Go Back   NeuroTalk Support Groups > Health & Related Topics > Caregivers Support

Caregivers Support A place for people who are a caregiver to another to find help and support.

ppms

Reply
 
Thread Tools Display Modes
Old 05-28-2012, 04:20 PM   #1
sadsister
Junior Member
 
Join Date: May 2012
Location: South Africa, Johannesburg
Posts: 19
Unhappy ppms

My sister was diagnosed with ppms 4 years ago,
She went for treatment, but it only made the progression of ms worse,
The doctors said there is nothing more they can do for her, what is the road ahead going to bring us? I wish there was something I could do for her!
sadsister is offline   Reply With Quote
"Thanks for this!" says:
tamiloo (06-06-2012)
Old 05-28-2012, 04:40 PM   #2
paulapepper
Junior Member
 
Join Date: Jun 2010
Posts: 30
Default Fahr's

Quote:
Originally Posted by sadsister View Post
My sister was diagnosed with ppms 4 years ago,
She went for treatment, but it only made the progression of ms worse,
The doctors said there is nothing more they can do for her, what is the road ahead going to bring us? I wish there was something I could do for her!
I am dealing with an incurrable disease, too. It is a real bummer. Think how fortunate you life has been up til now..... paulapepper
paulapepper is offline   Reply With Quote
"Thanks for this!" says:
tamiloo (06-06-2012)
Old 05-29-2012, 12:28 AM   #3
Sparky10
Member
 
Sparky10's Avatar
 
Join Date: Sep 2006
Location: Iowa
Posts: 674
My Mood:
Default

Sadsister, I'm sorry to hear about you sister's condition. What medication was she on that made her worse? None of the MS Disease Modifying Drugs (DMDs) are designed to improve the patient's condition; only to slow progression. And none of them are known to work on Primary Progressive MS because it is a different animal and even less understood than the other types.

How about asking your question in the MS forum? Maybe someone can give you better advice than mine, which is to be your loving sisterly self!
__________________
Secondary Progressive Multiple Sclerosis (or maybe RR), diagnosed '00

"Life is a lemon and I want my money back!"
Meatloaf

"No more turning away from the weak and the weary.
No more turning away from the coldness inside.
Just a world that we all must share.
It's not enough just to stand and stare.
Is it only a dream that there'll be no more turning away?
"
Pink Floyd
Sparky10 is offline   Reply With Quote
"Thanks for this!" says:
tamiloo (06-06-2012)
Old 05-31-2012, 12:02 AM   #4
sadsister
Junior Member
 
Join Date: May 2012
Location: South Africa, Johannesburg
Posts: 19
Frown

Thank you sparky!

She was on chemo therapy called Mitoxantrone, it was supposed to slow down the progression of the MS.

I think the hardest thing for me is that my sister has become a complete different person.
With the MS came a new personality and even new looks!
I found a photo of her that was taken a year before she got sick and I could not believe how much she has changed!
Another thing is she is now like a child of 12 (she will be 31 in June).
And ever since she got sick a kind of had to become the 'big' sister.
How I miss those days when I asked her for advise and talked about my problems! Which obviously I can not do anymore!

and the sadest thing of all is she keeps on asking when she is going to die, because she overheard me telling my parents that there is nothing more the doctors can do for her, I sometimes don't know how to handle these situations! No matter how hard I try, I just cannot get used to the idea of her being sick and that there is no cure!
sadsister is offline   Reply With Quote
"Thanks for this!" says:
tamiloo (06-06-2012)
Reply

Thread Tools
Display Modes

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off
Forum Jump

Similar Threads
Thread Thread Starter Forum Replies Last Post
PPMS sufferer Gertrude Multiple Sclerosis 10 11-11-2011 03:10 PM
PPMS only - need answers Gertrude New Member Introductions 2 10-28-2011 09:48 PM
Neurologist has given up. Looks like PPMS. legzzalot Multiple Sclerosis 20 04-09-2010 10:08 AM
RRMS or PPMS? Thumper2 Multiple Sclerosis 5 04-13-2009 11:43 PM
hello out there -- new with PPMS bbarbick New Member Introductions 7 01-27-2008 10:29 PM


All times are GMT -5. The time now is 01:32 AM.
Brought to you by the fine folks who publish mental health and psychology information at Psych CentralMental Health Forums

The material on this site is for informational purposes only, and is not a substitute for medical advice, diagnosis or treatment
provided by a qualified health care provider. Always consult your doctor before trying anything you read here.


Powered by vBulletin • Copyright ©2000 - 2013, Jelsoft Enterprises Ltd.


All posts copyright their original authors • Community GuidelinesTerms of UsePrivacy Policy
NeuroTalk Archives