Disaboom.com Connecting the millions touched by disability
Sign in | Sign up
 
Search
  • health
  • living
  • community
  • marketplace
  • news
  • store
  • jobs
  • Blogs  |
  • Groups  |
  • Galleries  |
  • Discussions  |
  • Organizations
Text Size
A
A
A
 Green Nation Today

Forums

View all members
Posts you have not read
Forum Subscriptions
Disaboom » Health » Multiple Sclerosis » The Many Faces of MS

The Many Faces of MS

Last post Fri, May 16 2008 11:36 AM by Michele McHenry. 39 replies.


Page 3 of 3 (40 items) < Previous 1 2 3
Sort Posts:
  • gymstyie2 gymstyie2
    Posts: 2
    • permalink Re: The Many Faces of MS

    • Posted: Sat, Mar 15 2008 10:13 PM

    • hi i am a mother of daughter who has ms and it has been a very diffcult. she has lost part of her sight and abuilty to walk, she uses a walker. she is 23years old and also has a 2year old daughter. I am helping her with as much as i can, or let me say as much as she will let me she is angry depressed, and sometimes down righ mean. My family; my husband and other 2 daughter dont know what els to do for her I have even suggested she ge some outside help with the emotions she's going throug but nothing helps. what do you do for someone who you love wont let you in and how do i help her with out going crazy myself.

       

      gwen


    • gymstyie2
    • Reply Contact
  • SGoodwin SGoodwin
    Posts: 8
    • permalink Re: The Many Faces of MS

    • Posted: Sun, Mar 16 2008 12:02 PM

    • Hi, I'm brand new to this site.  I was diagnosed with MS in 1993 due to vision problems.  I had many other things in the years leading up to that, but it was vision issues that finally got me to a neurologist and an MRI.  I have had those tests you are talking about and have a wonderful neuro-opthamologist.  None of trhe tests i have had done on my eyes was painful.  I usually spend all day at her clinic and have many different tests done so she can determine changes/progression of the optic involvement and she then sends her results and opinions to my neurologist (who is a specialist in MS).  Don't be worried about the tests.  Diabetes can certainly be the culprit.  I have done a lot of reading on the issue and you can find a lot out about it on the internet.


    • boopsie
    • Reply Contact
  • gorolltide123 gorolltide123
    Posts: 5
    • permalink Re: The Many Faces of MS

    • Posted: Wed, Mar 19 2008 5:07 PM

    • Thank you so much for your reply. That makes me fill alot better. I just hope it is nothing serious. I am sorry it took me so long to respond but I have been out of town since saturday. Sorry to hear about your diagnosis. Thank you once again.                            gorolltide123


    • Reply Contact
  • WEDRESSFORLESS WEDRESSFORLESS
    Posts: 1
    • permalink Re: The Many Faces of MS

    • Posted: Sun, Mar 30 2008 3:56 PM

    • I MYSELF WAS ON AVANEX SHOTS ENDED UP IN THE HOSPITAL FROM BEING  SO SICK NEXT TIME I DID LESS EVEN THOUGH DOCTOR TOLD ME NOT 2  .I COULDNT HELP BUT 2  PUT LESS AND IT WORKED DID HALF WORKED MY WAY UP 2 A FULL SHOT STILL GET SICK BUT NOT LIKE B4.THAT WAS 3 YEARS AGO THERES THIS NEW MEDICATION OUT  IT REVERSES SOME OF THE MS SYMPTOMS  ALOT OF BACK PAIN THE FIRST SHOT  IS THE BEST FELT LIKE I NEVER HAD MS  BEST FEELING I HAVE EVER HAD .ONLY PROB IS HARD 2 GET VERY ITS CALLED IMMUNOSYN CORP THATS THE  COMPANY   STOCK  SYMBOL IF U WANT 2 LOOK UP WHATS GOING ON WITH THE COMPANY IMYN ITS BEEN IN STUDY 4  13 YEARS NOW AND NO SIDE EFECTS


    • Filed under: MS_Treatment, MS Multiple_Sclerosis
    • Reply Contact
  • RandallFlagg RandallFlagg
    Posts: 3
    • permalink Re: The Many Faces of MS

    • Posted: Thu, Apr 03 2008 6:34 PM

    • I was dx'd in 1991 when I was 16 years old, after a year of struggling with symptoms, and except for having PPMS, I am in almost perfect shape. I have had more than half a lifes time experience dealing with people who think that because you are physically disabled you are also stupid. You will find a lot of people who are very courteous and helpful, but they will never think of you as a "normal human being". Hold your head up and keep remembering there are others worse off than you. Your own PMA will be the most effective treatment.

    • Reply Contact
  • Daniel502 Daniel502
    Posts: 431
    • permalink Re: The Many Faces of MS

    • Posted: Fri, Apr 04 2008 12:40 PM

    • Even LPs (lumbar puncture/spinal tap) are not 100% accurate. Symptoms can come on well before a positive test. 


    • Reply Contact
  • Betsy Betsy
    Posts: 14
    • permalink Re: The Many Faces of MS

    • Posted: Mon, Apr 14 2008 1:18 AM

    • Hi All. I have not posted or visited lately due to many symptoms and having three back teeth pulled recently. Ouch. I'm wondering if anyone here has had their facial cheeks harden  up? Wierd I know, believe me  Other than that, I'm on Rebif now for almost a month and it's not so bad.. No results yet but I'm patient. I'm also on Baclofen  to help the twitching and tremors. My head bobs sometimes and says yes or other times it will  say no. Great when you are  having a conversation with someone. Eventually someone's going to punch me over it but it's ok........they will break their hands on my hard little cheeks. Blessings! Betz


    • Inspired. Encouraged. Enlightened. Unstoppable. Unpredictable. Unfrightened.
    • Reply Contact
  • Daniel502 Daniel502
    Posts: 431
    • permalink Re: The Many Faces of MS

    • Posted: Tue, Apr 29 2008 1:52 PM

    • Maybe this is just a flare up or it could be new symptom. Monitor its changes, and see when it is better/worse. Maybe keep a journal if you deem it a good idea and definitely tell your doctor about it. 


    • Reply Contact
  • Michele McHenry Michele McHenry
    Posts: 18
    • permalink Re: The Many Faces of MS

    • Posted: Fri, May 16 2008 11:29 AM

    • fretlessman71:

      There's at least one person here who has complained of MS related "shocks" going down their arms.  It's not the first time I've heard of it.  If I were you, or your mom, I would get a 2nd opinion.  Do not pass GO, Do not collect $200, go STRAIGHT to the phone book and set up a separate appointment.  Better yet, see if you can find the MS Society near you and find a doctor that people have had good luck with.  Keep us posted on your progress! 

      I experience this phenomena a lot.  It is like someone puts a cord in my arm that runs from my neck to my middle finger and someone presses a button....zzzzzaaaaap!  Then I also get it going down the back when I bend forward.

      Sometimes my arm will be in pain along with ONLY my middle finger....wierd.  But this whole disease is wierd and after the first couple of years before being diagnosed and being called "crazy, depressed, drug seeker...etc, etc" I thought I actually was. 

      A doctor said to me once early on, well good news! It is NOT MS! Isn't that great!  Well...what is it I asked?  Well I don't know, but, you can be happy to know it is not MS.  How the hell can a person who is suffereing so bad, be happy about not knowing what is wrong?  Tell me it is MS, heck, tell me it is cancer, but, don't tell me to be happy it is NOTHING and I am dreaming this stuff up. I look like an idiot feel like I was hit by a truck and  I should be happy to know I have nothing wrong with me.

       Being diagnosed, was the most difficult, embarrassing, excruciating experience of my life. And the drugs they gave me, almost killed me.

      If anyone is going through the process of finding out what is wrong and having doctors say you are crazy, or be happy we did not find anything....hang in there.  Life is worth living and you will find the truth soon. It just takes a while and the right test at the right time. Keep up the strength, and keep going to the right docs. Even Dr. Smith will tell you how difficult and how much time it takes to diagnose MS.

      Good luck, and let us know.

       


    • Michele McHenry
    • Reply Contact
  • Michele McHenry Michele McHenry
    Posts: 18
    • permalink Re: The Many Faces of MS

    • Posted: Fri, May 16 2008 11:36 AM

    •  

      gymstyie2

      She has nothing to look forward to in her life except doom and dependance.

      I think if she were able to have a purpose in her life, she would regain her spirit and soul and love for life.

      It took me a while..but, I found things I can do and want to do, so now I don't feel so worthless to myself and everyone around me.

      Good luck, I hope she can reach out and get the help she needs to find herself and what makes her spirit whole again.


    • Michele McHenry
    • Reply Contact
Page 3 of 3 (40 items) < Previous 1 2 3
rss feed

 



 

Home | About Us | Terms of Use | Privacy Policy | Contact | Advertise With Us