I just got back home an hour and a half ago from my neurologist appointment with my new neuro!
Taking the county commuter bus which has handicap accessibility was nerve-racking and scary as hell. And bumpy. But coming back was not as bad and I think I'm going to use it for a couple more things soon. Plus I think it was a deal at $37 to take me to the dr. and back in a privately reserved bus? I feel pretty privileged.
So she wants to get me on Tysabri. I have to have the test for the JC virus ASAP and she seems to think that I shouldn't worry about Time I'm going to pay for this drug. And I also figured out how to get my blood tested while fasting, which would otherwise be impossible for me to do as a hypoglycemic, and that is to use my private bus! That's the only way I can get out of the house without having anything to eat all night, is to just plan out of bed onto the power chair and I have to get back off until I'm back home.
She said that I have moderate to severe MS and I have a lot of lesions. Of course I know exactly how many I have and I kind of knew that I have moderate to severe MS is well. She said that some people can experience dramatic improvement of symptoms taking this drug Tysabri.
So I am going to be reading on here about anyone who has experience this is that was extremely uplifting to hear this possibility. And I will do everything I'm expected to do I need to do on my part to make sure it could happen. But now I'm exhausted so I have to go but I just wanted to let those who were following my previous thread know how everything went today. And I'm really happy. I'm so happy! Oh and she also gave me a prescription for Zoloft and I didn't even have to ask, she just said I'm depressed and she could see that clearly and wanted me to take this. And she also has me getting tests for vitamin D deficiency and vitamin B12 deficiency.
I hope everyone has a good night! Thank you all for your support and concern!
Taking the county commuter bus which has handicap accessibility was nerve-racking and scary as hell. And bumpy. But coming back was not as bad and I think I'm going to use it for a couple more things soon. Plus I think it was a deal at $37 to take me to the dr. and back in a privately reserved bus? I feel pretty privileged.
So she wants to get me on Tysabri. I have to have the test for the JC virus ASAP and she seems to think that I shouldn't worry about Time I'm going to pay for this drug. And I also figured out how to get my blood tested while fasting, which would otherwise be impossible for me to do as a hypoglycemic, and that is to use my private bus! That's the only way I can get out of the house without having anything to eat all night, is to just plan out of bed onto the power chair and I have to get back off until I'm back home.
She said that I have moderate to severe MS and I have a lot of lesions. Of course I know exactly how many I have and I kind of knew that I have moderate to severe MS is well. She said that some people can experience dramatic improvement of symptoms taking this drug Tysabri.
So I am going to be reading on here about anyone who has experience this is that was extremely uplifting to hear this possibility. And I will do everything I'm expected to do I need to do on my part to make sure it could happen. But now I'm exhausted so I have to go but I just wanted to let those who were following my previous thread know how everything went today. And I'm really happy. I'm so happy! Oh and she also gave me a prescription for Zoloft and I didn't even have to ask, she just said I'm depressed and she could see that clearly and wanted me to take this. And she also has me getting tests for vitamin D deficiency and vitamin B12 deficiency.
I hope everyone has a good night! Thank you all for your support and concern!
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