Keep peddling, keep going forward into the New Year

The new year is upon us and I want to reflect on the many things for which I am thankful.
  
2013 has been a good year for me. I was bless to find an exceptionally skilled surgeon that was able to remove the tumor from my brain last January 10, to have a wonderful supportive husband, and to have many supportive friends during my recovery.  I am thankful for my improving health, which is so much better than a year ago.  While I continue to have some challenges, I am slowly getting my life back in order.  

My eyes are learning to adapt to my work at the University of Oregon. I continue to work part time as my brain continues to heal and I learn adaptive life skills. Thank goodness for my special prism glasses that allow me to see single vision directly in front of me.  I continue to have super sensitive hearing, similar to Superman. I have been tested and the audiologist confirmed I hear sounds that most people do not hear. Due to my auditory sensitivity, I wear custom fitted ear plugs in public. I can still hear everything, but sounds are a bit duller and more comfortable for me to handle. 

My latest milestone is that I have recently started to ride a bicycle. My doctors suggested if I want to ski this year, I should get use to visually handling motion by riding a bicycle. That is because my eyes and brain still have trouble processing motion and spotting objects quickly while I am in motion. The experience of processing peripheral motion on a bike will be similar to what I will need to visually process on the ski slope. I had my first bike riding adventure a couple weeks ago and it was much like when a 5-year-old child first learns to ride a bike. I started out wobbly, but after a couple of pumps of the peddles I started riding in a straight line. Now, I am up to about 4-5 blocks.  Afterwards, I am over stimulated and worn out, but it is very exciting to be back on a bicycle again. 

The next year is full of promise and of goals yet to achieve, but with God’s help, and the loving support of my husband and friends, anything is possible.

Eye spy with my little eye...

Each week brings hope and challenges as I continue on my road to recovery. 

Last week, I was able to increase my time at work up to 5 hours a day. I am trying to slowly increase my work hours without jeopardizing my recovery.  I feel good that I was able to achieve this goal but I am very exhausted after 5 hours and continue to take long naps each afternoon. Between working part time and doing my physical and eye therapy there is not a lot of spare time in my day. I am behind on emails, I will try to do better on my blog as that is easier than doing individual emails for now. 

I am gaining strength each week and learning to adapt to my new lifestyle. I miss being out and about with friends and events. I am still challenged in public with noise and motion.  I have attempted it a few times, and I tend to pay the price by getting extremely exhausted, dizzy, nausea and loud ringing of the ears. This week I am to get my new custom earplugs. (Goodbye ugly neon orange and green foam earplugs!) I am very excited as this should help some with my over-stimulation in public and events.

I had my 2 month follow up appointment with my neurologist last week and I have some good news. He said I am continuing to heal since my last appointment. My eyes are tracking movement better and my pupils are constricting when focusing on his finger as he moved it close to my eyes and away. It appears my eyes are still healing, and my new prism glasses and visual therapy are working!

I continue to push the envelope of what I can do, whenever possible. I have signed up for Oregon Adaptive Sports to downhill ski with their visually disable program as I have a limited field of vision and lack depth perception. Watch out Bunny Hill, here I come! This should prove to be very exciting! I got my Mt. Bachelor 4 Pack Pass this week and ready to go as soon as the snow arrives!

Thank you all for your support, I appreciate you all being on my journey with me!

Hi ho hi ho its off to work I go!

It has been two months since my last my last entry and 9 months since my brain surgery.

Since my last post I have continued to make gradually improvements.  I am getting used to my prism glasses. At my last eye appointment we learned that my eyes can maintain single vision in a 8" x 10" area directly in front of me and a little bit below and to the right of me. Outside that area my vision remains a bit jumbled and doubled. The good news is that my sweet spot for vision is perfect for computer work. I continue to work with a Vision Therapist to try to further improve my vision and to learn strategies to navigate more independently.

A month ago I returned to work 4 hours per day at the Center for Teaching and Learning / University of Oregon. It is good to be back at work! My co-workers have been very supportive and helpful with my re-entry. My office is conducive to my recovery because it allows me to work in a quiet and calm setting. With time I will be increasing my work hours. But for now, I come home from work and head straight to bed for a long power nap in the afternoon. After my nap I am able to make dinner and work on my balance and vision therapies. Doing my therapies daily is my other regular job.

I do not drive but have become very adept at riding the local city bus. I continue to have difficulties being in the public or in large groups, because my eyes are have difficulty tracking motion and I am sensitive to loud and ambient noises. Yes, I still have supersonic hearing.  Last week I heard Rod’s cell phone vibrate upstairs in his office while I was downstairs napping. To help address my over-stimulation from sounds I hear, I am having special custom earplugs made. I will receive them in a couple weeks.

I am often asked how long will it take for you to get back to normal, or if my hearing and visual limitations are permanent?  Well, if I had a magic crystal ball I could answer that question. Unfortunately, we really don’t know how much more recovery to expect and when. My recovery is slow, but it is happening!  Compared to where I was last year at this time -- when I was in in extreme pain, using a cane and having rapidly deteriorating health -- my current health condition is a cakewalk. I firmly believe in neuroplasticity, which involves the brain's ability to reorganize itself by forming new neural connections throughout life. Rod and I continue to see improvements and we remain optimistic about my future. We also accept that I might have some long-term limitations in life but that will present new life experiences for me.

Getting Better, But Not Yet Ready For Prime Time

Last month was a busy month for me due to a family emergency, so I was unable to do a blog update. Now things are getting back into a normal routine.  I have been progressing nicely in the past couple months, but I still have some deficits.  My eyes are still having some issues and I can get over stimulated easily.

It has been six months since my brain surgery. Day by day I don't notice the difference, however when I look back at how I was 6-7 months ago, I am amazed at my progress.

Since the last blog, I am no longer using a cane during the daytime. I still use a cane sometimes in the evenings, or times I am over stimulated by noise or excess ambient movement, such as in large crowds.

My balance has much improve and I am able to hike with Rod's help. We have done a couple hikes over 6 miles and I am hiking the Ridgeline trail behind our house more often. It is so great to be active again!

I am getting out in the public some and going into some stores. Loud voices, ambient noise and/or a lot of movement can cause me to get over stimulated.  I wear earplugs and sunglasses in public to protect me from being over stimulated.

Some friends look at me and think I have fully recovered. However, I cannot see and hear things the way others perceive things. Sounds are intensified and I have troubles visually tracking movement. Hence if you see me in public it is best to approach me front-on slowly and not to the side so I can recognize you. Perhaps say “Hi” first and your name as my eyes move upwards slowly and I don’t often recognize friends immediately. If you see me in public, please come by and say “Hi.”

I am neither driving nor working at this time. I am not sure when I will drive again. I have gotten more comfortable taking the city bus around town and Rod makes an effort to chauffeur me whenever possible. I am working hard on my physical therapy daily; presently it is my full time job. Along with my intense eye therapy, and I have new prism eyeglasses for distance and computer work that seems to be helping. I plan to return to work in September.   

Not yet ready for prime time, but getting there!

The journey is more fun with company.

It has now been 4 months since my brain surgery. 

Recently I was talking with a friend, we were discussing the possibility that things in life sometimes happen for a reason. Sure, the recovery from brain surgery has not been easy but the journey with friends and family has been comforting. Every cloud has a silver lining and my friendships and support by loved ones has been 24 karat lined!

I continue to get stronger each week. I enjoy my walks around the neighborhood and around Eugene. The last few weeks with the wonderful weather, I found myself venturing out in our yard puttering about pulling weeds and cutting back the ferns. With my eyesight some ferns got more of a haircut than I had planned!

My vision is about the same, so I decided to move forward in improving my vision. I tried some temporary prism lens for my vision but they were not exactly right. I recently started to see a new eye specialist that is working on my vision. She believes I need three pairs of prism glasses for distance, computer and reading. After I get the new prism glasses, I will be starting eye therapy.

My balance is better per my physical therapist. I still use a cane or walking poles for getting around in public and going on walks. I have been using a Wii station daily and doing balance and yoga to increase my coordination. I am hoping my ski score on the Wii will equal my ability on the ski slopes some day!

My days are never dull as they are full of physical therapy exercises in the morning and afternoon. I treat my physical therapy like a full time job and we continue to feel optimistic about my recovery. I am still not able to get out into big crowds as the noise levels and motion are visually difficult for my brain to process as I get over stimulated, causing nausea and then exhaustion. I do miss getting out and about with my friends but each week I am doing more and getting stronger.

April showers bring May flowers

As my fellow Oregonians know we have had quite the downpour of rain the past few days. That is OK as we needed the rain for the flower show that is going on this spring.

Sometimes, you have to be patient when life gives you downpours but you know in the long run the best is yet to come. This is true with my recovery. 

I am working hard daily doing physical therapy exercises, taking long walks, going to physical therapy appointments to continue working on my eyes and balance, and acupuncture for post surgery issues and healing the eyes. All the work is yielding progress, slow but noticeable changes are occurring weekly.

My recent MRI scan report was good. The surgeon, Dr. Shihinian, said all was healing nicely and no major issues. There is still some slight swelling at the base of the brain due to the surgery but no concerns as it will go down in time.

Rod continues to be  my constant helper, patiently encouraging me to try new things, and my main supporter when my progress seems slow. He has a great attitude and I know with him at my side, that I will indeed fully recover. 

We are optimistic next year Rod will be able to return to the ski slopes more often.  As he sacrificed his ski season to take care of me and for that, I will be forever grateful! Hopefully, I will be able to join him but I might have to start out slow on the bunny hill. Watch out below, here I come!

Next stop Bakery and Recovery

As of two weeks ago, I am now doing all of the cooking.  Recently I made yummy Eggplant Parmesan and my first pie post surgery.  Personally, I think making a pie each week would be good therapy, but probably not good for my waistline.

New milestone, since I am not driving, I explored taking the LTD city bus about 2 miles to a local bakery in my neighborhood by myself.  It was a challenge to see my bus stop, but I got close enough and walked the rest of the distance.  Of course I had to reward myself for completing this task with a delicious gluten free orange cranberry muffin!  I am not able to use the bus to go across town yet.  I just tried it out in a familiar location near my home.  It felt good to get out and explore a little on my own.

 

I had my first post surgery MRI last Tuesday. The MRI is to check that all is healing properly.  I will learn the results during my consultation with Dr. Shahinian, my brain surgeon, on Thursday.  We are optimistic that all is healing well for this stage of recovery.  I will need to have yearly brain MRIs for the next five years as a precaution.

I continue to walk as much as possible and regularly go to physical therapy. I was asked what are they doing for me PT-wise since I can walk? The PT is mainly for my eyes and balance.  I still have double vision, depth perception deficits and vertigo.  My physical therapist is teaching me how to move my eyes from object to object smoothly and to re-learn how to focus my eyes again.  My eyes are a lot like a newborn baby's eyes.  I need to re-learn how to move my eyes where I want them to go and how not to get nausea or loose my balance in the process.  I am making progress and learning tricks to cope with every day living, but the deficits with my eyes are taking a while to improve. My surgeon explained that the eye symptoms are sometimes the last to improve.  We are optimistic that I will have a full recovery, as small progress is being noted week to week.

Each day is a blessing and I am so fortunate to have had my surgery. I can't imagine what my life would have been like without the surgery.

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Becki is Healing!

I have been busy healing since my last post.  Or at least that is what my neurologist proclaimed this week, "Good news! You are healing!"

I cannot see the progress daily, but each week I am noticing that I can do a little more.  I am still seeing double with blurriness and have sensitivity to light, but I am starting to wear my sunglasses less indoors each week.  Some have asked, what do your eyes see? Here is an example of what my vision is like:

Another question I'm asked, when will you get your vision restored?  I wish I knew.  Dr. Shihinian told me that everyone heals at a different rate...some in a few weeks and others in a few months. The good news is that I can tell my vision is improving each week.  I remain optimistic that my vision will eventually be restored ... with patience … all in due time.

As I have gotten stronger, my physical therapist has increased the amount of physical therapy I receive.  I receive therapy for my eyes as well as for my balance.  I cannot go upstairs yet without assistance, but hopefully in a week or two that will change.  Our house has two stories and I miss having full access to the house.  I am still walking daily and am starting to cook more.

Recently, I started venturing out into the public. I went to a small quiet church service and had pizza at small intimate pizza parlor with Rod (sunglasses and ear plugs still required).

Each day I count my blessings.  I have no more migraines and I am getting stronger all the time.  Rod continues to be my constant companion and has provided me strength and encouragement throughout my journey.  I owe so much of my  recovery to my wonderful husband.

This Week's Mission was Transition

It has been 5 weeks since Becki's surgery and recovery continues to go well. This was a transition week as Rod returned to work.

Becki is continuing to walk daily about 3 miles, now with a walking pole. She has had to take a break from walking hills as they were aggravating her vertigo.

As Rod returns to the workforce, Becki is trying her hand in the kitchen. She started this off by making a chocolate soufflé. Rod still does a lot of the meal preparation, but Becki is starting to help out as long as it does not involve using knives. We don't want to have a Dan Akyord/Julia Childs moment http://www.dailymotion.com/video/x7tnc9_the-french-chef_fun#.USAqlBG9KK2

With Rod going back to work, he has not been as available to Becki to do all the things around the house and to take her to all of her medical appointments. On the upswing, Becki has very much enjoyed seeing friends this week as they took her to medical appointments and helped her around the house. It was the highlights of her week to see friends.

Clip Clip Here, Clip Clip There

Week four - I am writing this blog entry, which is my first entry since my surgery. I am using "Dragon Speak", dictation software and "text to speak" feature on the iPad to create this blog entry.

This week's milestones consist of the following three things:

1. My lifting limitation has been increased to 15lbs, so my cat Simon is now in the range (pretty much) to be lifted for hugs.

2. Rod and I have done daily walks of about 3 miles, with a couple of days of about 4 miles that included a hill. (At times I am able to walk without a cane on the smooth straight stretches or when holding Rod's hand for stability. And sometimes I just hold Rod's hand because...)

3. Wednesday I had my first outing (non-medical related) since my surgery. I got my first hair cut in 6 months - clip clip here, clip clip there. I felt like Dorothy in the Wizard of Oz.

www.youtube.com/watch?v=8nlD_BQnAFw

I was very excited about getting my hair done by Christina at Lush after so long a wait. Whew, it felt wonderful to have my hair styled and tidied up!

I should explain that I halted all hair appointments back when I first learned I had a brain tumor and might be having surgery. I did so because I thought I would be losing some or all of my hair when I had surgery. I learned only a few weeks before the surgery that only a small credit card size patch near the base of my neck would be shaved and the top of my hair would cover the surgery point of entry. If you saw me you would not be able to tell from my hair that I had brain surgery.

This week was my second PT baseline assessment for vision and balance deficits. The testing aggravated my visual senses, causing me to relapse for a couple of days. This was a reminder that my recovery is not a straight line. It was advised that I should not go out in public for another month due to my difficulty in handling sensory stimuli.

Thank you to all of you for the words of encouragement during my journey.

Good Bye to the Overstuffed Chair

Hurray, Becki has completed three weeks of recovery! This is important because for the first three weeks she has had to deal with various restrictions, including always sleeping upright in an overstuffed chair to minimize brain swelling. Starting Friday she began sleeping in a bed. She had been looking forward to that day for some time! She also had her 3 week review with the Skull Base Institute and had her 5 pound restriction upped to 10 pounds. With her lifting restrictions she has not been able to pick up her cats, and it still might be a couple more weeks until she can pick up Simon, not that he has a weight issue!

Becki's energy and strength continues to increase. On Wednesday she was able to shower and dress herself for the first time. She is also able to tolerate longer walks, in fact she is up to 2 miles on sidewalks daily with small inclines. However, she still continues to enjoy her regular cat and bunny slipper naps. Overall, her recovery is progressing well.

Becki's tumor was located in a very sensitive area of the brain. Her recovery's biggest challenges are the stabilization of her various senses that were impacted by the tumor and the effects of the surgery. She continues to experience significant sensitivity to light, with double vision and blurriness that fluctuates in intensity. She has hyper-sensitivity to smell, taste and to sound. She needs to wear ear plugs to tolerate basic household sounds. She also experiences some difficulties with swallowing which requires that she focus on swallowing when eating. We anticipate that these symptoms will eventually improve during her recovery. Due to Becki's heightened senses, she is not able to go out into the public yet. She does miss her friends and is able to talk briefly by phone. Becki's recovery is coming along but she has a ways to go for a full recovery. She enjoys the encouraging words by her friends during her recovery and looks forward to eventually seeing them in person.

Recovery - Week Two

The intense migraine headaches Becki had every day for over four months prior to surgery are gone, as is the severe nerve pain she was experiencing in her left arm. And, the head pain from the surgery is greatly improved. However, as previously noted, recovery from brain surgery does not involve steady forward progress. Becki has had good days and days that have not been as good. It is like a dance of two steps forward and one step back. The good news is that over time Becki is making forward progress.

Highlights this week include Becki getting outside for brief walks and having a very slight improvement in her sensitivity to light, but she does continue to require shades. She also continues to experience double vision and blurriness, but her doctor advised her this week that her eyes were tracking together so she does not need an eye patch - so no dressing like a pirate ... Arrrrr! Becki's doctor said that only time will tell what improvements she will have with her vision deficits and that the maximum improvement could take quite some time. The important thing to watch for with nerve damage is that Becki continue to show gradual improvement. Becki remains positive that she will eventually have an excellent recovery. In the meantime she continues taking lots of cat naps and Rod continues to provide excellent care.

Thank you again for everyone's support and encouragement. It means so much to Becki. Please note that she continues to be unable to respond to emails because of her vision deficits.

Cat naps

During Becki's recovery she has been taking a lot of naps. It was recommended that she take several naps a day to help with her recovery. Becki is following doctor's orders. In fact, we've noticed she has taken a couple cat naps at one time or was it a couple of cats with naps at one time?

For those of you who haven't met Becki and Rod's cats, Zoenobia is sitting in front and Simon is laying down in the back.

Home Sweet Home

We are now home and getting settled into our new routine. Becki's new routine is focused on getting healthier and stronger one day at a time. Rod's new routine is taking care of Becki's every need.  We are slowly getting acclimated back to Oregon's weather after having had endless days of sunshine in California.

 

The surgery was a success and it was great to say goodbye to the bubble. Since the surgery, Becki's eyes have been dilated and she has sensitivity to light. As her future remains bright, she continues to wear shades. Becki also experiences some double vision and blurriness but all her eye symptoms are expected to gradually improve with time. In the mean time, Becki has great difficulty reading emails or responding to them.

The surgeon told us that having brain surgery is a bit like being hit by a Mack truck. Becki's body is busy trying to heal from that event. She is recovering as expected at this time. We are very optimistic for an excellent recovery, but it will take some time. Becki may not be on the ski slopes this year, but she is already thinking ahead to next ski season.

Thank you to everyone who offered encouragement and support to us while we were in California. It felt like you were along with us on our journey.  We would especially like to thank Uncle Chuck and Nancy for all they did for us during our time in California.  

Up, up and away

We are sending Becki and Rod back from LA to Eugene-- here's a shot of Becki at their boarding gate VIP Lounge at LAX. Takeoff 1:00 pm.

I see Becki is holding up six fingers which could mean two things that I can think of --- either she's excited because it's only six more hours til her next dose of pain meds or six hours 'til she gets home.

Whether she needed it or not, their plan was for Becki to wear the ice mask on her head the whole way so they would be catered to- and if that didn't work they would say "brain surgery" loudly in conversation.

We are so blessed, Chuck and I, to have been part of this successful story -- and I will be turning in my chief blogger badge now for a seat in the audience with you ;)

Xox and love to all and thanks for ur great comments and support of Becki and Rod.

Nancy

Cleared for Take-off!

Doctor gave Becki the thumbs up. The pathology report was all clear -- it was benign. This is fabulous, fabulous news-- and Becki and Rod will be headed to LAX airport together in a limo at 9:30 am tomorrow-- Wednesday.

Will add more "color" after dinner -- but this is short, sweet and the news we were all waiting for !

Xox, Nancy

Dancing with the star!

Becki reports a much better day today,

1. Got in several cat naps as advised by Dr. Caryn ..

2. Nibbled on chocolate to help with her recovery.

3. Completed a few short walks down the hallway with a walker.

4. Now this is Kleenex material- Becki did a few dance steps with Rod as part of her physical therapy, which was the highlight of her day.

Becki will be seeing her surgeon tomorrow to hopefully get cleared to fly home on Wednesday.

We will keep you posted... She LOVED UR Comments ! Keep 'em coming!

Until tomorrow , nancy

3 does not equal 10

Becki reports that as expected, recovery is not a straight line, and day three was not a top ten day. According to the doctor, at day three the brain is having its worst day of swelling with blood rushing to the brain to work on healing.

She has been resting all day today and sitting up to help reduce the swelling--and the pain meds are doing their job. The Doctor is monitoring her condition and is in touch with Rod for ANY concerns or questions about what is normal.

Good news-- this part of the process is par for the course-- and if anyone is going to master the course, it's Becki -- a role model for us all !

And Bravo to Rod for Oscar winning caregiving!

We are ALL optimistic that tomorrow will be a better day.

Words of encouragement from her friends and family to the blog comment area make her feel really good. !!!!

Tune in tomorrow for more news from the Bubble Busting front.... Nancy

Zzzzzzz

Becky is safe and sound in the Residence Inn, exhausted and sound asleep.

LIz, Becki's Mom, just called me and said that when she saw the singing In the rain blog she knew Becki's Dad, Erle, must be finding a way to connect spiritually with his beautiful daughter. Why ? Because when Erle was in the navy , he was in the same troop as Gene Kelly who starred in the Singing In The Rain movie!! Very cool. I totally believe that is true. No such thing as coincidence.

Liz also says it's 28 degrees in Oregon! Yikes-- we think 45 is sub-zero here in LA. Maybe Becki and Rod will just send for their things ;)

Chuck and I will drive over tomorrow to visit Becki and Rod ---Sunday --and bring a treat or two.

Please make blog suggestions of what you would bring her if you were here !!

Xox.. Until tomorrow ;) nancy

Singing in the rain (shower)

It is Departure Day for Becki from the Surgical hospital! Doctor has given her the thumbs up.

It's 1:00 in California and Becki is scheduled for release in one hour to head back with Rod to their hotel.

Rod's report this morning was very encouraging -- Becki is taking pain meds for the headaches and she is experiencing much less pain than she has had in a very long time . APPLAUSE SIGN.

And she's singing in the shower -- just being able to take a shower has been the highlight of her day so far....

Rod has promised to stage another photo op when they are safely settled back at the Residence Inn -- so there will be another update later in the day!

Over and out for now. Nancy

Pictures worth 3,000 words

Day two report from the Celebrity surgical spa....

After an understandably uncomfortable night, Becki reports that she had a pretty good day and the headache pain is down to a 7 out of 10. Remarkable, I'd say, to any other of us other mortals ---

She had some breakfast, sat up in a chair, walked with the Physical therapist down the hall , around the corner and back to her room and even put on street clothes!

Becky's eyes still need to stay closed for awhile due to expected light sensitivity and double vision which will improve with time. So it's either the ice mask or celebrity sunglasses for now .

Rod is with her every step of the way, and talked to her doctor who said that recovery is not a straight line -- and she can expect to have a little tougher day tomorrow. He is pleased with her progress and says she is on schedule to be released tomorrow to go back to the Residence Inn and sit around eating chocolates.

Becki says she is listening to a "fluff novel" on audio books called "Major Pettigrew's Last Stand."

MOST IMPORTANTLY -- she is delighted to hear from you via the blog -- so keep those comments coming!!!!!


Over and out for today, Nancy

Becki Photo Op -- around 1:00pm California time

Hello! Still Nancy here blogging for Becki. Wow what an amazing woman our Becki is! Brain surgery in the morning and entertaining visitors after lunch. This picture shows Becki in her hospital room. Important things to look for...

1. Becki giving thumbs up to everyone
2. Ice mask over eyes to help with headache
3. Oxygen mask (required)
4. Fancy pre-warmed blankets

During my 20 minute visit, Becki was talking up a storm, wanting to know all of the details of her surgery and exactly what the pictures of "the bubble" looked like. Much to her chagrin, she cannot open her eyes for a while until the ice mask is off and Dr. says it is OK to open them. None-the-less, she was delighted to hear that the "after" bubble photo showed a completely clean slate --- and to what my non-technical eye looks like a delightfully healthy brain.

Becki still has quite a headache, but is delighted to report that overall from before surgery to now the pain seems to be diminished.

She is in wonderful spirits, Rod is SOOOOOO delighted.. And will betcha he sleeps better tonight than he has in a longtime.

Major thumbs up -- a successful day for a strong woman and a strong and devoted husband, Rod.

Nancy

Transfer in progress

Becki is now being moved out of post-op room into a hospital room. She can have one person at a time visit her quietly, and even though Chuck and I did not expect to see her today, she has requested a visit and a photo-op for her blog -- so she can give you all a thumbs up herself.

On my way now to her room.

Good News

Surgery went well .. There were no complications!

Becki is in a post-op room with nurses and Rod.

She has a bad headache which she describes as a 9 out of 10, and feeling sick to her stomach -- both of which were expected. She is being given meds that address both of these issues, and the goal right now is to keep her awake so they can monitor all aspects of brain functioning. This is the normal procedure.

Rod showed us before and after four-color pictures of the cyst --- it sure looked nasty in the before picture -- but it is totally all gone in the after picture. I will not include those in the blog unless Becki approves.

So great, great news... Becki is awake, talking, and we will post hourly updates.

Bless you all!

Rod is being briefed now 10:35am

Hi everyone --- I know you are tapping your toes and waiting for news. The doctor has called Rod back into the surgery area for a report and undoubtedly to see Becki. I'm not sure how long he will be back there -- but I know he will want to be getting a very detailed report and will want to sit with Becki as long as they will let him. So hang in there --- be back soon...

Nancy

All's Quiet on The Western Front

Nancy updating here from the waiting room next to the dapper Rod Robinson, who I believe could at the correct camera angle be mistaken for the news comedian Jon Stewart.

Last word from the operating room is that all is going well and on schedule!

More soon.

Thumbs Up,

Xox

Becki In Progess

Hi all Becki Family and Friends! Nancy here blogging for Becki....

It is 8:15 am California time... And Becki's surgery has been underway now since 7:30. Everyone is very positive. We will be able to report in about an hour when Rod is called from the operating room about how things are going.

Chuck, her uncle, me, Chuck's wife, and Rod her amazing hub are sitting in the surgical center waiting room that looks like the lobby of a fancy spa resort.

Speaking of fancy, the facility picked up Becki and Rod this morning at 5am in a BIG BLACK LIMOSINE at 5:05 am. The security guard greeting them at the faculty entrance and escorted them to the waiting room.

Rod just showed me Becki's lucky charm that has a saying that has been bringing her comfort from Winnie the Pooh .. Something Christopher Robin told Winnie ...

"Always remember you are BRAVER than you believe, STRONGER than you seem, and SMARTER than you think."

Becki passed this to Rod when she went into the operating room at 6:24.....

So prayers all around and I will be back up as soon as we get the next word.

Thumbs up!

Xox

"Surfin Safari" to "Don't Worry Baby" - Beach Boy Days

This post is covering yesterday's and today's events as Dr. Rod says Becki must rest and get ready for the big day on Thursday. After this post, Becki's uncle's wife, Nancy, will be taking over the blog for the next week.

Tuesday we enjoyed a leisure day and a break from medical appointments. After a nice leisurely morning, we decided to have a Surfin Safari and drove to Malibu beach. We had a nice long romantic walk along the beach, admiring the gorgeous houses of the rich and famous. Rod was checking out the houses while Becki was watching all the various seabirds. We were even able to get up close and personal with some of our feathered friends. Afterwards, we had a delicious meal at Moonshadows (once an old surfers's hang out, now a chic romantic restaurant). From the outside deck of the restaurant we enjoyed the panoramic ocean view, birds and even porpoises swimming by. The afternoon was filled with great conversations, sharing future dreams, positive thoughts and laughter as we enjoyed each other's company. Definitely a top ten day in life.

Later that evening, we had a hot night...no not that kind of hot night. Our hotel room's thermostat went bizzerk, making things hotter than we could handle. By 9 pm, with the room at 80 degrees and the heating/cooling system still blowing hot air, we convinced the desk clerk that we had to be relocated to another room. They had only one room left and it was not their finest, but at least the temperature was conducive for sleeping. Also the temporary room had no G3 and very low wifi, hence no blog update yesterday. We are now in a much nicer room with a working thermostat and just chilling today (literally).

Tomorrow's surgery has been move up to 7am, with a 5 am check-in at the hospital. That is really early for Rod. Becki will have to convince him that he is getting up early tomorrow to ski Mt. Bachelor, as they are expecting 6" of fresh powder tomorrow. That should get him out of bed in a hurry! Too bad we are heading for the hospital and not Mt. Bachelor. Oh well, all in good time!

Some have asked if Becki is scared or worried about the surgery. She is doing quite well despite the serious nature of her surgery. Her faith in God has been steady and she has believed He has walked by her side from the very beginning and will continue to be holding her close at this time. We appreciate all the well wishes, prayers and positive thoughts. Please continue to pray or think good thoughts, or even eat a piece of chocolate during Becki's surgery time of 7-9 a.m. Thursday.

"I can do all things through Christ, which strengthens me." - Philippians 4:13

In and Out of Beverly Hills

At 6:45a.m. we were whisked away in a black limo to Beverly Hills to meet with Dr. Shahinian at the Scull Base Institute. I guess if you are going to have brain surgery, it is best to do it with style. (Compliments of Dr. Shahinian)

Thank goodness for our driver as we entered Beverly Hills during rush hour but still arrived for our appointment on time. The driver must have received driving lessons from Mario Andretti, as we could not have maneuvered around in traffic at his skill level, nor would we want to. Becki came down with some post surgery nausea pre surgery... burp* Fortunately, this will be our only drive to Beverly Hills during this trip.

We met in person with Dr. Shahinian for the first time. We were impressed with his professionalism and his confidence in performing this complex surgical procedure.

We spent the early afternoon looking for our hospital for pre-admit testing and paperwork. We initially drove to Los Robles Hospital in Thousand Oaks thinking that was where the surgery would be performed, but it turns out the surgery will be performed at the Thousand Oaks Surgical Hospital, a smaller but very nice hospital. After locating the correct hospital and completing all the pre-admit formalities, Becki returned home for a refreshing nap.

The future so bright, I gotta wear shades.

Today was a travel day and we arrived in L.A. with blue skies, and fortunately I was already wearing my shades. By the time we arrived at our hotel in Westlake Village, CA, the Oregon clouds were here to greet us and make us feel right at home. Westlake Village is a really nice area and we have a comfortable hotel room, which is a good thing because I will be spending a lot of time in our hotel room. This afternoon I tested out the bed for a nice long 3 hour nap, and I think it will do nicely.

Tomorrow morning I meet Dr. Shahinian face-to-face to discuss the surgery and any last minute pre op testing that may need to be done. From there I go to the hospital for more blood work and to meet with the anesthesiologist. I hope it all goes well, so I can have the next two days to rest up for the surgery on Thursday. I doubt I will be going to Disneyland on this trip. Due to my symptoms and medications, I feel like I am already on the Teacup and the Matterhorn rides!