Hi everyone,
Next week i have to go to Brussels again, to see my docter KDM.
I am already 1 year in treatment and last summer we discoverd that i have an hhv6 infection.
I already saw some storys about valcyte, but i am almost bedridden and cant stay long with the computer.
So my question, can somebody say anything about there experience with valcyte???
Or give me a link to storys about it?
I am from holland, and on that forum only 2 people use it, so i really want more experiences because this treatment is so expencive.
So i really need to know if this is a good decision and i my body can handle this heave drug.
Please someone any experience??? Or know someone who is taking valcyte?
Thanks very much
Next week i have to go to Brussels again, to see my docter KDM.
I am already 1 year in treatment and last summer we discoverd that i have an hhv6 infection.
I already saw some storys about valcyte, but i am almost bedridden and cant stay long with the computer.
So my question, can somebody say anything about there experience with valcyte???
Or give me a link to storys about it?
I am from holland, and on that forum only 2 people use it, so i really want more experiences because this treatment is so expencive.
So i really need to know if this is a good decision and i my body can handle this heave drug.
Please someone any experience??? Or know someone who is taking valcyte?
Thanks very much