It seems like it has been forever that I have updated the blog. As most of you know, we will not be going back to Houston for treatments. My mom always told me I should never hate anyone or anything, but folks I have to say, "I HATE CANCER"! It has been so hard seeing Michael in pain again. The pain has been as bad or worse than it was when we first went to Houston. I feel so inadequate as a mother when he is in such pain.......I just pray that God give him painless days ahead. We have started with Hospice at home to help in controlling the pain. They are such wonderful folks. Had them with my mom and now with Michael. Michael is pain free due to the excellent medical expertise of Hospice.
When we were given the results of the last PET Scan, Michael decided he was very tired of being sick from chemo and he made the decision with the help of Dr. Mankins, our pastor Andy Graham, and Dr. Ravi that he just wanted to be pain free from here on. We were told that we did not need to wait until January to take the cruise we had booked, so I got busy and had the cruise rescheduled and we took it last week. We went to Jamaica, Grand Cayman Islands, and Cozumel. Our original cruise was to stop in Cozumel and Progresso. Michael and I had some wonderful time together. Thanks to Joe, Almyra, Heavenly and Jose for going along to help me. We really enjoyed the time on the ship, but needless to say Michael and I were ready to get back on Olney soil. When you don't feel well, there is no place like home. Michael was in a lot of pain during the cruise, but was able to enjoy the trip.
If you would like to stop by the house and visit him, please feel free to do so. He is having several visitors daily and loves every one who stops by. The only thing we ask is if you have a cold, please wait until it is over. We do have some hand cleaner on the end table by the door and don't mind you using it.
He is sleeping a lot, but wake him up if you find him asleep. He doesn't want to miss you.
Continue to remember him in your thoughts and prayers. He is one tough boot and plans to take another cruise in a few years.
God Bless everyone for all your have done for the Wippermans.....Love to all
Merry Christmas
Terri and Michael
Thursday, November 4, 2010
Michael has had a pretty good week other than being tired all the time. He has been eating some and his blood counts were down some on Monday when blood work was done.
We did journey to Houston on Tuesday, October 27, had a PET Scan on Wednesday morning, and saw our Doctor on Thursday afternoon. It was so late when we saw the doctor, we decided to go ahead and spend the night and head home on Friday morning. Went by the Blue Bell Plant for the second time and found that tours were cancelled for that day. What a bummer..........next time before we drive to Brenham we will call to see if they are having tours or not.
We arrived home about 6:00pm and wasn't too long before we hit the hay. We had stopped about every 50 miles for Michael to get out and stretch his legs but he still was hurting pretty bad.
We have started the pain patches again. We are waiting to see what Dr. Ravi recommends for us to do now as we know the cancer is growing in the pelvis again. It is 66 days until we sail and are praying that Michael will be able to make the cruise.
Keep the prayers going......
We did journey to Houston on Tuesday, October 27, had a PET Scan on Wednesday morning, and saw our Doctor on Thursday afternoon. It was so late when we saw the doctor, we decided to go ahead and spend the night and head home on Friday morning. Went by the Blue Bell Plant for the second time and found that tours were cancelled for that day. What a bummer..........next time before we drive to Brenham we will call to see if they are having tours or not.
We arrived home about 6:00pm and wasn't too long before we hit the hay. We had stopped about every 50 miles for Michael to get out and stretch his legs but he still was hurting pretty bad.
We have started the pain patches again. We are waiting to see what Dr. Ravi recommends for us to do now as we know the cancer is growing in the pelvis again. It is 66 days until we sail and are praying that Michael will be able to make the cruise.
Keep the prayers going......
Wednesday, October 20, 2010
Thought I would give you an update on the happenings in the Wipperman household. We went to Houston last Wednesday, October 13, 2010 for a CT Scan on the 14th of October. Saw our favorite oncology team on Friday afternoon the 14th. The scan was actually better than Dr. Ravi anticipated since we had not had treatments for a period of time. The tumor is growing, but not at the rate suspected. Since Michael had been out of the hospital for only a month and had not improved very much, Dr. Ravi said he could not start the chemo again with Michael in the low state that he is. He wanted to do a PET Scan so that he could seek the advice of the radiation oncologist to see if the growth was in a location in the pelvic area where they could target with radiation since he was in no shape to start chemo again. They set us up for a PET Scan today. We were going back to Houston this morning for a scan this afternoon, but was called yesterday and told that Blue Cross Blue Shield would not approve the PET Scan and needed more information from Dr. Ravi before making a decision. So, they had put the Scan on schedule for Friday morning. Received another call from the Sarcoma dept. finance office this afternoon and said that Dr. Ravi had talked with BCBS of TX and they needed more information on Michael's cancer and past treatment in order to make a decision. So it's back to the drawing board again ......waiting for a high school drop out probably sitting behind a desk trying to make a decision as to whether my son needed a PET Scan or not in order to treat him. Right now I am on pins and needles waiting for a decision to be made by someone who probably doesn't know what Ewings Sarcoma Cancer is and how aggressive it is. If I were a betting person, I bet they would feel the same way I do if it were their son or daughter.
Michael has no stamina whatsoever. The least little bit of activity wears him out. He went with Andy this afternoon to one of his leases and he has been in the recliner ever since. We are looking to go back to Houston in the near future....they tell us it possibly could be a month before we hear anything from BCBS regarding the approval of the PET Scan.
'
I am sorry you have to listen to me vent....but I am very down tonight regarding the scan..........Looking for a better day tomorrow.
Michael has no stamina whatsoever. The least little bit of activity wears him out. He went with Andy this afternoon to one of his leases and he has been in the recliner ever since. We are looking to go back to Houston in the near future....they tell us it possibly could be a month before we hear anything from BCBS regarding the approval of the PET Scan.
'
I am sorry you have to listen to me vent....but I am very down tonight regarding the scan..........Looking for a better day tomorrow.
Wednesday, September 29, 2010
Just a short update about the Wolfman. He is feeling better each day and his counts are coming up each day. We are having blood work done twice a week to keep tabs on the platelets, hemoglobin, potassium, and magnesium. The swelling in his feet has left giving him some much needed relief when he walks. He still doesn't have much of an appetite.....he has gone from 248 lbs on September 13th to 203 lbs on September 28th.....so you can imagine how swollen he looked. His kidneys are working great and his creatinine count is 2.9 as of yesterday. The doctors told us it probably would not get under 3.5 any more, but we have witnessed another miracle. I am so fortunate to have a son with such a wonderful attitude regarding his illness. There are days it is hard for me to realize my son has cancer, but then there are days that I could crash. But with the support of the town of Olney, it is much easier to hold your head up.
Some of you may be unaware, but some of our friends in town have had t-shirts made for purchase to support Michael in his fight of this terrible disease. They say " 'Team Wipperman' with God all things are possible" on the front and on the left sleeve they have Michael's initials with a wolf. They can be purchased at the First National Bank here in Olney for $15.00 .....Dianna Kunkel is the contact there. The medical expense account has been activated once again to help with medical expenses to and from Houston. Small town living is wonderful and we are proud to call Olney HOME. The past 18 months have been rough, but with the help of our friends who are like family to us, have been made easier because we have not had to worry about financial expenses for meals, fuel, etc. This Friday beginning at 9:00am the town will be having a bake sale for Michael to help with Medical expenses at the First National Bank.
The food that has been brought to the house has been delicious. Michael has a standing order with the Hubbards for brisquet and sausage and Zola Mae Owens for mac and cheese. Thanks to everyone.....
Our hearts are overwhelmed with the outpouring of love from our friends and family. There are no words that can describe our heartfelt thanks for everything our friends have done. The monetary donations, prayers and calls are abundant.....and we can only say God Bless You and we love each and every one of you.
I was praying for a cure for Cancer, but now I am specific in praying for a cure of the cancer my son has residing his body.....Ewing Sarcoma. I think God wants us to be specific, so this is my prayer each hour of the day.
Some of you may be unaware, but some of our friends in town have had t-shirts made for purchase to support Michael in his fight of this terrible disease. They say " 'Team Wipperman' with God all things are possible" on the front and on the left sleeve they have Michael's initials with a wolf. They can be purchased at the First National Bank here in Olney for $15.00 .....Dianna Kunkel is the contact there. The medical expense account has been activated once again to help with medical expenses to and from Houston. Small town living is wonderful and we are proud to call Olney HOME. The past 18 months have been rough, but with the help of our friends who are like family to us, have been made easier because we have not had to worry about financial expenses for meals, fuel, etc. This Friday beginning at 9:00am the town will be having a bake sale for Michael to help with Medical expenses at the First National Bank.
The food that has been brought to the house has been delicious. Michael has a standing order with the Hubbards for brisquet and sausage and Zola Mae Owens for mac and cheese. Thanks to everyone.....
Our hearts are overwhelmed with the outpouring of love from our friends and family. There are no words that can describe our heartfelt thanks for everything our friends have done. The monetary donations, prayers and calls are abundant.....and we can only say God Bless You and we love each and every one of you.
I was praying for a cure for Cancer, but now I am specific in praying for a cure of the cancer my son has residing his body.....Ewing Sarcoma. I think God wants us to be specific, so this is my prayer each hour of the day.
SATURDAY, SEPTEMBER 11.2010
I wanted to write a note and tell everyone where we are in the roller coaster ride. First of all, we had the scopes done yesterday afternoon after a 4 hour dialysis procedure that morning. Things are looking up somewhat, and with God grace, we may get to come home next week sometime. I am physically and mentally exhausted and really thought I was hold up pretty good until today and have had a hard time trying to concentrate on anything I try to do.
We had a colonoscopy and and upper GI yesterday after receiving a bag of platelets. Our platelet count was 40 day before yesterday and 27 yesterday. After they transfused the platelets they immediately took him into the unit to do the scopes. He was really scared since he had been passing blood for the past 2 1/2 weeks. The doctors (3) who did the scopes are supper nice guys and really make Michael feel at ease. After they completed the scopes the head surgeon came out and told me that he had found the cause of the bleeding and it was very rare. I told him that didn't surprise me that my son was pretty rare as well. They found that he has Mallory Weiss Tear which is a tear in his esophagus from vomiting so much and so hard.
He was also diagnosed with Ischemic colitiS. I have added what these two conditions entail as it is very difficult to make sense in my own words what they are. Long story short...they anticipate that time will correct both problems.
Ischemic colitis is a medical condition in which inflammation and injury of the large intestine result from inadequate blood supply. Although uncommon in the general population, ischemic colitis occurs with greater frequency in the elderly, and is the most common form of bowel ischemia.[1][2][3] Causes of the reduced blood flow can include changes in the systemic circulation (e.g. low blood pressure) or local factors such as constriction of blood vessels or a blood clot. In most cases, no specific cause can be identified.[4]Ischemic colitis is usually suspected on the basis of the clinical setting, physical examination, and laboratory test results; the diagnosis can be confirmed via endoscopy or by using sigmoid or endoscopic placement of a visible light spectroscopic catheter (see Diagnosis). Ischemic colitis can span a wide spectrum of severity; most patients are treated supportively and recover fully, while a minority with very severe ischemia may develop sepsis and become critically ill.[5]
Patients with mild to moderate ischemic colitis are usually treated with IV fluids, analgesia, and bowel rest (that is, no food or water by mouth) until the symptoms resolve. Those with severe ischemia who develop complications such as sepsis, intestinal gangrene, or bowel perforation may require more aggressive interventions such as surgery and intensive care. Most patients make a full recovery; occasionally, after severe ischemia, patients may develop long-term complications such as a stricture[6] or chronic colitis.[7]
We are still struggling with roller coaster blood counts. He is suffering quite a bit today from the neupogen shots he has been receiving daily for his low white blood count which is very important regarding his immune system. Once his white blood count starts going up, it will help with the red blood count and the amount of platelets. I did not realize how important one count was to the other counts, but when one is out of whack, everything is out of whack. His bones feel like he has the flu so they are injecting pain medication to keep him from suffering so much.
His kidneys are improving daily and hopefully we can have the catheter removed for the dialysis before we come home. His feet are swelled so bad the look as if they are going to burst. It is very hard for him to stand on them.
All the doctors have asked me if I really knew how sick my son was when he was airlifted to Houston and I told them I did. They cannot believe he is the same person they saw the first day he was here. God is good and we give him all the glory and honor for the turn around that Michael has made.
Keep on praying......
Terri
We had a colonoscopy and and upper GI yesterday after receiving a bag of platelets. Our platelet count was 40 day before yesterday and 27 yesterday. After they transfused the platelets they immediately took him into the unit to do the scopes. He was really scared since he had been passing blood for the past 2 1/2 weeks. The doctors (3) who did the scopes are supper nice guys and really make Michael feel at ease. After they completed the scopes the head surgeon came out and told me that he had found the cause of the bleeding and it was very rare. I told him that didn't surprise me that my son was pretty rare as well. They found that he has Mallory Weiss Tear which is a tear in his esophagus from vomiting so much and so hard.
He was also diagnosed with Ischemic colitiS. I have added what these two conditions entail as it is very difficult to make sense in my own words what they are. Long story short...they anticipate that time will correct both problems.
Ischemic colitis is a medical condition in which inflammation and injury of the large intestine result from inadequate blood supply. Although uncommon in the general population, ischemic colitis occurs with greater frequency in the elderly, and is the most common form of bowel ischemia.[1][2][3] Causes of the reduced blood flow can include changes in the systemic circulation (e.g. low blood pressure) or local factors such as constriction of blood vessels or a blood clot. In most cases, no specific cause can be identified.[4]Ischemic colitis is usually suspected on the basis of the clinical setting, physical examination, and laboratory test results; the diagnosis can be confirmed via endoscopy or by using sigmoid or endoscopic placement of a visible light spectroscopic catheter (see Diagnosis). Ischemic colitis can span a wide spectrum of severity; most patients are treated supportively and recover fully, while a minority with very severe ischemia may develop sepsis and become critically ill.[5]
Patients with mild to moderate ischemic colitis are usually treated with IV fluids, analgesia, and bowel rest (that is, no food or water by mouth) until the symptoms resolve. Those with severe ischemia who develop complications such as sepsis, intestinal gangrene, or bowel perforation may require more aggressive interventions such as surgery and intensive care. Most patients make a full recovery; occasionally, after severe ischemia, patients may develop long-term complications such as a stricture[6] or chronic colitis.[7]
We are still struggling with roller coaster blood counts. He is suffering quite a bit today from the neupogen shots he has been receiving daily for his low white blood count which is very important regarding his immune system. Once his white blood count starts going up, it will help with the red blood count and the amount of platelets. I did not realize how important one count was to the other counts, but when one is out of whack, everything is out of whack. His bones feel like he has the flu so they are injecting pain medication to keep him from suffering so much.
His kidneys are improving daily and hopefully we can have the catheter removed for the dialysis before we come home. His feet are swelled so bad the look as if they are going to burst. It is very hard for him to stand on them.
All the doctors have asked me if I really knew how sick my son was when he was airlifted to Houston and I told them I did. They cannot believe he is the same person they saw the first day he was here. God is good and we give him all the glory and honor for the turn around that Michael has made.
Keep on praying......
Terri
THURSDAY, SEPTEMBER 9,2010
Sorry I haven't posted anything on the blog in a few days. Things are beginning to look a little better from Houston we thought. We have slowly improved since we started dialysis, but things are still not really good. We were to have some scopes done this afternoon. He drank 1/2 gallon of the colon prep solution GoLYTELY last night and has not had anything to drink or eat since 10PM last night. We got up this morning and went to dialysis and came back thinking we were going to have the scopes done. Much to our surprise, the GI doctors came by and said that the platelets had bottomed out again and were not high enough to have the scopes done this afternoon. So guess what, another night of the wonderful drink "GoLYTELY" beginning at 6:00pm and nothing to drink or eat after that until after the scopes are completed tomorrow. Hopefully in the morning. This has been one more trip. I am so tired of this place. This little 12X14 room is beginning to get the best of me. I am looking forward to seeing my bed. We have been told that they may kick us out of here next week.....depending on what the counts do between now and then. We appreciate your continued prayers for Michael and I am looking forward to bringing my son home. When I left Wichita Falls on Monday after the ambulance crew left the hospital with him, I really had a doubt that I would ever talk to him again, but God is so good to him and we give Him all the glory and praise for this another miracle in Michael's life.
August 23, 2010 to September 1, 2010 Our Roller Coaster Ride
This has been one week that I wish I didn’t remember. On Monday, August 23, we began our second week of chemo in Wichita Falls. We were taking the IV chemo that we had taken several cycles before with the addition of an oral chemo called Temador. We thought Michael was tolerating it pretty well until we took diarrhea and vomiting on Monday, August 23, 2010. We were not feeling real well when we went to see our oncologist that morning and he authorized us to continue the chemo for the second week. Tuesday wasn’t too bad with the diarrhea and vomiting, but Tuesday evening things got pretty bad. Michael was sick all night Tuesday evening and was just a little scared and slept with me. We didn’t get but about 1 hour sleep that night. Talked about taking him to the emergency room in Olney that night, but decided we would be going to get chemo on Wednesday morning and we would make them aware of Michael’s sickness. The diarrhea got so bad, we had to stop at Target and buy clothes before we could go on to the cancer center.
Michael could not walk he was so week, so we wheeled him in to the center and he was immediately place in a bed. Counts were low on Monday, but extremely low Wednesday. When we saw the doctor he sent us directly to the hospital next door where Michael was admitted. They immediately started pumping his body with fluids to stop the diarrhea and vomiting, but had no success. By Thursday morning he was throwing up bile and his stool had some darkness to it. They called in a kidney doctor as his output was not good, and an infectious disease doctor. Ran some cultures on him, but was unable to determine any infection so they started him on a broad spectrum of antibiotics. Wednesday night he was given some phenergan IV injection and had an allergic reaction to it and he was so bad I didn’t know if he would make it or not. They called the doctor four times during the night because of his condition.
Saw our oncologist on Thursday and was told that another oncologist would see him on Friday, Saturday, and Sunday while he was away. Michael continued to lose ground through the weekend and on Sunday; the kidney doctor suggested we put him on dialysis as his kidney function was bad. At that point, I contacted Dr. Ravi, our oncologist at MD Anderson and he said to have one of the staff at the hospital in W.Falls get in touch with him immediately, which we did. They advised me we would have Michael transported to Houston on Monday which I agreed.
On Sunday afternoon, they transfused a unit of platelets to Michael and he had an allergic reaction to them and had whelps come up all over his body. His body was on fire and he was clawing like he had poison ivy. We finally got him calmed down and he slept most of the night due to so much Benadryl . This whole two weeks, he had not eaten solid food. He was getting weaker and weaker.
To make a long story short, he was transported by a medical airplane from Ok City and took him to Houston where his medical team met him at MD Anderson. He was placed in CCU where they observed him until Tuesday afternoon and they moved him to a private room. Had a pretty good afternoon on Tuesday and Tuesday night he started bleeding. They have give him numerous units of platelets and blood and the diarrhea has slowed down and the vomiting has stopped, but the kidney function is less than 10%. We will start dialysis on Thursday morning, and when his counts are high enough he will have some scopes done to see where the blood is originating. Hopefully when his platelets come up, the bleeding will stop.
God is so good and has performed another miracle in Michael’s life. Please continue to lift him up in prayer as we are going to get through this with God as our Great Physician.
Michael could not walk he was so week, so we wheeled him in to the center and he was immediately place in a bed. Counts were low on Monday, but extremely low Wednesday. When we saw the doctor he sent us directly to the hospital next door where Michael was admitted. They immediately started pumping his body with fluids to stop the diarrhea and vomiting, but had no success. By Thursday morning he was throwing up bile and his stool had some darkness to it. They called in a kidney doctor as his output was not good, and an infectious disease doctor. Ran some cultures on him, but was unable to determine any infection so they started him on a broad spectrum of antibiotics. Wednesday night he was given some phenergan IV injection and had an allergic reaction to it and he was so bad I didn’t know if he would make it or not. They called the doctor four times during the night because of his condition.
Saw our oncologist on Thursday and was told that another oncologist would see him on Friday, Saturday, and Sunday while he was away. Michael continued to lose ground through the weekend and on Sunday; the kidney doctor suggested we put him on dialysis as his kidney function was bad. At that point, I contacted Dr. Ravi, our oncologist at MD Anderson and he said to have one of the staff at the hospital in W.Falls get in touch with him immediately, which we did. They advised me we would have Michael transported to Houston on Monday which I agreed.
On Sunday afternoon, they transfused a unit of platelets to Michael and he had an allergic reaction to them and had whelps come up all over his body. His body was on fire and he was clawing like he had poison ivy. We finally got him calmed down and he slept most of the night due to so much Benadryl . This whole two weeks, he had not eaten solid food. He was getting weaker and weaker.
To make a long story short, he was transported by a medical airplane from Ok City and took him to Houston where his medical team met him at MD Anderson. He was placed in CCU where they observed him until Tuesday afternoon and they moved him to a private room. Had a pretty good afternoon on Tuesday and Tuesday night he started bleeding. They have give him numerous units of platelets and blood and the diarrhea has slowed down and the vomiting has stopped, but the kidney function is less than 10%. We will start dialysis on Thursday morning, and when his counts are high enough he will have some scopes done to see where the blood is originating. Hopefully when his platelets come up, the bleeding will stop.
God is so good and has performed another miracle in Michael’s life. Please continue to lift him up in prayer as we are going to get through this with God as our Great Physician.
Tuesday, August 17, 2010
We started our new round of chemo yesterday in Wichita Falls at the Texoma Cancer Center. Saw our Wichita Falls oncologist and then to chemo. Received word that the MRI taken last Thursday did not show any cancer in the knee. We are so thankful. Started the oral chemo of Temador and then through IV's we got the Ifosfamide, Irinotecan, and Vinicristine. The only new one is the Temador and we think maybe it is the one that is causing Michael's loss of appetite. Yesterday was a rough one, but think the sickness was from them having to try to hit a vein so many times before they actually got one that wouldn't leak. The iv chemo causes killing of the tissue around the place of leakage if it leaks, so we definitely have to be careful so that the iv doesn't leak.
We are so thankful that we found the new little activation of the sarcoma when we did as we can get a handle on it.
We will be making daily trips to Wichita Falls Monday through Friday of this week, next week and then will have a couple of weeks off before we start the next cycle. We are scheduled to go back for scans the end of September, but will probably have to reschedule since we are going to have two weeks off chemo instead of one as planned.
We are so thankful that we found the new little activation of the sarcoma when we did as we can get a handle on it.
We will be making daily trips to Wichita Falls Monday through Friday of this week, next week and then will have a couple of weeks off before we start the next cycle. We are scheduled to go back for scans the end of September, but will probably have to reschedule since we are going to have two weeks off chemo instead of one as planned.
Thursday, August 12, 2010
Well, the CT Scan was done this morning to see about the situation in Michael's right let. We had it done in Wichita Falls and they will mail it to Houston for Dr. Ravi and the radiologist there to read it. We are to begin round 1 of 2 of the new chemo on Monday if we get the oral chemo pills. So far they have not been ordered or shipped to us. I guess i am just an over anxious mom wanting to get the ball rolling to kill out this stuff.....I am working very hard in trying to swallow my pride for this weekend....Michael has asked to do several things and I am really not comfortable in doing some of them, but am trying to swallow my pride so that my son can do some things that other boys his age have done. Please pray that God will give me some peace and allow me to swallow my pride and let my son experience some things he wants to do.
I will tell you about it next week. It is a surprise for Michael so will have to wait until it has happened.
Terri
I will tell you about it next week. It is a surprise for Michael so will have to wait until it has happened.
Terri
Friday, August 6, 2010
We traveled to Houston on Wednesday, August 4, 2010 for scans. We were 300 miles from home and received a call from MDACC that BCBSTX would not approve the PET Scan that our oncologist had ordered. They would approve a CT Scan, but not the PET Scan......cheap insurance company! We had the CT Scan last night about 8:00pm and when Michael came out of the scan, he told me, "Mom I just feel like something is wrong." Don't know if he heard them talking about the scan or what,but he was definitely a little worried. We met with Dr. Ravi this morning and he advised that the scan showed some active sarcoma in the pelvis area again and we told him about the on and off pain Michael had experienced in his right knee area. He immediately went to schedule a MRI for that leg, but couldn't get one done until next Friday, August 13, 2010. So we got a x ray of the knee and he wrote orders for us to get it done in Wichita Falls next week and to start chemo again asap. So we faxed the orders to Dr. Reddy in Wichita Falls to start asap. We have been on the mountain top for the past 3 1/2 months, so God saw that we were a little less dependent on Him and thought we needed some discipline. We are continuing to trust in Him for another battle and know that He is in control.
Tuesday, July 20, 2010
Thought I had better take the time to post on the blog. We have had a very busy summer. It is very hard to do anything outdoors as the heat just nearly wipes Michael out. He has gone through a week or two with pain in his back, and we were really scared, but seems as though it is lessening daily so feel is is probably some sore muscles. The least little bit of pain will really get me worried. It is wonderful to get back into the swing of things. Life is so much better when things are pretty much normal if you can call it that.
We are so excited for Christmas and then January to get here as we have scheduled a Carribean cruise out of Galveston for the 8th of January. I will have some mixed emotions about the cruise and this is something that Marc and I talked about taking before he passed, but Michael is excited and the time will we wonderful as we make some memories. We will be traveling to Cozemel, Progresso and then back to Galveston. Michael is very interested in history so we thought a tour of the Ruins in Cozemel would be something he would enjoy.
We will be leaving next week to make our trip to Houston to visit Dr. Ravi and Nurse.
This week we plan to go to the Ranger game on Friday night with some friends from Olney and spend the night. Go Rangers!
It is so nice that God has blessed us with Michael's good report and he can enjoy some things. He has never been much of a person to want to do any sightseeing, but God has opened his eyes and he is now ready to enjoy what God has given us. It is sad that we have to go through what he has been through the past year to make us realize the beauty that God has laid before us.
Hope you all are having a wonderful summer and rested for another good year at school. We are ready for some cooler weather but then we would be wanting it to warm up. Have a blessed week.
We are so excited for Christmas and then January to get here as we have scheduled a Carribean cruise out of Galveston for the 8th of January. I will have some mixed emotions about the cruise and this is something that Marc and I talked about taking before he passed, but Michael is excited and the time will we wonderful as we make some memories. We will be traveling to Cozemel, Progresso and then back to Galveston. Michael is very interested in history so we thought a tour of the Ruins in Cozemel would be something he would enjoy.
We will be leaving next week to make our trip to Houston to visit Dr. Ravi and Nurse.
This week we plan to go to the Ranger game on Friday night with some friends from Olney and spend the night. Go Rangers!
It is so nice that God has blessed us with Michael's good report and he can enjoy some things. He has never been much of a person to want to do any sightseeing, but God has opened his eyes and he is now ready to enjoy what God has given us. It is sad that we have to go through what he has been through the past year to make us realize the beauty that God has laid before us.
Hope you all are having a wonderful summer and rested for another good year at school. We are ready for some cooler weather but then we would be wanting it to warm up. Have a blessed week.
Thursday, June 10, 2010
Well, it seems like it has been months since I last updated this blog. My mom always said, "No news is good news", so guess that is what I have been trying to say with no posts. Michael is doing well. The heat nearly wipes him out, but he is doing well otherwise. He worked every day week before last, and had some set backs from that, but he is improving. I have never seen a boy his age want to work sooooooooo bad, but hopefully he has realized he just isn't up to it right now, especially in the heat. We have another appt in Houston on July 30, 2010 for an appointment with our Primary Doctor and hopefully will get a good report again. It is hard to realize that he has been through so much and look as healthy as he does. He is still a very sick young man with no stamina for very long; but, we are improving daily. We covet your prayers daily as we still have a very long road ahead of us.
Love you all,
Terri and Michael
Love you all,
Terri and Michael
Friday, April 29, 2010 from MD Anderson Cancer Center
News we have been ready to hear for one year. ..............NO MORE CHEMO AND NO MORE LOVENOX SHOTS FOR THE BLOOD CLOT! Our God is AWESOME!
WOW! From Day 1 until now I wondered if we would ever hear the words we heard today. Dr. Ravi said from the start, that the cancer has progressed further than he would like for it to, but ......we will try and if he responds well to the chemo we might have a chance.......I have said all along that God is on our side and that He is still in control of our situation. It has been a hard year but He never puts more on us than we can handle......but I have to tell you there have been some days I didn't think we could do it anymore. Some days, more than I like to think about, I didn't know if I could make the right decision or not. But, we have an awesome team who treats Michael and there has never been a moment that I didn't respect their treatment plans. They are like family........Dr Ravi's assistant came out after we left the examining room today and said this was her last day at the center in Houston. She and I both cried as she has been a light to a dark situation ever since we met her. She is definitely called of God in the position she is in.
WOW! From Day 1 until now I wondered if we would ever hear the words we heard today. Dr. Ravi said from the start, that the cancer has progressed further than he would like for it to, but ......we will try and if he responds well to the chemo we might have a chance.......I have said all along that God is on our side and that He is still in control of our situation. It has been a hard year but He never puts more on us than we can handle......but I have to tell you there have been some days I didn't think we could do it anymore. Some days, more than I like to think about, I didn't know if I could make the right decision or not. But, we have an awesome team who treats Michael and there has never been a moment that I didn't respect their treatment plans. They are like family........Dr Ravi's assistant came out after we left the examining room today and said this was her last day at the center in Houston. She and I both cried as she has been a light to a dark situation ever since we met her. She is definitely called of God in the position she is in.
Thursday, April 22, 2010
Well, guess I need to be a little more consistent with my updates than I have been the past three months. It is sooooo nice to be home and enjoying the time we have there. We are completing our 17th or 18th round of chemo tomorrow. Next week we will be journeying to Houston on Wednesday, Scans on Thursday and Results on Friday. We are looking forward to some good news from Dr. Ravi regarding our chemo treatments......keeping our fingers crossed that we can stop for a while. The Cancer Center in Wichita Falls has been super in taking care of Michael the past few months. We have really learned to love those people and their interest in my hero. Dr. Reddy is a good oncologist and we really like him. We will keep you posted about the scans and results next week.
Thursday-April 8, 2010 from Olney
Well, one more day til the weekend. Looking so forward to tomorrow evening when we will be going to the Relay for Life in Archer City. The Hubbard Team will be walking for Michael along with some others. We are still selling chances for the Cross Made by Paula Kunkel at $1.00 each or 6/$5.00. The cross is beautiful......sure would like to win it myself....as I love crosses. Michael has looked forward to this for some time and wants to walk.
We have had a pretty good two weeks since the last chemo cycle. Will start another cycle on Monday, April 12, 2010. Hopefully we will get a little time off after this cycle. Have a trip planned to Houston on Wednesday, April 28, scans on April 29, and consultation with Dr. Ravi on Friday, April 30. Looking for another GREAT report. Michael is so ready to go back to work on a regular basis. He has tried several days but give out pretty easily. I think when the chemo is over, he will be more able to withstand the standing. I just wish we had more people who want to work as bad as he does. His daddy would be very proud of him and I am thankful to call him SON. He has blessed my life so much before all this and especially in the past year.
We have had a pretty good two weeks since the last chemo cycle. Will start another cycle on Monday, April 12, 2010. Hopefully we will get a little time off after this cycle. Have a trip planned to Houston on Wednesday, April 28, scans on April 29, and consultation with Dr. Ravi on Friday, April 30. Looking for another GREAT report. Michael is so ready to go back to work on a regular basis. He has tried several days but give out pretty easily. I think when the chemo is over, he will be more able to withstand the standing. I just wish we had more people who want to work as bad as he does. His daddy would be very proud of him and I am thankful to call him SON. He has blessed my life so much before all this and especially in the past year.
Saturday, March 27, 2009-Olney, TX
My oh my, where has the past year gone? Seems like only yesterday that I thought my world was coming to an end. Most devastating news that any mother has ever heard, "I'm sorry Mrs. Wipperman, but your son has a malignant football size tumor in his pelvic area and it has spread to his lungs and it is a very rare form of cancer. . . .Ewing's Sarcoma and only three hospitals in the US specialize in treating it ! Where would you like to go? " MD Anderson in Houston, Mayo Clinic, or some other hospital and I don't remember where it was. Even through the worst storm of our life, God is still in control. He arranged for us to have an appointment in Houston within 2 weeks, and treatment so successful that only He could have done it. Excrutiating pain went away the second day of the first round of chemo, pain patches x 2 were removed that day and no pain since other than side effects from injections. A place to sleep and feel welcome for the past year. My brother-in-law and Michael's Uncle, and his family have been so wonderful to us, it is hard to put into words our thanks for all they have done. Thanks also to Lydia for her unselfishness of going with us to appointments the first week until we got familiar with the area.
We have had some up and downs during the past year with the aggressive treatment that Michael has had to endure, but God has got him through it with very little side effectss. We have laughed, we have cried many times, we have been irritable at times, and we have thought we couldn't do it ONE more minute. Times when I laughed about my stalker were funny to me, but not very funny to Michael. There have been times I just didn't think I could make a particular decision on my on, but with the help of friends who would hear me out and then encourage me to do what I thought was best, it made it easier. I finally realized in the early stages of our roller coaster ride that God was always with me and I really felt the presence of Marc with me. Just wish I had had him with me physically, because I sure could have used some embraces and someone to wipe the tears from my eyes. Michael and I would like to thank our Pastor, Andy Graham, for being there for us 24/7 and checking on us every day while we were away from home.
We are beginning the second year of our battle. The enemy is always in the back of our minds, but we are ready and willing to face whatever he has to put forth. We have the Great Physician on our side and no one can win but us since He is on our team.
We will be attending the Relay for Life in Archer City this April 8 and 9. The Hubbard team will be walking in Honor of Michael as a one year survivor and anyone who would like to buy a raffle ticket for a cross made by Paula Kunkel, please let me know or Janell Hubbard. I will try to get a photo of the Cross and put it on the blog so you can see what it looks like.
We thank you all for your continued prayers and thoughts as we embark on Year 2. God bless all of you.
MY SON IS A SURVIVOR!!!!!!!!!!!!
Love to all, Terri and Michael
We have had some up and downs during the past year with the aggressive treatment that Michael has had to endure, but God has got him through it with very little side effectss. We have laughed, we have cried many times, we have been irritable at times, and we have thought we couldn't do it ONE more minute. Times when I laughed about my stalker were funny to me, but not very funny to Michael. There have been times I just didn't think I could make a particular decision on my on, but with the help of friends who would hear me out and then encourage me to do what I thought was best, it made it easier. I finally realized in the early stages of our roller coaster ride that God was always with me and I really felt the presence of Marc with me. Just wish I had had him with me physically, because I sure could have used some embraces and someone to wipe the tears from my eyes. Michael and I would like to thank our Pastor, Andy Graham, for being there for us 24/7 and checking on us every day while we were away from home.
We are beginning the second year of our battle. The enemy is always in the back of our minds, but we are ready and willing to face whatever he has to put forth. We have the Great Physician on our side and no one can win but us since He is on our team.
We will be attending the Relay for Life in Archer City this April 8 and 9. The Hubbard team will be walking in Honor of Michael as a one year survivor and anyone who would like to buy a raffle ticket for a cross made by Paula Kunkel, please let me know or Janell Hubbard. I will try to get a photo of the Cross and put it on the blog so you can see what it looks like.
We thank you all for your continued prayers and thoughts as we embark on Year 2. God bless all of you.
MY SON IS A SURVIVOR!!!!!!!!!!!!
Love to all, Terri and Michael
Tuesday, March 16, 2010
Happy rainy Tuesday to everyone. Looks like God isn't finished giving us some rain. I really feel for the farmers and ones who have to drive in the mud. But God is good and we will take what He wants us to have.
We started our 16th round of chemo yesterday. Michael is wondering if this will ever end. . . . I keep telling him as long as the cancer isn't growing not to complain. It is hard for him to understand the continuation of chemo if the cancer is dead. His poor body is worn out from all the chemo and he wants to go to work and his counts are too low to be in public.
We will be getting the next two rounds of chemo in Wichita Falls and then back to Houston for scans and hopefully some time off from chemo. That is the plan right now. Continue to lift Michael up in your prayers......God is good.
We started our 16th round of chemo yesterday. Michael is wondering if this will ever end. . . . I keep telling him as long as the cancer isn't growing not to complain. It is hard for him to understand the continuation of chemo if the cancer is dead. His poor body is worn out from all the chemo and he wants to go to work and his counts are too low to be in public.
We will be getting the next two rounds of chemo in Wichita Falls and then back to Houston for scans and hopefully some time off from chemo. That is the plan right now. Continue to lift Michael up in your prayers......God is good.
Tuesday, March 2, 2010
Wow! What an awesome day! Thought we would be on our way home, but still in Houston. Will leave in the morning after we talk with Dr. Ravi's nurse. He wanted Michael to see a dermatologist, but the earliest we can get an appointment is Friday morning, so we will cancel that appointment and see a dermatologist in W. Falls this week or Monday of next. Can see the Oncologist who is treating Michael in W. Falls about the rash on his leg.
On to the more important business of the day. Had a PET Scan done yesterday, Dr. Ravi's remarks today regarding the scan was "AWESOME". That is the word we like to hear. We will have two more rounds of Chemo and then back to Houston and possibly get some much needed time off from Chemo.
We still think we have the best medical team that practices at MD Anderson Cancer Center in Houston, TX. You all are wonderful.
Thanks to all for your prayers and thoughts during the past year. I have a son who will be a one year survivor in less than a month. Praise God and we are anticipating many more years of survival with the Best of Sons. His scans are awesome because he is AWESOME and a true fighter.
On to the more important business of the day. Had a PET Scan done yesterday, Dr. Ravi's remarks today regarding the scan was "AWESOME". That is the word we like to hear. We will have two more rounds of Chemo and then back to Houston and possibly get some much needed time off from Chemo.
We still think we have the best medical team that practices at MD Anderson Cancer Center in Houston, TX. You all are wonderful.
Thanks to all for your prayers and thoughts during the past year. I have a son who will be a one year survivor in less than a month. Praise God and we are anticipating many more years of survival with the Best of Sons. His scans are awesome because he is AWESOME and a true fighter.
Saturday, January 23, 2010
Sorry I have been so lax in updating the blog. We have had a unusual two weeks. Put Michael back in the hospital yesterday because of low hemoglobin and potassium. They are giving him straight potassium through his CVC line as well as Potassium Chloride. He feels pretty good tonight and sent me home to rest. I slept in his bed at the hospital most of the afternoon ......was afraid they might not know who the patient was so didn't want to sleep too soundly. I am ready to "hit the hay" so I will write more later.
Thursday, February 11, 2010
Well, thought I had better let everyone know we are still alive. This week has been one of the worse since we started our cancer roller coaster....Michael had a real close encounter of serious illness this week but has rebounded like he always does and is feeling much better. He was completely dehydrated and had to be taken to the hospital by ambulance from between Archer City and Olney on Tuesday evening. Actually ate some solid food today without it coming up or down.......so he is better. We are to start another round of chemo next Monday...and then to Houston for scans.....Keep the prayers coming......thanks for everything everyone does and continues to do on his behalf.
Saturday, January 23, 2010
We traveled to Houston this past Wednesday, had scans on Thursday and saw our Oncologist on Friday at 1:00 pm and arrived in Olney at 10:15pm. We were truly blessed this week when we received the results of Michael's most recent P.E.T. Scan. From the radiology report......"Dominant features of the previously noted metastatic lesions in the lungs and primary tumor in the pelvis and soft tissues are stable with no metabolically active tumor at these sites and no change in these features compared to 11-19-09 Scan. Chest X-Ray ---No sign of metastatic disease." No new tumors and all old tumors are inactive........WOW this is awesome and never dreamed we would see this within a year of his being diagnosed. All Dr. Ravi could say was, "This boy is AWESOME!" We go back to Wichita Falls on Monday to start another round of chemo. So far there have been no side effects of the lesser dose of chemo......could deal with it if we had to since it is doing its job.....Thanks everyone for all your thoughts and prayers.....keep em up.....We love all of you.
Monday, January 11, 2010
Thought we had better let everyone know we are still breathing. Michael finished his 10th round of chemo last Friday, January 8. He really likes being able to do it and still be at home. We have been leaving around 1:00pm for our chemo appt at 2:00pm. We are off for a couple of weeks and have a conflict with the schedule in W Falls and the schedule in Houston....they are working this out....Not sure what is next on the agenda for us, but will post as soon as we find out. Michael has been a little under the weather the past weekend....don't know if it is from the chemo or has had a little touch of the virus that is going around.
Monday, January 11, 2010
Thought we had better let everyone know we are still breathing. Michael finished his 10th round of chemo last Friday, January
Monday, January 11, 2010
Thought we had better let everyone know we are still breathing. Michael finished his 10th round of chemo last Friday, January 8. He really likes being able to do it and still be at home.
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