Tuesday, March 25, 2014
One Little, Two Little...
Two little chickens gone... :-(
Remember these chickie doos?
I went out to tuck my chickies in, and counted to six. Two were gone. So I went out to the yard to see if they had gotten locked out of our automatic door and found one dead - and it had been dead a good while. I never did find the other, but I know *when* my chicken disappeared because I do a head count morning and night - and often a couple of times a day.
We were gone all day Sunday. We have had stray dogs (dumps) running around and a few weeks ago, Frankie, my Roo chased one off. I guess this time, they critters got one and left the other - probably because Frankie was not being nice to them. On his best days, he isn't a nice guy:
Anyhoo, that is how chicken math works... you gain a few, name a few, loose a few.
Sad for this chicken mom, but I have learned that is part of farm life. We were amazed we got those eight babies to this stage without losing any.
And I cannot be here all of the time.
It was probably two hens they got - just my luck.
But I will never know.
Monday, March 24, 2014
Making a Flower Bed... Can We Do It?
We are finally getting around to making our place 'ours' by making flower gardens. Today I will start showing your our progress. This is what we started with - nothing! Those ugly planters were in front of the house when we moved here. I put chrysanthemums in them, but they are still butt ugly. I left them just because... I was too lazy to move them:
My chickens wreak havoc in my flower beds. This used to be all nice and pretty, complete with gorgeous hostas, but between the chickens and the winter, it sure leaves a lot to be desired now:
So we set about trying to figure out a design for a garden with a water hose:
As you can tell, we might not be gardeners...
But we are gonna give it our best shot.
Tomorrow we will see if we made progress!
My chickens wreak havoc in my flower beds. This used to be all nice and pretty, complete with gorgeous hostas, but between the chickens and the winter, it sure leaves a lot to be desired now:
So we set about trying to figure out a design for a garden with a water hose:
As you can tell, we might not be gardeners...
But we are gonna give it our best shot.
Tomorrow we will see if we made progress!
Sunday, March 23, 2014
Proud Moma
Every single night, I 'tuck' my chickens in. I count heads, make sure everyone is inside, roosting and safe. I have never, ever missed a night. It is part of what a chicken moma does.
I went to tuck my chickens in last night and found all eight of my 6-week-old chicks had figured out how to roost all by themselves.
It is the little things that make me smile: :-)
Meet my chicks: left to Right: Sara and Hazel. I haven't named the little peeps yet - I still don't know which are boys and girls. The yellow one is a guy - I am almost certain. And psst! Just so you know, he doesn't look like the others - he is YELLOW. Something is amiss in the chicken pile.
I wish you could see Sara's fluffy cheeks. I will have to get a picture of them soon...
My big chickens were roosting happily under the 'family portrait' wall:
From left to right: Ella (she is my 'special' chicken - she isn't the brightest crayon in the box), Clara (she is the eight little peeps moma), Aunt Bea, Frankie, Cole and Gloria.
Yes, I love my coop and my chickens. They might be a bit spoiled. I might be a tad insane decorating their coop, but, it is mine and I love doing it. I am always watching out for chicken portraits.
Those are all my chicky doos that I have right now - all except one - who is broody and sitting on 6 wooden eggs... I keep telling Charlotte that her eggs will not hatch, but she keeps them warm just in case. Silly girl! I have no idea where her picture went - I took one, but it didn't download.
Just imagine a black chicken in a dishpan 'growling' here...
I have 5 more babies coming in the week of April 15th.
And tomorrow, I promise, it will not be about chickens.
But it is true - my life revolves around my chickens. They make my world twirl.
Saturday, March 22, 2014
Good Morning From the Farm
These are my 'farm smiles'... the many reasons I love being a 'country girl':
Some mornings, I simply sit outside and enjoy the chickens chattering and pecking...
Thought I would share a few moments of my day.
Thursday, March 20, 2014
A Very Loved Cookbook
The best Banana Nut Bread recipe ever:
A well loved cookbook with a triple tried recipe and a few adjustments:
One hour in the oven:
A few minutes to cool and cut:
A nice slab of butter on the warm bread:
Makes for "YUM!"
Just in case you want to try it out:
A well loved cookbook with a triple tried recipe and a few adjustments:
One hour in the oven:
A few minutes to cool and cut:
A nice slab of butter on the warm bread:
Makes for "YUM!"
Just in case you want to try it out:
My Banana Nut Bread
½ c margarine
1 c sugar
2 eggs
2 c flour
1 c mashed bananas (about 3)
1 teaspoon soda
3 Tablespoons buttermilk OR 3 T milk mixed with 1 teaspoon
vinegar
½ teaspoon salt
1 cup cut up PECANS
Melt margarine, mix margarine and sugar, add eggs and
mix. Add remaining ingredients. Fill
greased loaf pans a bit over half full and bake in 350 degree oven for one
hour.
Let
the bread cool for about 15 minutes then take a couple of tablespoons
of margarine and put over the top. I usually just take a dab of
margarine, stab it with a fork and run it over the top of the warm
bread. It melts and makes the bread even more yummy.
Wednesday, March 19, 2014
The 'Berryhill' Sale
I entered an estate sale with a couple of friends of mine who actually make a living hosting estate sales. We had decided we would go junking on Fridays; estate sales, garage sales and junk stores just to entertain ourselves, but today we get first hand before the estate sale. So we enter this estate sale with anticipation, but, once we got in, we saw the enormous amount of stuff this family had. Walls and walls full of things, loot stacked to the brim on everything in sight, junk leaned up in stacks against the walls, beds overloaded with piles of... stuff. Nooks and crannies had items in it - there were years of collections stuffed EVERY where!
Most estate sales are very organized, well priced and it's easy to access all the items. It was obvious to my friends and I that this person was a hoarder and even though everything had been sorted, cleaned and priced, there was entirely too much to be able to display it nicely in this very small home.
Each room we strolled through got deeper and deeper. Customers were having 'cheek talks' to get around each other. At one point, I looked at my friend and thanked her for not taking and having THIS sale. We laughed about that sale for the next month or two.
On one Friday, I picked her up and she was unusually quiet. She kept looking sheepishly at me, until she finally said, "I need to take you to Berryhill". Come to find out, 'Berryhill' was the sale she had accepted the day before. So she took me to Berryhill.
Let me back up a bit; she has been in business for 40 years doing estate sales and she was my mom's best friend. Since I am near her, she asked if I would be interested helping out. As my energy allows (it mostly doesn't), I go to her newest estate sale and help (?) organize for it for the upcoming sale.
I was not prepared. Her daughter was not prepared. Browsing through the top floor, it was a piece of cake. They (we?) could easily whip it out in no time.
Ha! Then we went downstairs...
It is actually pretty fun going through other people's loot, however, this latest - "the Berryhill sale" - was overwhelming! It is quite a (hoarders) challenge.
Here is what we were faced with going in:
Two floors, two outdoor patios and one barn chock full of STUFF.
Yes, she had taken the job. As I said, I try to help, but until I get to Bethesda and find out what I need to know, I have not forced myself beyond what I feel like doing. Until then, I go when I feel like it, whip through one itsy, bitsy pile or corner and pray I never hoard things like this woman has done.
I cannot even get IN to take pictures in most of the rooms!
Yes, the lady who has this house is still alive. She is 92. I figure she has been hording for 72 of those years in this very house. Yes, she still comes in to see what we have uncovered. And yes she still takes some to her new home - which is a problem since the ones HOSTING the sale have uncovered mounds of stuff, cleaned it, cleaned the room, set it all up to look wonderful for the sale - and then the owner comes in and takes this - and that - and that - and this... yet WE have done all the work, so the money earning items she has taken takes away from the percentage the estate sale seller could earn.
Thankfully her daughter brings most of it back.
And we laugh about it being my fault my friend accepted this sale, because I started it that fateful day by saying, "Thank you for not taking this sale!" I challenged her and -
She did.
Only worse.
'We' hope to have the sale ready by May 1st.
I think it may be a pipe dream.
It will definitely be a challenge.
Challenge accepted.
And blamed on me. Lol...
Most estate sales are very organized, well priced and it's easy to access all the items. It was obvious to my friends and I that this person was a hoarder and even though everything had been sorted, cleaned and priced, there was entirely too much to be able to display it nicely in this very small home.
Each room we strolled through got deeper and deeper. Customers were having 'cheek talks' to get around each other. At one point, I looked at my friend and thanked her for not taking and having THIS sale. We laughed about that sale for the next month or two.
On one Friday, I picked her up and she was unusually quiet. She kept looking sheepishly at me, until she finally said, "I need to take you to Berryhill". Come to find out, 'Berryhill' was the sale she had accepted the day before. So she took me to Berryhill.
Let me back up a bit; she has been in business for 40 years doing estate sales and she was my mom's best friend. Since I am near her, she asked if I would be interested helping out. As my energy allows (it mostly doesn't), I go to her newest estate sale and help (?) organize for it for the upcoming sale.
I was not prepared. Her daughter was not prepared. Browsing through the top floor, it was a piece of cake. They (we?) could easily whip it out in no time.
Ha! Then we went downstairs...
It is actually pretty fun going through other people's loot, however, this latest - "the Berryhill sale" - was overwhelming! It is quite a (hoarders) challenge.
Here is what we were faced with going in:
Two floors, two outdoor patios and one barn chock full of STUFF.
Yes, she had taken the job. As I said, I try to help, but until I get to Bethesda and find out what I need to know, I have not forced myself beyond what I feel like doing. Until then, I go when I feel like it, whip through one itsy, bitsy pile or corner and pray I never hoard things like this woman has done.
I cannot even get IN to take pictures in most of the rooms!
Yes, the lady who has this house is still alive. She is 92. I figure she has been hording for 72 of those years in this very house. Yes, she still comes in to see what we have uncovered. And yes she still takes some to her new home - which is a problem since the ones HOSTING the sale have uncovered mounds of stuff, cleaned it, cleaned the room, set it all up to look wonderful for the sale - and then the owner comes in and takes this - and that - and that - and this... yet WE have done all the work, so the money earning items she has taken takes away from the percentage the estate sale seller could earn.
Thankfully her daughter brings most of it back.
And we laugh about it being my fault my friend accepted this sale, because I started it that fateful day by saying, "Thank you for not taking this sale!" I challenged her and -
She did.
Only worse.
'We' hope to have the sale ready by May 1st.
I think it may be a pipe dream.
It will definitely be a challenge.
Challenge accepted.
And blamed on me. Lol...
Monday, March 17, 2014
The Long Story of Why
It never seems enough... what I have to say about things going on in my life these days is a struggle.I love where we live, love my hubby and my family, so that isn't the problem. The problem is whatever is going on with my body.
I have trouble seeing now, my eyes are blurry from lack of tears. Not from crying, but from whatever I am dealing with... my mouth stays consistently dry, and no I don't have diabetes. Literally, my tear ducts have gotten smaller and smaller as the eyes get dryer and dryer. Because of that, I have trouble focusing - and some days are much worse than others. For that reason, I don't get on the computer much at all - which is also the problem with blogging. I do miss doing it, but to be honest, about 5 minutes on the computer is all I can master right now. I went in to an eye Dr and he gave me some drops to use after Bethesda. We don't want to mess up any testing being done there... we will see how the drops help.
I go to the National Institute of Health in Bethesda, MD in April to see if they can help me. So many problems... I have trouble holding things and typing now. My hands don't work from some kind of weird arthritis (?) that set in after taking sulfa drugs. I have been off of them for months now and I still have this problem, which also adds to me not being on the computer. Typing has become an issue. I can do it for short terms, but not for long and so many mistakes... Between that and the eyes, I just don't play on the computer.
I swear I feel like I am falling apart. Some days I get up and know it is an awful day. Unfortunately, they are getting more and more common. It breaks my heart to see Steve in the morning and have to tell him it is another crappy day. I am sick of me - how can he not be?
So about Bethesda. How did I get to go there? It all started with sinus problems. One side of my sinuses stays blocked all the time. I went to an Ear/Nose/Throat Dr and he tried helping me with no luck. He referred me to an immunologist/allergist. I went, she questioned me and immediately said I had an immune problem. However, she did allergy testing on me, but told me prior to testing that she suspected it would come back negative. It did. Even the false positive was negative. I ran into that problem at another allergy clinic in Baton Rouge YEARS ago. However, this immunologist didn't let it rest with, "hmmm, this is weird..."
She took blood. And she called for me to go back and give more blood... and more... I have LOTS of blood. 59 vials when I finally started counting!
My blood work looks all peachy and great... my bad cholesterol is good, my good cholesterol is good, sugar is great... everything looks super - until you get to the lymphocytes. I have gone for an extensive health exam every year for 10 years now. There have always been some questionable things on my blood. Lymphocytes were always a 'little' off, and my C-Reactive proteins were always way off. However, not one Dr questioned the lymphocyte problem. Not one! Apparently, maybe they thought I had a little infection going on each time, but no one realized I had 10 years of crappy lymphocyte counts!
This Dr saw my lymphocytes were down and she did a subset count - dividing the different sets of lymphs and seeing which part was down. My CD4+ count was non-existent and another set was low. She didn't believe the results and tested again. They were lower. So, she tested for AIDS/HIV.
NEGATIVE.
She called another Dr. They retested for AIDS/HIV.
NEGATIVE.
They did other testing and a different blotter test for AIDS/HIV. Ask me if I am panicked at this point.
HELL YES!
EVERY test has come back NEGATIVE on AIDS/HIV. Confirmed negative, cross checked, double checked and triple checked by every AIDS/HIV test available. The tests are negative.
So my blood work was turned in to the CDC. They confirmed all the results. I am definitely AIDS/HIV negative. They turned it over the National Institute of Health in Bethesda, MD. Ask how scary it was to call Jewish Medical Center and National Institute of Health (NIH) and they already had all my records and they have been 'confirmed'...
When I finally braved it up enough to contacted NIH, they were already in the process of putting together a 'team' and were getting ready to call me. HUH?! They took 1.2 nano seconds to 'invite' me to Bethesda for further testing. So, that is how I got accepted.
I am scheduled for multiple CAT scans, blood work, DNA testing, x-rays, a biopsy of my saliva glands (complete with stitches), numerous other tests and I will see at least 7 Drs while I am in Maryland. They are going to try to see if there is some other reason my CD4+ count is so low. They suggest I may have a mast cell problem as well as my blood disorder... or Sjogren's Syndrome. Not sure what the mast cell problem is and too skeered to ask. Sjogren's makes some sense - and I do have 10 of those symptoms - but it is a result of my CD4+ count - not the cause of it.
Anything I have is secondary to my blood disorder. My blood disorder, in case you are interested is once again; Idiopathic CD4+ Lymphocytopenia. If you read up on it, it is not serious - unless you have a CD4+ count like mine - it is 61. 300-350 is critical. There is no cure; IGiV's will not help, blood transfusions won't help... nothing to help the count grow. Apparently, once it is this low, there is no fixing it. Had it been discovered before the 'critical' level, they could have helped. Not now. Every stinking Dr I see says the same thing.
So, since October 31st, Steve and I have been 'processing' what is going on with my body and what to expect. We have stayed on top of my continuous sinus infections, bladder infections and any other infection I might have pop up. Simple little things like if I get a scratch that gets inflamed, my body cannot fight infection because it doesn't have a clue there is a problem.
That leads to another problem I am having. ANY antibiotics I take seem to make the 'arthritis' problem worse! I have to take antibiotics to live, so how can we deal with this other problem?
We are trying to find Drs to work with Bethesda when I return. Not an easy chore... no one knows what to do with me exactly. I have a few good days, but mostly really crummy days where I feel like crawling under the covers and sleeping it off. We both agree staying busy will help. I try to stay as busy as I can, but sheer exhaustion stops me in my tracks. I have never felt fatigue like I do right now.
So that is my long story.
Steve and I had a weekend where we talked a good bit. I am discouraged because I have let my blog go as long as I have and I don't really know where to start it. I decided to let you know the crappy things going on in my life and start there first so you can have some idea of what we are dealing with.
I will post as soon as we get the results from Bethesda. Thankfully, I am staying with a dear friend over there. We will try to see a bit of DC while we are there, but I don't think we will try to see much. I am just not up to it.
The next few months will be sketchy posts with random stuff that has happened in the last six months and what is going on now trying to catch you up. It probably won't make a lot of sense, but I am bound and determined I am going to get it up and running again so I can regularly post.
I guess that is all I can do unless you have other suggestions. Feel free to offer them. This post has taken me weeks to finally get out. I want to blog! But I had to get this crummy stuff out in the air.
And say a few prayers for me. I think my blood could sure use them. :-)
I have trouble seeing now, my eyes are blurry from lack of tears. Not from crying, but from whatever I am dealing with... my mouth stays consistently dry, and no I don't have diabetes. Literally, my tear ducts have gotten smaller and smaller as the eyes get dryer and dryer. Because of that, I have trouble focusing - and some days are much worse than others. For that reason, I don't get on the computer much at all - which is also the problem with blogging. I do miss doing it, but to be honest, about 5 minutes on the computer is all I can master right now. I went in to an eye Dr and he gave me some drops to use after Bethesda. We don't want to mess up any testing being done there... we will see how the drops help.
I go to the National Institute of Health in Bethesda, MD in April to see if they can help me. So many problems... I have trouble holding things and typing now. My hands don't work from some kind of weird arthritis (?) that set in after taking sulfa drugs. I have been off of them for months now and I still have this problem, which also adds to me not being on the computer. Typing has become an issue. I can do it for short terms, but not for long and so many mistakes... Between that and the eyes, I just don't play on the computer.
I swear I feel like I am falling apart. Some days I get up and know it is an awful day. Unfortunately, they are getting more and more common. It breaks my heart to see Steve in the morning and have to tell him it is another crappy day. I am sick of me - how can he not be?
So about Bethesda. How did I get to go there? It all started with sinus problems. One side of my sinuses stays blocked all the time. I went to an Ear/Nose/Throat Dr and he tried helping me with no luck. He referred me to an immunologist/allergist. I went, she questioned me and immediately said I had an immune problem. However, she did allergy testing on me, but told me prior to testing that she suspected it would come back negative. It did. Even the false positive was negative. I ran into that problem at another allergy clinic in Baton Rouge YEARS ago. However, this immunologist didn't let it rest with, "hmmm, this is weird..."
She took blood. And she called for me to go back and give more blood... and more... I have LOTS of blood. 59 vials when I finally started counting!
My blood work looks all peachy and great... my bad cholesterol is good, my good cholesterol is good, sugar is great... everything looks super - until you get to the lymphocytes. I have gone for an extensive health exam every year for 10 years now. There have always been some questionable things on my blood. Lymphocytes were always a 'little' off, and my C-Reactive proteins were always way off. However, not one Dr questioned the lymphocyte problem. Not one! Apparently, maybe they thought I had a little infection going on each time, but no one realized I had 10 years of crappy lymphocyte counts!
This Dr saw my lymphocytes were down and she did a subset count - dividing the different sets of lymphs and seeing which part was down. My CD4+ count was non-existent and another set was low. She didn't believe the results and tested again. They were lower. So, she tested for AIDS/HIV.
NEGATIVE.
She called another Dr. They retested for AIDS/HIV.
NEGATIVE.
They did other testing and a different blotter test for AIDS/HIV. Ask me if I am panicked at this point.
HELL YES!
EVERY test has come back NEGATIVE on AIDS/HIV. Confirmed negative, cross checked, double checked and triple checked by every AIDS/HIV test available. The tests are negative.
So my blood work was turned in to the CDC. They confirmed all the results. I am definitely AIDS/HIV negative. They turned it over the National Institute of Health in Bethesda, MD. Ask how scary it was to call Jewish Medical Center and National Institute of Health (NIH) and they already had all my records and they have been 'confirmed'...
When I finally braved it up enough to contacted NIH, they were already in the process of putting together a 'team' and were getting ready to call me. HUH?! They took 1.2 nano seconds to 'invite' me to Bethesda for further testing. So, that is how I got accepted.
I am scheduled for multiple CAT scans, blood work, DNA testing, x-rays, a biopsy of my saliva glands (complete with stitches), numerous other tests and I will see at least 7 Drs while I am in Maryland. They are going to try to see if there is some other reason my CD4+ count is so low. They suggest I may have a mast cell problem as well as my blood disorder... or Sjogren's Syndrome. Not sure what the mast cell problem is and too skeered to ask. Sjogren's makes some sense - and I do have 10 of those symptoms - but it is a result of my CD4+ count - not the cause of it.
Anything I have is secondary to my blood disorder. My blood disorder, in case you are interested is once again; Idiopathic CD4+ Lymphocytopenia. If you read up on it, it is not serious - unless you have a CD4+ count like mine - it is 61. 300-350 is critical. There is no cure; IGiV's will not help, blood transfusions won't help... nothing to help the count grow. Apparently, once it is this low, there is no fixing it. Had it been discovered before the 'critical' level, they could have helped. Not now. Every stinking Dr I see says the same thing.
So, since October 31st, Steve and I have been 'processing' what is going on with my body and what to expect. We have stayed on top of my continuous sinus infections, bladder infections and any other infection I might have pop up. Simple little things like if I get a scratch that gets inflamed, my body cannot fight infection because it doesn't have a clue there is a problem.
That leads to another problem I am having. ANY antibiotics I take seem to make the 'arthritis' problem worse! I have to take antibiotics to live, so how can we deal with this other problem?
We are trying to find Drs to work with Bethesda when I return. Not an easy chore... no one knows what to do with me exactly. I have a few good days, but mostly really crummy days where I feel like crawling under the covers and sleeping it off. We both agree staying busy will help. I try to stay as busy as I can, but sheer exhaustion stops me in my tracks. I have never felt fatigue like I do right now.
So that is my long story.
Steve and I had a weekend where we talked a good bit. I am discouraged because I have let my blog go as long as I have and I don't really know where to start it. I decided to let you know the crappy things going on in my life and start there first so you can have some idea of what we are dealing with.
I will post as soon as we get the results from Bethesda. Thankfully, I am staying with a dear friend over there. We will try to see a bit of DC while we are there, but I don't think we will try to see much. I am just not up to it.
The next few months will be sketchy posts with random stuff that has happened in the last six months and what is going on now trying to catch you up. It probably won't make a lot of sense, but I am bound and determined I am going to get it up and running again so I can regularly post.
I guess that is all I can do unless you have other suggestions. Feel free to offer them. This post has taken me weeks to finally get out. I want to blog! But I had to get this crummy stuff out in the air.
And say a few prayers for me. I think my blood could sure use them. :-)
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