Saturday, August 15, 2009

Update on Lisa

Hi you all, I hope you haven't given up on checking in on Lisa. I was able to text with her for a few minutes yesterday afternoon and so I am going to give you an update on what she told me. I don't understand all the medical "lingo" so I hope I can actually give you the information correctly. She continues to press on under much pain. She is on so much pain medication to cope with these migraines she gets and is just trying to keep out of the hospital as much as possible. Lisa's last chemo treatment is next week and then she will under go radiation treatment every day for the next 7 weeks. In the mean time, she now has a new head doctor outside of Kaiser. He has looked over Lisa's records and seen some areas of concern regarding her treatment at Kaiser. First, she has had two spinal taps done with reports stating there is too much pressure.( I'm not sure where but I believe it is the brain). He wanted to know what Kaiser did about this. Lisa replied to him that she never got results from them regarding these spinal taps. He said that spinal fluid on the brain is normally suppose to be a count of 10-20, with a 20 being extremely high. Lisa was at a 25 and that was over a year ago. This would apparently explain the bad eye sight she has developed and how certain medicines work for her or not. She said she will have another spinal tap soon (I think to assess her numbers again) and then possibly surgery to remove the pressure. This might be the source of her migraines and as you can well imagine the frustration of all the time and money they have spent and put into her care when something could have been done to relieve her of this problem. So, aside from her battling cancer, I think her main source of pain and discomfort has been from these migraines. This is what keeps her from being able to keep in touch with many of us, because she is on so many pain medications so that she might be able to stay at home, she can't drive let alone concentrate on being able to answer us all. I know she covets all the texts and messages she can get and the encouragement she receives from them, so thank you for that!

Please continue to keep her in your prayers, for this doctor to be able to help relieve her of these migraines. For her last chemo session and for the next 7 weeks of daily radiation treatments. Please continue to pray for their family and for the kids. I know Lisa would say thank you and that she loves and misses everyone!

Monday, June 15, 2009

Chemo Rounds

I didn't just want to leave the last post in with out some kind of update, but there is not much I can tell you right now. Lisa needs all our prayer to get through these rounds. I have realized that it takes all her strength just to get from one round to the next and that was with her going every other week. I understand they intend for her to have weekly rounds as well, so it might get even quieter when that happens. Just know that she is trying her best to hang in there and stay out of the ER. She told me she is on so much medication that I am sure it is hard to do anything else. Precious "well" time will obviously be spent with the kids as much as she can. I'm sure she appreciates all the encouragement she can get from us texting her even if she can't find the strength to text back right now, so keep on giving her that! I know that when she gets on the other side of this she will have so many words of wisdom and an incredible story to tell us, but for now we wait...

Love you Lisa, here's to seeing you soon! Praying so much for you and your family!

Love,

Suzi

Tuesday, June 2, 2009

Hospitalized Again

Hi, I heard from Lisa yesterday, I know she has been trying to catch up on her texts so you might be updated already but,she returned to the hospital on Friday and is hoping to go home today. She will have another round of chemo on Thurs.

The main complication Lisa is having seems not to be so much from the cancer itself, but more the migraines. She has been going to Kaiser and they are now going to refer her to UCLA as they can't seem to do anything else for her migraines there.

As always she stays up lifted on her messages and always asks how we are doing. She even said she had been worried about me, lol, and I was like "you have to be kidding me." (In a teasing way) She continues to fight this cancer and the complications with a positive attitude. When she is home it is precious time with her family and sleeping.

Thanks so much for praying for her!

Love,
Suzi

Friday, May 29, 2009

Chemo Yesterday

I know we get concerned when we haven't heard from Lisa in a bit and usually our concerns are very valid, well the same holds for this post. I texted Kaitlyn this morning for an update on her mom and she said that Lisa had been sleeping A LOT and then went for another round of chemo yesterday and the same side affects happened again. The intense vomiting and the migraines. They are currently back in the ER. As soon as I get some more info, I will update here and please feel free to Facebook me a message if you get an update from her and I will post it here.

Love,

Suzi

Sunday, May 17, 2009

Lisa's return to the Hospital

Well, Lisa did get to go home, for about 6 hours and then she ended up back in the ER with severe bone pain, a high fever and vomiting, so back in she went. She said her chemo treatment for tomorrow had been canceled, the doctor felt it was too much for her body. They also inserted a pick line so that her poor arm can heal and hopefully this will be a better option for her. She said maybe she'd get to go home tomorrow and that her counts were up today.

Through this all she still continues to think of asking how others are doing and never complains.

Love,

Suzi

Saturday, May 16, 2009

Lisa Went Home!

Ok, so I could not share the great news with you all because I was not home, but yesterday afternoon, Lisa was awaiting Scott, Kaitlyn and Matthew's arrival with cake for his birthday and the doctor came in and said she could go home!

God is good and answers prayers! Stay encouraged Lisa!

Love,

Suzi

Friday, May 15, 2009

Quick Update

So, Scott, Kaitlyn and Matthew are at the hospital with Lisa having a small family party for Matthew today! Yeah!

Love,

Suzi

Thursday, May 14, 2009

Matthew Turns 4 Tomorrow

This is Suzi updating you a bit sooner this time :)

So, you notice the title of this post? This is Lisa's prayer request, that she can go home to be there tomorrow morning when Matthew wakes up on his 4th birthday. Can you imagine how hard this is? My son, Coby and I after getting her update were in the car and just stopped and prayed. This is the verse we took to heart and boldly approached His throne for her today.

Hebrews 4:15-16,

"For we do not have a High Priest who cannot sympathize with our weaknesses, but was in all points tempted as we are, yet without sin. Let us therefore come boldly to the throne of grace, that we may obtain mercy and find grace to help in time of need."

As of this morning Lisa's platelets were still low but the doctor she saw today did not think a transfusion would be the best thing for her as he felt it would open her up to more infections. So, it can be a bit frustrating when one doctor says one thing and another counters it, but I trust they will give her the best care she needs. She has been getting Nupigen shots to increase her white cell counts which she said are up to a 2. She said this is better but not great.

Before letting her go home she had to be able to hold down a meal. This meal started for her this afternoon with a liquid lunch, which I have yet to hear from her if she held that down. They also wanted to make sure that her headaches were in a tolerable state. The last we "texted" she was getting ready to go for a Brain MRI and that was 2:45 ish this afternoon. As soon as I hear how this went I will let you know if she is not able to do so.

So, you could see why she so badly wants to be released tonight. I think she was determined to escape if they refused. Please be in prayer for whatever they want to see happen that it will happen, even maybe if it meant a one day trip home for Matthew's birthday.

On a personal note from me, please pray for her upcoming chemo treatment on the 18th and soon she will begin weekly treatments and her body needs strength that only comes from the Lord. He is able to do all things, even that which would seem impossible.

Love you Lisa!

Wednesday, May 13, 2009

Praying for Lisa-Update

Hi, this is Suzi giving you an update on what is going on with Lisa. I thought I would check in with her today and see how she was doing and so I am going to relay to you what we ended up "texting". If you have time and feel led please be praying.

Here's what she told me... Lisa went in for her chemo treatment on Monday, May 4th. The plan was that after chemo they would admit her so that they could better help treat the horrible effects she has from the treatment. They admitted her on the 4th and she came home on Friday, May 8th.

Lisa was re-admitted last night for her migraines and vomiting. They have also determined her white cell count is extremely low and they have her in isolation. Her platelets are very low at 8.7. Just so you know they give blood transfusions at a count of 8, so this looks as if it will be a high possibility for her.

I told her to "hang on" and she said "she is trying". Lisa has amazed me at her positive attitude and strength amidst weakness and when we touch base she always wants to know how I am doing. She never outwardly complains, you'd not know all she is going through by talking to her. She amazes me! Praying for you dear friend!

Thursday, April 30, 2009

Questioning God....

Hey there!

First, you know I have to thank you all for the wonderful warm comments, thoughts, cards, FB comments, prayers, just everything, it's been amazing how many people are thinking and praying for little old me! I just don't feel deserving, but I want you to know I am just so grateful!

I know God is listening and taking everything under advisement (haha). I know a few of you have some questions for Him right about now, but I don't. Although, I do have to say, it is a bit strange that you never hear of some mass murder or child predator or someone like that dying from some horrible disease....am I right? What's up with that? Well, the reason that I don't question God about my having Stage III breast/vascular cancer is because I just really believe that we are all put here on earth to do a job, you know, do something that is going to make a difference somehow. Maybe not, worldwide, save the earth kind of job, but we're all put here for a reason. I've ALWAYS thought my reason was one: Kaitlyn. She truly is the most incredible person I've ever met. She's draws these amazing pictures and has a beautiful voice and has a smile that lights up a room! She's truly beautiful inside and out. It was her and I for quite a long time and I know her so well. Much better than I'm sure she'd ever be willing to admit. And I know, mom's always think their kids are amazing and the best and rightly so. But Kaitlyn is just something different, something special. Those that know her, know she hasn't had the easiest life and a lot of that is because of me and poor decisions I've made. Everything I've done has been for her because quite frankly, she's the best thing I've ever done. I truly feel that God put me here on this earth so that SHE could be on this earth. Sure, at times, she's driven me crazy and I know I've driven her crazy, but we've NEVER doubted our love for each other and I remind myself of that when I'm frustrated after 6 hours of shopping for a prom dress. I'm so very grateful God let me have her and help her grow and I pray that He is happy with how I've raised her...mistakes and all. She is the love of my life. So, that's it, my work on earth was done! I had her, that was my reason.....

Then, I had Matthew. Really GOD? TWO PERFECT CHILDREN? Matthew, who is so incredibly full of life and so, so smart! He loves everything and everyone! Every sport and every musical instrument. Every dandelion and every dinosaur! He has the deepest chocolate brown eyes I've ever seen and when you look into them, you can see his soul. He brought home a plant that they had grown at preschool yesterday...and he named him Arthur. He had his dad go out to the car at 10:45pm last night to get Arthur out of the car because he was afraid Arthur would grow so big in the middle of the night that it would burst through the roof on dad's car and break it. So, he thought it would be best if he put it in his room next to Toby his fish, who could keep an eye on it during the night. Matthew never fails to make us smile, even on the worst days imaginable. So, as you can see, I have two loves of my life now. I remember when he was hospitalized when he was just two weeks old and crying to my mom. I remember telling her that when Matthew was born, I always wondered how long God would let me keep him. Well, Matthew will be turning 4 in just 2 weeks. I can hardly believe it, he's so beautiful!

So, no, I don't question God. I am grateful. Grateful He has given me these two amazing beautiful children to be here on earth and to be able to touch other people, each in their own way. I don't pray to God and ask Him to help me through this cancer (well admittedly I have called on Him a few times in ER with my migraine pain.) or to help me get past the chemo or vomiting, etc. I just pray to Him that my kids will stay safe and loved and cherished.

Love & Blessings to you all!
Lisa

On a side note: I am having chemo on Monday. At this point, they have decided to admit me into the hospital for a few days in order to try to control the violent vomiting, severe migraines and dehydration. I will have my blackberry, so you can still text me or FB me. If I don't answer...I'm a little preoccupied! lol

Monday, April 20, 2009

Its Been Too Long!

Guess who? Just little old me. I'm actually sitting here at the hospital waiting for my chemo treatment. My appt. was actually at 10:50a.m.and its now 1:22pm & they haven't even started yet! Unbelieveable!

My original chemo appt was for Thursday last week but guess what??? Yep, I had another one of my lovely migraines. It started Wednesday night & Scot took me to the ER. We spent all night there while I was being pumped full of pain & nausea meds. We left there just in time to drive home, shower & head back down for chemo. Except that by the time I got there my migraine was back full force along with the severe vomiting. My oncologist decided I wouldn't be able to handle the chemo. So they layed me in the back & hooked me up to ivs of demerol. We were there 6 hrs before they would let me leave.

I spent the weekend trying to recoop & rest up for today. Oh! They finally called my name! Chemo here I come! WoooHooo!

Love you all! Promise to update soon!

Thursday, April 9, 2009

WTF.....where's my hair!?!?!?!?

Ok, so see my new haircut? That was just last week and today I'm going to get the rest completely shaved off. It hasn't been very fun, but I haven't freaked out or anything. It's hair, right? Of course, they don't tell you is how freakin' painful it is! I've never heard anything about it actually hurting. Really, it makes sense though, I mean my scalp hasn't seen the light of day...ever! So even my pillowcase hurts. I'm pretty sure it'll be fine once the hair is completely gone and my head can "toughen up" a little. Other than that, I've been hanging in there. Trying to do a few things, like take Matthew for a haircut or do a little housecleaning (fun!). If I overdo it, which is sooo me, then I pay for it the next day or two and am usually in bed. This time around, I haven't had a bad migraine yet, so that's is FANTASTIC!!! They do have me on pretty heavy meds to avoid it, but hey, whatever works at this point, I'm game! :) Still nauseous most of the time, but dealing with it better too.

Oh, the best news ever is that my best friend from Seattle came down to see me! She flew in yesterday and is here thru Saturday. We haven't seen each other since her wedding in Vegas almost 2 years ago. We are just hanging out and taking it easy. Luckily, she's been down here several times, so the whole site seeing thing isn't necessary! :)

Thanks to everyone who is sending me good wishes, comments and most of all prayers! I appreciate each and every one of you! It might not seem like a big deal to leave a comment for me, but I can't tell you how much it brightens my day, so please...keep them coming!!!

Love & Blessings,
Lisa

Thursday, April 2, 2009

Chemo...the day after!

Hi everyone,

Well, I made it through chemo yesterday! Good news, no asthma attack...bad news...I started vomiting before treatment was even over..not a good sign. But they gave me an additional medication called Ativan via i.v., which is supposed to help nausea and general all over calming down. It did help me for the ride home.

I did talk to my oncologist, well the dr. who was filling in for my dr. who was on vacation. Anyway, we discussed my issues from past treatment, severe migraines & nausea. He did say that it was probably inevitable that this will happen every time I have treatment. Oh YEAH! He feels meds aren't working too well for me because my liver produces a very high level of enzymes. Basically, my liver doesn't give the meds a chance before they have time to get into my system. Meds usually work for me by i.v. because they go through my system first..then to my liver. Makes sense, by why have my previous doctors in the migraine clinic nor my neurologists ever said anything..just kept giving me more meds? We asked if there was anything they could do to decrease the enzyme levels in my liver. He said I'd need to talk to my regular oncologist and find out what he would want to do. So, for now they are giving me a different nausea medication and giving me the pain med that I usually get via i.v. when I'm in the ER, in pill form to take home, so we'll see.

I seem to be doing better today. I am nauseous, but not vomiting and I do have a bad headache, but not a migraine...so far so good!

One more bit of news....I began loosing my hair Tuesday night. Which is right on target, because they warned me it would be about 2 weeks after chemo began. I have to say I am pretty bummed about it. I mean I've ALWAYS had long hair and a ton of it! But I'm not freaking out...I mean it's hair for pete's sake and it does grow back! I'm going to call my hairstylist Lindsey and find out if she can cut if off so I can give it to Locks of Love. I'd rather do that, than have it fall out chunk by chunk and be useless! So...if anyone has any good ideas on what I can start wearing on my head, that would be much appreciated! I don't think bald is gonna look too hot on me! lol!!!

Thanks to everyone for their kind "words of encouragement" prayers, texts and LOVE! I do so very much appreciate it!!!

Love & Blessings,
Lisa

Sunday, March 29, 2009

Rough Patch....

Well, I'm grateful that this weekend is just about over. It's definitely been rough the past few days. As many of you know, I've been battling with migraines for quite some time now and it appears that they have decided to persist. Late Thursday night my headaches started increasing. By Friday morning, I knew I was in trouble. I got Matthew ready and took him to school, but before I could even make it home, the vomiting started. It became uncontrollable, along with the pain, so Scot rushed me to the ER. They had done blood cultures and some test that I don't recall the name of, came back that I was at a 9% level of a serious infection. The doctor didn't want me to wait until Wednesday, when I see my oncologist, but insisted that I go back in to Urgent Care the next day to have more blood drawn to see where my level of infection was at. In any case, they spent 6 hours trying to get the vomiting and pain under control and finally released me.

Not 15 mins. after I got home, I started vomiting again. Every 15 mins for 5 1/2 hours. This of course brought my migraine right back to where it was, so late Friday night, it was back down to the ER. This time they admitted me and were worried about dehydration (obviously) and infection. They drew more blood and ran a CAT scan of my brain just in case. They tried a different nausea medication and this seemed to work. They kept me for a while, made me eat jello and I was released on Saturday.

I was happy to be home and resting in my own bed. My goodness, hospitals are so incredibly noisy...the LAST place one can actually rest! I was grateful that Kate had spent the night at a friends house and they took her to her track meet at Mt. Sac. She ran the 800m, which was only her 3rd time ever running the 800m and she took 5th place and got a medal! I am so very proud of her, but so bummed I wasn't there to see her and cheer for her! She's been going through her own battles lately between her surgery, strep throat, ear infections, etc. but she's been giving 100% and I'm so proud of her! Can you tell?? :)

Well, Wednesday, April 1st is my next chemo treatment. I'm going to be talking with them to find out if there are different meds we can use to help me through the nausea better and my migraines, so I'm hoping they come up with something.

I do have a confession to make. On Friday, on our way down to the ER, I was praying to God, asking Him if He could just, please, give me a break...just a little one. That I absolutely couldn't handle the pain in my head anymore. I instantly felt guilty for that. First off, I know God wasn't giving me the pain, nor has He given me cancer. There are so many more people out there suffering much, much more than me and I realize that I CAN handle this. I had a few minutes, ok hours, of weakness there, but I'm going to try not to let that happen again. Besides, I know God heard me, because I happened to get the Head of ER doctor waiting on me...and he was there again when I went back...so God gave me the best doctor I could get. So, thank you God, for looking after me.

Love & Blessings,
Lisa

Wednesday, March 25, 2009

Taking Matthew to school!

Yes! I was actually feeling good enough to take Matthew to school today! I got to get him dressed, comb his crazy hair, get his cereal...and pack his little lunchbox for Lunch Bunch! I know, I know parents do it every day, right? No big deal..only today, it was. Believe me, I've had those days when I've been impatient with him and frustrated at the craziness of how sometimes mornings can be...but today, I relished it! I dropped him off at school and got the best hug from him and the cutest little smile...ahhh! Made my heart melt.

I am happy because I still have a full week before my next treatment, so I'm hoping to get some fresh air, do a little reading and spend time with my babies. :)

Hope everyone has a great day!
Love & Blessings,
Lisa

Monday, March 23, 2009

March 23, 2009

Ok, so I'm slowly starting to return to the land of the living. Very rough weekend. Seriously, I think every single pore hurt! Still can't seem to get away from the nausea for some reason. I spent the entire weekend in bed and away from my sweet kids :( Poor Kaitlyn came down with strep and a bilateral ear infection and little Matthew hasn't been too bad, just a little cough. Even though I kept them (mostly) at arms length, my throat is hurting, which can't be real good. But, I'm drinking fluids and will keep aware if it gets any worse.

I'm really glad I got my Blackberry because friends & family have been checking in and saying hi to me the last several days and that makes me smile to know you guys are thinking of me.

Scot's been a trooper. Matthew's been his little buddy this last week. I'm so greatful they have such a bond and love to be together!

Just want to say thanks for all the good wishes & prayers! Keep them comin'!!!!

Love & Blessings!
Lisa

Thursday, March 19, 2009

A quick update

Hey everyone! Thank you Suzi for updating my blog for me. The last two days have been difficult, but today is a little better. Still nauseous, which I got some different meds for and my migraine is still hanging on but not quite a "10" yet.

I think Suzi caught you all up to date. Only one more thing is that I also have to start giving myself injections in my tummy about 4 days before my next treatment. This will hopefully incourage my bone marrow to produce more white cells. If my count gets too low, they will hold off on chemo and put me in the hospital until the are up enough to continue with treatment. So, I would much rather the shots work!

I have to say that I honestly didn't realize how much is involved with chemo and how live changing it is. I kinda just thought, get chemo, get sick, hair falls out, etc., etc. but we found out its much more than that. Nothing I can't handle though!

I see quite a few people are reading my blog, but not commenting back. I would REALLY appreciate hearing back from all of you...just say hi, or something silly or what you are up to...anything really, ok? I would LOVE it! Oh and you can either sign up for an account (it's free) in order to get my updates, or you can just comment me as anonymous and then sign your name in the body of the comment so I know who it's from.

Well, I'm worn out, so I'm gonna go get some rest. Thanks for all the continued prayers!

Love & Blessings!
Lisa

Wednesday, March 18, 2009

Lisa's Results

Hi, this is Suzi and I am a friend of Lisa's. Lisa asked if I wouldn't mind posting her update this time as she knows some of you are waiting for the results. It's been two very long days for Lisa. The results of the scans showed that her bones are clear of cancer as well as her major organs. This is truly a praise. The concern is that the cancer is in her Vascular system. So, as she explained to me, it it in the blood which means it can travel any where and they can not track that so, the plan of attack is going to be a more aggressive plan than she had thought. The plan will be for Lisa to have four rounds of chemo, the next one being April 1st and then she will go in for chemo weekly for 16 weeks. Then she will revisit the prospect of another surgery, radiation and more chemo. So, this will be an aggressive attack on her body. There are a couple of other factors that cause her complications in treatment. First, Lisa has asthma and yesterday at chemo she had an acute attack, which took an extra half hour while they gave her shots of steroids and gained control of her breathing so that they could continue. Then this morning Lisa had a migraine and Scot had to take her into the ER to which she had just got home around 4 this afternoon. She is really exhausted as I am sure you can understand. She is holding up very well and is an inspiration to me. Things we can be praying for are:

-for her immune system to hold up, with chemo she has to be very careful of germs and she
needs her white counts to stay high for each treatment
-that she recovers from each treatment quickly, she is a mom who desires to keep things as
normal for her children as possible
-that these migraines decrease and that she will not have asthma attacks that further
challenge her
-for their family and for strength,energy and health

Lisa thanks you so much for your love and concern. She will post again as soon as she has rested up a bit from yesterday and today.

Tuesday, March 17, 2009

The day it all begins...

Well, today is the day! I find out the results of my bone scan & CAT scan. Also, I will be getting my first round of chemo today. For some reason, I'm not nervous at all. One day at a time, right? Ok, well wish me luck! I'll let you all know how it goes!

Ciao!

My Story....to date (cont'd)

Part 2

On January 26, 2009, it was confirmed. I had breast cancer in my left breast. After that, it was a bit of a blur. I remember telling my 16 year old daughter, Kaitlyn that it wasn't good news. I don't remember if I actually said "cancer" at that time but she knew what it meant. I remember calling my mom and her being so very upset. After all, they'd already lost my brother 32 years before, almost to the day, from cancer. After that, it was a bunch of doctor appts., including a plastic surgeon. That's right, the doctor that told me I had cancer, was suggesting a double mastectomy and having my ovaries removed. This sounded a bit drastic to me. They suggested genetic testing, which I did...but said it would take up to a month to get those results back. If they came back positive they wanted to take both breasts and ovaries for sure. The only problem was, I didn't have a month to wait for surgery.

About 2 weeks passed and guess what, yep I felt another lump. This time under my arm. I had already gotten a second opinion about my breast cancer and felt more comfortable with my new doctor. So, I had Dr. Nora take a look (or feel) at the second lump. He immediately ordered a biopsy on the lymph node. That came back positive as well. His suggestion was that we just do a lumpectomy on the mass in my breast and remove the lymph node involved and he would then map the cancer and we would discuss what to do from there.

So, on February 17, 2009, I had surgery. They removed the mass from my breast and it turns out it had spread to 5 of the 8 lymph nodes located in the breast and to an additional node under my arm. Surgery was what they consider a success. I've been recovering just fine from that. Some pain and numbness and lots of fatigue, but that's to be expected. I went back to the surgeon a week later and then a week after that and I'm healing nicely. The doctor was happy with my progress, but said that without question, I will need chemotherapy & radiation.

Since then, I have been to two separate oncologists: one for hematology (chemo) and one for radiology (radiation). My oncologist that will be handling my chemo, is worried that it may have spread beyond my lymph nodes at this point. Supposedly, all the signs point to that....whatever that means. So, I was scheduled for a bone scan and an full body CAT scan last week. I am supposed to get the results tomorrow when I see my oncologist and the plan, as of right now, is to start chemo then as well. I guess depending on the results, he will decide an exact schedule. As far as I know, I will be getting treatment every other week for 20-24 weeks....if it hasn't spread. Then after that, 7 weeks of daily radiation, to stop the actual breast cancer from spreading.

In all this time, I've not 'freaked out', cried, been scared, nervous..nothing. I'm not exactly sure why. I know I'm not in denial. I'm well aware that I have breast cancer and am able to talk about it with friends and family. Some of my friends have even said how great I sound or how strong I am. I don't look at it that way. I've thought about it and I'm really ok with it. With having cancer I mean. My take on it is, well, if it's me, then maybe, just maybe that means someone else doesn't have to go through it. I'm not afraid of it or the treatment. In fact, I've asked my doctors if I really NEED to have chemo. I mean, if it hasn't spread, then how will they know if I'm responding to it, right? Answer is, they won't. They have no idea. They won't know until the cancer comes back.

Ok, I do have one worry...or two...my kids. My darling Kaitlyn and my adorable Matthew. I truly don't want them to see me go through chemo and what it will do to me. Matthew won't understand it at all and it will be so rough on Kate. The last 1 1/2 years they've watched me with my severe migraines and on heavy meds, I can't tell you what that did to them. I lost all that time with them. I don't want them to now have to deal with this! Ya, ya, I know, kids are resilient. If I do this, it might give me more time with them, right? BUT, will it be quality time? It's a question that really can't be answered and I know this. You have to admit though, it's a good question, right? Anyway, that's my worry, my kids....everything else...I can handle!

I realize God didn't do this to me. Although I have to admit, sometimes I do wonder why you never hear of murderers or child predators dying from cancer. A special person made me think the other day...that maybe this isn't a "test" or "trial" for me, maybe this is more about others and what I can do for them. I really love that thought.

I have amazing friends and family that will be there for me and be praying for me. Everyone is asking me what they can do for me, but really, I just want everyone to count their blessings and hug their loved ones just a little bit tighter next time their in your arms...especially the little ones!

I will keep my blog updated. I would love to hear from everyone...even just a hello!

Love & Many Blessings!

Lisa

Monday, March 16, 2009

My Story....to date.

Part 1

So, you know how amazing it feels to have your 3 year old run up to you and give you a huge hug? The best feeling ever...right? Well, that is exactly what my son did one day shortly before Christmas this last year. He'd done it dozens of times before, but this time was different, this time...it hurt. I flinched a bit, but not enough to end the glorious hug I was receiving from Matthew. Once he turned around and took off running, as 3 year olds often do, I immediately put my hand where I felt the pain. I didn't have to search at all, there was a large lump in my left breast. At first I thought, well that's weird! I'd had swollen glands before, but this was much harder and really hurt. I didn't put much thought into it after that, I just hurried to catch up with Matthew, who by this time was yelling after me, "Can't catch me!".

The next morning, I woke up and felt a dull pain. Again, I felt my left breast..yep, the lump was still there. Oh well, I had other things to think about. I was still dealing with my migraines and because of all the constant meds I'd had over the last year, I now had high blood pressure to deal with. I knew I had a neurologist appt. coming up and after that, if the lump was still there, I'd make an appt. with my general. Another week went by. I had the appt. with my neurologist, where at that time, my blood pressure was so high, they made me an appt. to see my general doctor.

Finally, on January 14, 2009, I went to see my general to do something about my continued high blood pressure. I was pretty upset about this because I knew it was caused from all those migraine meds and nothing else. Now I would have to take another medication for BP...not happy! So, I spoke to the dr. about my BP and "..oh yeah, by the way, I've had this lump in my breast for about 3 weeks now, can you check it for me?". Which of course, he did. He didn't have to search for it either, it was very obvious. He asked me if I'd ever had a mammogram, which just turning 40 in November, I had not. He told me he was scheduling me for one right away. "How long before I get an appointment do you think?" I asked. "You are going now, immediately! I need to you drive to Kaiser in Panorama City, to get an emergency mammogram & ultrasound. They will be waiting for you." I'm thinking, ok wait, I was just supposed to see you about my BP, now I'm having an emergency mammo & ultrasound? I called my husband Scot and explained it to him. He left work immediately and met me at the hospital. We ended up being there for about 4 hours. I had 3 different sets of mammograms taken and 2 ultrasounds. By the time we left the doctors office, it was obvious I had a large mass (apricot size), but we didn't know what it was. I think at that point, I knew.

I was scheduled for a biopsy for the following week. It wasn't super fun, but not so horrible either. I wasn't nervous...it is what it is...right? The doctor said it was 24-48 hours before we would get results. Well, this was a Thursday and if they didn't get back to me on Friday, then I would be waiting all weekend. Scot took the call Friday night, I wasn't even home. He told me later that night that the doctor wanted to see us first thing on Monday. I remember him crying when he told me, but I didn't cry at all. I just kept saying, "It's ok!".

continued in Part 2