Posts - My MSAA Community | HealthUnlocked

My MSAA Community

9,019 members • 20,711 posts

All posts for August 2016

Hello Everyone - New Member, but not new to MS

Hi ! I'm a new member on this site and I just wanted to say hello and say I hope this finds everyone as well as can be expected. I was dx with RRMS back in...

Hi ! I'm a new member on this site and I just wanted to say hello and say I hope...

•8 years ago

Recently diagnosed in the last few years?

I was diagnosed in July 2014 and have gained support, understanding and information from others who have been recently diagnosed. I had intense vertigo, facial...

I was diagnosed in July 2014 and have gained support, understanding and informat...

•8 years ago

tingling in my head

Hi my name is Sandy I'm new here so glad to find this site :-). I have been diagnosed since 1993 been on Copaxone for over 9 years just changed to the 40 ml...

Hi my name is Sandy I'm new here so glad to find this site :-). I have been dia...

•8 years ago

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MS and marriage-ongoing

I want to say that I appreciate all of your comments. For those of you who inquired I do have two people: my sister in law and a neighbor who is a CNA who...

I want to say that I appreciate all of your comments. For those of you who inqu...

•8 years ago

Hello Everyone

Hello everyone, I was DX April 2013 with RRMS, I am stubborn and put my cane down because I just don't want to depend on it. I walk funny but I believe I will...

Hello everyone, I was DX April 2013 with RRMS, I am stubborn and put my cane dow...

•8 years ago

NEVER GIVE INTO MULTIPLE SCLEROSIS

I'm Just Another Person in This Great Big World- THAT HAS MS MULTIPLE SCLEROSIS.. MY GRAMPS TOLD ME AT AN EARLY AGE "THESE WORDS" YOU WERE BORN WITH 2 FEET---...

I'm Just Another Person in This Great Big World- THAT HAS MS MULTIPLE SCLEROSIS....

•8 years ago

Long day ahead

The last couple days have been ridiculously tough. I have been fighting through spasms in my lower back which are painful, but now I have the same painful...

The last couple days have been ridiculously tough. I have been fighting through ...

•8 years ago

Multiple MS therapies?

Hello All, I am wondering your thoughts if my MS life is "normal"? I was diagnosed in 2013. Doc put me on Rebif (#1) and said we'd do an MRI after a year to...

Hello All, I am wondering your thoughts if my MS life is "normal"? I was diagnos...

•8 years ago

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MS and marriage

Hello, I am new to this site but have been reading hundreds of posts on various sites. Does any of them address the problems when the husband doesn't stay,...

Hello, I am new to this site but have been reading hundreds of posts on various ...

•8 years ago

Caretaker/Spouse

My husband has MS. I am a stay-at-home caretaker of both my husband and mother.

My husband has MS. I am a stay-at-home caretaker of both my husband and mother. ...

•8 years ago

Trigeminal Neuralgia

Hi everyone! Just started having really bad shock-like pain in my lower jaw on the left side. The pain is especially bad when I eat, brush my teeth or touch...

Hi everyone! Just started having really bad shock-like pain in my lower jaw on t...

•8 years ago

Body movement disorder

Hi everyone,. I'm still waiting for my official diagnosis but wanted to know if anyone has experienced whole body jerks and sometimes uncontrollable shaking....

Hi everyone,. I'm still waiting for my official diagnosis but wanted to know if ...

•8 years ago

Help.....Android users unite! Please develop an app for us too.

Please work on an app for Android phones, not just I-phones. Thanks. Fancy1959

Please work on an app for Android phones, not just I-phones. Thanks. Fancy1959

•8 years ago

MSN maryland

I am new to the site I've had a ms for years I count myself lucky because I can still walk I'm always tired always achey. I'm afraid of losing my ability to...

I am new to the site I've had a ms for years I count myself lucky because I can ...

•8 years ago

New member

Hi ya'll my name is Karen I have been DX with MS, anxiety,PTSD,depression and so much more. I am a military wife with you beautiful girls. I...

Hi ya'll my name is Karen I have been DX with MS, anxiety,PTSD,depression and so...

•8 years ago

Ending drug therapy due to side effects

If I decide to terminate drug therapy because of side effects destroying my quality of life, what will my neurologist most likely do? Drop me as a patient...

If I decide to terminate drug therapy because of side effects destroying my qual...

•8 years ago

A Good Day

Today is going to be a good day. If l keep saying it , it will happen lol. Will it be a good day for you?

Today is going to be a good day. If l keep saying it , it will happen lol. Will ...

CommunityAmbassador•8 years ago

MS for at least 36 years

My MS was diagnosed in 1980 after several years of symptoms. I was on Avonex for 3 years (2001-2004) and then Copaxone (2006-2009) but currently am taking no...

My MS was diagnosed in 1980 after several years of symptoms. I was on Avonex for...

•8 years ago

New here

Hi, my name is Vicki, I live in Northern New York with my husband, Jim and our 17 yr old daughter, Sarah. I'm originally from Utah, which is where I met my...

Hi, my name is Vicki, I live in Northern New York with my husband, Jim and our 1...

•8 years ago

Facial Paralysis on one side of face.

Hello, I'm new to this blog. I was wondering, has anyone experienced Hemifacial spasm?

Hello, I'm new to this blog. I was wondering, has anyone experienced Hemifacial...

•8 years ago

Anyone 18 yrs old and taking Copaxone?

My daughter will start Copaxone soon. She was just diagnosed in June and I was wondering if anyone her age was on Copaxone too and how you're doing?

My daughter will start Copaxone soon. She was just diagnosed in June and I was w...

•8 years ago

Ms Strong

Multiple Sclerosis Awareness #msstrong #curems #msawareness #msmam via MS Memes and more Multiple Sclerosis Information

Multiple Sclerosis Awareness #msstrong #curems #msawareness #msmam via MS Meme...

•8 years ago

Being so tired

Would love to here about what you do about being so tired. I have no energy to do anything. And will sleep for 3 days sometimes. My boyfriend doesn't...

Would love to here about what you do about being so tired. I have no energy to ...

CommunityAmbassador•8 years ago

Have you heard about HSCT? Stem cell transplants for MS?

Hematopoietic stem cell transplants use chemotherapy and your own stem cells to stop MS in it's tracks and reverse disability for many! And yet we hear so...

Hematopoietic stem cell transplants use chemotherapy and your own stem cells to ...

•8 years ago

40 years of adapting

My husband has MS. He was diagnosed in 1977. As we sat with our 6 month old daughter the Dr. came into the room announcing, " I have bad news and I have...

My husband has MS. He was diagnosed in 1977. As we sat with our 6 month old d...

•8 years ago

Is it ms? That 5 CT scans 12 years ago missed? MRI 2 days away

I'm being tested once again for m.s. I have tested with electrodes and do have neuropathy. It's been 12 years since my last test. They can miss MS with CT...

I'm being tested once again for m.s. I have tested with electrodes and do have n...

•8 years ago

Hi

Hi like most of you lm new here and new to MS. Was told last yr that l had it. I'm 50 yrs old and guess l hit the cut off. I don't know. I don't know about you...

Hi like most of you lm new here and new to MS. Was told last yr that l had it. I...

CommunityAmbassador•8 years ago

Dental decay and MS or is it Medication

My son has MS. He takes copoxone every three days by injection. His teeth have become so brittle that they have broken off at the gum . Any input or help on...

My son has MS. He takes copoxone every three days by injection. His teeth have...

•8 years ago

Decisiones un life!!

Hello everyone!! I have decided to be HAPPY, because It is GOOD For MY HEALTH. Voltaire

Hello everyone!! I have decided to be HAPPY, because It is GOOD For MY HEA...

•8 years ago

Working with MS

I was diagnosed with MS in 2014. My symptoms can be traced back to 2007. I started on Copaxone, then Tecfidera, and am now on Tysabri. I have only 3 lesions...

I was diagnosed with MS in 2014. My symptoms can be traced back to 2007. I start...

•8 years ago

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