My verse....

"I will still be joyful and glad, because the Lord God is my savior. The Sovereign Lord gives me strength.
He makes me sure-footed as a deer and keeps me safe on the mountains."
Habakkuk 3:16-18

Wednesday, July 8, 2015

I'm finished with Radiation!!

 Today was my last radiation treatment and I am so happy to be finished.  I met with Dr. Baseman yesterday and he is really pleased with how I've done with it all.  Have a share a couple of pictures.

This first one is with Lorene, my radiation therapist.  Missy was the other therapist but she wasn't there today.  Lorene said when she got sent to one of their other locations, Missy moaned that she would "miss Mrs. Lipe's last treatment."  I hate I didn't get to tell her good-bye.  These two ladies were so good to me!!
This next shot is with Kathy, the nurse, with us holding a completion certificate they gave me.  She was always concerned with my radiation burns and my healing!
It is SO good to be finished.  I hope in  2 or 3 weeks my energy level will pick up some, too.

On Monday I also completed the last physical therapy on my knee.  I will continue to do exercises they gave me and will continue to see improvement, but at least I don't have to go to PT anymore. Yea!!

Now I am looking forward to seeing Dad and my family this weekend as we gather to celebrate his 95th birthday!  I have only seen him once since Christmas so I can't wait. 

I will report back in to you after I see Dr. Harkness, my oncologist, on July 22.  Let's hope things are looking up then!!

Thanks again to all of you who have continued to pray for us so faithfully.  It means so much to know that we have you prayer warriors lifting us up in prayer.  It's been a LONG 10 months, and I've hit a wall several times, but always one of my family or friends were there with a call, an e-mail message, a card, something to help light my way.  Thanks to the ladies at church who have continued to write up the Sunday News for me each week--Pam, Martha, Karla, Paula!! (I haven't publicly thanked these ladies yet.) What a blessing. 

I am now seeing the light at the end of that dark tunnel we've been walking through all this time.  It is so great to come out into the sunshine!!  I could not have made it through all this without all of your love helping to light the way for us!!!  So a big Thank you!!!  And much love to you all.
Smiles, Laura

Tuesday, June 30, 2015

Still going...

Still going on the radiation treatments, that is.  Of course I am still going, too.  After I posted that last entry and had treatments through June 19, my chest was so burned (and my spirits so low because of the pain) that the oncologist suggested I take a week off before we started the last phase (of 6 treatments).  I don't think I could have taken any more had he not suggested this.  Frank was all for my quitting, because seeing the outer skin damage, he was so worried about what it might be doing to my internal organs.  We met with the dr. and he assured us all was OK internally.  He said I had actually done very well and lasted for 6 weeks when some women burned like me would ask for a break at 3 weeks.  He said I had some "nasty cancer" with many lymph nodes infected and they wanted to "hit it hard" to make sure it does not come back.  All I know is I was in real pain with burns that looked like you had sat a hot iron down on my chest.

That week off sure helped.  Here is a shot of some of the area 11 days after the last treatment.   Still looks like the point of an iron burned me in that one spot.  But it is scabbing over.  And darn it, it is up high enough that in shows in all my tops.

I still have some other pretty raw places, too, but when I saw the oncologist today, he said I was doing great and seemed like my old self again.  I decided to have a treatment today.  I will have 3 treatments this week (they will be closed Friday for the 4th), will have a 3-day rest, and then will have the final 3 treatments next week.  I will be so glad to have this over.  These last 6 do not cover my entire left chest, all the way to the clavicle, but rather just the area of the lumpectomy.  I am not sure if the dosage is the same or not, but at least it is not as wide an area! 

I also saw my orthopedist today and he is very pleased with how my knee is healing.  When the physical therapist measured my extension last week, I have 141 degrees in that knee, which is all you could ask for--outstanding!!  It is still a bit weak about my walking on it, but it is getting there!! I have 3 more therapy appointments, finishing up next Monday.  Just think, by Wednesday, I will be finished with both PT and radiation treatments.  Praise the Lord!!  He said it will be awhile--1 to 2 years--before I can kneel because of the lower area with the patella piece missing but I can just do without kneeling.  (I tried kneeling the other day to find something I thought might have rolled under the bed and yikes, pain on that spot!  Fortunately Frank volunteered to look for me.

I have some other things to go through with the oncologist.  Of course the radiation oncologist will continue to see me for awhile, he said, to see how I'm healing.  And the regular oncologist, Dr. H., will see me for the Zometa injections every three months.  But basically as my energy level comes back, I will be able to do what I want and not have so many doctor visits to make!

What I want most is to have my energy back!  I still get really tired sometimes, but as friend Pam Deacon told me, "you don't have to do ANYTHING except rest and get well."  I think of her encouragement every time I'm tired and think I SHOULD feel like doing something.  I have stopped "should-ing" myself!  You SHOULD clean the bath.  You SHOULD dust.  You SHOULD mop the floors.  No, I just have to get my energy back

On a lighter note, we have been dog sitting Gabby's sister Chelsea since June 19 and it's been so much fun to have them both here together.  Chelsea loves going for walks with us, running behind the 4-wheeler, and of course keeping me company.  Here they both are while I am posting this entry:
  These Schnauzers are loving little dogs and they stay right with their "humans".  What a joy!!  

Thanks for reading this latest entry.  And thanks for continuing to pray for me and for your cards and messages and calls.  I love each of you!!
Smiles, Laura

Friday, June 12, 2015

Two-thirds of the way through with radiation treatments...


Well, one thing you can count on: time passes!  I can remember back in April, laying in the hospital and wishing it was already June.  Wow, time seems to have passed quickly and here we are.

My knee is doing much better.  I still have some pain and walk with a slight limp, but it is improving daily.  Monday I will start physical therapy to help me do "step-over-step" when climbing steps.  That seems to be the hardest thing for me to do yet.  Right now I am "dragging" that leg up the steps.  Dr. Lemel wanted me to start therapy sooner but this is the first appointment they had in physical therapy.  So I am looking forward to that.  I don't know if I can kneel or not, but really didn't do much of that before I broke the knee and don't plan to start now.  But I can do most other things I want to do, except the steps.  I have to watch and not spend too much time standing/walking as it gets painful, but I know a few more weeks will help.  It has been 10 weeks yesterday since I broke the knee and I feel I'm on target.  Dr. Lemel is very pleased with my rotation (over 115 degrees already).

As of this morning, I was two-thirds of the way through my radiation treatments.  I had 11 of the 33 treatments yet to go, and had one of those at noon today.  I am to the point that the radiation is really burning my chest.  Here are some pictures I took 4 hours after treatment today:

Doesn't look too good, huh?  Well, at this point, this is how it gets with 5 straight treatments so thankfully I have the 2-day weekend to heal.  It will look better before they start on Monday.  And just 10 treatments to go!!  I can see the end in sight.

Had to share a selfie I just took, too.  I normally would not say this, but it looks better to add a head, right?  Ha!  I still have very short hair on top/front, so am still wearing caps.   But I can tell it's growing.  Maybe by the middle of July (when we celebrate Dad's birthday) I will begin going without a hat/cap.
Thanks for continuing to pray for me!  It means so much to me and my mental well being.  I have been reading articles on how important it is for friends and family to help keep up the spirits of a cancer person and you all have done a GREAT job of helping to cheer me!!  I love you all so much!!
Smiles, Laura

Monday, June 1, 2015

Almost half way there!

Well, a friend of mine reminded me at church yesterday that I have not posted to this blog in a bit and some of you are using it to keep up with my progress!  As of this coming Thursday, I will be half way finished with the 33 radiation treatments.  So far, so good.  They are coming along fine.  I am using hemp oil cream on my skin after each one and so far no redness or burning.  Dr. Baseman sees me every Friday after the treatment and thinks I am doing fine.  He asks me if I am feeling any fatigue.  Well, yes I am, but am not so sure that it is not from the chemo.  It takes a person a long time to get their energy back after chemo.  But I have the added issue of the broken knee and what that has taken out of me!  I'm telling you, it has been tiring to walk around with the heavy brace and with crutches.  The fatigue I am feeling is bearable and probably caused by a combination of all I've had going on this year.

I see Dr. Lemel tomorrow.  It's been 8 weeks since I broke  the knee and he is taking my healing very slowly.  I am pushing the limit, though.  He told me I could walk with the brace and one crutch out of the house and without the brace and with one crutch inside.  Well, for a couple of weeks now, I haven't worn the brace at all and am now only using my cane for walking outside and nothing to aid me inside.  Yesterday Frank and I even walked on the state road where we usually walk.  Of course I didn't go quite as far as we usually do, but still Gabby loved us walking with her after so long a time.  I can't wait to show Dr. Lemel how well the knee is doing.  (A church friend reminded me "those fellows have degrees for a reason, you know" so I hope I haven't pushed the limit too much.)  I probably am getting about 110 to 115 degrees rotation already, which is great.  But I still have pain in the knee when I walk too much or hold it in one position too long, or get up after sitting a long time, etc.  I just think I need to get started on some physical therapy to work the gluts so they are strengthened.  We'll see what Dr. Lemel tells me tomorrow!

Thanks for continuing to pray for me and to ask about my progress.  I know all this will be behind me before too long and then I can spend time getting my strength back and doing some household chores I have let go too long!

Frank and I love and thank God for all our friends!!  Keep the faith for/with us!!  And keep offering up prayers; we feel them!
Smiles, Laura

Wednesday, May 13, 2015

Finally started radiation!

Well, the old knee is healing and I am hobbling around pretty good.  I saw the orthopedist on Monday and he was pleased with my progress.  He gave me 70 degrees range of motion (but I think I can actually do 90 degrees with the knee brace off), is letting me sleep without the brace now, I can stand in the shower, I can walk without the crutches inside the house (using one when outside) and best of all, he is letting me drive now!! It will be so good to drive myself around without having to impact Frank.  Of course when I get out at a store to shop (like the grocery store) it is very wearing on me and the knee tends to swell later in the day, but at least I am showing improvement!

I wanted to share pictures of the knee because it is amazing how far I've come in 6 weeks!  This first one was taken on my iPhone by the EMT in the ambulance on the way to the hospital.  Ewee!  Looks as painful as it felt!  You can see the patella broken into two pieces.  Broke it on April 1, but it was no April's Fool joke!
 This shot was on April 3, the first time I saw it after the surgery.  That's 19 staples in there!  You can see the bruise, too.
 This shot was on April 8, one week after I broke it!  Lots of swelling!
 This shot was taken April 28, after the staples had been out a week or so.  I skipped alot of time taking shots, as I was more focused on healing and didn't realize I'd want to see the progress later.
 And this shot was this morning.  You can see the heavy, adjustable brace, but also how well the incision is healing.  I will have a scar but not too bad and of course at my age, who worries about scars and their legs anymore! Ha!
 When I fell, I bruised my left hand pretty badly, too.  They thought at first I had broken my little finger but the x-ray showed I had not.  Here are shots on April 1 of my hand, the night of the fall.

 This shot shows the hand on April 7.  It has done lots of healing but was still sore to use.  Just glad it didn't break, too.
OK, thanks for bearing with me on the knee shots!  Ha!  Just documenting, folks!

I also went on Monday,May 11, to have my first radiation treatment.  Unfortunately they needed to take two more x-rays for the doctor to use to set my positioning correctly, so no treatment that day.  So I had my first treatment yesterday (May 12) and it was interesting and not painful.  Of course I had been told I would not feel anything.  I think the effects are cumulative and I will notice it more as treatments progress.  I am so glad to be started with these treatments!!

I did get so tired of laying with my arms over my head for 30 minutes.  I did not know all this, so I will share if you in case you did not know and are interested.  They lay you on a table and make a mold of you from your shoulders up (for breast treatment radiation) and you have to have your arms over your head.  They mark 3 or 4 spots and take pictures of how you are laying, and then do a CT scan. The radiation oncologist uses this to plot exactly where the treatment will be administered.  Each time you go for a treatment, they position you in that mold in exactly the same position to administer your radiation.  When they made my mold, they just said, "raise your arms over your head" and I thought they were going to do the CT scan--had never heard of the mold.  So I was not in a comfortable position with my shoulders and every time they have taken x-rays, lined everything up, or administered my radiation, I had been in that same uncomfortable position.  Guess I can stand it for 32 more times!  Just wish I had been warmed that this position was to be used for a mold for my positioning.  Oh, well.

I had a great Mother's Day on Sunday.  Meg and Dillon and Jessica came out for lunch and to celebrate not only Mother's Day, but Dillon's 17 birthday which was last week.  We had a nice visit.  You might have seen these pictures on my Facebook page, but here they are again if not.
 Jessica is almost as tall as Meg and of course Dillon is alot taller than Meg or me! 
 Just had to include a picture of me with my little sweetie Gabby.  She has been with me constantly while I've been healing the broken knee, laying on the bed all those long hours with me.  I don't know what I'd do without her!
Well, hope this post was not too boring for you.  Just wanted to report the radiation has started, I can drive again, and my spirits are lifted! 

I continue to thank God for all my many friends who had sent cards, have called, brought food, and just sat with me!  I love you all more than I can express.
Smiles, Laura

Monday, April 20, 2015

Broken knee setback...

Well, I was on target to start my radiation and then, for those who have not heard, on April Fools Day, April 1, I twisted my right ankle, fell and broke my left knee cap.   I know, I know, how could I do that!!  Well, it was just a bad accident.  I had dropped Gabby off at her groomers and was heading to my car when I stepped on a stone and down I went.  It was so bad I had to call an ambulance to come get me.  Of course it required surgery.  The lower half was in 5 pieces so that the doctor finally gave up trying to put them together after 45 minutes and just took them out and drilled holes in the upper knee cap half and tied it in with my tendons.  Bummer!

I spent several days in the hospital and have been convalecing at home.  Needless to say,  it has been painful but is healing.  Friday they took the 19 staples out and my incision looks good.  They want me  to go another week without bending it before I start physical therapy.  I know what is ahead of me from when I broke the other knee 18 years ago, but will get through the PT and have use of it again. 

So many of my sweet friends have surrounded me with love. I had 17 visitors at the hospital on Easter Sunday, with many bringing flowers, candy, cookies, etc.  Since then 3 friends have brought supper for us.  It is so gratifying to have so many wonderful friends.  I will never be able to thank people enough.

In the meantime, I saw my oncologist and he says I am still OK on the radiation, but wants me to start it within 6 weeks of the end of chemo.  So this Thursday I will see the Radiation Oncologist for tattooing the spot for the radiation and hope to start that next week or the following one.  My cancer treatment comes before anything to do with the knee! 

Guess I will be doing therapy and radiation treatments at the same time.  Thanks for your continues prayers.  Sometime we wonder why these things happen, but I know God has a plan.  I just hope things get back on track soon and I am not tested with any more trials.!
Love to all of you!!
Laura

Thursday, March 26, 2015

Chemo is completed!!

Monday I completed my last chemo treatment and am so happy!!  It was a fun day, not because it was my last treatment, but because of the many friends I saw during my treatment!!  But first, here is the chemo chain my friend Jill Monte made for me when all this started.  Look at it with no links remaining!!! 
Here it is when we first started with chemo:
All those links! I thought we'd never get through them all!  We have come a long way from that chain with 16 links on it to be removed.  I'm glad the chemo is over but treasure the time I had with the nurses and other ladies I met there. 

Here are some of them.  This first beautiful lady is Hope and she is on her second round of chemo, having had her first in 2012.  She is such a beautiful heart and I pray for her daily.  I did not even get her last name, but we talked several times during chemo and she has a positive spirit in spite of the fact that she's going through chemo a second time.  I want total healing for her.
This next lady is Teresa Wheeling and her is her sister Jamie.
The first two times I saw Teresa, she had her hair, long pretty hair, and was sad to think of losing it.  But she has now and her spirit is so beautiful who even notices!  Frank and I talked to Teresa and Jamie a couple of times and she had treatment Monday, too, and came to tell me good-bye before she left.  Hard to think of not seeing these brave women each week.

My friend Sharon Kelly stopped by to see me on my last day, too. She was there for her blood work. Her last treatment was to be March 25, yesterday. Yea, Sharon!!  She just glowed and I think she felt better than she has in a long time.  Sharon's husband was a co-worker of mine, so I know we will stay in touch.  I pray for great outcomes for both of us. 

Then there are the wonderful nurses who administer chemo every day at the Hope Center.  I have already posted a picture of Tamara who was my nurse several times. She has left Hope Center to go back to school for her BS in Nursing.  Here are my other wonderful nurses:
 This is Kristie.  She did my final treatment.  Kristie is the nurse who so graciously cleaned up the coffee my sister Becky spilled.  So patient with us!!  Becky sent a special thank you to Kristie!
These are Debra and Joyce.  Both of them have administered my treatments, too.  Joyce got the call the morning I took the wrong drug!  What a scare that was to them all (not me, I was "out of it" at home).  We laugh about it now.  I don't think they will forget the lady who took 10 of the WRONG pills and was "out of it" for a day or so.  Now they say at least they know someone CAN survive taking so many of those pills but they don't see how!
This is Melissa.  I called her Michelle for 3 or 4 visits until I heard her say "Melissa" on the phone one day.  Never did she correct me! What a honey she is.  She brought me pillows and blankets and so graciously opened the combination door for Frank when he had to go out and come back in. Melissa is the receptionist and scheduler.  She tried her best to schedule me for the days and times I wanted.  Love her!!

On the last day, when treatment was over, the nurses all brought me my completion certificate and blew bubbles all over me and clapped for the finish!!


See all the bubbles in the photo?
The last nurse on the right is Judy.  I didn't get a shot of her and me together, except with the group, but Judy was absolutely wonderful to me, too.  Just think, these nurses treat people with cancer every day, some of whom are VERY sick and don't have a lot of promise for getting past it, but still these ladies stay cheerful and are so very nice to all of us in that room.  What a blessing they are to so many!!  I just had to include their pictures to give them the credit they deserve!

And lastly my friend Judy Thompson who drove me to 5 of my 16 treatments.  (I have to mention that sweet hubby Frank took me to 7 of my 16 treatments himself and was so patient with me!  Love him so much!!)  Judy is a jewel and also took the above pictures for me.  So I have to include a picture of her.  She's a dear, dear friend whom I love very much!!
So we are finished with the chemo---I PRAY forever!  When I started, I thought 16 treatments over 5 months was SOOOOO long, but you know, I met ladies who are HER2 positive who have been in chemo treatments for 4 years and are still going.  I pray for these ladies!! 

Some of my friend from church (we call ourselves "the Birthday Girls" since we all celebrate our birthdays with lunches together) and I went to lunch the day after my last chemo to celebrate.  Here are those precious friends:
Front row, Helen, Marge, Sandy and Pam.  Back row, Pam, me, and Mimi.
 We had a delightful lunch and fellowship that day.  What in the world would we do without sweet friends!

I meet with my oncologist Dr. Harkness on April 10 to see how he feels things are going.  His nurse did call to tell me that the results of the CT scan were good, no new tumors showed up.  (Well, I'd be REALLY upset if I had new tumors to come while having all this chemo!  I'll see what Dr. H. says when we meet.)  And I have the gene testing on April 22 and will be very interested in those results.

I don't know the dates, but will probably start radiation around the middle of April.  That is going to be very confining, since it is 5 days a week, every week for a couple of months.  I am getting mixed messages about radiation and the fatigue factor.  Some who have had it say it really fatigues you, but others say it's a "piece of cake" so I'll see how it affects me.  And report back.  Oh, and I can't remember if I reported or not, but my hair has started growing back in and yes, it's still white.  It started about February 14 (Valentines Day) and of course isn't thick nor very long yet, but at least I am getting hair back.  Yea!!

I hope this long post has not bored you too much.  I use this blog to document things so I won't forget details later so all this is probably more for me than for my readers, but I did want to show you the fun last day of treatment.  I know many others are much weaker and cannot enjoy the time like I did.  I praise God that I have done pretty well during all these treatments.  I am trusting in Him to heal my body completely so that this will be my only experience with all this.  But I continue to pray for all those who are going through chemo for so long and with so much sickness!  Precious souls!

Thanks for continuing to pray for me and Frank.  We feel your love!
Love to all, Laura