Mom is doing well. She is a asymptomatic at this point with her Chemo treatments. Her Doctors continue to be impressed by Mom's physical, emotional and mental strength at this point. Mom's energy, attitude and humor is all present and shared with all.
Mom, though she is sharing her hospital room, is enjoying having the extra company. Her roommate has a lot of company throughout the day and they visit with Mom as well. It was funny to hear Mom say they are a loud family. I think she has forgotten her roots. I know I have not, wink. Anyway, Brian and Poppie continue to visit Mom in the evenings for several hours. Mike and Cindy drive into the city to see Mom when possible. Mike does speak with Mom daily to check in and chat about "life." Mom, now has mastered using Skype on the laptop and calls every few hours to check in or we call her.
Overall, Mom is fighting hard in many ways to resume her life as it presents itself. She has allowed herself to see, feel and experience what ever presents itself to her with a strong mind. I am so very proud of her. She is a true warrior and now a bit less of a worrier.
Mom will be attending a dinner party with Kimmy and I in San Diego this evening. Yes, I now bring my laptop everywhere so Mom is able to share and vicariously get out and about.
Hugs and Love,
Karen
Sunday, January 31, 2010
Saturday, January 30, 2010
Trying to Stay Positive
Mom was admitted into Strong Memorial Hospital yesterday for her 3rd round of Chemo treatment. Yes, I am in San Diego attending to my own medical, personal and professional responsibilities. It is very difficult for me not to be at Mom's side. She and I refer to my absence as being bitter sweet. If I could only clone myself everyone would be much happier.
Mom is being strong and is trying to maintain a positive attitude. She has accepted that fighting to get her AML into remission and then keeping it there is simply going to be her life here on in. Yes, Mom has windows of anger attached with deep sadness, but she no longer stays in that mental space very long. She and I speak in the morning, the afternoon and then the evening to ensure her emotional calmness. It also helps me to feel I am still able to support her though from 3000 miles away.
Yesterday, Brian and Poppie had visited Mom for several hours in the evening. Brian, brought in his video cam on his laptop so Mom, Kimmy and I are able to see and talk as much as possible. Since the end of October, that has been how we kept in touch with Kimmy when she was back in SD. Mom really enjoys watching Shayna Punum playing in our back yard, seeing the San Diego sunshine and our tropical backyard theme with palm trees, bamboo walls, water falls etc.
This morning Mom received her second round of Chemo IV. She is doing well. She is not experiencing any adverse side effects. She is being check several times a day by her nurses and visits by her Oncology team.
Mom enjoyed this evening with us on Skype. Mom was so excited to have the Oncology Team and Staff say hello on Skype. It really made Kimmy and I feel as if we were there with Mom in the hospital room. It is so nice to see the person I am speaking with. Mom was pretty tired by 8:30pm East Coast time. We all said good night and we would chat on Sunday.
Three cheers to Momma Ruthie's strength and desire to overcome this horrible disease.
All my warmth and love,
Karen
Mom is being strong and is trying to maintain a positive attitude. She has accepted that fighting to get her AML into remission and then keeping it there is simply going to be her life here on in. Yes, Mom has windows of anger attached with deep sadness, but she no longer stays in that mental space very long. She and I speak in the morning, the afternoon and then the evening to ensure her emotional calmness. It also helps me to feel I am still able to support her though from 3000 miles away.
Yesterday, Brian and Poppie had visited Mom for several hours in the evening. Brian, brought in his video cam on his laptop so Mom, Kimmy and I are able to see and talk as much as possible. Since the end of October, that has been how we kept in touch with Kimmy when she was back in SD. Mom really enjoys watching Shayna Punum playing in our back yard, seeing the San Diego sunshine and our tropical backyard theme with palm trees, bamboo walls, water falls etc.
This morning Mom received her second round of Chemo IV. She is doing well. She is not experiencing any adverse side effects. She is being check several times a day by her nurses and visits by her Oncology team.
Mom enjoyed this evening with us on Skype. Mom was so excited to have the Oncology Team and Staff say hello on Skype. It really made Kimmy and I feel as if we were there with Mom in the hospital room. It is so nice to see the person I am speaking with. Mom was pretty tired by 8:30pm East Coast time. We all said good night and we would chat on Sunday.
Three cheers to Momma Ruthie's strength and desire to overcome this horrible disease.
All my warmth and love,
Karen
Tuesday, January 26, 2010
Bone Biopsy Results
Mom's positive thinking is paying off. This afternoon, Mom and Poppie waited with anticipation for her Oncologist to share last weeks bone biopsy results. Mom continues to put smiles on her Doctors faces. Her results are showing that her body is fighting hard. She is at 4% range with blasts (white cells). Anything under 5% is good. This means Mom has a good chance to get into remission after her 3rd round of Chemo.
This Friday or Monday Mom is expected to be admitted into the hospital for what is called a Consolidation Period of Chemo treatment. This is for 6 days of Chemo and then the patient is sent home. Yes, if the patient develops a fever or other complicating outcomes, the patient will be re-admitted into the hospital immediately for treatment and observation.
Here is the process of Consolidation. After the 6 days of receiving Chemo the patient is sent home. Monday and Thursday's the patient has an In service Nurse drawing blood and checking all vitals and present condition of the patient. Tuesday and Friday's the patient goes back to the hospital for any IV transfusions that may be needed according to the previous day results.
I will add more as the specific days unfold.
Today is a new path for more good news to follow as her treatment begins. Keep your positive thinking, healing energy, and prayers flowing. I know, Mom will be enjoying life to its fullest, traveling and enjoying with friends and family in all settings in months to come.
I will post again when Mom is admitted back into the hospital.
All Our Warmth and Love,
Momma Ruthie, Poppie, Mike, Cindy, Brian, Reece, Kimmy and I
This Friday or Monday Mom is expected to be admitted into the hospital for what is called a Consolidation Period of Chemo treatment. This is for 6 days of Chemo and then the patient is sent home. Yes, if the patient develops a fever or other complicating outcomes, the patient will be re-admitted into the hospital immediately for treatment and observation.
Here is the process of Consolidation. After the 6 days of receiving Chemo the patient is sent home. Monday and Thursday's the patient has an In service Nurse drawing blood and checking all vitals and present condition of the patient. Tuesday and Friday's the patient goes back to the hospital for any IV transfusions that may be needed according to the previous day results.
I will add more as the specific days unfold.
Today is a new path for more good news to follow as her treatment begins. Keep your positive thinking, healing energy, and prayers flowing. I know, Mom will be enjoying life to its fullest, traveling and enjoying with friends and family in all settings in months to come.
I will post again when Mom is admitted back into the hospital.
All Our Warmth and Love,
Momma Ruthie, Poppie, Mike, Cindy, Brian, Reece, Kimmy and I
Friday, January 22, 2010
Mom's finding her way
Mom and I stayed up together on Wednsday night till our eyes simply had to close. We both felt me leaving was "bitter sweet." Though I am able to return at any time, she wants me to focus on my health, family, profession and personal needs. I agree, but it is so difficult to leave. Saying "See you later" was extremely difficult for Mom and I yesterday. She has a lot of wonderful support around her. She simply needs to reach out and ask for it. Example, massaging her, hanging out to watch a movie, doing her exercises with her, chatting about the bizarre topics, playing games, sharing and enjoying various foods, and much more.
Mom is doing pretty well. She is anxious to receive the results from the previous Bone Bipopsy. She is also having trepidation regarding her 3rd round of Chemo. She so badly wants this to be the last treatment that throws her into REMISSION! She has so many interests and traveling which she wants to do.
I will write in the blog after we are informed about her Bone Biopsy results next Tuesday, January 26th. Until then, thumbs up to Mom for beinga able to handel the strongest Chemo Treatment. Yes, this a treatment that is often given to no one older than 55 years old and is the last prior to receiving a bone marrow transplant. Unfortunelty, a bone marrow transplant Dr.'s informed us they still do not perform on individuals older than 60.
Well, have a beautiful weekend.
All my Love and gratitude for all your support,
Karen
Mom is doing pretty well. She is anxious to receive the results from the previous Bone Bipopsy. She is also having trepidation regarding her 3rd round of Chemo. She so badly wants this to be the last treatment that throws her into REMISSION! She has so many interests and traveling which she wants to do.
I will write in the blog after we are informed about her Bone Biopsy results next Tuesday, January 26th. Until then, thumbs up to Mom for beinga able to handel the strongest Chemo Treatment. Yes, this a treatment that is often given to no one older than 55 years old and is the last prior to receiving a bone marrow transplant. Unfortunelty, a bone marrow transplant Dr.'s informed us they still do not perform on individuals older than 60.
Well, have a beautiful weekend.
All my Love and gratitude for all your support,
Karen
Wednesday, January 20, 2010
Emotionally Feeling Slightly Weakend
Today was a difficult day for Mom to awaken to. She so badly wants to awaken from this terrible dream of being diagnosed with AML. The mental exhaustion for her trying to stay "positive" catches up with her from time to time. I am very proud to share with you how well she is able to snap herself out of her natural desire to be negative and pessimistic. She now is able to gather her thoughts and feelings and redirect her self talk to embrace and control her path towards getting into remission.
Mom was a star today entering the procedure room for her 3rd Bone Biopsy. A few tears of fear of the unknown did creep up and out for a short time. She allowed herself to "feel" and then began to allow the unknown to present itself. Mom was prepared to embrace the new information. She realized the procedures and tests are performed to simply assist her towards and into remission.
Mom's positive thinking brought good news today. Post the Bone Biopsy we were informed the Doctor, for the first time, was able to extract a small amount of marrow, yes that is "liquid." They also took two more bone chips to analyse. Mom, was not in any discomfort post the procedure. She simply was tired and hungry.
As I mentioned yesterday, on January 26th Mom has her follow up appointment with her Oncologist regarding the Bone Biopsy results. January 29th, Mom is re-admitted for another Chemo induction called a consolidation period. We all are confident Mom will respond as well with this Chemo treatment and better as the last.
Tomorrow, I must return back to San Diego to address my medical, professional, and personal responsibilities. If Mom takes a u-turn for the worse, which I know is an extremely slim chance, I and Kimmy will return to Rochester immediately. Yes, leaving Mom's side is extremely difficult for she and I. We decided to try to pull an all nighter. You would think being glued to the hip for over three weeks we would run out of things to talk about or want space from each other. Well, NO! Poppie, Brian, Mike, Cindy, Reece, and our cousins will all be continuing to support Mom as they have since November.
This evening Brian surprised Mom and the rest of us with her favorite Chinese food. We all indulged, enjoyed sharing stories and laughed a lot together. I will continue to share Mom's updates while in San Diego. The information will be through the eyes of Mom and the family. I will miss being on site, in person and being able to hold and care for little Momma Ruthie.
Again, thank you for all your love, warmth, healing energy and prayers.
Lets give another Big Cheer for Mom to SHINE through this 3rd Chemo treatment and enter REMISSION!
All Our Warmth and Love,
Momma Ruthie, Poppie, Mike, Cindy, Brian, Reece, Karen and Kimmy
Karen
Mom was a star today entering the procedure room for her 3rd Bone Biopsy. A few tears of fear of the unknown did creep up and out for a short time. She allowed herself to "feel" and then began to allow the unknown to present itself. Mom was prepared to embrace the new information. She realized the procedures and tests are performed to simply assist her towards and into remission.
Mom's positive thinking brought good news today. Post the Bone Biopsy we were informed the Doctor, for the first time, was able to extract a small amount of marrow, yes that is "liquid." They also took two more bone chips to analyse. Mom, was not in any discomfort post the procedure. She simply was tired and hungry.
As I mentioned yesterday, on January 26th Mom has her follow up appointment with her Oncologist regarding the Bone Biopsy results. January 29th, Mom is re-admitted for another Chemo induction called a consolidation period. We all are confident Mom will respond as well with this Chemo treatment and better as the last.
Tomorrow, I must return back to San Diego to address my medical, professional, and personal responsibilities. If Mom takes a u-turn for the worse, which I know is an extremely slim chance, I and Kimmy will return to Rochester immediately. Yes, leaving Mom's side is extremely difficult for she and I. We decided to try to pull an all nighter. You would think being glued to the hip for over three weeks we would run out of things to talk about or want space from each other. Well, NO! Poppie, Brian, Mike, Cindy, Reece, and our cousins will all be continuing to support Mom as they have since November.
This evening Brian surprised Mom and the rest of us with her favorite Chinese food. We all indulged, enjoyed sharing stories and laughed a lot together. I will continue to share Mom's updates while in San Diego. The information will be through the eyes of Mom and the family. I will miss being on site, in person and being able to hold and care for little Momma Ruthie.
Again, thank you for all your love, warmth, healing energy and prayers.
Lets give another Big Cheer for Mom to SHINE through this 3rd Chemo treatment and enter REMISSION!
All Our Warmth and Love,
Momma Ruthie, Poppie, Mike, Cindy, Brian, Reece, Karen and Kimmy
Karen
Tuesday, January 19, 2010
Mom is still in the game
Mom had her Oncology appointment today. She met with two Oncologists and a Nurse. All three of them expressed how pleased and astonished to how well Mom's body has and is taking the previous 2 Chemo treatments. Mom is not in remission yet. We all know she will be there soon, wink. She is soon to step into round 3 of Chemo treatment.
Mom continues to fight head on with her Leukemia. She does not have any pain, discomforts, fevers, nausea, headaches, nor additional skin outbreaks or lesions. Mom only has to battle fatigue after slight-moderate exertion. Mom continues to focus on Poppie's health and her own exercise regime.
Mom's entire system is holding its own and fighting at this point. Her numbers are good though low in some areas. She is showing that her body is producing all that is needed to fight against the AML. Her blood at this point is not showing any Leukemic cells. Prior to Round 3 of Chemo, Mom must complete the following:
Tomorrow, January 19th, Mom will be heading in for her 3rd Bone Biopsy. This time, she is being sent to Radiology. Here, she will be sedated and not receive a local of Lidocane as in the past two procedures. The Doctor will be using a special machine that will be able to explore and hopefully be able to gather more information. Yes, again we hope Mom's body is able to produce "liquid" to be extracted for testing. We will see.
.
Mom, continues to have her Visiting Nurse weekly to have her blood drawn. On January 26th Mom returns for a follow up regarding her Bone Biopsy with her Oncologist. She will receive the findings on this day. On January 29th Mom begins her 3rd Chemo treatment. Note, the previous two "Inductions of Chemo" were for an expected 30 day stay in the hospital. This induction is referred to as "Consolidation Chemo Treatment." This is for 6 days of Chemo and then the patient is sent home. Yes, if the patient develops a fever or other complicating outcomes, the patient will be re-admitted into the hospital immediately for treatment and observation.
Here is the process of Consolidation. After the 6 days of receiving Chemo the patient is sent home. Monday and Thursday's the patient has an In service Nurse drawing blood and checking all vitals and present condition of the patient. Tuesday and Friday's the patient goes back to the hospital for any IV transfusions that may be needed according to the previous day results.
I will add more as the specific days unfold.
Please continue to send your healing energy towards our Energizer Momma Ruthie.
All our Hugs and Love,
Karen
Mom continues to fight head on with her Leukemia. She does not have any pain, discomforts, fevers, nausea, headaches, nor additional skin outbreaks or lesions. Mom only has to battle fatigue after slight-moderate exertion. Mom continues to focus on Poppie's health and her own exercise regime.
Mom's entire system is holding its own and fighting at this point. Her numbers are good though low in some areas. She is showing that her body is producing all that is needed to fight against the AML. Her blood at this point is not showing any Leukemic cells. Prior to Round 3 of Chemo, Mom must complete the following:
Tomorrow, January 19th, Mom will be heading in for her 3rd Bone Biopsy. This time, she is being sent to Radiology. Here, she will be sedated and not receive a local of Lidocane as in the past two procedures. The Doctor will be using a special machine that will be able to explore and hopefully be able to gather more information. Yes, again we hope Mom's body is able to produce "liquid" to be extracted for testing. We will see.
.
Mom, continues to have her Visiting Nurse weekly to have her blood drawn. On January 26th Mom returns for a follow up regarding her Bone Biopsy with her Oncologist. She will receive the findings on this day. On January 29th Mom begins her 3rd Chemo treatment. Note, the previous two "Inductions of Chemo" were for an expected 30 day stay in the hospital. This induction is referred to as "Consolidation Chemo Treatment." This is for 6 days of Chemo and then the patient is sent home. Yes, if the patient develops a fever or other complicating outcomes, the patient will be re-admitted into the hospital immediately for treatment and observation.
Here is the process of Consolidation. After the 6 days of receiving Chemo the patient is sent home. Monday and Thursday's the patient has an In service Nurse drawing blood and checking all vitals and present condition of the patient. Tuesday and Friday's the patient goes back to the hospital for any IV transfusions that may be needed according to the previous day results.
I will add more as the specific days unfold.
Please continue to send your healing energy towards our Energizer Momma Ruthie.
All our Hugs and Love,
Karen
Monday, January 18, 2010
Tomorrow is the BIG DAY
Mom is anxious regarding meeting with her Oncologist for her appointment tomorrow. She will have more blood drawn and will be given her results from her reports on her present status of health. We will be presented with her next set of options for care.
I will keep you posted in tomorrows blog.
Mom and the rest of us had a wonderful long weekend. The days consisted of taking car trip tours around to see gorgeous sites, we hung out at home, we watched movies, went through family pictures, cooked some creative meals and chatted up a storm. Sunday, Mom and I hung out, played scrabble with Poppie and watched the 4:30pm football game. Yup, Mom smiled ear to ear when the Jests beat the "Choking Chargers." Mom showed great sportsman conduct towards me. Actually, we both we sad the Chargers, once again, BLEW IT! We still had fun together.
Well, please hug yourself from us. We truly appreciate your love and support the past several months.
Momma Ruthie, Poppie, Mike, Cindy, Brian, Reece, Kimmy and I xoxo
I will keep you posted in tomorrows blog.
Mom and the rest of us had a wonderful long weekend. The days consisted of taking car trip tours around to see gorgeous sites, we hung out at home, we watched movies, went through family pictures, cooked some creative meals and chatted up a storm. Sunday, Mom and I hung out, played scrabble with Poppie and watched the 4:30pm football game. Yup, Mom smiled ear to ear when the Jests beat the "Choking Chargers." Mom showed great sportsman conduct towards me. Actually, we both we sad the Chargers, once again, BLEW IT! We still had fun together.
Well, please hug yourself from us. We truly appreciate your love and support the past several months.
Momma Ruthie, Poppie, Mike, Cindy, Brian, Reece, Kimmy and I xoxo
Saturday, January 16, 2010
Mom is feeling "normal"
The past three days Mom has been feeling almost "normal." She is back to herself minus her decreased endurance of energy. She continues to have her playful outlook and desire to engage in anything. We have been watching home videos, exercising, playing with several new wigs, and taking outings in the car.
Today, Mom, Poppie, Brian and I spent the day at Mike and Cindy's place in Naples. Mike and Cindy have a beautiful home set on 25 acres with a gorgeous panoramic view. It was a beautiful day. The weather was in the mid 40's with a light breeze, the sun was shining, the deer where out and all, but I, was happy to see the snow melting. I still would fully enjoy many feet high of fresh snow. Yes, after 20 years in San Diego, I have become a typical West coaster. "Let it Snow, Let it Snow, Let it Snow."
We spent the better part of the morning into the afternoon on Skype with Kimmy and Shayna Punum. Mom, and the rest of us, have great pleasure watching Shayna Punum and Kimmy playing. Overall, Skype seems to decrease the absence of someone in person. The 7000 miles a part is not felt as much being able to view and talk with each other.
Tomorrow Sunday, will be a kick back day. Yes, it is Football Sunday. Poppie will spend the day reading and probably running errands. Reece will be working. Mike and Cindy will be cuddled up watching the games at their place. Brian will be swinging by Mom and Poppies to say hello. Mom and I will be glued to the TV to watch the Chargers and the Jet game. Hmmm, who will win, wink. Go Chargers!
Lots of Hugs and the best health possible,
Karen
Today, Mom, Poppie, Brian and I spent the day at Mike and Cindy's place in Naples. Mike and Cindy have a beautiful home set on 25 acres with a gorgeous panoramic view. It was a beautiful day. The weather was in the mid 40's with a light breeze, the sun was shining, the deer where out and all, but I, was happy to see the snow melting. I still would fully enjoy many feet high of fresh snow. Yes, after 20 years in San Diego, I have become a typical West coaster. "Let it Snow, Let it Snow, Let it Snow."
We spent the better part of the morning into the afternoon on Skype with Kimmy and Shayna Punum. Mom, and the rest of us, have great pleasure watching Shayna Punum and Kimmy playing. Overall, Skype seems to decrease the absence of someone in person. The 7000 miles a part is not felt as much being able to view and talk with each other.
Tomorrow Sunday, will be a kick back day. Yes, it is Football Sunday. Poppie will spend the day reading and probably running errands. Reece will be working. Mike and Cindy will be cuddled up watching the games at their place. Brian will be swinging by Mom and Poppies to say hello. Mom and I will be glued to the TV to watch the Chargers and the Jet game. Hmmm, who will win, wink. Go Chargers!
Lots of Hugs and the best health possible,
Karen
Thursday, January 14, 2010
2nd Day Home and Happy
Mom continues to feel happy and spunky that she is back in her home.
Mom and I spent yesterday morning attending to her hygiene needs. She was in heaven being back in her own shower again. Mom continues to enjoy being being able to take whatever food of choice at any time of the day and night. Mom spent the day finding her rhythm again. She enjoyed roaming around the house making sure all is in its correct place. She, best of all, enjoyed not being interrupted by having to have her vitals taken, to have to take medications, to have to order food, to have housekeeping make noises while she was napping or sleeping.
Yesterday, Mike came in the city for a long visit with Mom. This kicked her day off well. Mom continued to have a great day. Poppie allowed her to do as she wished with him. She told him what he could and could not eat and made sure he relaxed with her. The spent several hours kicked back in bed with together. They both had there feet up on pillows, their feet and legs in their compression stockings, watched movies together and napped on and off together. Mom and I exercised a bit and then cuddled up and watched several other movies into the late night.
This morning, Mom has her visiting Nurse coming over. More to come as the day unfolds. I must run to get Mom ready for her Nurse.
Hugs to all,
Karen
Mom and I spent yesterday morning attending to her hygiene needs. She was in heaven being back in her own shower again. Mom continues to enjoy being being able to take whatever food of choice at any time of the day and night. Mom spent the day finding her rhythm again. She enjoyed roaming around the house making sure all is in its correct place. She, best of all, enjoyed not being interrupted by having to have her vitals taken, to have to take medications, to have to order food, to have housekeeping make noises while she was napping or sleeping.
Yesterday, Mike came in the city for a long visit with Mom. This kicked her day off well. Mom continued to have a great day. Poppie allowed her to do as she wished with him. She told him what he could and could not eat and made sure he relaxed with her. The spent several hours kicked back in bed with together. They both had there feet up on pillows, their feet and legs in their compression stockings, watched movies together and napped on and off together. Mom and I exercised a bit and then cuddled up and watched several other movies into the late night.
This morning, Mom has her visiting Nurse coming over. More to come as the day unfolds. I must run to get Mom ready for her Nurse.
Hugs to all,
Karen
Tuesday, January 12, 2010
Bitter Sweet with Discharge Today
Mom, Poppie and I just got home. She is settling in and resting. Mom has been so excited to get home. Her energy, strength and mental state is outstanding. Her medical status is wonderful. She was discharged without having to fill any prescriptions this time. Her immune system is working strong on its own. Yes, she continues to amaze the medical staff.
It was amazing to see so many Doctors, Nurses, Technicians, Food Service staff came to Mom to say good-bye and good luck. Several of the Nurses and Technicians wanted Mom's number to call and say hello. Many of the staff expressed how much they were going to miss their conversations with her and simply her self motivating outlook on getting into remission. As we were leaving, some of the staff walked us out. It was very heart warming.
Tuesday, January 19th, Mom has an appointment with her primary Oncologist. She will get her blood drawn and receive her new treatment plan. We will be informed when she will receive her next bone biopsy. I will keep you posted as we find out.
Again thank you for all the support. Please continue to send your prayers for Mom to have a good bone biopsy. We trust this biopsy the Doctor is able to collect fluid to test. We also pray she will soon get into remission.
Lots of love and hugs,
Karen
It was amazing to see so many Doctors, Nurses, Technicians, Food Service staff came to Mom to say good-bye and good luck. Several of the Nurses and Technicians wanted Mom's number to call and say hello. Many of the staff expressed how much they were going to miss their conversations with her and simply her self motivating outlook on getting into remission. As we were leaving, some of the staff walked us out. It was very heart warming.
Tuesday, January 19th, Mom has an appointment with her primary Oncologist. She will get her blood drawn and receive her new treatment plan. We will be informed when she will receive her next bone biopsy. I will keep you posted as we find out.
Again thank you for all the support. Please continue to send your prayers for Mom to have a good bone biopsy. We trust this biopsy the Doctor is able to collect fluid to test. We also pray she will soon get into remission.
Lots of love and hugs,
Karen
Monday, January 11, 2010
Marvelous Monday
This morning Mom again surprises her Doctors. Her numbers continue to rise, her energy & endurance continue to improve and she is being discharged tomorrow afternoon. Her discharge Nurse has already put the process in motion.
Mom is no longer on IV antibiotics. Tonight she will receive her last injection of Neupogen. Her "bumps" have decreased in size, color and in tenderness. She has not had a fever for 48 hours.
Mom and her staff have permanent smiles and exude uncontrollable excitement for her being able to return home. Poppie and I brought in two big barrels of different snacks for the staff. This is Mom's little way of expressing her warmest thank you for everyone taking wonderful care of her.
Mom and I spent the afternoon chatting, what's new, taking short walks around the Oncology floor, visiting with all the staff and watching DVD movies on my laptop. Today was her first day she felt able to focus and was fully relaxed.
This evening, Brian, Poppie and I shared in celebrating Mom's "Last Supper" with her in the hospital. We all spent several hours talking about various topics, taking walks, and yes talking about planning a Panama Canal Cruise. At least gathering information so when she enters remission we can head out ASAP. This has been a dream cruise they have spoken about for years.
Mom was fading and we took off for home around 8:30pm. We all want a good night sleep for the big day tomorrow. Poppie and I will be at the hospital around 9am to await the discharge together and speak with her Medical team for the next plan of treatment care.
To all a good night and happy dreams,
Hugs,
Karen
Mom is no longer on IV antibiotics. Tonight she will receive her last injection of Neupogen. Her "bumps" have decreased in size, color and in tenderness. She has not had a fever for 48 hours.
Mom and her staff have permanent smiles and exude uncontrollable excitement for her being able to return home. Poppie and I brought in two big barrels of different snacks for the staff. This is Mom's little way of expressing her warmest thank you for everyone taking wonderful care of her.
Mom and I spent the afternoon chatting, what's new, taking short walks around the Oncology floor, visiting with all the staff and watching DVD movies on my laptop. Today was her first day she felt able to focus and was fully relaxed.
This evening, Brian, Poppie and I shared in celebrating Mom's "Last Supper" with her in the hospital. We all spent several hours talking about various topics, taking walks, and yes talking about planning a Panama Canal Cruise. At least gathering information so when she enters remission we can head out ASAP. This has been a dream cruise they have spoken about for years.
Mom was fading and we took off for home around 8:30pm. We all want a good night sleep for the big day tomorrow. Poppie and I will be at the hospital around 9am to await the discharge together and speak with her Medical team for the next plan of treatment care.
To all a good night and happy dreams,
Hugs,
Karen
Sunday, January 10, 2010
Sunday as it "should be"
This morning Mom received wonderful news. Her cat scans all came back negative. Also, the bumps that had surfaced the past few days began to decrease in size. We will be informed tomorrow if the Doctors want to follow up with any further tests regarding to the bumps. Mom received several IV's of antibiotics, an IV of blood. This evening she had her Neupogen Injection and lots of attention from all the staff. It is wonderful to see so many of the staff caring for Mom as their own Mom or Gramma.
All day, Mom was in a good mood though she exhibited limited energy. She had a strong appetite for all three meals. Mom walked several times in the day with me. Each walk was only a few minutes in result of being winded quickly. It was adorable to see Mom and Poppie walk around the Nurses station holding hands this evening. Poppie was as red as young man on his first date. It was so cute to hear the staff comment with endearing statements and see the beaming smiles as Mom and Poppie continued to circle around the station.
Mom started to doze on and off starting around 7:30pm. Brian, Poppie and I gave Mom a kiss and said we would see her tomorrow. Mom quickly grabbed her face mask, wrapped her shawl around herself and walked the three of us down the hallway towards the elevators. This is a routine for Mom when we leave and she is feeling up to it.
Well, we all pray that tomorrow brings only good news and Mom continues to gain her strength.
Sleep well,
Karen
All day, Mom was in a good mood though she exhibited limited energy. She had a strong appetite for all three meals. Mom walked several times in the day with me. Each walk was only a few minutes in result of being winded quickly. It was adorable to see Mom and Poppie walk around the Nurses station holding hands this evening. Poppie was as red as young man on his first date. It was so cute to hear the staff comment with endearing statements and see the beaming smiles as Mom and Poppie continued to circle around the station.
Mom started to doze on and off starting around 7:30pm. Brian, Poppie and I gave Mom a kiss and said we would see her tomorrow. Mom quickly grabbed her face mask, wrapped her shawl around herself and walked the three of us down the hallway towards the elevators. This is a routine for Mom when we leave and she is feeling up to it.
Well, we all pray that tomorrow brings only good news and Mom continues to gain her strength.
Sleep well,
Karen
Saturday, January 9, 2010
Roller Coaster of Emotions
This morning Mom awoke with pain under her chin and in her right calf. She explored her body and found a bump on right calf. She noticed with palpation and weight bearing she experiences pain and tenderness. She then explored her body and noticed a reddish bump on her left. She shared her new findings with her Nurse. He immediately contacted her Dr. and a series of tests where requested to be done this morning.
She had more blood drawn, she had a cat scan done (this included a contrast dye and a scan to see from above heart, chin, throat, sinuses, forehead, and crown of her head. Monday she will receive and ultrasound for her right calf.
This afternoon, Mom received an IV of fluids. Her heart rate was low and she was dehydrated from the past 72 hours of fever. She is in better spirits and actually walked a good 5 minutes. Her Dr.'s are not surprised she needed the fluid(antibiotic and then sodium chloride). They are concerned with the new findings, hence the tests being ordered.
Yes, today Mom is emotionally trying to gather herself and be in the present and wait for results. It is challenging to hurry up for tests and then wait. A positive today is that Mom slept through most of the night, her appetite is back and food tastes good. This alone is making her smile.
Unfortunately, we found another unknown bump with redness on her upper side of the thigh that looks like the left hip from this morning. She also is showing more unknown red spots on her legs. All is being watched closely. The Doctor at this point, gave Mom a complete body check. Nothing else was found on Mom, which relieved her.
Mom received her Neupogen injection and another IV of anti-biotic this evening. i gave Mom her nightly foot and leg massage. She seems to unwind and fall into a light sleep when I give her this. Poppie, Brian and I left Mom around 8:45pm tonight feeling relaxed emotionally and physically. She was actually ready to fall into bed and sleep.
She is looking forward to feeling much better tomorrow, getting more walking in and have no NEW surprises.
Lots of good health and warmth to you,
Karen
She had more blood drawn, she had a cat scan done (this included a contrast dye and a scan to see from above heart, chin, throat, sinuses, forehead, and crown of her head. Monday she will receive and ultrasound for her right calf.
This afternoon, Mom received an IV of fluids. Her heart rate was low and she was dehydrated from the past 72 hours of fever. She is in better spirits and actually walked a good 5 minutes. Her Dr.'s are not surprised she needed the fluid(antibiotic and then sodium chloride). They are concerned with the new findings, hence the tests being ordered.
Yes, today Mom is emotionally trying to gather herself and be in the present and wait for results. It is challenging to hurry up for tests and then wait. A positive today is that Mom slept through most of the night, her appetite is back and food tastes good. This alone is making her smile.
Unfortunately, we found another unknown bump with redness on her upper side of the thigh that looks like the left hip from this morning. She also is showing more unknown red spots on her legs. All is being watched closely. The Doctor at this point, gave Mom a complete body check. Nothing else was found on Mom, which relieved her.
Mom received her Neupogen injection and another IV of anti-biotic this evening. i gave Mom her nightly foot and leg massage. She seems to unwind and fall into a light sleep when I give her this. Poppie, Brian and I left Mom around 8:45pm tonight feeling relaxed emotionally and physically. She was actually ready to fall into bed and sleep.
She is looking forward to feeling much better tomorrow, getting more walking in and have no NEW surprises.
Lots of good health and warmth to you,
Karen
Friday, January 8, 2010
Day 17 and feeling exhausted
Mom at 4:30am awoke soaking with perspiration. Her fever had broke. She continues to receive an IV of antibiotics. She waits to hear about the results from the cultures taken. Mom did not need any transfusions today.
Mom has eaten very little for breakfast and lunch. She has not had the strength to walk today. She has been dozing on and off since the morning. Unfortunately, Mom has had a low grade fever since the later part of the morning.
This afternoon, Mike was able to have a nice long visit with Mom. Yes, this perked her right up. Poppie also has had a wonderful day sharing naps with Mom into the evening. Brian, as every night, showed up around 5:30pm for a nice visit. Mom, Poppie and I continue to be amazed with all the stories Brian has to share. Yes,they are his life stories. So many them are simply too funny. I love seeing Mom and Poppie have tears in their eyes from laughing.
Mom had a fever way into the evening. The Nurses took additional blood to culture, Mom had X-Rays of her chest, and then the Nurses settled Mom in for the night with another IV of antibiotics. I gave Mom another foot and leg massage. She always seems to doze off into a relaxing sleep. Shortly after, Brian, Poppie and I left so Mom can sleep and rest.
Have a beautiful weekend,
Karen
Mom has eaten very little for breakfast and lunch. She has not had the strength to walk today. She has been dozing on and off since the morning. Unfortunately, Mom has had a low grade fever since the later part of the morning.
This afternoon, Mike was able to have a nice long visit with Mom. Yes, this perked her right up. Poppie also has had a wonderful day sharing naps with Mom into the evening. Brian, as every night, showed up around 5:30pm for a nice visit. Mom, Poppie and I continue to be amazed with all the stories Brian has to share. Yes,they are his life stories. So many them are simply too funny. I love seeing Mom and Poppie have tears in their eyes from laughing.
Mom had a fever way into the evening. The Nurses took additional blood to culture, Mom had X-Rays of her chest, and then the Nurses settled Mom in for the night with another IV of antibiotics. I gave Mom another foot and leg massage. She always seems to doze off into a relaxing sleep. Shortly after, Brian, Poppie and I left so Mom can sleep and rest.
Have a beautiful weekend,
Karen
Thursday, January 7, 2010
Day 16 Not such a good day
Mom around 1:30 am had a low grade fever. Throughout the early am she was feeling the onset of mild joint acheiness, mild nausea, sinus pressure, and pretty fatigued. This am around 8:30 am all symptoms remained and increased slightly. She barely ate her breakfast (scrambled eggs, English muffin and tea) and could not get the energy up to walk. I gave Mom another foot and leg massage and she fell right into a deep sleep.
Mom continued to stay in bed and rest till 2:30pm. She was running a 101 fever. She received an IV of red blood cells, an IV of platelets, and and IV of more aggressive antibiotics. Her appetite is not present. I was able to get her to eat a small baked potato, some chicken soup and finish another hot tea and yes, she is also drinking water.
At 3:15pm, Mom and I took a tour around the nurses station. All the staff smiled and were calling Mom's name out with encouragement that she get herself up to walk. It was very heart warming to see and feel the love so many new people in Mom's life hold for her. Mom settled back into bed exhausted. Poppie arrived at 3:30pm. after a few minutes of conversation, Mom and Poppie took a nap until 5:15pm. It was cute to see they still are napping together and snoring in harmony.
Brian had arrived with Mom's favorite Chinese ribs in hand. Poppie and I were beaming and Mom was struggling to find an appetite. Mom with resistance, did take a rib and gobbled it up with a big smile. We all hung out and chatted and shared stories till about 7:30pm. Mom had dozed off again and we three decided to pack our stuff up and head out. We left Mom feeling only a queasy stomach. She, thankfully, had no fever, no bodily aches, no headache and was ready for a good night sleep.
Mom is excited for tomorrow. Though Mike calls everyday to speak with Mom, he has not been able to get to the hospital for a visit. Tomorrow he is able to drive into Rochester and spend time with her. It will be nice for all of us to be together with Mom tomorrow.
Sleep well and pleasant dreams,
Karen
Mom continued to stay in bed and rest till 2:30pm. She was running a 101 fever. She received an IV of red blood cells, an IV of platelets, and and IV of more aggressive antibiotics. Her appetite is not present. I was able to get her to eat a small baked potato, some chicken soup and finish another hot tea and yes, she is also drinking water.
At 3:15pm, Mom and I took a tour around the nurses station. All the staff smiled and were calling Mom's name out with encouragement that she get herself up to walk. It was very heart warming to see and feel the love so many new people in Mom's life hold for her. Mom settled back into bed exhausted. Poppie arrived at 3:30pm. after a few minutes of conversation, Mom and Poppie took a nap until 5:15pm. It was cute to see they still are napping together and snoring in harmony.
Brian had arrived with Mom's favorite Chinese ribs in hand. Poppie and I were beaming and Mom was struggling to find an appetite. Mom with resistance, did take a rib and gobbled it up with a big smile. We all hung out and chatted and shared stories till about 7:30pm. Mom had dozed off again and we three decided to pack our stuff up and head out. We left Mom feeling only a queasy stomach. She, thankfully, had no fever, no bodily aches, no headache and was ready for a good night sleep.
Mom is excited for tomorrow. Though Mike calls everyday to speak with Mom, he has not been able to get to the hospital for a visit. Tomorrow he is able to drive into Rochester and spend time with her. It will be nice for all of us to be together with Mom tomorrow.
Sleep well and pleasant dreams,
Karen
Wednesday, January 6, 2010
Day 15 is a Good Day
Mom continues to be primarily positive emotionally and is focused on doing all she can do to get into remission. Daily, Mom visits her anger and fear of dealing with having AML. She is working hard to "feel" and then allow herself to find comfort in taking one day at a time. She is eating well, walking a mile plus a day, and taking many naps.
Today, Mom did not need any transfusions, she received her second injection of Neupogen (stimulates the production of white blood cells), her numbers show slight increase from yesterday, and she is still receiving antibiotics to prevent infections.
Mom, Brian, Poppie and I enjoyed our visit tremendously tonight. Brian was on a roll tonight sharing stories that made us laugh and had us in amazement. He really has a lot of adventurous things he has done in his lifetime. Mom loved the stories and we all loved getting to know another side of Brian.
I just finished giving Mom a foot and leg massage. She is all tucked into bed and is in a deep sleep. I am spending the night with her. Yup, a slumber party at her hospital "dorm" room. Tomorrow will be more exercise, massages, eating, walking, sharing stories and visiting with the family.
To all a good night. Sleep Well,
Karen
Today, Mom did not need any transfusions, she received her second injection of Neupogen (stimulates the production of white blood cells), her numbers show slight increase from yesterday, and she is still receiving antibiotics to prevent infections.
Mom, Brian, Poppie and I enjoyed our visit tremendously tonight. Brian was on a roll tonight sharing stories that made us laugh and had us in amazement. He really has a lot of adventurous things he has done in his lifetime. Mom loved the stories and we all loved getting to know another side of Brian.
I just finished giving Mom a foot and leg massage. She is all tucked into bed and is in a deep sleep. I am spending the night with her. Yup, a slumber party at her hospital "dorm" room. Tomorrow will be more exercise, massages, eating, walking, sharing stories and visiting with the family.
To all a good night. Sleep Well,
Karen
Tuesday, January 5, 2010
Hope is back and Mom is smiling
Mom awoke feeling pretty good today with a strong outlook. She continues to eat well, walk many times in a day, and loves to share with me about her childhood stories. Mom experienced a little spa day by me today. Tomorrow will be her massage. Her head leukemia bumps are completely gone. The 2 biopsy's on her head are a good 80% healed. She exhibits no pain nor discomfort.
Early afternoon one of Mom's Doctors on her team came by to inform her that she is at her low point in numbers. The Dr. complimented Mom on how well she has and is responding to the advanced Chemo treatment. Her doctor also informed her at this time the blood tests are showing NO blast cells (NO leukemic cells)are in her blood. Yes, this means there is presently NO cancer cells showing up. Mom shrieked with excitement and big smiles.
Mom received her first of several injections of Neupogen this evening. She will receive an injection daily for the next week. Neupogen assists to elevate Mom's numbers. We hope to see in 7-10 days her numbers show a considerable increase. Mom then can rely on her own system to fight off bacteria, fungal and viral infections. She then can home safely. After her numbers reach a certain level she then will be heading back for another bone marrow biopsy.
Mom was tired and ready to get some shut eye by 8:00pm. Brian and I tucked her in and shortly left there after.
I will add more tomorrow. Enjoy "hump" day.
Lots of Hugs and Good Health,
Karen
Early afternoon one of Mom's Doctors on her team came by to inform her that she is at her low point in numbers. The Dr. complimented Mom on how well she has and is responding to the advanced Chemo treatment. Her doctor also informed her at this time the blood tests are showing NO blast cells (NO leukemic cells)are in her blood. Yes, this means there is presently NO cancer cells showing up. Mom shrieked with excitement and big smiles.
Mom received her first of several injections of Neupogen this evening. She will receive an injection daily for the next week. Neupogen assists to elevate Mom's numbers. We hope to see in 7-10 days her numbers show a considerable increase. Mom then can rely on her own system to fight off bacteria, fungal and viral infections. She then can home safely. After her numbers reach a certain level she then will be heading back for another bone marrow biopsy.
Mom was tired and ready to get some shut eye by 8:00pm. Brian and I tucked her in and shortly left there after.
I will add more tomorrow. Enjoy "hump" day.
Lots of Hugs and Good Health,
Karen
Monday, January 4, 2010
An Emotional Day
Mom was informed that her bone biopsy will be postponed. Her Dr. prefers to have her numbers start to climb. As you know, it is difficult for Mom to switch gears after she sets something in her mind. She understands why, but now she needs to rethink her game plan once again. Today, she is sad that she will never have her old life back being "healthy."
Mom is on day 13 with her Chemo. Her body continues to be responding very well. Her numbers are continueing to drop. Around day 20 to day 22 her numbers are expected to be at their lowest level. It is here where her numbers are expected to rise. At this point, Mom will be re-evaluated to take her off antibiotics to prevent infections. Her body at this point will be avle to fight fungal and bacteria infections on its own. Mom remains in the hopsital to be monitored.
Reece came to visit today for a good hour and half. Brian and Poppie came for a good portion of the night. They both show up every evening around dinner time. Poppie still says the hopsital food is a five star restauarnt. THey both took off around 8pm. Mom and I after walking them to the elevators took another 20 minute walk and then did some upper body exercises. I like to hang out with Mom till she falls asleep. She rests best having company into the night.
Have a great evening and a wonderful day tomorrow.
Hugs from the Baskin's
Mom is on day 13 with her Chemo. Her body continues to be responding very well. Her numbers are continueing to drop. Around day 20 to day 22 her numbers are expected to be at their lowest level. It is here where her numbers are expected to rise. At this point, Mom will be re-evaluated to take her off antibiotics to prevent infections. Her body at this point will be avle to fight fungal and bacteria infections on its own. Mom remains in the hopsital to be monitored.
Reece came to visit today for a good hour and half. Brian and Poppie came for a good portion of the night. They both show up every evening around dinner time. Poppie still says the hopsital food is a five star restauarnt. THey both took off around 8pm. Mom and I after walking them to the elevators took another 20 minute walk and then did some upper body exercises. I like to hang out with Mom till she falls asleep. She rests best having company into the night.
Have a great evening and a wonderful day tomorrow.
Hugs from the Baskin's
Sunday, January 3, 2010
Count Down to the Next Bone Biopsy
This morning Mom's Oncologist and the Team came in to discuss her present status. Mom continues to be weathering the Chemo very well. Her numbers are dropping as expected. Her head is healing well from her biopsy's. Mom's energy is pretty good and walks after every meal. She walked a bit over a mile today. Mom is eating like a champ and is keeping her spirits up.
This coming Tuesday, Mom heads in for another bone biopsy. We hope the procedure goes well and there is some fluid in her bone to extract and then test. This procedure is now at the fore front of Mom's thoughts. I and others are trying to keep her "minds eye" focused on seeing the fluid in her bone.
Today, Poppie and I had lunch with Mom. Then, Mom and I took off for a walk and then did upper and lower body exercises. She really "LOVES" to feel her body work. It is so cute to see her inspire that staff on the floor. Brian and I accompanied Mom for dinner time. The three of us enjoyed watching "The Funniest Home Videos." It really is a warming feeling to hear Mom laugh from deep down and forget what is going on for her.
Brian headed home around 8:30pm. Mom and I walked Brian to the elevators. She and I continued to walk for 20 minutes. We then went through another series of upper and lower movement exercises. I spoiled her with a foot and leg massage. At 9:30pm Mom wanted me to head home to be with Poppie. The other reason was, she did not want me too tired while driving. The roads have been pretty bad all day due to all the snow fall and low double digits since yesterday night.
She is resting now and is sound asleep.
Again, THANK YOU for all your prayers and healing thoughts,
Karen
This coming Tuesday, Mom heads in for another bone biopsy. We hope the procedure goes well and there is some fluid in her bone to extract and then test. This procedure is now at the fore front of Mom's thoughts. I and others are trying to keep her "minds eye" focused on seeing the fluid in her bone.
Today, Poppie and I had lunch with Mom. Then, Mom and I took off for a walk and then did upper and lower body exercises. She really "LOVES" to feel her body work. It is so cute to see her inspire that staff on the floor. Brian and I accompanied Mom for dinner time. The three of us enjoyed watching "The Funniest Home Videos." It really is a warming feeling to hear Mom laugh from deep down and forget what is going on for her.
Brian headed home around 8:30pm. Mom and I walked Brian to the elevators. She and I continued to walk for 20 minutes. We then went through another series of upper and lower movement exercises. I spoiled her with a foot and leg massage. At 9:30pm Mom wanted me to head home to be with Poppie. The other reason was, she did not want me too tired while driving. The roads have been pretty bad all day due to all the snow fall and low double digits since yesterday night.
She is resting now and is sound asleep.
Again, THANK YOU for all your prayers and healing thoughts,
Karen
Saturday, January 2, 2010
Mom staying positive
Mom continues to push herself to all she can to put her AML in remission. She is eating well, walking about a mile a day, and is encouraging all her medical staff to be pro-active with his/her own health. Many of them are now going to Mom to get direction with creating a healthy lifestyle.
This morning Mom had an IV of platelets. Her numbers continue to drop as expected. She is not exhibiting any physical symptoms from her Chemo expect fatigue and getting tired with walking and mild exertion. Mom is trying to stay hopeful that this Chemo will put her into remission.
This afternoon my cousin Jody surprised Mom with her favorite soup and brought her a new beautiful shall. Mom wore it all day with a big smile. I brought Mom a pedometer today. She now knows exactly how far she walks. She loves to track her achievements. This evening a childhood friend of mine, Suzanne, came by to visit with Mom. Mom beamed to see Suzanne and reminisce about the early days when we were kids. Poppie also chimed in and enjoyed. Mom then had another highlight of the night. Brian stopped in with Mom's favorite Chinese ribs. Yup, the five of us enjoyed in quiet while we devoured the ribs.
It is wonderful to hear Mom engage, laugh, and simply enjoy. It was a wonderful evening for all of us.
Have a good night. I will chat tomorrow.
Hugs and good health always,
Karen
This morning Mom had an IV of platelets. Her numbers continue to drop as expected. She is not exhibiting any physical symptoms from her Chemo expect fatigue and getting tired with walking and mild exertion. Mom is trying to stay hopeful that this Chemo will put her into remission.
This afternoon my cousin Jody surprised Mom with her favorite soup and brought her a new beautiful shall. Mom wore it all day with a big smile. I brought Mom a pedometer today. She now knows exactly how far she walks. She loves to track her achievements. This evening a childhood friend of mine, Suzanne, came by to visit with Mom. Mom beamed to see Suzanne and reminisce about the early days when we were kids. Poppie also chimed in and enjoyed. Mom then had another highlight of the night. Brian stopped in with Mom's favorite Chinese ribs. Yup, the five of us enjoyed in quiet while we devoured the ribs.
It is wonderful to hear Mom engage, laugh, and simply enjoy. It was a wonderful evening for all of us.
Have a good night. I will chat tomorrow.
Hugs and good health always,
Karen
Friday, January 1, 2010
Feeling Strong and Hopeful
Mom and I thoroughly enjoyed awaking together this morning in her "dorm" room. Both of us turned towards each other, our eyes connected and we both had big smiles. We both shared what it meant for ourselves to be able to bring in the New Year together. We both treasured this experience of sharing.
Mom feels confident that she is ahead of the game and in control of her AML. This morning her Medical Team reviewed her blood reports and evaluated her physical strengths and weaknesses, and expressed what she may be experiencing in the next few days. All four doctors present had smiles on their faces.
Her lead Dr. began with "Ruth you are amazingly doing well. You are a rock! We are all very pleased."
He expressed her blood test are showing expected numbers to be dropping. Her red blood cells are below normal and her platelets are below normal. All of this is expected and she is receiving the appropriate IV's to resolve the below normal levels. Every day, Mom has her blood tests reviewed, her eyes checked, her balance & coordination evaluated and her emotional and mental state is assessed.
Today, Mom walked a good mile. She completed this triumph by walking several laps in the early morning, in the late morning, in the early afternoon, in the late afternoon, in the early evening and in the late evening. The medical staff is in awe of her personal focus and dedication to be in control of her AML. She continues to educate the staff on the importance of eating well, getting daily exercise, using their mind, and trying to keep stress in check. The staff simply adore and have adopted Mom. Her staff continue to visit her daily with smiles and hugs. Mom and they are enjoying each other so much. This is WONDERFUL for me to observe and be a part of.
Brian, Poppie and I joined Mom for dinner in her room this evening. It is wonderful that she is NOT feeling all the terrible symptoms yet. We all trust she will weather this re-induction well. After dinner, we all took a long stroll around the Nurses station and up and down a hallway with Mom. It really feels that we now have an extended family.
Well, hugs to you. Again, thank you for keeping in touch.
2010 is about reaching for all your dreams and creating new ones.
Karen
Mom feels confident that she is ahead of the game and in control of her AML. This morning her Medical Team reviewed her blood reports and evaluated her physical strengths and weaknesses, and expressed what she may be experiencing in the next few days. All four doctors present had smiles on their faces.
Her lead Dr. began with "Ruth you are amazingly doing well. You are a rock! We are all very pleased."
He expressed her blood test are showing expected numbers to be dropping. Her red blood cells are below normal and her platelets are below normal. All of this is expected and she is receiving the appropriate IV's to resolve the below normal levels. Every day, Mom has her blood tests reviewed, her eyes checked, her balance & coordination evaluated and her emotional and mental state is assessed.
Today, Mom walked a good mile. She completed this triumph by walking several laps in the early morning, in the late morning, in the early afternoon, in the late afternoon, in the early evening and in the late evening. The medical staff is in awe of her personal focus and dedication to be in control of her AML. She continues to educate the staff on the importance of eating well, getting daily exercise, using their mind, and trying to keep stress in check. The staff simply adore and have adopted Mom. Her staff continue to visit her daily with smiles and hugs. Mom and they are enjoying each other so much. This is WONDERFUL for me to observe and be a part of.
Brian, Poppie and I joined Mom for dinner in her room this evening. It is wonderful that she is NOT feeling all the terrible symptoms yet. We all trust she will weather this re-induction well. After dinner, we all took a long stroll around the Nurses station and up and down a hallway with Mom. It really feels that we now have an extended family.
Well, hugs to you. Again, thank you for keeping in touch.
2010 is about reaching for all your dreams and creating new ones.
Karen
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