Friday, June 8, 2012

So...it's on!

Well, the electrode thing for my head is on! I got my head shaved on Wednesday first by the hair lady and then yesterday by the doctor to be extra smooth. It was a little more than I was expecting. We entered the doctor's room and there were things everywhere that we had to be learn how to use and when to use it. We (well, technically it was my dad, but still!) had to literally move a giant black luggage piece, a bag full of wires, shaver etc, and back-up supplies of extra batteries and devices. My mind is kinda reeling from that even today!

My doctor put on the first four batches of these electrode things. We have to change them every 4-7 days. They gave me four battery packs and a unit that plugs into the wall, so I can plug-in 18 hours a day. I wish my camera was working right now, so I could give you all a better description!

The funny thing is that there was a little misunderstanding with the manufacturer and insurance company. Apparently, I was supposed to hear from this guy from their company last week before this whole treatment starts. So this morning I heard that the insurance company is still in process approving me for this machine! The guy somehow misunderstood or the misunderstanding was with the doctors involved, but anyways, the company that makes it will take care of the balance if there is one and insurance doesn't approve me.

My dad calls me "Magneto" from X-Men and my sister calls me the evil queen from Captain E.O. And my mom just calls me "special" since I am one of two people using this thing in the Northwest.

 


Saturday, June 2, 2012

You're never going to believe this!

So, I was so excited yesterday because I finally got a haircut with color. My hair looks so cute right now! That is until next Thursday, when I have to shave my head! My insurance went through for the electronic  head cap. I'm so excited, true - its experimental, but at least it gives me more hope.

Wednesday, May 30, 2012

Last Few Days

Just wanted to give you all an update. My doctor has decided that I needed to choose between treating my brain or treating my spinal cord. There are cancer cells in both, so it was tough deciding. I decided to keep treating my brain since I know what that involves. It's an infusion called Avastin that I get every two weeks.   

The other kind of treatment for my spinal cord involves putting an ommaya port in my brain (which I had so many complications with last year) and then the doctors don't even know if that chemo would work that well. 

The last treatment my doctor mentioned is an experimental one that hasn't been approved yet for my tumor. It is like a magnetic field that attaches to my scalp, which will have to be shaved again for this one!  My insurance company is working with the manufacturer to see if they can set me up with this. 

Anyways, those are my treatment options! Please pray that I'm choosing the right one and that it works out alright!

Monday, May 7, 2012

What Happens This Week?

Hi everybody!

So, this week I am supposed to get another Avastin on Thursday. True - I haven't heard from the hospital yet, but I am ever optimistic! :)

Now this past week, I got shingles, which is fabulous! (pun intended!) I think I can get Avastin, but I am not too sure about the interthecal chemo, which goes into my back. Everything is in the air right now!

Wednesday, April 18, 2012

Patient Story

I just wanted to pass on my patient story at the Seattle Cancer Care Alliance. I think it just got published today. Here is the website: http://www.seattlecca.org/patient-story/tiffany-kennard-survivor.cfm
Thanks for checking it out!

I'll keep you updated on my MRI tomorrow. I should know something by tomorrow afternoon. Keep those prayers coming!

Sunday, April 15, 2012

Another Couple of Those Days

Well, I should have known better than to expect chemo three weeks in a row! All of my blood levels were too low last Thursday and so chemo was withheld for another week.

Then, on Friday, I had to go to the ER for another seizure. I had some difficulty with answering questions this time and it lasted longer than normal. They did a CT scan and spoke to the neurologist at the UW Medical Center and decided that I could go home since the seizure had abated.

Other than being incredibly tired, the rest of the weekend went well.

I have an MRI and more labs scheduled next week to see what is going on and whether chemo can be restarted, so I would really appreciate prayers!

Friday, March 30, 2012

Another Good Thursday!

I had another good chemo yesterday. I did have some minor side effects, but it's going away now. I actually had an interview yesterday for the Seattle Cancer Care Alliance. It went pretty well. I'll send you the link when it's finished.

I know it sounds contrite, but thank you all so much for your prayers for me and my family! We really appreciate it!