We joke around here about what the poor man substitutes for the more expensive things. I've used canned salmon to make Salmon Pesto Pasta (a delicious dish that Nona made for us a couple years ago). Nona uses salmon fillets and we do too, when we have them. But this particular evening, we didn't have a meal planned and Daddy was almost home. So, I cooked the pasta and dumped in salmon and pesto and served it. The only bad thing about it was that the salmon broke up into little pieces.
The other day, Katie was cooking and I taste-tested for her (we do it all the time around here). I was surprised because it tasted like mushrooms and I knew that we had used up the mushrooms in the fridge. Then Katie said that it was a eggplant tart with a potato crust. Now I guess the poor man has eggplant for his mushrooms!
Hannah
One Big Adventure
An opportunity to log in some of the thoughts and activities of our homeschooling family of eight. We love books and good food and aspire to a Christ-centered, multi-generational, agrarian life.
An opportunity to log in some of the thoughts and activities of our homeschooling family of eight. We love books and good food and aspire to a Christ-centered, multi-generational, agrarian life.
Wednesday, November 4, 2009
Tuesday, November 3, 2009
That little red hairbrush
Daddy has a little red hairbrush that he's had for as long as I remember. When Owen was a little boy, about 4 years old, he loved Daddy's hairbrush and would borrow it whenever he could. Finally Daddy and Momma got him a little red hairbrush of his own, so that Daddy could find his.The other day, James found Daddy's hairbrush and immediately attached himself to it. And then it disappeared. James hasn't been able to find it yet. I guess he hid it to keep us from finding it and taking it away and hid it too well. It seems that James might be getting old enough to get a little red hairbrush of his own. Maybe for his 5th birthday in December. My, how time does fly!
Hannah
Hannah
Labels:
daily life,
family traditions,
memories,
stories
Monday, November 2, 2009
Minor change in plans
After talking with Vern and the folks at the clinic, we have decided to just go to Atlanta and have counts done there. We'll just pop in, get James' finger pricked and be on our merry way. Doing it this way, we can be sure that everything is looked at by the right folks and all the results are in the right place so those that need them (the surgeon, in particular) can get to them.
So, on Thursday, we will be taking field trip. Not sure yet what all of our stops will be, but hopefully it will be a nice day.
The nurse called today from the Day Surgery unit about James' tests and procedures on Monday. We have to be at Day Surgery at 6 in the morning.
So, we have two prayer requests:
1. That James' counts would be excellent and everything would look great (and be great).
2. That we can get a room at the Ronald McDonald house near the hospital for Sunday night. We won't know for sure until Saturday morning if they will have a spot for us.
So, on Thursday, we will be taking field trip. Not sure yet what all of our stops will be, but hopefully it will be a nice day.
The nurse called today from the Day Surgery unit about James' tests and procedures on Monday. We have to be at Day Surgery at 6 in the morning.
So, we have two prayer requests:
1. That James' counts would be excellent and everything would look great (and be great).
2. That we can get a room at the Ronald McDonald house near the hospital for Sunday night. We won't know for sure until Saturday morning if they will have a spot for us.
Labels:
James update,
prayer requests
Saturday, October 24, 2009
969 days later
Edited: James' off treatment pictures weren't showing up for some reason. Hopefully it's fixed and y'all can see Mr. Handsome. If not please leave a comment and we'll try to figure out what's going on. Thanks, Hannah
On February 25th, 2007, Momma posted that for some reason, she had this feeling that we had several more big weeks ahead of us. And she was right. Though, none of us would have thought it would have turned out this way. Those several big weeks turned into 2 years and 8 months!
But yesterday, James took his very last chemotherapy pill at 7:10pm and is now officially OFF TREATMENT! In a way, I am so thrilled, for James, and me and our family. But it brings more unknowns... and unknowns are.... well, unknown. But not for God and that is full of comfort. Before we close the chapter on leukemia, I would like to share some pictures of James before, during and after treatment. GO JAMES!!!
***************************************************************************************
On February 25th, 2007, Momma posted that for some reason, she had this feeling that we had several more big weeks ahead of us. And she was right. Though, none of us would have thought it would have turned out this way. Those several big weeks turned into 2 years and 8 months!
But yesterday, James took his very last chemotherapy pill at 7:10pm and is now officially OFF TREATMENT! In a way, I am so thrilled, for James, and me and our family. But it brings more unknowns... and unknowns are.... well, unknown. But not for God and that is full of comfort. Before we close the chapter on leukemia, I would like to share some pictures of James before, during and after treatment. GO JAMES!!!
***************************************************************************************
Before leukemia and with hair....
(January 2006)
During Treatment
(March 2007)
(May 2007)
(December 2007)
(May 2008)

(August 2008)
(September 2008)
(February 2009)

(September 2009)
And now.... Officially OFF TREATMENT


(January 2006)During Treatment
(March 2007)(May 2008)
(August 2008)
(September 2009)
And now.... Officially OFF TREATMENT


|
As I put this 'in review' post together I saw so many other pictures I would love to have shared with you. If you want to see more pictures and to read James' journey through treatment, the best place to start is in February of 2007 and then finish up here.
Labels:
Down syndrome,
James update,
memories,
pictures,
stories
Friday, October 23, 2009
Shin splits
I haven't been doing any real running recently. A couple of days ago, Owen was going to run up to where the chickens are and move the pens and I asked to go along, because I wanted to get out and stretch a bit. So Owen and I ran pretty much all the way down and back. The next day, my shins started hurting and I thought it was just sore from where James had sat on me. The next day, my shins felt like there was a bruise and someone was pushing down on it all the time, except there wasn't a bruise and I couldn't think of anything I had done that would make my shins hurt this long. So I told Momma what was hurting and what it felt like and Momma said "That kind of sounds like shin splits." so I asked how would one get it and you'll never guess what she said... running or walking after not exercising much. I checked on Wikipedia and now I have shin splits and they hurt! Next time, I think I'll walk, in my sneakers, not my boots!
Hannah
Hannah
Labels:
daily life,
memories,
stories
Wednesday, October 21, 2009
I'll bet you didn't know
What the difference is between bird flu and the swine flu.
For bird flu, you need tweetmint and for swine flu? oinkment.
Hannah
P.S. Thanks Aunt Donna for this great laugh!
For bird flu, you need tweetmint and for swine flu? oinkment.
Hannah
P.S. Thanks Aunt Donna for this great laugh!
Sunday, October 18, 2009
Camping tonight
Tonight in the south (where we haven't felt 'global warming' in nearly a year), Katie, Owen, Becca, Carrie and I are going camping in the yard. It seems that all us children set up our 8 person tent and sleep in it about once a year. Usually, we set it up in the livingroom/diningroom. But this time we are actually going to sleep outside. Some of us (including me!) are wimps when it comes to camping and we wimps decided to take our mattresses out and sleep on those, smothered in our sleeping bags and piles of blankets. Hopefully we'll stay warm, it's supposed to get down to 39* tonight.
Owen has built a fire and beds and bedding is set up. We even decorated with pine boughs inside and outside the tent and we have boards at the entrance, so that we don't track in sand. Carrie is all dressed up in her flannel pantelettes, red turtleneck, blue couch-pouch and two pairs of socks. Becca has her horse sweatshirt, a denim shirt, flannel pantelettes, sweatpants and two pairs of socks on. They both look too cute for words and are eagerly looking forward to sleeping in the tent tonight. Maybe I should go take pictures, so we can share our experience.
Hannah
Owen has built a fire and beds and bedding is set up. We even decorated with pine boughs inside and outside the tent and we have boards at the entrance, so that we don't track in sand. Carrie is all dressed up in her flannel pantelettes, red turtleneck, blue couch-pouch and two pairs of socks. Becca has her horse sweatshirt, a denim shirt, flannel pantelettes, sweatpants and two pairs of socks on. They both look too cute for words and are eagerly looking forward to sleeping in the tent tonight. Maybe I should go take pictures, so we can share our experience.
Hannah
Labels:
family time,
family traditions,
fun,
memories,
stories
Saturday, October 17, 2009
Mendelssohn's 200th Birthday
This evening, Momma, Katie and I went to a concert given by GCSU, celebrating the 200th birthday of the famous composer, Felix Mendelssohn. It was very pleasant to listen to the choral groups and finally the orchestra play. We heard 'There Shall A Star From Jacob Shine Forth' from his unfinished oratorio, Christus and some from the oratorio, Elijah, and then the orchestra played first movement of Mendelssohn’s famous E Minor Violin Concerto (there are clips of the concerto on the link), which was awesome to listen to. We ended up leaving during the intermission, because it was already 8:40 pm and we had things to finish up at home. As we talked on the way home, we agreed that James would love going to listen and it would have been neat to hear more of Mendelssohn's music. Going tonight inspired me to learn more about Mendelssohn and perhaps get some, if not all, of his music from the library to listen too.
Hannah
Hannah
Labels:
daily life,
family time,
fun,
home education,
memories,
music
Wednesday, October 14, 2009
A recent dessert
This is what I made for a quick and relatively healthy (wink) treat recently.... Chocolate Pudding, whipped coconut cream and fresh mint leaves on top. Yummy!!!
Labels:
family time,
family traditions,
fun,
good food,
memories
Monday, October 12, 2009
James--endings and beginnings
We actually have a date for James' last chemo. Friday, October 23rd. He will finish the last pills and we will be done with chemo. The week of Nov 2nd, we'll get James' counts checked locally and the results will be sent to the oncology team and the surgeon. (Please pray with us for GREAT counts!)
The surgeon is in the loop now to start the process of reversing (hopefully and Lord willing) the ileostomy James had to have at the beginning of treatment. If the problems were caused by the chemo AND all is well with the pieces and parts after 2.5 years of chemo and non-use, then they should be able to put our little guy all back together again. Which is, of course, what we are hoping and praying for!
Assuming all is well with counts, James will have a fluoroscopy of his colon on Nov 9th. This will ensure there are no blockages or anything strange with all this non-use. Later that day, James will have procedures in Day Surgery. The oncology team will check his bone marrow and spinal fluid one last time. (Pray all is CLEAR... no more leukemia... EVER, Lord willing!)
During the surgery time, the surgeon will do a rectal biopsy to be sure that James still has all the important cells that should allow him to 'work like the rest of us'. The surgeon will also do a scope of the colon and check the health of James' colon and the mucosal lining. If all is well, he will flush the colon (via James' mucous fistula) and see how things work. Then we will figure out where we stand on the road to repairing James' ileostomy. (Please pray for a healthy colon with great mucosa, all the right cells in all the right places, and that there would be no blockages and things would flow JUST like they are supposed to.)
As we get closer to procedure day, I'll ask for prayer that either James would tolerate the fluoroscopy well, or they would be willing to sedate him for the test.
When James started chemo, it seemed like it would be FOREVER before we finished. Treatment is 130 weeks and we are now in week 128. With the end of treatment, brings the beginning of other new things... so we have endings and beginnings and we have James with us still. Which, if you had seen him 2 and half years ago, you would know that that is nothing short of a miracle. We are so grateful for God's mercies!
The surgeon is in the loop now to start the process of reversing (hopefully and Lord willing) the ileostomy James had to have at the beginning of treatment. If the problems were caused by the chemo AND all is well with the pieces and parts after 2.5 years of chemo and non-use, then they should be able to put our little guy all back together again. Which is, of course, what we are hoping and praying for!
Assuming all is well with counts, James will have a fluoroscopy of his colon on Nov 9th. This will ensure there are no blockages or anything strange with all this non-use. Later that day, James will have procedures in Day Surgery. The oncology team will check his bone marrow and spinal fluid one last time. (Pray all is CLEAR... no more leukemia... EVER, Lord willing!)
During the surgery time, the surgeon will do a rectal biopsy to be sure that James still has all the important cells that should allow him to 'work like the rest of us'. The surgeon will also do a scope of the colon and check the health of James' colon and the mucosal lining. If all is well, he will flush the colon (via James' mucous fistula) and see how things work. Then we will figure out where we stand on the road to repairing James' ileostomy. (Please pray for a healthy colon with great mucosa, all the right cells in all the right places, and that there would be no blockages and things would flow JUST like they are supposed to.)
As we get closer to procedure day, I'll ask for prayer that either James would tolerate the fluoroscopy well, or they would be willing to sedate him for the test.
When James started chemo, it seemed like it would be FOREVER before we finished. Treatment is 130 weeks and we are now in week 128. With the end of treatment, brings the beginning of other new things... so we have endings and beginnings and we have James with us still. Which, if you had seen him 2 and half years ago, you would know that that is nothing short of a miracle. We are so grateful for God's mercies!
Labels:
chemo tidbits,
James update,
prayer requests
Thursday, October 8, 2009
Heading to Atlanta
In a few moments, Momma, James and I will be on our way to Atlanta. James has his regular once-a-month clinic visit to the oncologist and another appointment with the surgeon who placed his ileostomy. Hopefully, I can post about the trip tomorrow, because I'm sure that we'll be tired by the time we get home.
Love, Hannah
Love, Hannah
Labels:
James update,
prayer requests
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