Welcome

Welcome to all who visit this Blog whether you suffer from Multiple Sclerosis or have a loved one who does. Hopefully this will help all who read understand that they are not alone even though MS affects us all in very different ways. Maybe it can help open eyes of those around who do not know the unpredictability of daily life with MS.
The purpose of this blog is to offer support and inspiration. Please feel free to share any useful information that you have gathered along your journey and words of inspiration. It is hard to overcome all the obstacles we must face and it is nice to hear ways people have adapted. Inspirational stories and anectedotes are especially sought after.
If you post and suffer from Vision disabilities you are welcome to post in all capitals and no one will think that you are shouting.
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Monday, November 15, 2010

Doctors

Today I am going to see the neurologist, not my MS doctor.  It's a little stressful for me to go to all these different appointments.  I actually hate going to the doctors, as often as I have to go.  I hate being poked and prodded.  I hate being on display.  That's what it feels like.  With this neurology clinic, I never see the same doctor.  I usually see either a medical student or a resident, and then they bring in the attending doctor.  I have to tell my story all over again.  Why do I go to them then?  Because I can't afford my medications any other way.  Utilizing this clinic allows me to afford my Copaxone.  With just my health insurance, my copay is $250 a month, but through this clinic my copay is only $8.
I am struggling today.  I am sick of taking medications, so many for different things that all relate to MS.  A couple for other diagnosis. I can't stand taking medications, especially that shot.  I know that I can't control the course of this illness, but I take the medications so that hopefully it will slow down my progression.  I want to be able to participate in life, not sitting on my butt, but actively participating.

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