I'm doing everything I can to reduce stress. My dad brought me a T.E.N.S. machine that I can put on to rub, knead, push, acupuncture, etc. They're giving me random massages. I have lavender and peppermint in the room. Whatever I can. I'm still in the hospital doing the steroids. I'll be here for a few more days. After that, it's on me.
Wednesday, April 10, 2019
Tuesday, April 9, 2019
No Sensation
Well, happy Tuesday. First of all, yes I've scheduled my appointments with my Neurologist and Primary Care Physician. The lack of sensation has moved up to my waist. The bottom of my feet feel like i'm walking on wood. Unstable to say the least. My arms have some loss of sensation but not as much as the rest of my body. I've had headaches all week. My body feels REALLY tight around my waist.
And guess what? *drumroll* We're having another baby! Remember the last time we had this conversation? Well, the plus about it is, I haven't been on any medication to cause an issue. The bad part is, I'm in the MIDDLE OF A MS FLARE. I thought this couldn't happen.
And guess what? *drumroll* We're having another baby! Remember the last time we had this conversation? Well, the plus about it is, I haven't been on any medication to cause an issue. The bad part is, I'm in the MIDDLE OF A MS FLARE. I thought this couldn't happen.
Monday, April 8, 2019
Losing Sensation
I was scheduled to leave to head back to Puerto Rico today. But I started feeling a little weird after Saturday's MS Walk. I started losing sensation in my lower extremities. My legs didn't feel right, to touch. So I decided to go to the Emergency Room. The last time I opted to fly back to work, April 2014, I ended being diagnosed with MS. So I figured something was 'wrong.'
Unfortunately my visit to the ER didn't give me much. My potassium and magnesium was low so I received a refresher and was sent on my way. But remember, I've not been on any medication for a couple of months now. I know I know!
Anyway, I'm not going back to work just yet. I need to make an appointment with my neurologist and get to the bottom of this. I'm now thinking back to my last MRI, where my lesions are and what areas of the body they impact.
Unfortunately my visit to the ER didn't give me much. My potassium and magnesium was low so I received a refresher and was sent on my way. But remember, I've not been on any medication for a couple of months now. I know I know!
Anyway, I'm not going back to work just yet. I need to make an appointment with my neurologist and get to the bottom of this. I'm now thinking back to my last MRI, where my lesions are and what areas of the body they impact.
Saturday, April 6, 2019
Walk MS 2019 - Tallahassee
This year's walk has been sort of rushed. I didn't put as much work into making it come to. It DID but it wasn't as together as I'd liked. I was tired. Drained. Stressed. But we made it through. It was actually sorta dreary. I'd gotten in late the night before, from Puerto Rico. Oh yeah, did I mention I'd working in PR now?! No shirts though. Everyone was to wear their favorite sports team.
I felt good. I got my laps in!
Theme: Play To Win
#TeamTasha #OnMyNerves
I felt good. I got my laps in!
Theme: Play To Win
#TeamTasha #OnMyNerves
Monday, March 4, 2019
Neurology - San Juan
As I mentioned before, I had the opportunity to network with some people in San Juan that allowed me to get in to see a neurologist on the Island. I'd been in Puerto Rico, almost permanently, since January and need to find a doctor to coordinate my first dose (restart) of the Gilenya. I got in to see Dr. Chinea. It was a great visit. We discussed my symptoms and issues. He talked to me about the work/research (MS in people of color) he'd been doing with the University of Miami and looked forward to seeing me again.
Saturday, March 2, 2019
MS Walk 2019 - San Juan, PR
I like participating in the walks in different cities/states. My coworkers joined me this morning in San Juan, Puerto Rico. The walk here is different than in the states. They have ONE BIG walk on the island. Everyone from all over comes here with the teams. It was really nice to see. I was also able to network with representatives from Novartis and the The Fundación de Esclerosis Múltiple de Puerto Rico (MS Foundation) to see a doctor on the island.
#TeamTasha #OnMyNerves
#TeamTasha #OnMyNerves
Thursday, January 31, 2019
Co-Payment Renewed | Let's Go
... now send me my medication. :-)
I'm reaching out to a local (stateside) Neurologist to set up my first dose observation and you know what they told me (before doing research, apparently), "I didn't know you had to do that!" So what you're telling me is, you have no idea about the medications that MS patients take. You don't have knowledge of other medications and presumably stick to the few that you do have knowledge of. That's discouraging. How am I supposed to feel comfortable talking to my doctor about something that concerns my health and you (or your staff) don't do the due diligence to perform the 'procedure'?
Ok, so now what?
I'm reaching out to a local (stateside) Neurologist to set up my first dose observation and you know what they told me (before doing research, apparently), "I didn't know you had to do that!" So what you're telling me is, you have no idea about the medications that MS patients take. You don't have knowledge of other medications and presumably stick to the few that you do have knowledge of. That's discouraging. How am I supposed to feel comfortable talking to my doctor about something that concerns my health and you (or your staff) don't do the due diligence to perform the 'procedure'?
Ok, so now what?
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