Michael is eating and drinking. He still needs to eat more to gain weight. He went to visit church for a short time this morning. He is playing with Daddy and Mom. He wanted us to play with blocks so we built him a chair out of blocks. He is giving dad lovings and drinking his hot tea.
My grace is sufficient for you, for My strength is made perfect in weakness.
2 Corinthians 12 :9
When storms arise in our life, it is comforting to have those around us who are familiar and safe—a spouse, children, or close friends. But when we are alone and facing uncertainty, we must remind ourselves that God controls not only the wind and the waves created by nature, but those created by life as well. We are never truly alone and facing the elements by ourselves; God will always walk through the storm with us. Words of David Jeremiah, but so true. I don't know how often I have thought this myself.
Thanks for all the prayers,
Cathy
Sunday, August 30, 2009
Posted by michael dyer at 8:57 PM 0 comments
Friday, August 28, 2009
Michael is doing well today. Smiling and playing with his brother and sister. He even was acting like he was vacuuming the floor while Amy Mills was here helping out. She did a great job helping me clean the house. Thanks a lot Amy. The kids followed her around trying to help but really getting in the way. We all went to Taco bell and Michael decide he wants to walk around the restaurant and was playing with a couple other children there. We came home and it was time for naps and quite time for Makayla. Soon it will be time for them to get up and the noise and play will begin again. Dad is making it easy on me tonight and is bring dinner home. Thanks you daddy.
Don't miss the little blessing that are around you everyday. They are there! Just look or them. You might be surprised how many you have in just one day.
Keep the prayers coming and you will see a miracle before you soon. Keep spreading the word about Michael. We need the rest the Western USA to pray for Michael. We also need many other countires to pray for him.
Posted by michael dyer at 3:56 PM 0 comments
Thursday, August 27, 2009
Michael is back from the hospital and is doing well. His blood counts and immunity is doing good. Makayla and Tristan had a wonderful time with the Darlings. Thank you Barb and Steve for entertaining the children today they went to see the new kittens, then to the zoo and even had a picnic. They were talking about it for some time after getting back. Michael was excited to see his brother and sister when they came back.
I was reading something from David Jeremiah, "When storms arise in our life, it is comforting to have those around us who are familiar and safe—a spouse, children, or close friends. But when we are alone and facing uncertainty, we must remind ourselves that God controls not only the wind and the waves created by nature, but those created by life as well. We are never truly alone and facing the elements by ourselves; God will always walk through the storm with us.
During the uncertain and frightening storms of life, let us do as the Psalmist "…in the shadow of Your wings I will make my refuge, until these calamities have passed by""
(Psalm 57:1).
We must remember that God is truly the wind beneath our wings. That he is in control and that when we go through the storms in our lives he is teaching us special things.
What a blessing to see that Michael is back to his old self. We have to get him to eat a bit more food so he can gain weight.
God Bless,
Cathy
Posted by michael dyer at 6:16 PM 0 comments
Thankyou Barb and Steve
Thanks for taking Tristan and Makayla for the day.
God bless you both.
Michael continues to do well on this cycle of chemo
Russ
-- Post From My iPhone
Posted by michael dyer at 6:16 PM 0 comments
Wednesday, August 26, 2009
Michael, Tristan and Makayla are all playing together in the living room. They made a tent in the middle of the floor. They try and make it different every time. They seem to be having fun. Michael is playing with the toys while the other two play hide and seek from him in the tent.
We are trying to get Michael to gain some weight again. Since this chemo is not as hard on him, we hope he will gain a few pounds before starting the first type of chemo again in a couple of months. Michael will have one more round of Irinoteacan and Vincristine, then another scan to see the response from these two chemo treatments. We have had great results from the other chemo drugs (cisplatin, doxorubicin, 5-FU, and Vincristine), but they are highly toxic.
We will be off to the hospital again tomorrow for Vincristine. Makayla and Tristan are excited that Mrs. Darling will be coming to spend time with them.
Thank you everyone that gave food this week. It turned out that Russ and I were both sick. We hope that Michael does not get sick as well. We find out on Thursday if his immunity is still good or has dropped down. We are not sure what to expect since this chemo is not supposed to affect his bone marrow as much.
Thanks again for the prayers. We ask that you continue to keep praying, the prayers are working.
God bless you,
Cathy
Posted by michael dyer at 11:44 AM 0 comments
Wednesday Update
Michael is going strong and ready for another shot of chemo tomorrow.
Posted by michael dyer at 11:34 AM 0 comments
Monday, August 24, 2009
Back Home
Michael breezed through todays chemo.
Posted by michael dyer at 2:46 PM 0 comments
Morning update
Cathys taking Michael down this morning for another chemo infusion.
He is still doing great on this chemo round.
-- Post From My iPhone
Posted by michael dyer at 8:56 AM 0 comments
Saturday, August 22, 2009
Michael is back home
We are home.
Michaels progress is very good.
The scans show the cancer spots in his lungs to still be there but there is hugh reduction in size and numbers. Many are gone.
His liver tumor is less than half the size and about 1/4 to 1/5 the volume it was 2 cycles ago. This is fantastic. It is now the size of a super bouncy ball, before it was probably the size of a softball. The doctors said the MRI report shows signs that the tumor is dying.
Michael still needs even more prayers as he goes through his chemo and this cancer shrinks away. Michael goes in for outpatient chemo tomorrow, Monday and Thursday. After two cycles of this chemo he will have another MRI/CT.
Praise God, and thank you great medical staff.
I'll be at church tomorrow with Tristan and Makayla.
Russ
-- Post From My iPhone
Posted by michael dyer at 4:19 PM 0 comments
Friday, August 21, 2009
Michael did very well today. He slept most of the day and finally got active around 5:00pm. He seems to be tolerating this new chemo very well. At about 9:00pm we got a preliminary report that stated that he still has the cancer in the lungs and liver. The ones in the lungs look as tho they have gone down to 3mm in size, but have to wait for the doctor to confirm in the morning. The mass in the Liver also seem like the report is saying that it has reduced down about 30% more. That would mean his liver tumor has gone down 60% since May. From the report it seems to be saying that the tumor is dying, but we still have to have that confirmed by the doctors tomorrow. We will be talking to them about this tomorrow mid morning. We will update the blog tomorrow with more information. I am very tired and will brush mine and Michael's teeth and go to bed. Hopefully to not be awoken in the middle of the night. Thank you for all the prayers for Michael.
Good Night and God Bless. Keep the prayers coming!
Posted by michael dyer at 10:00 PM 0 comments
Back inroom
Michaels back in the room.
No rest results yet.
Getting more chemo and doing well. Probably begone tomorrow.
Russ
-- Post From My iPhone
Posted by michael dyer at 3:15 PM 0 comments
Recovery
Michaels in recovery after his MRI and CT.
-- Post From My iPhone
Posted by michael dyer at 2:03 PM 0 comments
MRI and ct in progress
Michaels gone infor his MRI and ct.
On aside note, the anesthetist is from New Zealand.
Mire later.
-- Post From My iPhone
Posted by michael dyer at 12:40 PM 0 comments
Update
Chemo going very well.
No issues and it looks like Michael will be discharged tomorrow to come home.
His scans are scheduled formidable day today.
His bless
Russ
-- Post From My iPhone
Posted by michael dyer at 11:16 AM 0 comments
Michael's blood pressure actually went down to 63 for the top number last night. So his blood pressure was checked a little more(2:00am, 3:00am, etc). Michael was not to happy with that. He would say awhee when it would squeeze his arm, his way of protesting. I woke him up at 5:30am so he would be able to eat something before his MRI/CT scans today. He then went back to sleep and is still sleeping this morning. He will go down and get ready for another hours sleep in just about one hour. They have to put him out for the MRI/CT because he can not move. The scans will be finished around 1:00pm and he will be able to start eating and drinking all he wants then. We should know something by tonight. So we will have a lot of calls to family and update our faithful friends on our blog with the news.
Keep PRAYING, the prayers are really working. Don't be a stranger, you can comment and let us know you are thinking of us or praying for us. You can even ask us questions. We love hearing from all of you.
Love and God Bless
Posted by michael dyer at 9:47 AM 0 comments
Thursday, August 20, 2009
Michael did very well so far with his new chemo. He has had a lot of energy and has played with Tristan and Makayla in the playroom at the hospital today. This is a first for Michael. He usually does not go in the playroom and if he does want to leave as soon as he enters the room. He then slept for only one hour and went up to listen to Bob play his guitar. He has been running around the floor pushing the button to open the doors and playing in the park section of the 7th floor. He was climbing up and playing in the fire truck there and was really enjoying himself. He did not want to go back to the room, but I think he is finally starting to slow down and get sleepy. Tomorrow is the big day. He gets his MRI and CT scan. Please PRAY for Michael tonight and tomorrow that God will heal him completely. Thanks everyone God Bless
Posted by michael dyer at 10:25 PM 0 comments
Chemo started
Michael started his new chemo at 5 pm.
-- Post From My iPhone
Posted by michael dyer at 6:19 PM 0 comments
unpacking
Room 76 , 7 th floor , Motts Childrens Hospital.
His blood tests were good so the chemo will start today.
God bless
Russ
-- Post From My iPhone
Posted by michael dyer at 1:36 PM 0 comments
At Motts
Michaels getting his blood test.
Next to the clinic for a consult and then check in.
They have the room ready already. Dont know number yet.
Posted from moBlog – mobile blogging tool for Windows Mobile
Posted by michael dyer at 10:52 AM 0 comments
on the way to hospital
We are driving in to the hospital for michaels blood test and then to check him in for the next rd of chemo.
I'll post the room number when we get checked in which will probably be this afternoon sometime.
Posted from moBlog – mobile blogging tool for Windows Mobile
Posted by michael dyer at 9:39 AM 0 comments
Wednesday, August 19, 2009
Wednesday Update
Michael was super happy last night. Even walking around by him self unassisted which he hasnt done for a while. Recently he had been very scared of falling and wanting to hold your hand when walking but last night he was having so much fun he began walking around by himself a bit.
Posted by michael dyer at 10:56 AM 0 comments
Tuesday, August 18, 2009
update - no changes today
Michaels doing well today. His Levels are all good and he is on zero meds apart from the Calcium until thursday.
Posted by michael dyer at 12:18 PM 0 comments
Monday, August 17, 2009
Morning Update
Hes had his blood tests so now we have to wait for the results to see if any meds are needed before thursday.
Posted by michael dyer at 11:32 AM 0 comments
Sunday, August 16, 2009
Michal is home and eating a snack
Michaels eating a little late night oatmeal snack.
He's got a little trip out tomorrow for blood tests but apart from that should be home till thursday when we check him into the hospital for more chemo.
friday is the big MRI / CT scan day so please pray that the scans show big improvements.
god bless
Russ
Posted by michael dyer at 8:22 PM 0 comments
Morning update
Michaels sleeping.
He will he at church for the main service this morning.
God bless
Russ
-- Post From My iPhone
Posted by michael dyer at 8:30 AM 0 comments
Saturday, August 15, 2009
Evening update
Michaels had a good day. Out and about with Cathy in the morning and relaxing at home this evening.
Enjoying the days at home.
Russ
-- Post From My iPhone
Posted by michael dyer at 6:36 PM 0 comments
Friday, August 14, 2009
Almost bed time
Michaels had a good day. Some walking and lots of talking.
No meds this weekend exceps calcium .
God bless
Russ
-- Post From My iPhone
Posted by michael dyer at 9:17 PM 0 comments
Michael is doing well today. He is playing on the couch and enjoying time with dad. He is eating better and still loves his English hot tea. He is smiling and playing a lot more. This morning he was playing with crayons. Putting them in the crayon bin and dumping them out. He would then play with Makayla and Tristan most of the morning. Tonight he is tickle daddy and sissy's feet. He slept pretty good last night. Michael is losing most of his eye lashes, but his still has his hair and eye brows. We don't know is the new chemo will make him lose his hair more. I guess we will see soon. Pray that Michael will do well with this new chemo., that it will not cause the severe diarrhea that can happen with the side effect. Also, pray that his Red, White and Platelets will call come back up well. Also, that his immune system will come up more.
Posted by michael dyer at 6:12 PM 0 comments
Thursday, August 13, 2009
Update
No chemotherapy today. Michael will get blood and then we are back home.
Michael will get a blood test on monday and then check in on Thursday next week for chemo , an MRI. and a CT scan.
Michael is also no longer needing infusions if electrolytes each day.
Have a nice day
Russ
-- Post From My iPhone
Posted by michael dyer at 11:51 AM 0 comments
Morning update
Still at Motts.
Here's a brief history of his AFP levels (cancer number)
05/01/09. 64244.4
05/09/09. 22992.1
05/15/09. 12801.9
05/22/09. 566.4
05/29/09. 610.6
06/04/09. 649.0
06/12/09. 97.1
07/06/09. 59.5
07/16/09. 20.7
08/13/09. 20.6
Normal level is 0.0 - 7.9
Pray we continue to progress to the good range
God bless
Russ
-- Post From My iPhone
Posted by michael dyer at 10:44 AM 0 comments
Wednesday, August 12, 2009
evening update
Michaels Sleeping.
Posted by michael dyer at 9:06 PM 0 comments
Morning Update
Michaels got an easy day today. At home resting for the trip to the hospital tomorrow.
Posted by michael dyer at 7:37 AM 0 comments
Tuesday, August 11, 2009
Morning Update
Michael was still sleeping as I left for work.
Posted by michael dyer at 7:18 AM 1 comments
Monday, August 10, 2009
Bloodtests done
Waiting for call with results.
Michael well today.
-- Post From My iPhone
Posted by michael dyer at 1:20 PM 0 comments
Sunday, August 9, 2009
Evening update
Michael had a good nap, finished a small dinner and is sitting on cathys lap playing with a toy.
He's had all his meds Also for today.
Blood tests tomorrow.
God bless
Russ
-- Post From My iPhone
Posted by michael dyer at 6:53 PM 0 comments
Morning update
Michael was a little restlass last night. We are at church and enjoying Yves sermon.
Michael is doing well today .
-- Post From My iPhone
Posted by michael dyer at 11:38 AM 0 comments
Saturday, August 8, 2009
Saturday update
Michaela aost done with his afternoon nap.
He's hooked up to his potasium and sodium phosphate drip which should go for another half hour.
He ate some chocolate pancake for breakfast and cheeto's and cookies for lunch along with his hot tea with milk and sugar.
Michaela doing well overall and was even crawling around on the floor last night playing with Tristan and Makayla, his brother and sister.
Have a good weekend all,
God bless
Russ
-- Post From My iPhone
Posted by michael dyer at 3:08 PM 0 comments
Friday, August 7, 2009
Morning Update
Michael slept soundly through the night.
Posted by michael dyer at 10:10 AM 0 comments
Thursday, August 6, 2009
Evening update
Michael is doing well. Still needs to eat a little more but is enjoying his time at home.
He is sleeping well at night and will be in bed shortly
God bless
Russ
-- Post From My iPhone
Posted by michael dyer at 9:53 PM 0 comments
Wednesday, August 5, 2009
Michael will not go to the hospital tomorrow
Well, Michael's platelets are not strong enough for him to start his new chemo. We had to let him have a one week break. Hopefully his platelets will recover before next Thursday. They have him planned to go in by 8:00am next week. This new chemo will be easier on his kidneys and bladder, but still gives nausea and diarrhea. Micheal seems to be enjoying toys,and playing the new game that Virginia gave the kids, and dancing with the little bunny Dorthy gave him. Keep praying that his Blood counts will recover and that he will get a better appetite. He has lost 2 1/2 pounds since we started.
Posted by michael dyer at 6:56 PM 0 comments
Tuesday, August 4, 2009
Evening update
Great evening for Michael.
Very happy, playful and talkative.
Blood test tomorrow then checking into hospital Thursday.
God bless
Russ
-- Post From My iPod Touch
Posted by michael dyer at 10:16 PM 0 comments
Morning update
Michael slept fairly well.
He has a couple more rest days before the new chemo.
Looks like he will get a MRI and CT scan this week also.
More later.
-- Post From My iPod Touch
Posted by michael dyer at 10:26 AM 0 comments
Monday, August 3, 2009
Update - sort of
Michaels down at Motts getting his infusion.
Cathy forgot her cellphone so I'm not sure how it's going. They should be home this afternoon.
-- Post From My iPod Touch
Posted by michael dyer at 1:05 PM 0 comments
Sunday, August 2, 2009
Evening
Michael very well today.
Low immunity sono church or outside travels.
Blood tests and infusion tomorrow at Motts childrens hospital.
I'll try to post a pic soon
Russ.
-- Post From My iPod Touch
Posted by michael dyer at 9:13 PM 0 comments
Saturday, August 1, 2009
Sad Good bye
Well the sad day has come and Grandma and Granddad Dyer are on their way back to New Zealand. Gramme and Granddad are on their way to Tennessee and we will need the help of friends once again. Virgina is coming to visit on Monday and stay with Tristan and Makayla while Michael is getting is Chemo treatment. Michael should be starting his new chemo on Thursday and will probably be in the hospital for 5 days at least. The doctors said that this chemo. treatment is not as bad as the previous. It should not affect his body has much.
If our children know you and you can help during the day, please let us know by emailing Russ or calling the house.
Please pray that Edith and Selwyn get back safely and that Edith surgery goes well. Pray that we have additional strength and energy to get through the day. We both will need it now more then ever.
Posted by michael dyer at 1:21 PM 0 comments