Friday, April 14, 2006

Chemo starts today

Mom moved up to the sixth floor at St. Lukes today which specializes in cancer care. The room is set up to accommodate two beds, but right now it only has one, so she'll have some privacy as she recuperates from these procedures. She's going back to Faxton about 2p for the next radiation and that will continue for two weeks. The chemo is a one time thing that will be repeated again in 21 days. I'm sure at some point they'll do additional MRI testing and cat scans to see what impact all this is having, but she's definitely moving forward quickly with the treatments, and we'll hope for the absolute best outcome.

They haven't said anything about going home yet, but depending on how her system reacts to the chemo, it might be possible that she could go home next week. One doctor mentioned to her, "sorry to keep you through the Easter weekend," which seems to me that she might be able to go home soon thereafter. She'll need to get back up to Faxton for the radiation treatments each day, and Jen has been able to arrange her schedule to be there a lot during the day and will be able to assist with transportation. (Good thing she got her driver's license!)

Gail and I will be traveling back to Happy Valley next weekend with Nate, so we're looking forward to spending time with Mom again and letting her see how Nate has grown.

As TJ's almost 5, he's understanding more and knows that something is up, and he's having some difficulties. He seems to have some kind of bug right now as he's running a fever, but the stress has likely impacted his immune system and made him more susceptible to illness. Please include him in your prayers as he's going to need support through all this as well.

Craig

Thursday, April 13, 2006

second radiation treatment today

Today mom had her second radiation treatment today. I rode over with her in the ambulance and waiting in the waiting room and she was in and out in about 20 minutes. There has been no talk yet as to when the chemo is starting but the port is there and is ready. It is nice they can run her iv through the port and they don't have to poke her arms or hands anymore. She is in very good spirits and is very positive. She will be moving to the 6th floor which is where the chemo unit is, we are not sure when though.

Jen

Progress

Mom was back to her room at St. Lukes last night. She didn't get to eat anything after breakfast, so she was pretty hungry. She went over to Faxton Hospital in the afternoon for a radiation consultation and treatment. They discussed doing the targeted seed radiation, but the decision was ultimately made to use external radiation. They described it as something similar to the machine that takes the X-Ray at the dentist's office. It's a very targeted tool. She's going to be getting radiation treatments every day in this fashion, but she's not yet certain how long this will continue.

She also had the port installed that will be used for the chemotherapy regimen. She will likely be in the hospital until their at least finished with the radiation and to see how she reacts to the overall treatment plan. If all goes well, she'll be able to go home in between chemo treatments to rest and recuperate.

The staff at the hospital told her that they can't believe how healthy she looks, so we're considering that to be a positive. The radation and chemo will be challenging for her body to take, so it's good that she's in good health otherwise.

Wednesday, April 12, 2006

Bad News

I'm still hoping for some good news to report, but so far, we just keep getting more bad news...

I spoke to Mom last night and she got the results that the growth on her adrenale gland is also cancerous. She didn't hear any results from the lung tap, but since the cancer has spread to the adrenale gland, then that rules out surgery to remove her lung.

The next step is radiation treatment to hopefully reduce the size of the tumor in her left lung and allow it to function normally again. The concern there is fluid developing in the lung that can't get cleared because it's currently collapsed. After that, she'll start some type of chemotherapy regimen and should be able to do most of that from home.

Her spirits are high and she's going to hang onto every hope for a miracle so that's what we'll all have to hope for.

Tuesday, April 11, 2006

Tests were run as planned

I spoke to Mom last night, and she sounded good. They were able to do the two tests they had planned for yesterday. They drew some of the fluid that has collected around her left lung, and they did a biopsy of the growth on her adrenale gland. If these are negative for cancer cells, then they'll likely proceed with removing one or both of the left lobes. If they are positive for cancer cells, that means the cancer has spread and they'll move right to chemotherapy and radiation treatments.

We're hoping that the cancer HAS NOT spread, as surgery is the preferred option at this point. Gail read that the non-small cell cancer is slower to advance, but it sounds like this tumor has been growing for some time, and the doctors have just had difficulty in diagnosing it.

We'll just keep thinking positive and hope for the best. The test results should be back by tomorrow, but since they performed the test yesterday morning at 8.30a, then we might hear something back later today.

Monday, April 10, 2006

Latest News

News from this past weekend. We got the news on Friday, and Mom had a lot of visitors this weekend. We got a lot of news, which clarified some earlier issues.

There is a tumor in her left lung which has closed off the windpipe, and the lung collapsed as a result. This made it difficult to determine how big the tumor is at this point. We heard yesterday that it is a non-small cell lung cancer, which is the type which is supposed to be slower to spread, but it's still questionable as to whether or not it has.

There is fluid around the lung which is not typically present, and there is a separate growth on her adrenale gland. Each of these things could be unrelated, or they could also be cancerous. Mom is having both of these tested today. They will be drawing fluid from the lung, and performing a biopsy of the growth on the adrenale gland.

We're hoping that these both come back as negative, which will mean that the cancer has not spread beyond the lung. If not, then it sounds like they plan to do a radiation treatment to reduce the size of the tumor to allow air into the lung. This will reduce the chance of pneumonia developing and allow them a better view of how big it is.

They will then proceed with removing the one or both lobes of the left lung. She has been breathing with one lung all week and by this past weekend, her body has seemed to adapt well, and her pulse ox was normal with no supplemental oxygen and just one lung!

If the cancer has spread, then they will proceed with a combination of radiation and chemotherapy.

The results of today's tests should be available by Wednesday and that will outline what the next steps are.

Please keep her in your prayers and we'll hope for the absolute best. She is determined to beat this and will need lots of support to do so.

Love

Craig

Saturday, April 08, 2006

Liz Backus updates

Well here we go again - this sucks. Anyhow - Liz was diagnosed with lung cancer late yesterday - the 7th. We were getting some conflicting information about having to remove her entire left lung and if or how they will do treatments.

The doctors have determined that the cancer has spread and therefore will NOT REmove her lung. So that doesn't sound good. However, they will be doing treatments chemo and probably radiation - I assume all over. We do not know where the cancer has spread at this time.

Liz is staying at FAxton - St. Luke's hosptial in Utica, NY and her room number is 173.

Please tell friends about this website that may know Liz. I realize most people that check may be our family - but we'll pass this along to the Backus gang as well.

Its important we keep her in our prayers - she's a wonderful woman and very strong. If anyone can beat this cancer- its Liz. She's a fighter and has a LOT to look forward to in life and she's young. So we are focusing on all those positives right now.
Love,
Gail

Saturday, March 11, 2006

Woo HOo

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Wednesday, February 01, 2006

new year

Ok - a little late - but we have been running around in January.

Anyhow - you can check out Nate's 18 month pictures on the picture link. We are still going to download all the ones from the holidays.

Hope this new year is good to everyone so far.

Yes - Nate is 18 months - and starting the "terrible 2's" a little early. He's also teething - hence not as many happy smiles in his pictures this time around. He refused to pose. But enjoy - we have a few - bruises on the forehead and all. He's all over the place and a true boy! Its great.

Love,
Gail

Saturday, December 24, 2005

Merry Christmas!

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Wednesday, December 21, 2005

Merry Christmas

Well this is Nate's 2nd Christmas and he's totally not into Santa at all this year. He just looks at him like - who in the world are you Mr? Its cute and funny. We didn't push it - he held on to one of us with his death grip indicating - don't you dare put me closer to that guy!

anyhow - we are ready for the holidays - and just can't wait to spend some time with family and just chill out and relax. I have all next week off to spend with Nate and visiting friends and family.

We wanted to wish everyone a very Merry Christmas and happy (and safe) New Yaers!

love,
Gail, Craig and Nate (and even Fudd)

Saturday, December 03, 2005

Mmmmm ice cream

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Thursday, December 01, 2005

First Hair Cut & More

Well Nate finally had enough hair that required a hair cut. We saved the special moment to do with grandma Backus and Aunt Jen in NY over Thanksgiving weekend. Nate really didn't care for it much at all - squirmed and cried. they really only cut the back a little bit and tried to get around the ears. It was cute - we have pictures somewhere at home of the fun.

We hope everyone had a good Thanksgiving holiday with family, friends and loved ones. As I mentioned - we were in Ny with the Backus clan - it was fun. Just a LONG 12 hour drive home sunday. We are all trying to get caught up from that. Its amazing just sitting in a car makes you tired and worn out. Not fun.

This weekend we are hoping Nate won't be afraind of Santa - we are attending my works Breakfast with Santa party. It should be fun - sold out - so I'm sure TONS of kids! i can't wait. Hopefully my friend Barb's kids will help Nate visit Santa for a quick picture. Hopefully

Alright - just had to send a quick update. Other than all that - we joined a new church a few weeks ago - really happy about that. Work - its work for us both. Craig's swamped at his job - and me - just plugging along.

I'll hopefully post more this month.

Sunday, November 06, 2005

My new hat

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Saturday, November 05, 2005

Hi from Chicago

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