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Primary Progressive MS and Copaxone???

 
 
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Old 03-06-2009, 01:37 PM #9
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DizzyLizzy DizzyLizzy is offline
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Location: Minnesota
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DizzyLizzy DizzyLizzy is offline
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Join Date: Dec 2008
Location: Minnesota
Posts: 222
15 yr Member
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Originally Posted by SallyC View Post
I think Neuros can't really be sure it's PPMS, so some recommend a DMD. Copaxone could be helpful for you and I hope it is....and I hope you don't have PPMS..

Would yu have to pay for all of the Copaxone? Do you not have any insurance? It could be, that you may qualify for financial help in paying for it.
I do have insurance, but it is not the greatest but ok. I actually think that I am within $50 of my deductible this year already anyway, but I didn't want to contact the insurance company, because I don't want them to "label" me as an MS patient yet....maybe I am hoping that this is all a big joke?!
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DO WHAT makes you happy, Be with WHO makes you smile, Laugh as much as you breathe & LOVE as LONG as you LIVE



.

July 2006- First significant SXs, suspect it started back in mid 1990's
1/21/09 - Positive MS Dx
2/17/09 - 2nd Positive MS Dx
4/2/09 - MS Dx 3rd Neuro - finally found the Dr. who has the characteristics I was looking for
.

10/8/09-optic neuritis flair, Cog Fog, chronic headaches
5/4/09 - 12/15/09 Copaxone
1/15/2010 - First Tysabri Infusion - 3/25/16 - Last Tysabri Infusion
3/3/16 - signed the documents to start the Lemtrada journey
4/25/16. Lemtrada begins.
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SallyC (03-06-2009)
 

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