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rivernb
Newbie
Joined: 19 Mar 2010 Location: Canada Online Status: Offline Posts: 21 |
![]() Topic: My daughter needs helpPosted: 11 Aug 2010 at 10:11am |
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I was recently diagnosed with MS..just put my script in and will be starting copaxone..I am nervous and didn't expect the reaction I've had (emotionally). All in all tho, I think I will get thru it. My 9 year old had a big breakdown the other day..said se's afraid and doesn't know what's going to happen when I start the needles. I explained it would make me better kinda. I'm wondering if the MS society or someone can tell me how to get her someone that can talk to her. I have reading material and we've talked..but I think she may need more
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sammee
Senior Member
Joined: 27 Jul 2007 Location: Canada Online Status: Offline Posts: 385 |
![]() Posted: 12 Aug 2010 at 11:36am |
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hi rivernb. I can relate as my daughter too reacted She was 16 at the time, but the emotions are the same. Now, almost four years later, she is giving my my needle of avonex once a week, says she needs to help me. The MS Society has great people for this very reason Contact your chapter right away or if you have a great family DR to talk to her. Also this forum has a place for kids to vent with other kids. Siberbian Husky can help with that one.. Take care rivernb. Sending you and your daughter a
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worry about tomorrow when it is today, and forget it when it is yesterday
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strong
Newbie
Joined: 18 Feb 2010 Location: Canada Online Status: Offline Posts: 30 |
![]() Posted: 14 Aug 2010 at 6:25pm |
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Hi Rivernb my daughter is 13 years old and it was a day before her 13 birthday that I was diganosis been a quiet child she told me after she was afraid I was never going to walk....I am in NL and the MS nurse at the hospital gave me a book for my daughter title My Mum is Special. My daughter and I read this book each night to her and we talk about MS and what it can do...But contact the MS society or the MS chapter in your area and they will get your daughter help. The MS society has a section on their site for children of parents with MS. Good luck to you both and keep strong!!!
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