Monday evening, 6:20 P.M. We just got home from a full afternoon of doctor's appointments, Greg had one at 4:00 after mine at 1:40. Anyway, here's the scoop on my neuro appointment.......he thinks it's possible that I may be progressing, but he doesn't want to say for sure until after a MRI, which should be done sometime in the next couple of weeks. He says that part of my problem could be that I have been so lax about my betaseron shots lately, and I do agree with him. So for the next 6-10 weeks, I'm going to be very faithful on my shots, Greg will make sure of that, and when I see him again the first week in April, we will discuss my options then. He will have the MRI results by then. He mentioned that if there are major changes in my MRI, he will want to discuss Tysabri, he has a good number of patients on it and he is extremely pleased with how they are doing. He thinks it's the best thing out there today. So time will tell, y'all please keep me in your thoughts and prayers. I'm feeling ok today, just a little down about all this, and for some strange reason today I'm really missing my dog. I need some dog therapy, lol.
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Hi Deb, I hear that Tysabri is great. Many good benefits from it. I asked my Dr about it before the chemo and he said it was not for me.. Hang in there. We have our good and our bad days that is MS...but do take your shots...Greg best stay after you. I will pray that all goes well for you. Take Care, LOL
Dog therapy, ok, here you go;
Bark, bark, bark, ruff, ruff, growl growl, bark ruff (Take your damn shots when you are suppose to)
Rufus
LMAOOOO, yessir Mr. Tex, errrr....Rufus
Wish I could send Maddie to love you up. She loves cuddling and would cheer you right up. I\'m sure hoping your better compliance of Beta will improve your symptoms so you maybe won\'t hav to do the Ty.
Be a good girl and do your shots. I am thinking of you and sending warm fuzzies your way. Peace too.
Love ya girl, Jani