Posts - My MSAA Community | HealthUnlocked

My MSAA Community

9,351 members • 21,120 posts

All posts for August 2016

Hi 🙂 Just Joined

I was diagnosed with MS in 2014. I had symptoms since 2010 when my feet went numb, i was getting fatigued easily, and headaches with the fatigue. My original...

I was diagnosed with MS in 2014. I had symptoms since 2010 when my feet went num...

Astrea

•8 years ago

2 Replies

MS and facial spasms

I was recently diagnosed with MS and I currently have Hemifacial twitching. I just started my medication. I have relapsing remitting. It's getting pretty...

I was recently diagnosed with MS and I currently have Hemifacial twitching. I ju...

Katyw46

•8 years ago

4 Replies

Primary Progressive MS

I have been diagnosed with Primary Progressive MS! I have suffered from the symptoms for 4-5 years. I currently take high doses of Gabapentin, Lyrica and...

I have been diagnosed with Primary Progressive MS! I have suffered from the symp...

Chris_Percival

•8 years ago

44 Replies

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Hot flashes and MS

Hello my name is Yvette. I am new to this. I guess my story starts in 2006 I had a lot of fatigue, pain and weakness in my arms and went to several doctors...

Hello my name is Yvette. I am new to this. I guess my story starts in 2006 I ha...

Cocoasmom

•8 years ago

15 Replies

Lady DI - I am new to this site .

I was diagnosed with MS 23 years ago. I have had many Exacerbation 's & have used all the Injectable Medications over the years. I can't use Interferons...

I was diagnosed with MS 23 years ago. I have had many Exacerbation 's & have use...

LADYDI0317

•8 years ago

19 Replies

ACCESS TO EXPENSIVE MS TREATMENTS

I am new to this site, so I would like to introduce myself. I am a retired lawyer with Relapsing MS. I was diagnosed 6 years ago. My current disease...

I am new to this site, so I would like to introduce myself. I am a retired lawy...

Sukie427

•8 years ago

24 Replies

Never give up! Never stop fighting! Never give into this fire - breathing monster called MS!

Hello everyone! I'm Fancy 1959. I am new to this site but not new to MS. I am in my 15th to 20th year of fighting this MS monster and over the past year I...

Hello everyone! I'm Fancy 1959. I am new to this site but not new to MS. I am i...

Fancy1959

•8 years ago

4 Replies

I am scared. What will happen to me in a year.

I have had MS for 16 years. But when I was DX my doctor said it looked like I had it for 10yrs. 19 lesions in brain and spinal cord! RRM.

I have had MS for 16 years. But when I was DX my doctor said it looked like I ha...

KKlynch5096

•8 years ago

6 Replies

New here.

Hello everyone. I'm Ryan. I have been fighting MS all mylife. I'm 37 and just moved to Mohave Valley AZ. I was diagnosed with secondary progressiveMS...

Hello everyone. I'm Ryan. I have been fighting MS all mylife. I'm 37 and just...

Sleek78

•8 years ago

7 Replies

Anyone like me out there?

I'm 78 years old and a newbie here. Had my first MS exacerbation on April 18, 1979. Was diagnosed via an MRI in 1989 and by 1995 moved into SPMS and began...

I'm 78 years old and a newbie here. Had my first MS exacerbation on April 18, 1...

KayV

•8 years ago

7 Replies

Bored in the Mountains

Hi everyone I am new here . I live in PA and I was diagnosed 24 years ago and have been on Copaxone for 15 years . Recently had to stop working because I...

Hi everyone I am new here . I live in PA and I was diagnosed 24 years ago and ...

sweetjayne

•8 years ago

2 Replies

Just diagnosed

Hi my name is Colleen and I was just diagnosed with ms on May 2, 2016. I just signed up to msaa yesterday. I hope I can learn from all the post and also...

Hi my name is Colleen and I was just diagnosed with ms on May 2, 2016. I just si...

Lucille3

•8 years ago

16 Replies

MS and Autoimmune Liver Disease

Hi! I'm new here and sure hope I can figure out how to respond to any posts as well as find my way back to this website. I'm wondering if anyone else has been...

Hi! I'm new here and sure hope I can figure out how to respond to any posts as w...

WAshingtongirl

•8 years ago

17 Replies

Adult Trike is a great tool for MSers

Hey MSers, if you have difficulty walking or fatigue easily but still want to get around on your own locally to run errands, get some exercise, etc., consider...

Hey MSers, if you have difficulty walking or fatigue easily but still want to ge...

TrikeMan

•8 years ago

4 Replies

ALASKA GIRL/MS WORLD

Hello everyone, my name is Karen and I'm from Anchorage Alaska. Well lived in Alaska over 22 years, I'm originally from Laguna Hills California. Once you've...

Hello everyone, my name is Karen and I'm from Anchorage Alaska. Well lived in A...

Happykp56

•8 years ago

3 Replies

Help me please

I need some help My MSAA Community https://www.crowdrise.com/sue-is-running-out-of-time1

I need some help My MSAA Community https://www.crowdrise.com/sue-is-running-out-...

suewaters1

•8 years ago

5 Replies

Have sec progressive MS

Hi my name is Shan. I have secondary progressive Ms for 2 years and RRMS for about 25 years. I can walk with a walker in my house. But use my wheelchair when I...

Hi my name is Shan. I have secondary progressive Ms for 2 years and RRMS for abo...

Shan58

•8 years ago

6 Replies

¡¡Hola a todos!!

Desde México los saludo Tengo esclerosis múltiple hace 22 años. Tengo una hija de 8 años y ella es mi motivación para no darme por vencida. No es fácil pero...

Desde México los saludo Tengo esclerosis múltiple hace 22 años. Tengo una hija ...

Lucycg

•8 years ago

8 Replies

The Grand Canyon

Hi All, Was diagnosed 3 years ago with primary progressive. It took ten years to get to that point. I now get around with a walker (my chariot). Just spent a...

Hi All, Was diagnosed 3 years ago with primary progressive. It took ten years to...

Peterdawolf

•8 years ago

Be the first to reply

Multiple Sclerosis

MS over 25 years. Use walker or cane. Received Lemtrada. Believe in remaining Positive, adapting to situations and Keep on FIGHTING.

MS over 25 years. Use walker or cane. Received Lemtrada. Believe in remaining Po...

Gypsy91

•8 years ago

1 Reply

Container for needles.

I use a laundry detergent bottle it takes a long time to fill. Then i duct tape it after I close it.

I use a laundry detergent bottle it takes a long time to fill. Then i duct tap...

ascmartin30

•8 years ago

3 Replies

MS

Hello, my name is Patricia. I am 62 yo and was dx'd w/MS in November 2013. Don't care for the way it affects my life and limits my ability to participate in my...

Hello, my name is Patricia. I am 62 yo and was dx'd w/MS in November 2013. Don't...

whitchurch54

•8 years ago

2 Replies

MS challenges

I have had MS almost 25 years. I have been on all the shots over the years and am currently not on any DMD. Pretty good until about 7-8 years ago, after two...

I have had MS almost 25 years. I have been on all the shots over the years and a...

KDenes

•8 years ago

3 Replies

Surgery Recovery w/ MS (knee replacement)

Anyone else with MS have knee replacement surgery? I'm having trouble trying to decide what is MS and what is just recovery pain.

Anyone else with MS have knee replacement surgery? I'm having trouble trying to ...

Nana_B

•8 years ago

2 Replies

New to this Community.

Hello everyone. I am 56 yo, and was diagnosed with RRMS 16 years ago. I had to finally give up working in 2008. I have 4 adult children and we are raising 3...

Hello everyone. I am 56 yo, and was diagnosed with RRMS 16 years ago. I had to f...

RhondaK8930

•8 years ago

2 Replies

My Life With MS - BITTERSWEET

I was diagnosed in 1988 (doctors thought I had MS since 1978) and am new here. There were times I didn't think I would recover from a serious relapse....

I was diagnosed in 1988 (doctors thought I had MS since 1978) and am new here. T...

revcarm

•8 years ago

2 Replies

Nett1959

I was diagnosed with MS in the '80 that's over 30 years. I am so glad I have other patients to talk to. Thank you for inviting me to your community.

I was diagnosed with MS in the '80 that's over 30 years. I am so glad I have oth...

Nett1959

•8 years ago

3 Replies

Chris

Hello my name is Chris I'm 49 years old and have had Ms since I was 13 16 years old I am married and have 2 children I own and operate a horse farm my Ms in...

Hello my name is Chris I'm 49 years old and have had Ms since I was 13 16 years ...

Chris-26

•8 years ago

Be the first to reply

New to this forum and not used to reaching out...

Hi! I'm new to the community. My name is Cindy. I'm 48y.o. and was diagnosed with RRMS in 2015. The symptoms began in 2006 with double vision, R hand...

Hi! I'm new to the community. My name is Cindy. I'm 48y.o. and was diagnosed w...

cindyrn68

•8 years ago

8 Replies

Living my life with multiple autoimmune diseases!

I'm new to posting on forums but this sounded interesting so I'm giving it a shot. I hate all of the negativity that is posted on sites. I'm not talking about...

I'm new to posting on forums but this sounded interesting so I'm giving it a sho...

Couragewarrior

•8 years ago

1 Reply

Posts - My MSAA Community | HealthUnlocked

My MSAA Community

All posts for August 2016

Hi 🙂 Just Joined

MS and facial spasms

Primary Progressive MS

Hot flashes and MS

Lady DI - I am new to this site .

ACCESS TO EXPENSIVE MS TREATMENTS

Never give up! Never stop fighting! Never give into this fire - breathing monster called MS!

I am scared. What will happen to me in a year.

New here.

Anyone like me out there?

Bored in the Mountains

Just diagnosed

MS and Autoimmune Liver Disease

Adult Trike is a great tool for MSers

ALASKA GIRL/MS WORLD

Help me please

Have sec progressive MS

¡¡Hola a todos!!

The Grand Canyon

Multiple Sclerosis

Container for needles.

MS

MS challenges

Surgery Recovery w/ MS (knee replacement)

New to this Community.

My Life With MS - BITTERSWEET

Nett1959

Chris

New to this forum and not used to reaching out...

Living my life with multiple autoimmune diseases!

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