Thursday, December 17, 2009
Great Week
Monday was a day of being connected to a machine for collection and she was not able to even get up to go to the bathroom! Hence, no liquids for her those 7 hours.
On Tuesday, she and my Dad jumped in the car and went to Mammoth. She is so happy to be there--no skiing for her, but the weather is perfect and being in the mountains is a nice change.
Anyway, she is feeling like things are going her way. Christmas should be great, then on to chemo #6 on the 28th. Hmmm...not so sure about New Year's. HAPPY HOLIDAYS TO ALL!!
Tuesday, December 8, 2009
The waiting game continues...
My poor mom has STILL been waiting to get the final schedule for her transplant, but things continue to be up in the air. She just received an email from UCSD. I'm going to include part of it because let's face it, I'm just as confused as you all.
"I received a new e-mail from Dr. Castro. He DOES want you to have cycle 6 of chemo. So we are going to collect your precious stem cells, put them in the freezer, have your bone marrow recover a little, ( Dr. Castro to determine the time line, usually it's 1-2 weeks) and then have your chemo with Dr. Helton, then come back to us for the autologous stem cell transplant."
So there it is in all its vagueness. I'll let you know when we know FOR SURE when all of this is going to be happening. Let's pray for a Christmas miracle and hope she has this all behind her by February!!!! The lady is just desperate to get on with her life.
**I just checked the comments from the previous post. Thank you so much for offering to help. When it all finally starts we will definitely be needing you all! I'll keep you posted!**
Wednesday, December 2, 2009
Stem Cell Transplant Info
I wanted to update everyone on my mom's schedule for the next month, though it still is up in the air a bit. This is what she knows for sure:
December 3rd: Catheter gets put in
December 4th: Chemo at UCSD
Decemeber 14th-18: Stem cell collection at UCSD
This is the part that may change:
December 30: admitted to the hospital where she will get more chemo, then her stem cells will be put back
January 20: released from the hospital
For the next month, she's going to need round-the-clock care. Nancy Logan will be putting together a calendar of volunteers to come over to give my dad a much deserved break!
She is going to have crazy diet restrictions so I will post those later. Thanks in advance :)
Friday, November 6, 2009
Oops, another lie...
So, last month I said my mom didn't have to undergo the final two treatments, which actually turned out to be untrue. Don't blame me, though. It's been very difficult to get both of her doctors on the same page about this (especially when one is vacationing in Italy). This week she found out that before she starts the stem cell transplant process she has to finish out her two rounds of chemo. She had the first one yesterday and it looks like the final one will be the week of Christmas. Needless to say, we will be having a very mellow holiday season this year. Luckily, Ashley and Damian are hosting Thanksgiving so she wont have to worry about anything other than whether or not Ashley has enough Fall decorations up :)
During the time in between treatments they will harvest her stem cells and then the transplant will take place in January. I say this all very loosely because it seems to change daily. Her schedule has been one big question mark lately and luckily she's become quite flexible and just takes it as it comes.
She has been studying the book that prepares her for the stem cell transplant and is really dreading that month she's going to have to spend in the hospital, so if anyone knows of some good hobbies to keep her hands busy she'd appreciate them! I personally think smocking baby clothes or knitting baby blankets are her best bets (which will then maybe pressure Ash and Damian to have a baby--just kidding, guys!)
I'll keep you all updated as we find more out (assumming that you guys haven't given up on me--I know I haven't been an active blogger lately).
Monday, October 12, 2009
Monday, October 5, 2009
Sunday, September 20, 2009
She and my dad went to lunch at Shutters and watched some football and then Ash, D, and I met them to go to dinner. We went to a great restaurant on the Santa Monica Pier called Lobster and after, we headed to Westwood to go to this place called Diddy Riese that Ash and D knew about. Oh. My. Goodness. I have never tasted anything so delicious! You can choose any kind of cookie and any kind of ice cream and they make you an incredibly yummy cookie sandwich! We were in heaven.
This morning I picked them up at their hotel and we drove through Brentwood looking at houses (our favorite thing to do) and then walked around Santa Monica. It was a great weekend and we're all so happy we have a wonderful new member of the family who just happens to accrue a gazillion Starwood points thanks to his job and was able to get our mama out of town :) Thanks Damian!!!
Monday, September 14, 2009
We did the math...
It's actually the beginning of Novemeber, so we're feeling pretty lucky!
Wednesday, September 9, 2009
We got a little prematurely excited by her doctor's appointment last week and were brought back to reality the following day. Her other doctor at UCSD said that she would in fact finish the 6 rounds of treatment, bringing the chemo to a close the week of Christmas. We were really liking her other doctor's plan of only one more round after today, but the UCSD doc said that she is handling the treatment so well that she may as well go to Decemeber. Handling it well?? I think my mom would argue otherwise :)
Happy Birthday!!!
This is a day late (blame it on my 6am flight back from NYC and exhaustion), but my wonderful mom celebrated her birthday yesterday!
This picture is from our trip to Italy a couple of years ago. The whole family went to Positano and my mom and I stayed longer and drove around Tuscany and toured Rome. She is my favorite travel companion and one of the most FUN people to explore new places with! We all agree that it was the best vacation we ever went on and we're looking forward to a time in the near future when my mom is healthy enough to travel again.
Happy (belated) Birthday to the most beautiful, funny, generous, loving, and creative woman I know! You are so incredibly strong and your positive attitude amazes so many of us every single day. We love you!!!
Monday, August 31, 2009
Great News!!
She meets with a doctor from UCSD tomorrow to discuss a possible stem cell transplant because it reduces the chances of the large diffused B-cell lymphoma from coming back in the future. The downside is, it doesn't prevent the low-grade lymphoma she had before from coming back.
Thursday, August 27, 2009
Tuesday, August 18, 2009
There's really not much to report- she's sleeping now and when I ask her how she's feeling she just says "fuzzy" and "weird." She was already sick around this time last cycle so it seems to me that she is handling it better this time around.
Her hair is really falling out so I just bought scissors to cut it even shorter--she isn't on board with a buzz cut so we are just going for a very VERY short pixie. She has some cute headgear, though. Damian's kind grandmother gave her lots of little hats and scarves and my sweet friends from SMU gave her an ADORABLE and colorful scarf. It's just been so amazing for us to see how generous everyone has been. I think we've eaten better the past month than we ever have before!!!
On another note, my dad started working on the organic garden so when she starts feeling better she'll start planting!
I'll let you know if anything changes, but she seems to be doing well so far.
Wednesday, August 12, 2009
It's Debbie- I figured I'd be out of commission next week (it's my second round of chemo) so I may as well update you all this time. I have had a really great week! I found out on Monday that my bone marrow is clear and my blood was where it needed to be to be ready for next week, so that's left me very hopeful and positive. I love my doctor and he is always so reassuring.
Yesterday I had the pleasure of meeting with Rob Wergin, Master Healer and Spiritual Teacher. His healing technique left me feeling lighter and relaxed. He provided me with a positive mantra to help put my mind where it needs to be to go through this whole healing process. As you can see, I'm open to a range of methods dealing with both my pain and my overall attitude.
My wonderful trainer Erin has been helping me keep up my strength- I out-crunched Lauren yesterday :)- and she has also provided me with gallons of Kangen water.
I've started to shed a lot and the fabulous Heidi and Amber have been working on my wig to get the right cut and color for me. I am so thankful to every one's generosity and support. It has meant so much not only to me but to my family as well.
We are at the beach house til the weekend and I'm enjoying this little vacation while I am feeling well. Lauren will update you next week. My chemo days are Monday and Tuesday and the rest of the week will be spent recovering.
Thanks again and lots of love from the entire Huddleston family!
Saturday, August 8, 2009
Tuesday, August 4, 2009
She's baaaaack!
Monday, August 3, 2009
Today we had to put down our sweet Shae. We found out two weeks ago that she had cancer and she was becoming so weak and uncomfortable we decided it was the right thing to do. We all seriously loved this little girl and were so sad to see her go. But, as with everything, something good is going to come of it. We had a little fenced off area for the dog in our backyard and my mom decided she wants to start an organic garden there. We all agreed that it is a great idea and would be something fun for my mom to fuss over!
On another note, she went in for more acupuncture today. I'm not sure that she really feels any better but she's also not feeling any worse, so that's at least something. She's shooting for at least one outing a day so we're going to hit up the grocery store pretty soon and back to the couch she'll go.
Over the weekend she developed sores in her mouth from the chemo. She said it was the worst thing ever, and she's a pretty tough lady so it must have been awful. Her doctor gave her a prescription mouth wash and it's thankfully starting to get a little better.
Thursday, July 30, 2009
Tuesday, July 28, 2009
I lied...
This morning she started the chemo and it may be too early to tell, but so far so good. She's been concerned about the nausea because, as she told the nurse, she was the woman who "threw up all nine months of both pregnancies." Despite that, the nurse told her that she shouldn't have a problem. They gave her both anti-nausea and hydrating fluids in her I.V. so we're all hoping that will do the trick. She's feeling a little fuzzy now and the nurse told her by tonight or tomorrow she will have a metallic taste in her mouth so we're going on a mission for bland food. The nurse told her she should lose her hair in 18-21 days, and she already has a super stylish wig on its way. For a second I thought she was going to reinvent herself as a blonde or a redhead, but alas she stuck to her brunette roots.
She's gotten some emails about people not being able to post comments and when Ash comes home tonight I'll get a tutorial so I can teach you all how!
Thursday, July 23, 2009
Pre-treatment diagnosis info
Much to my mother's dismay, I am starting a blog so she spends her time resting instead of on the phone updating you all ;)
I'm not entirely sure what I am supposed to write, so please bear with me as I figure it out.
For those of you who don't know, my mom found a small lump on her neck in June. After much poking and prodding, the Doctors determined that it is Large Diffuse B cell Lymphoma, a different form than she was originally treated for last year. Her most recent PET Scan showed that it has gone to her vertebrae and a lymph node in her groin, and a few more little lumps are popping up on various places on her body. She has gone to see a doctor at UCSD and most recently one at Stanford. Both have assured her that she is in good hands with Dr. Helton (who treated her last year) and her treatment plan is spot on. She loves her doctor and appreciates his office's proximity to our house.
I took her this morning to get her port in. It's petite and hardly noticeable and she is doing great. She's anxious to get the treatment started and get this behind her. She is in good spirits and is handling everything beautifully. She is the perfect patient- strong, optimistic, and maintaining that sense of humor!
That's about all for now! She starts chemo on Monday so send good thoughts her way! Ash is coming home so we'll all get to spend some time together as she gets her treatment.
Thanks to all of you for being such wonderful friends!