB

Welcome, Baltoric! We will become your extended family before you know it! You can share both good days and bad and we will totally get it!

bxrmom profile image
bxrmom

Welcome to the site Baltoric This is a great group of people here where you can chat with, vent. I am Jessie and I was diagnosed with RRMS 12 years ago after my vision went blurry suddenly. I was first on Copaxone daily until 3 times a week injection came out. I have now been on Tectifera for a little over a year and have been doing good. I will see a new Neuro in July and most likely have an MRI to see how my MS is doing with it.

Look forward to meeting you,

Jessie

Peruzzot profile image
Peruzzot

Welcome to the group.

RoseySawyer profile image
RoseySawyer

Welcome Friend! ☺🌷

goatgal profile image
goatgal

Baltoric You will find a community here. Many post frequently, others (me, for example) may do so only occasionally, but all of us understand in ways even our doctors do not, how MS impacts our lives. The Community Ambassadors are ever present and supportive, great resources. As for me, I start every day by reading the posts.

Yehealth profile image
Yehealth

Welcome to our ms family!!! This site has answered many questions that i may have regarding ms!! Welcome ☺

CraigS profile image
CraigS

Hi Baltoric,

Too bad you had to find us. But glad to share your experience with this thing.

I've found great comfort being able to share the format with such wonderful people. I wish you luck navigating your way through this.

Craig

Curran1970 profile image
Curran1970

Welcome to the site,great courageous people with lots of insight into this terrible disease.Plenty of lighthearted moments also & great place to leave off a bit of steam now & again.😀🍀.

Fancy1959 profile image
Fancy1959

Hello and welcome to our extended family Baltoric, from Fancy1959. We are glad you have found us. Welcome to our incredible chat room that is a safe place to come and ask questions, voice concerns, or simply speak to others who truly understand what you are going through. This chat room is full of some of the most caring, kind, and compassionate people I have ever met. The fellowship here runs deep as we all are forced down that winding and detoured filled.path that MS has set us upon.

Make sure you connect with jimeka, our birthday club ambassador and give her your birthday in any special interest you have. She will then put you down in our birthday Club and as families are want to do we will help you celebrate your special day! So Dive Right In and start asking questions, making posts, or simply respond to others questions, so we will get to know you faster. I am certain there is much we can learn from each other! Until we speak again please take care and I would like you to remember one important fact. And that is that together we are stronger! Fancy.

Welcome to a wonderful site

positiveness profile image
positiveness

Greetings! You have definitely come to a great place to hear and share stories about MS.

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