Saturday, September 28, 2013
Bakery Type Icing
3½ T flour
½ c milk
½ c shortening
½ c sugar
½ t salt
½ t vanilla
1½ c powdered sugar
Gradually blend milk into flour. Cook about 10 minutes or to a very thick paste. Stir as it scorches easily. Cool to lukewarm. Meanwhile cream shortening, sugar and salt. Add paste, beat until fluffy. Fold in vanilla and add powdered sugar.
In memory of Sye Sr.
Tuesday, September 24, 2013
Pineapple Fritters
1 cup flour, sifted
1 T sugar
1 t baking powder
¼ t salt
1 egg
½ cup milk
2 T melted Crisco
1 cup crushed pineapple, drained
Powdered sugar
Sift dry ingredients together. Combine egg and milk and stir into the dry mixture. Add melted shortening and pineapple. Drop by spoonfuls into Crisco heated to 365°F. Fry until golden brown 3-5 minutes. Sprinkle with powdered sugar if desired. Serve with ham, meatloaf or other meat.
Saturday, September 21, 2013
Maple Nut Twist
1 package Pillsbury Hot Roll mix
¾ c warm water
1 egg
3 T sugar
1 t maple flavor
6 T butter, melted
Filling:
½ c sugar
1 t cinnamon
1 t maple flavor
¾ lb English Walnuts, chopped
In large bowl mix yeast and warm water until yeast is dissolved. Stir in egg, sugar and flavoring. Add the flour mixture. Blend well. Knead on floured surface 2 or 3 minutes until smooth and elastic. Place in greased bowl. Cover and let rise in warm place until light and double in size. 30-45 minutes.
Divide dough in 3 balls on lightly floured board. Roll out one ball of dough to fit 12” pizza pan. Brush with 2 T melted butter and sprinkle with 1/3 of filling. Continue in the same manner, forming 2 more layers and ending with filling. Mark with glass to form a 2” circle in center. Cut through dough to outside of glass 16 wedges. Twist each of the 3 layered wedges 5 times. Let rise in warm place 30-45 min until double in size. Bake at 375°F for 20-25 min.
Drizzle while warm with powdered sugar glaze. Serve warm or cold.
Thursday, September 19, 2013
Tuesday, September 17, 2013
German Pancakes
Put ½ cup butter in heavy 8-9” fry pan. Let melt, don't brown. Mix 4 T flour and ¼ t salt, 2 t sugar, and ½ c milk. Beat smooth and add 4 eggs, one at a time. Beat well, pour into pan. Bake at 475°F for 1 min. Turn oven to 375°F and bake 8 minutes more.
Monday, September 16, 2013
September Results are...
I'm sorry I didn't keep my promise to post the results as soon as I got them. I do have the results but I don't know what they mean. It's all rather confusing and I've been trying to wrestle with feelings, emotions, and process the information that they provided. To say I am feeling confused and angry is pretty accurate maybe with a little bit of fear mixed in. It's such a dramatic change from how I was years ago. Confident to the point of cocky that something would and could be done about the cancer. I've expected the same this time around. OK this isn't going to make a ton of sense as it's jarbled and rambling and long but it is what I have to work with straight from the tape recorder.
I also get a T4a because of the size of the mass being far larger than anticipated but because they can't say how far beyond the original thyroid capsule it was they can't score me with this either. Since it didn't make it into the carotid artery or mediastinal vessels. I can't be a 4b, because both or at the very least one has to be involved and neither are with me.
I do get a N1 because it was in the general area of the thyroid and it was in the lymph nodes in that area and lower and metastasis was proven/shown/seen this time because of the size of the mass removed plus the cells it contained and it was in lymph tissue. But because of the lack of original tissue they can't say if it's an a or a b.
I do clearly have a M1 as it was distant and distinct metastasis (again lymph tissue being filled with it instead of thyroid gland tissue which is clearly because I don't have a thyroid any more.) so the best they can do is say the following. Since your under 45 yrs old with a M1 and a N1 and that means your most likely a Stage 2 M1.
But in the endo's gut, a Stage 2 M1 isn't accurate. Why? Because this isn't a first time occurrence of papillary cancer cells, it's in the lymph nodes but no one knows exactly why it's there. Was it present from before or after the surgeon removed the thyroid and surrounding lymph tissue 16 years ago? A questions I'd dearly love to have answered thank you very much.
When do I get to speak to an oncologist? I don't. I don't have any reason to bother an oncologist at this time because I don't have a true stage and clearly surgery corrected the problem.
Papillary or follicular or both? It was positive for papillary and no follicular showed in the sample that the pathologist received. Could the follicular cancer be lurking? Yes, but I'm not to think on it because it hasn't show up yet.
Mysterious lumps and bumps that I have should they be checked for cancer? No. It's not felt that they need investigated because while they are growing in size and some could be lymph involved due to location and they didn't show up on the MRI, PET, or CAT scans as pure cancer. When I said that this didn't show up as cancer either on the scans oh that's right was the response I was given. Well we won't worry about it until it gets bigger so don't you worry either. Nice try. I'm worried because when the first showed up they were the size of a pea, then they went to a quarter and now they are the size of a hen's egg. (Rhode Island Red if you want to be specific ) They show to ultrasound and they show like the mass in my neck did (in fact the mass in my neck that freaked everyone out is word for word written about these other ones). It's been advised to get them checked but not considered worth it at the moment; so no referral for further testing or guidelines as to what to make about them. This doesn't sit well with me.
What can I do to prevent a re-occurrence of this from coming back? Nothing. It will probably show up again because it's showed up now as there's no rhyme or reason as to why it showed up now. Since it's slow growing it will probably take at least 15 to 16 years and hopefully technology will have advanced enough to catch it next time. Everyone is convinced that there will be a next time but not convinced enough to refer to oncologist or to look further for treatment options.
Will I have to do the radioactive iodine treatment again? The endo and ENT are unsure if I will be able to do this. I've already had several doses of the radioactive iodine and I still had to have a mass of cancer cells removed so that would be up to an oncologist and yet, I don't get to see one.
When will I have to do it? They don't know as that's up to the oncologist but not for awhile because I need to heal and recover from the surgery in July still. I also need to get out of hypothyroidism.
Will I have a repeat ultrasound? Yes, a repeat ultrasound will be sometime down the road probably in the 3 to 6 month ranges in order to give my neck a chance to heal up from the surgery.
Will I have to repeat a thyroid scan? Yes, will probably be in 3 to 6 months depending on my labs or it could wait for 1 year.
Lab work will be done at the end of Nov for a mid December apt because of being on .900 thyroid meds.
Since I'm in the 1% of the population who has the cancer return; It appears there's not a lot known about why this happens or what to do. Each question and concern that I had was pretty much brushed off and dismissed as being irrelevant. I was told again to take every day as it might be my last. I probably have a year of good clean cancer free time. Yet, because of the lack of staging; they can't tell me if I am in the serious category or the minor category of the 1%.
I'm
no closer to having answers than I was three months ago. the only thing I have
an answer on is that I'm still hypo thyroid as I'm at an 11.? something the ink
smeared so the dr couldn't read the last part of the lab tests results. 11
something is a lot better than 60 or even a 100.
My thyroglobulin is
gone. This is a good thing. It was suspected that the surgery would
make it disappear so that's one positive from the surgery in July. It's also
indicates yet again that if thyroglobulin shows up that it's a red flag that
the cancer is coming back. He's hoping that I'll get at least 1 to 3 years
thyroglobulin free time min before it starts coming back if it's going to come
back. I don't know if that's possible because it was around 29 months that it
showed up last time and was dismissed until June of this year. He's increasing
my doses to like .900 daily for the next 3 months to try to get me out of
hypothyroidism.
The pathologist who did the peek at the mass that was removed didn't stage it. So I have an estimated stage. Apparently the lack of the thyroid gland itself means it couldn't accurately be staged so it wasn't worth the effort to stage it. I'm in the dark as to where I am on the scale. Unfortunately this is critical information if I want to be taken serious about getting a referral to an oncologist, the stuff with my dd's future, and a few other things like future health care.
The mass that was removed in July couldn't be staged because there was no thyroid to go along with the mass and due to the butchery from the original thyroidectomy 16 years ago. Because the original surgeon didn't do the surgery in July and the changes the original surgery did to the landmarks and grooves and some other things it's hard to get an accurate picture of just where this mass was and what it was doing. Without the original information and going just off of what was sent it was to hard to do a stage. So that means the doctors are going to stage me off of my age and the fact it was in the lymph nodes and not off the reality.
The pathologist who did the peek at the mass that was removed didn't stage it. So I have an estimated stage. Apparently the lack of the thyroid gland itself means it couldn't accurately be staged so it wasn't worth the effort to stage it. I'm in the dark as to where I am on the scale. Unfortunately this is critical information if I want to be taken serious about getting a referral to an oncologist, the stuff with my dd's future, and a few other things like future health care.
The mass that was removed in July couldn't be staged because there was no thyroid to go along with the mass and due to the butchery from the original thyroidectomy 16 years ago. Because the original surgeon didn't do the surgery in July and the changes the original surgery did to the landmarks and grooves and some other things it's hard to get an accurate picture of just where this mass was and what it was doing. Without the original information and going just off of what was sent it was to hard to do a stage. So that means the doctors are going to stage me off of my age and the fact it was in the lymph nodes and not off the reality.
Clear as mud? Will it be accurate no. The stage that I am
given will not be accurate and it could cause long term issues with far
reaching implications. It sets me up as looking like a first time
re-occurrence not a 2nd time re-occurrence. The endo is pretty
positive that this will impact my future treatment and my candidacy for dd's
guardianship but his hands are tied because the pathologist didn't stage it and
he can't really stage it because of lack of information in my files. Death and
retirement of medical providers stinks.
So this is how it breaks down per a Wolters Kluwer scale. I'm not sure what that is. I get a TX primary tumor cannot be assessed score. Why? It was removed 16 years ago. I get a T3 score because of it being over 4 cm in size but because of the original thyroid missing, I can't really have a T3 because 1. I have a TX 2. can't tell how this mass was laying in relation to the original cancer in the thyroid 16 years ago.
So this is how it breaks down per a Wolters Kluwer scale. I'm not sure what that is. I get a TX primary tumor cannot be assessed score. Why? It was removed 16 years ago. I get a T3 score because of it being over 4 cm in size but because of the original thyroid missing, I can't really have a T3 because 1. I have a TX 2. can't tell how this mass was laying in relation to the original cancer in the thyroid 16 years ago.
I also get a T4a because of the size of the mass being far larger than anticipated but because they can't say how far beyond the original thyroid capsule it was they can't score me with this either. Since it didn't make it into the carotid artery or mediastinal vessels. I can't be a 4b, because both or at the very least one has to be involved and neither are with me.
I do get a N1 because it was in the general area of the thyroid and it was in the lymph nodes in that area and lower and metastasis was proven/shown/seen this time because of the size of the mass removed plus the cells it contained and it was in lymph tissue. But because of the lack of original tissue they can't say if it's an a or a b.
I do clearly have a M1 as it was distant and distinct metastasis (again lymph tissue being filled with it instead of thyroid gland tissue which is clearly because I don't have a thyroid any more.) so the best they can do is say the following. Since your under 45 yrs old with a M1 and a N1 and that means your most likely a Stage 2 M1.
But in the endo's gut, a Stage 2 M1 isn't accurate. Why? Because this isn't a first time occurrence of papillary cancer cells, it's in the lymph nodes but no one knows exactly why it's there. Was it present from before or after the surgeon removed the thyroid and surrounding lymph tissue 16 years ago? A questions I'd dearly love to have answered thank you very much.
He's thinking I'm probably a Stage 4 because of the clear size,
lymph node involvement, the questionable follicular stuff, and the garbled
notes he's found from those involved in my care for thyroid cancer 16 years
ago. At this point and time it's still uncertain where my records are at from
the disappearance of 3 of the medical team members (death and retirement). Also
because of stuff going from paper to electronic.
I still can't get an answer to the question of Why didn't the cancer show up on the PET, MRI or CAT scan in 2010 and prior? no one knows why it didn't show up as clearly cancer just as tissue that might need to be watched. Everyone is in agreement that the size of the tissue removed it should have shown up in one of those tests. Especially since it tested positive for thyroid cancer. This does make them wonder how many other bumps and lumps I have that will also come back positive if removed and dissected. But since the thyroglobulin is gone there's no need to look further at these weird masses.
When do I need to get concerned about enlarged lymph nodes? When do I just ignore them? I am to not worry about lymph nodes in the future. This is less than satisfactory as the dentist is very concerned about the enlarged lymph nodes he's finding that have gotten bigger instead of smaller with the two month big gun antibiotics treatment I just went through. The dentist fears it's something more serious based on what July uncovered and my weird medical family tree.
I still can't get an answer to the question of Why didn't the cancer show up on the PET, MRI or CAT scan in 2010 and prior? no one knows why it didn't show up as clearly cancer just as tissue that might need to be watched. Everyone is in agreement that the size of the tissue removed it should have shown up in one of those tests. Especially since it tested positive for thyroid cancer. This does make them wonder how many other bumps and lumps I have that will also come back positive if removed and dissected. But since the thyroglobulin is gone there's no need to look further at these weird masses.
When do I need to get concerned about enlarged lymph nodes? When do I just ignore them? I am to not worry about lymph nodes in the future. This is less than satisfactory as the dentist is very concerned about the enlarged lymph nodes he's finding that have gotten bigger instead of smaller with the two month big gun antibiotics treatment I just went through. The dentist fears it's something more serious based on what July uncovered and my weird medical family tree.
When do I get to speak to an oncologist? I don't. I don't have any reason to bother an oncologist at this time because I don't have a true stage and clearly surgery corrected the problem.
Papillary or follicular or both? It was positive for papillary and no follicular showed in the sample that the pathologist received. Could the follicular cancer be lurking? Yes, but I'm not to think on it because it hasn't show up yet.
Mysterious lumps and bumps that I have should they be checked for cancer? No. It's not felt that they need investigated because while they are growing in size and some could be lymph involved due to location and they didn't show up on the MRI, PET, or CAT scans as pure cancer. When I said that this didn't show up as cancer either on the scans oh that's right was the response I was given. Well we won't worry about it until it gets bigger so don't you worry either. Nice try. I'm worried because when the first showed up they were the size of a pea, then they went to a quarter and now they are the size of a hen's egg. (Rhode Island Red if you want to be specific ) They show to ultrasound and they show like the mass in my neck did (in fact the mass in my neck that freaked everyone out is word for word written about these other ones). It's been advised to get them checked but not considered worth it at the moment; so no referral for further testing or guidelines as to what to make about them. This doesn't sit well with me.
What can I do to prevent a re-occurrence of this from coming back? Nothing. It will probably show up again because it's showed up now as there's no rhyme or reason as to why it showed up now. Since it's slow growing it will probably take at least 15 to 16 years and hopefully technology will have advanced enough to catch it next time. Everyone is convinced that there will be a next time but not convinced enough to refer to oncologist or to look further for treatment options.
Will I have to do the radioactive iodine treatment again? The endo and ENT are unsure if I will be able to do this. I've already had several doses of the radioactive iodine and I still had to have a mass of cancer cells removed so that would be up to an oncologist and yet, I don't get to see one.
When will I have to do it? They don't know as that's up to the oncologist but not for awhile because I need to heal and recover from the surgery in July still. I also need to get out of hypothyroidism.
Will I have a repeat ultrasound? Yes, a repeat ultrasound will be sometime down the road probably in the 3 to 6 month ranges in order to give my neck a chance to heal up from the surgery.
Will I have to repeat a thyroid scan? Yes, will probably be in 3 to 6 months depending on my labs or it could wait for 1 year.
Lab work will be done at the end of Nov for a mid December apt because of being on .900 thyroid meds.
Since I'm in the 1% of the population who has the cancer return; It appears there's not a lot known about why this happens or what to do. Each question and concern that I had was pretty much brushed off and dismissed as being irrelevant. I was told again to take every day as it might be my last. I probably have a year of good clean cancer free time. Yet, because of the lack of staging; they can't tell me if I am in the serious category or the minor category of the 1%.
The thing that
is being brushed off and over looked and is upsetting me the most is I had two cancers
in my thyroid and surround tissue that I shouldn't have had because of my
age the first time I was told I had thyroid cancer. I was in my 20s then and had fought for 7 years to be taken seriously that something wasn't right. That's when both types were found which usually don't
show up unless your older like not until the ages of 30 to 50. If it didn't
wait until I was the proper age to medically have it then.... if it can't be staged...,
then how accurate is it to base things like my treatment or lack of off my age
now? Because when that was done previously it missed getting it dealt with
sooner.
I was told repeatedly by several endos and an ENT that I was too young to have thyroid cancer. I was ridiculous to even consider that I might have it based on some lame high school genetics portion of my biology class. It gave the cancer a chance to grow and to spread. So that instead of
being all clear, I'm dealing with it now. Having me put it to him this way he
could see that the stage 2 means nothing and that I am more than likely a
higher stage but without the original tissue, records and notes I'm going to be
treated as if this is a first time age appropriate cancer happening. To sound a bit like a very spoiled two year old.... I don't think that's fair at all.
I don't know why but I can't help feeling/thinking they are missing something. Of course this was made a stronger feeling when the endo came in and introduced himself and said he was glad to meet me for the 1st time. Granted he was a little frazzled as it was almost 5 p.m. when he came in and I was his 2:45 p.m. patient.
I don't know why but I can't help feeling/thinking they are missing something. Of course this was made a stronger feeling when the endo came in and introduced himself and said he was glad to meet me for the 1st time. Granted he was a little frazzled as it was almost 5 p.m. when he came in and I was his 2:45 p.m. patient.
So there you have it. That's where I am at in this journey. I won't be able to update until sometime in December when the next step is under gone what ever that means.
Thank you for making it to the bottom and thanks for listening.
Saturday, September 14, 2013
Drop Doughnuts
1/3 cup sugar
½ cup milk
1 egg
2 T melted shortening
1½ cups flour
2 t baking powder
½ t salt
Blend together sugar, milk, egg, and shortening. Put flour, baking powder, and salt in the liquid mixture. Drop by teaspoons in hot grease for about 3-5 minutes.
Mix together: ¼ cup sugar, and ½ t nutmeg or cinnamon. When doughnuts are done, roll them in this mixture.
Tuesday, September 10, 2013
Fluffy Pancakes
Put in blender and blend on high speed.
5 slightly beaten egg yolks
1-2/3 cups buttermilk
1 t soda
Sift and add to blender then blend at high speed.
1½ cups sifted flour
1 T sugar
1 t baking powder
½ t salt
Add 3 t soft butter. Pour into a mixing bowl and blend in 5 egg whites beaten very stiffly. Fry on hot griddle, that's been lightly greased.
Saturday, September 7, 2013
Peach Ice Cream
2/3 cup Eagle Brand Sweetened Condensed Milk
½ cup water
1½ t vanilla extract
1 cup (½ pint) heavy cream
1 cup mashed fresh peaches or drained frozen peaches or drained canned peaches
In medium bowl, combine sweetened condensed milk, water and vanilla extract. Refrigerate. In medium bowl, whip cream to a soft custard like consistency. Fold into chilled mixture. Add peaches. Pour into two ice cube trays or a deep loaf pan. Freeze about 1 hour or until a firm mush forms. Turn into chilled large electric mixer bowl; break into pieces. Beat until fluffy but not melted. Quickly return to ice cube tray. Cover with aluminum foil. Return to freezer. Freeze until firm.
Make about 1½ pints
Variations:
Coffee Ice Cream
Fresh Strawberry Ice Cream
Peppermint Candy Ice Cream
Maple Nut Ice Cream
Vanilla Ice Cream
½ cup water
1½ t vanilla extract
1 cup (½ pint) heavy cream
1 cup mashed fresh peaches or drained frozen peaches or drained canned peaches
In medium bowl, combine sweetened condensed milk, water and vanilla extract. Refrigerate. In medium bowl, whip cream to a soft custard like consistency. Fold into chilled mixture. Add peaches. Pour into two ice cube trays or a deep loaf pan. Freeze about 1 hour or until a firm mush forms. Turn into chilled large electric mixer bowl; break into pieces. Beat until fluffy but not melted. Quickly return to ice cube tray. Cover with aluminum foil. Return to freezer. Freeze until firm.
Make about 1½ pints
Variations:
Coffee Ice Cream
Fresh Strawberry Ice Cream
Peppermint Candy Ice Cream
Maple Nut Ice Cream
Vanilla Ice Cream
Tuesday, September 3, 2013
Granola
5 cups oatmeal
2 cups wheat germ
1+2 cups coconut
1 cup almonds
1 cup any nuts, seeds, raisins, dates, etc.
½ cup salad oil
¼ cup brown sugar
½ cup honey
1 T molasses
2 T water
2 t vanilla
1½ t cinnamon.
Mix in a large bowl: oatmeal and wheat germ. Add if chosen coconut, almonds, or any other nuts, seeds, raisins, dates, etc. you want to use. Mix together salad oil, brown sugar, honey, molasses, water, vanilla, cinnamon. Pour over the oatmeal, wheat germ, coconut, almond, etc. mixture.
Spread in large pan, such as a broiler pan, and toast in 300°F oven for 30-40 minutes, stirring well every 10 minutes to prevent over browning.
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