Wednesday, December 30, 2009
PET Scan Tomorrow
Monday, December 28, 2009
Ready for a New Year!
Tuesday, December 22, 2009
Merry Christmas Y'all
Monday, December 14, 2009
Happy Happy Holidays!
Thursday, November 19, 2009
Thanksgiving
Wednesday, November 4, 2009
November is Here
Well it is November. I can remember back in July when I kept thinking "I can't wait for November" when this will all be over. It has finally come, and life is wonderful. Earl is practically back to normal. He still tires more easily than he did before but that doesn't slow him down. He is pretty active and keeps busy with his new toy. I am having everyone to our house for Thanksgiving so it will be fun & a little crazy. We spent so much of the year alone that I just want to surround ourselves with family and friends. Drew and Olivia are doing well and ready for the holidays too, and a break from school. I just want to say Thanks again for all the prayers over the summer. It's so nice to know how many people are pulling for you when the chips are down. Love you all. Donna
Thursday, October 29, 2009
Gettin Better Everyday
Wednesday, October 21, 2009
Earl is eating now
Monday, October 19, 2009
Grass Cuttin
Monday, October 12, 2009
Our weekend
We had a good weekend. Me, Mom and Olivia went to Atlanta for a girls weekend and Earl played in the member/member golf tournament at Pine Forest with his friend Jeff. It was a nice weekend for both of us and we were both very tired last night. Earl is eating pretty good now. He ate half a hamburger yesterday after the tournament and that is a big progress from soup. He is eating breakfast, lunch and dinner now, in small amounts. He did have a craving for a veggie pizza last night but by the time I picked it up the craving was gone and he couldn't eat it. That is usually what happens but he is improving. Hopefully when he goes back for his checkup next week he will have gained a few pounds. He is so skinny. I am really looking forward to the fall and the holidays. I can't wait to decorate for Christmas, I know it's too early now, but I am going overboard this year!!!! Love you all, Donna
Wednesday, October 7, 2009
A little normal
Monday, October 5, 2009
Earl's Present to himself
Thursday, October 1, 2009
Everyday is a new day
Earl is doing so great. He bought himself an '81-911 porsche (red) as a present for himself. He is like a kid in a candy store, so excited. It needs some work so that will give him something to do during his month of recovery. His Doc is taking the PEG tube out tomorrow, so that is more good news. He can't wait to get that out. We have a follow up tomorrow with the oncologist for just a check up. We get our CT scan on Oct 22, so please keep him in your prayers that all the cancer is gone and that it never returns and we live happily ever after. His Radiologist saw him Tuesday and she was so excited about how well he was doing she followed him all the way to his car, jumping up and down. A little crazy but a GREAT doctor. It is so nice to have our lives back to some normalcy. He still gets tired easy but doesn't really let it slow him down. Hope y'all have a super weekend. Love you all. Donna
Tuesday, September 29, 2009
Hooray for Progress
We are one week out of treatment and doing pretty good. Earl is now eating soup and soft food and not using his PEG at all. He is feeling really good. He played nine holes on Saturday. I am so Thankful that he is improving everyday. It is so nice to have him back. I know it will be a slow progress and he will not be fully back to himself for a while but it is so nice to have him up and around and feeling good. We all take our health for granted and sometimes we don't take very good care of ourselves and just think that we are always gonna have good health, but when you are down and sick and can't do anything for months you realize how important it is. Our next big hurdle is getting the PEG out. I called the DR today to see when we can and I am still waiting on him to call me back. Earl hates it so much that I just think that will be one last thing that will make him feel even better. I am just so excited each day to see him improving and I know by this weekend he will be even better. Thank you so much for the prayers. We love you all! Donna
Tuesday, September 22, 2009
It's a wrap!
Earl finished his final radiation today! All the Doctors and staff gave him a round of applause when he came out of the "room". I could hear him smiling over the phone when he told me. They let him bring his mask home, kind of creepy. Oh well, Halloween is right around the corner. He doesn't have to go back for four weeks. Now we can celebrate! Dr. Harper said she really doubted he would need any further surgery, so hopefully the PEG will come out soon. They just yank it out, OUCH! So yesterday when I got home from work he wasn't there. That was unusual because he is always in the same chair watching TV. Not today, he decided to go play a few holes. It was like he was a new person. Tired, but he did managed to finish six holes. He said it just felt good to get out. I suspect now he will do more of that. Besides the fact that he is a bag of bones, he really looks great. I will keep you all updated on his progress. Thank you all for the support over the last three months. I love you all! Donna
Monday, September 21, 2009
Great Weekend!
It was a super great weekend. It started with Friday, I took off to go to Earl's checkup with him. Doc was very pleased at how well Earl is doing, although he would not commit to a date when Earl can get the PEG out. Earl was feeling pretty good so we went and got his hair cut after the appointment. Thank you Lisa for our free hair cut, that was so sweet of you and his haircut really made him feel better. Olivia had a friend over Friday night and we went to dinner with Grandma. Earl went to bed pretty early Friday night but woke up a new person Sat morning. He ate breakfast (waffle) and took a shower and headed down to the driving range with his friend Jeff to watch Jeff hit some balls. Earl hit a couple but too weak to do more. He said it just felt great to get out. He felt good enough to go to Fleet for dinner Saturday night. It was my mom's birthday. Drew, Gracie and Olivia went too. Earl managed to eat some grouper and grits. It was a wonderful evening for the whole family. Tomorrow will be our last radiation treatment. I never thought the day would come. It has been so slow. So far Earl has lost about 20 to 25 lbs. He is very thin, but really looks good for all he has been through. Hopefully in a week or two he will improve significantly. Thank you all for your prayers. We love you all. Donna & Earl
Wednesday, September 16, 2009
GOOD NEWS FROM THE DOC
Earl saw his radiologist this morning after his treatment and she said the tumor is GONE! She said she can't feel anything and that she cannot see anything in his mouth either. That is such good news. She told him that most people can't handle the whole 7 weeks without taking a break so he has done REALLY good. He only has four more radiation treatments and NO more chemo. The end is near. We know we really have to wait until two months after the treatment for our final PET scan and a clean bill of health but this is some good news. She said in the beginning she was very concerned because the mass was big, but she is so impressed at how well it responded and she cannot believe it is GONE! God is Great! Earl looks like he has been to hell and back, and he has. He is so tired and weak but still has a great attitude. He is my hero. I love him so much, I am so excited about getting our lives back. Thank you all for keeping us in your thoughts and prayers, it really does work. Love you all! Donna
Monday, September 14, 2009
Monday Morning
Friday, September 11, 2009
Weekend is upon us.
Earl did pretty good through the night. He was a little queasy last night but after some good ol ginger ale he felt better. Went to bed early and slept well. We both feel if we just make it through the weekend without getting too sick then we are over the hump and well on our way to the end of this nightmare. Saturday is the Kenny Chesney concert and I am taking Olivia. She is so excited and so and I. Just a little sad that Earl can't go. We only have seven radiation treatments left. It's all downhill from here. I really hope he can get his PEG out before the end of the month. He wants that out more than anything. No cooking for me this weekend, I will have to go out in the mornings to get my coffee. The smell of any food or coffee makes him sick, I don't mind not cooking for a few days. Thank you for thinking of us, I will update you on Sunday at our progress over the weekend. Enjoy your family. Love you all. Donna
Thursday, September 10, 2009
Last Chemo Finished!
We finished our last chemo yesterday and as of today we only have eight more radiation treatments. We are so glad that we are done with the chemo. It is a long process. We were at MUSC yesterday morning at 8am and got home at 4:30pm. Earl is doing well today. If we can just make it over this hump then it will be all downhill from here. Hopefully by Oct. 1 Earl will be starting to get back to normal. We can't wait to ride the motorcycle and go have a beer. The weather will be perfect for riding. This has been such an incredible journey for us and we are changed, no doubt. Through this all I have become amazed at how awesome God is and how when you need Him the most He is there. Sometimes I am just so full of awe that I feel like I could explode with joy. You learn to take joy in the small things that most of us take for granted everyday. Thank you all for being here for us. I truly don't know what we would have done without our friends and family. Love you all. Donna & Earl
Tuesday, September 8, 2009
Countdown!
We had a fantastic weekend. Aunt Sis and Larry came down on Sunday and spent the afternoon with us. They have been at the beach and drove down for the day. It made Earl's day. We started our sixth week today. I can't believe the end is near. He is so ready to be done. The main thing he hates is just being tired all the time. He takes a shower and that wears him out. He has started eating more, so he can get the PEG out as soon as he's done with the last treatment. We will know this afternoon if they are going to do the chemo tomorrow. We only have 10 radiation treatments left. TEN!!! I went to the pool with mom yesterday. It was so nice and relaxing. My boy came home Sunday night, stayed about three hours, long enough for me to wash his laundry and feed him. I loved every minute of it. Hated to see him leave. Olivia got home from Alabama Sunday evening. She had a good time at the Auburn game. Earl and I did some yard work on Saturday afternoon. I cut the grass and he trimmed some hedges. All in all it was a super weekend. I will keep y'all posted on the chemo. Love you.
Friday, September 4, 2009
Labor Day Weekend
We have finished week 5. I am so excited that the end is near. Earl is doing great. He is so determined that he is pushing himself really hard. He is eating soup now and that is a big deal since he hasn't eaten food in over two weeks. He is still doing the feedings for extra calories and nutrition but he is really determined to get the PEG tube out ASAP. As you know the last chemo treatment keeps getting pushed back. I have just accepted that and we will get it done when he can handle it. It is the last one so no big deal. I want him to be as strong as possible anyway before he gets it. I can tell his energy level is improving everyday. He hardly takes any pain medicine, maybe only once or twice a day. His voice has completely come back, so that is good. Except for the weight loss, he looks great. So we have a long weekend, as no treatment on Monday. Olivia went to Alabama with her Dad, so we will be home alone. We will just enjoy each other's company and get him rested up for the last chemo. Oh yeah, and I will probably have to cut grass. I guess you're suppose to cook out on Labor Day, but since we can't grill soup, I guess we will have to skip that. I am so excited about the upcoming fall and holidays. I am anxiously waiting our new life. Thank you all for keeping up with our story. Love you bunches. Donna
Wednesday, September 2, 2009
Quiet Day at Home
Okay so here we are, a quiet day at home instead of getting our chemo. Yeah, that's right, postponed, AGAIN. We got up this morning at 5am, to be at MUSC by 7:30am. Went to the Lab and they said his count was not quite there. I had a small melt down in the office. This is the third time they have postponed it. No ones fault but it is frustrating. So we had the radiation treatment as scheduled and came home. We both took naps. That felt good. So we will try again on Wednesday. It is our last one so I am just ready to mark it off the list. Only 13 more radiation treatments now. Talked to the radiologist today, she said Earl is doing fantastic. She was very excited. Says she sees a lot of people getting the same treatment as him and he is doing so good. That made me feel better. I came home and opened all the windows, it feels so good outside. Back to work tomorrow. Love you all. Donna
Tuesday, September 1, 2009
Dancing in the Rain
I got an email from Sunny today and one of the quotes that I really like and thought I would share with you said, "Don't wait for the storm to pass, learn to dance in the rain. I really feel like we have been doing that. Even though we are in the middle of a storm we find time to "dance" everyday. Our chemo was postponed again yesterday to Wednesday.(white cell count still too low) It is a definite go tomorrow and it is our last! He is doing quite well today. His mouth is a little sore but other than that he feels pretty good. His weight is down to 169 lbs, so he has lost 11 lbs so far. My goal is to maintain it at that number but the last three weeks will be the hardest. Please pray that this last chemo doesn't hit him too hard. I am trying to encourage him to do as many feedings a day as he can. He really needs about 2500 calories to stay nourished and hydrated but he is actually only getting about 1500 and that's why he is losing weight everyday. He is not eating any food by mouth and only drinks a small amount so thank God we had the PEG tube put in before we started. He has completed 21 rad treatments so that means only 14 left. I was so glad to turn the calender to September today! We are in our finish month. Love you all! Donna
Friday, August 28, 2009
Thank God it's Friday!
Thursday, August 27, 2009
Light at the end of the tunnel
Tuesday, August 25, 2009
Storms a comin
Well we did not have chemo yesterday as scheduled. Earl's white cell count was too low. They postponed it for next week. However, we did get some good news, he will not need the third chemo so next Monday will be his last chemo. We are in week four of the radiation. He has completed 16 radiation treatments and has 19 left. So we are almost halfway there. He is declining somewhat, and I am trying to prepare myself for the worst. He is hoarse now and can barely talk. He is still eating pretty good and drinking good. He is just tired. He is starting to lose some of his hair, not from the chemo but from the radiation. I think I will have our hair dresser come to the house and give him a good hair cut so it doesn't annoy him. Olivia has a cold and had to take her to the DR yesterday, now I have to keep her away from Earl so he doesn't catch it. Wow, I am tired. On another note, Drew is all moved out and started college yesterday. His apartment is on St. Phillips St and he is on cloud nine. I miss him so much. All ya'll with little ones, enjoy them, they leave too soon. Thanks for your prayers, they really are working! Love you all, Donna
Tuesday, August 18, 2009
Week Three
Today is a good day! Earl had a good checkup yesterday with his chemo DR and today met with Dr. Harper (rad DR) and she said she was VERY pleased at how well the tumor is shrinking. He is having a minor sore throat but still eating and drinking pretty good. We are in our third week of radiation. By Friday we will only have four weeks left. Whew~ We had a fantastic weekend. Earl actually played golf Saturday with his friend Jeff, and shot even par. He was worn out by the evening but he was so happy. Olivia had her 13th birthday party with 10 of her closest friends and her cuz Madison. It was a nice evening. Earl's brothers and his sis-in- law, Sunny came up Sunday for a visit, we had lunch together and just spent the day visiting. Ain't nothin like family. School starts tomorrow for Olivia, it will be her last year at Summerville Catholic, she has been there 10 years (since K-4) I remember her first day she was crying and I couldn't get her out the car. Time flies! Drew starts college next week. He is looking for an apartment, I can't even talk about it without tearing up. I wish I could keep him around the house a little longer. Mom's never wanna let go. Anyway, Thank you for your prayers, they are working! Earl is doing so well and I am so thankful. Love you all! Donna
Thursday, August 13, 2009
One Day at a Time
Sunday, August 9, 2009
Sunday Update
It's been a long weekend. Earl is mostly tired and sleeps a lot, either in the chair or in the bed. He has not been sick, but has no appetite. The smell of everything makes him feel sick. He can't taste anything and has not eaten much over the weekend. It is so frustrating for me cause I just can't to anything to help. He barely slept at all Friday night. Saturday night was much better and he did sleep through the night. He is still very weak and tired oday. He is able to drink his ensure and gatorade and that's about all. He did eat some potato soup from ABC yesterday. I had to eat my lunch on the porch because the smell made him sick. I feel so helpless. When you hear someone going through chemo you really don't know how hard it is for them. Let me tell you IT IS HARD. I just keep telling myself that the tumor is shrinking and that he is getting better. This is just the beginning and the road is long. Six more weeks and he will be done with treatment. I love him so much, I just wish I could make it all better. Thank you for your prayers. Love you all. Donna
Friday, August 7, 2009
One week down
We have officially completed one week of treatment. Six to go. No sweat, yeah right. Earl is OK. Tired mostly. He had a headache yesterday and we determined it is from dehydration. Radiation dehydrates you really bad so he has to drink a lot of non-caffine drinks. We are looking forward to a weekend of no treatment. His next chemo is on the 24th. He will not have the energy to play in that golf tournament this weekend but that's okay. He needs to rest anyway. I was cutting grass last night and a man rode by on his motorcycle and it made me miss that so much. I can't wait til we can ride again. It's amazing how much you miss the simple things. If anyone wants to send him a card I know it would make his day. Our mailing address is 350 Prestwick Court, Summerville, SC 29483. Hope you all have a terrific weekend. Love you all. Donna
Wednesday, August 5, 2009
A little GOOD News
Hey Ya'll,
Today was day three of Radiation! Earl is feeling OK. Not good, but not bad. Well, that's okay. He's not suppose to feel good but I'll take "not bad". He went in for his radiation today and the Doc said that his tumor was responding very well and that it has already started shrinking. Yeah! He has done very well this first week. He is taking a lot of anti nausea medicine and it is working. He has been able to eat even though he says everything tastes like cardboard. Hopefully by Friday he will start to feel better and maybe he can even play in the golf tournament Saturday. I'm gonna caddy for him. Okay, here's a little something I found funny, Monday night after we finally got to sleep, Earl got a BAD case of the hiccups. Then had them almost all day Tuesday. Tuesday afternoon he called his chemo DR and he said it is a side effect that only a few people get. They actually had medicine for him for the hiccups. The medicine has helped but as soon as it starts to wear off, he starts to hiccup. God has a sense of humor. So no matter how bad things are there is always something a little funny to laugh about. Thanks for the prayers. Love you all, Donna
Tuesday, August 4, 2009
First Day of Treatment
Well all I can say about yesterday is we survived it all and today is a new day! We arrived at MUSC Hollings Cancer center on time and a little anxious. We were suppose to start treatment at 10am. We actually started at 12:30pm. Everything was a mess, no one knew why we were there and they kept sending us to different departments. Finally, the DR got it all worked out and we finished our first Chemo at about 4pm, then headed over to East Cooper to get radiation. That only took about 15 minutes. Earl did so good! He is my hero. I am so proud of him. He got a little flushed once but I think that was because he was hungry. We went to On the Boarder after Radiation and he ate very well. He has a lot of anti nausea medicine so the DR said only about 5% of patients get sick. I hope we aren't part of that 5%. So we came home, took showers, and tried to unwind. Got in the bed about 10pm, then Drew called at 11:30pm. He had ran off the road trying to answer his cell phone and hit a stop sign, some bushes and a ditch. Car had to be towed, but Drew is okay. Earl and I got to spend two hours on the road waiting for the police report and tow truck to come. So we finally got to bed at 2am. WHAT A DAY! Anyway, both of my men are fine today and I still feel so blessed. Here's a little note to all you-DO NOT ANSWER YOUR PHONE OR TEXT WHILE YOU ARE DRIVING. Love you all! Donna
Thursday, July 30, 2009
TGIF
Tomorrow is feeding tube day. We have to be at MUSC at 10:30am to have the feeding tube inserted. Short notice I know, but anyway it really did need to be done before we start treatment. It is only a 25 minute procedure but he has to spend the night just to make sure all is well. We also have to attend a class to learn how to care for it. We probably won't have to start using it for about four weeks. At least it will be there when we need it. I am feeling melancholy today, not really sure why, maybe because it's all getting so real now. I just wanna cry but see can't because I have to be strong for Earl. We probably won't go back until about 1pm. I will text ya'll when all is done. Deb, thanks for the card today. You always make me feel good. Love you all so much. Donna
Wednesday, July 29, 2009
May the Force Be with us!
Hey Everyone! We had a good day at our pre-run! I got to go in and see Earl with his mask on bolted down to the table. It kind of freaked me out but he was totally fine. We were able to see his CT Scan of his entire head and exactly where the tumor was. It has grown some since it was first discovered but that is normal. Dr. Harper called it an aggressive tumor but felt confident it would be eradicated and he will be cured. We feel good about his prognosis and I know we are surrounded by a great team of medical Doctors. So Monday, he will have chemo at the Hollings Cancer Center downtown which will take about five hours. We have to be there at nine am, which some of you know is probably a bigger challenge for Earl than the chemo. (He is not a morning person). The chemo treatment (cisplatin) will take about five hours(IV) and then we will head East of the Cooper to the Medical Center there for the Radiation which is only a ten minute appointment. Earl will be completely exhausted by the end of the day, I am sure. Then he will have radiation five days a week for seven weeks, with only two more Chemo treatments. Oh, yeah-we found a good little restaurant in Mt. Pleasant that will probably become his lunch spot, it's called Charleston's Cafe, so if you're over there, check it out. It's really good. I had the Fried Green Tomato & Pimento Cheese Sandwich. Good Lowcountry Eating. Well that's about it, we are gonna enjoy our weekend and just relax before life gets hectic. Earl has a great attitude and is very upbeat and positive about the whole thing. That is 2/3 the battle. Still no word on when we get the PEG tube in, I guess they'll call soon enough.
Thanks for checking up on us, Peace be with you! Donna & Earl
Tuesday, July 28, 2009
This is it!
check this out: csn.cancer.org
Thursday, July 23, 2009
Ready, Set, Go-almost!
Tuesday, July 21, 2009
Live.Love.Laugh
Monday, July 20, 2009
Boone Hall Plantation
Tuesday, July 14, 2009
Summer in July
We had a fabulous weekend doing nothing special but enjoying the great weather and a relative pain free weekend. Earl and I did yard work Friday night unitl about 8:30pm, trimming bushes and putting out pinestraw and cutting grass. It was such a nice evening and the yard looks so good. Then we had a little pizza and beer and chilled in the hot tub for about an hour. (Actually I had the beer.) Earl played golf Saturday and Sunday and played pretty good. I hung out at the pool with my mom and sister on Saturday afternoon. He has lost most of his stitches and can pretty much eat anything. Most of the swelling and bruising is all but gone and he is feeling pretty good. We went out on the motorcycle Saturday night and met up with his friends Lane & Joyce at the Dog & Duck. We grilled out burgers Sunday and my mom came over and ate with us. Drew was actually home for a change and ate dinner with us too. That's always a treat for me since I hardly ever see him. Olivia fed most of her burger to Cody ( the poodle). He doesn't mind. Monday-Back to work!!! He has his appointment today to get fitted for the mask and hopefully they will be able to get it done so we can get the treatment going. We are so ready to get it all going. The waiting really is the hardest part. I am guessing that if they scan for the mask today then treatment should start by August 1 or maybe sooner. In case you were wondering he will wear a mask during the radiation treatment to protect his head so they only radiate the part where the tumor is. The mask kind of looks like those masks people wear who sword fight (fencing). It's sci-fi looking but none the less necessary. I hope all of you are doing well. Thank you for keeping us in your prayers, may God Bless you with good health! Love, Donna