After Messaging My Neurologist On Friday About What I Have Been Going Through. He’s Not Doing One Thing In Helping Me Get A Mobility Device
to help me get around a little more better than I am now. I guess I’ll have to keep pushing through this mess on foot . This is hard to do and exhausting as well.
Dawn you’re not the first to say that. I’m starting to notice that I’m getting off balance quite a bit. I have all idea what it’s from. But it’s looking like I’m going to have to go through my gp if I want to get progress. He has my best interest anyway. I’ll see him in February of next year.
Bryan, I’m getting ready to contact my gps office to see what he suggests me do about this neurologist . As well what to do about theses symptoms I keep experiencing that I know are coming from what I’m taking. Do the fact they are listed in the literature that I get in the mail with my prescriptions and are also on site as well with the Mayo Clinic. So what does that tell you?
You Need To Speak To Your Medical Care Provider, Right Away
Toni that a good ways from me.
You should talk to your primary care doctor.
What Do You Do If Some Family Members Don’t Agree With You On What You Need To Help With Mobility?
This Weakness Isn’t Going Away In My Legs . The Simple Fact Is I Wake Up With It Every Morning And It Last Through The Day My Question Is
I Just Reread The Response I Got Back From My Dr Yesterday He’s Trying To Tell Me That The Side Effects I’m Experiencing Have Nothing To Do