All posts tagged acceptance

QOTD: Topic – Individuality

Published August 26, 2016 by lynn k scott

“Our uniqueness, our individuality, and our life experience molds us into fascinating beings. I hope we can embrace that. I pray we may all challenge ourselves to delve into the deepest resources of our hearts to cultivate an atmosphere of understanding, acceptance, tolerance, and compassion. We are all in this life together.” (Linda Thompson)



It’s time for a change

Published October 23, 2015 by lynn k scott

Could be it be true?  I’m back to blogging?

Yes, yes….it’s true.  No need for excitement.  I apologize for my disappearing act.  So much going on and so little time to blog while dealing with life.  Rest assured, I am here and I shall provide an exit blog should the time arise when I am no longer able to continue my ever-changing writing adventure.

So, as you can see, it’s time for a change.  This particular reference is in regards to our homeschooling journey.  After discussions with my daughter about her schooling preferences and her day and evening routines, we have made a change; hopefully for the better.

Starting on Monday, my lil miss will return to a brick and mortar school.  I still maintain my beliefs on the public school system and the shambles it’s in regarding quality education.  That being said, a private, Christian school has been located and appears to suit my daughter’s educational needs.

One, it’s not a public school and they don’t deal with Common Core (bonus points there).  Two, they have an American flag in each classroom and say the Pledge daily.  That might seem trivial to some, but it’s extremely important to this Army mom. Every school should be doing this, imo.  Three, she will have religion in her class.  While I am not overly religious, I find it important to have a foundation in faith; whatever that may mean to an individual.  Lastly, it’s a very small school.  My daughter will be the 10th child in her class.  The school holds K-8, but each grade only has one classroom.

For me, there’s a personal level and mirrors homeschooling, as close as possible, in a school environment.  Their goal is to teach during the day with no more than an hour’s homework per night, if at all.  Responsibility and accountability and coupled with the educational pursuit.

I was impressed when I inquired about the school, how they immediately invited me to come and take a tour.  I observed my daughter’s potential new class for 20 minutes and how I was able to have a private conversation with her potential new teacher.  I was impressed her tuition costs the same as what I was paying a friend to watch her during the day while I worked.

Change is scary but also necessary.  I have enjoyed homeschooling my daughter for the last two and a half years.  We will continue her art pursuit on our own.  She is nervous and excited to rejoin a brick and mortar school.  If this works out well, she will stay there through eighth grade.  At that point, we will see what charter schools are available.  If none meet our standards, then we can revisit homeschooling again.

The lil miss will still get the opportunity to hang out with her homeschool group friends.  We may not make every week’s meetup, but they have been a blessing the short time we’ve been involved with them and we’re glad to know we are still welcome to hang out when our schedule allows.

I firmly believe you cannot grow if you are not willing to change.  My daughter said this morning, her new school is a new door opening in her life.  How cannot I not be pleased with her acceptance of change?

Did you know…?

Published July 10, 2015 by lynn k scott

I’m sure you’ve heard of the “Stages of Grief”, but did you know who came up with them?

I, myself, didn’t know until December of last year.  The final day of my human development class; we passed a piece of paper around the class.  On this paper, was a variety of quotes from Elisabeth Kubler-Ross.  Each student chose a quote that got their attention and read it aloud.

Elisabeth Kubler-Ross was a psychiatrist and journalist and the stages were for terminally ill patients:  Denial, Anger, Bargaining, Depression and Acceptance.  Those stages apply to the majority of people, whether they themselves are terminally ill or they have lost someone close to them.  She spent a good part of her career observing, talking and being with those who were dying.

We had studied a bit of her just a couple weeks prior to the end of the semester.  I found her work very interesting and comforting.  I believe part of that was due to the fact I still had to write my final paper on “death and dying”.  As it was about my sister, my emotions were reeking havoc and I was an incoherent mess; to put it mildly.  One might think it’s a morbid topic, yet to read her work and observations is very enlightening.

I have posted two Quotes of the Day for today and tomorrow.  Both are by Kubler-Ross and they just seem really appropriate.  If you’d like to learn a bit more about her, I’ve provided a link for you.

Made It Through

Published July 1, 2015 by lynn k scott

I did it!  I survived another June.  I know I took myself out of the picture for a while there, but I just wasn’t coping as well as I had hoped.

It’s officially July and as anticipated, life continues.  I am redirecting some of my energy.  Some of that energy is focused on me.

I know some won’t understand, but I had a few “signs” from my mom over the last couple of weeks.  The signs misted my eyes but were still comforting and I was able to share a couple smiles with a friend here and there.

Over 15 years ago, my mother tricked me into telling her specific details of some cookware I saw on the HSN (Home Shopping Network).  She used that information to purchase the set as a birthday gift.  I still have all but 2 pans from the original set.

This past Sunday, I thought I was clicking on a cooking show, but it turned out to be cookware by Ming Tsai.  He’s a chef that I really enjoy watching; when time allows.  I had no idea he had a line of cookware.  I watched the television like a toddler would as if their favorite Disney movie just started playing.

I have looking for some new frying pans.  I was torn about ordering myself something new.  This set wasn’t a necessity.  Then I remember what my mom used to say, “Bills will always be there. You need to acknowledge what you need sometimes.”  I did need new frying pans and I chose this particular set.  Yes, there are cheaper sets available.  However, I have learned, good equipment yields good results.  I cook over 90% of our meals.  Takeout isn’t the norm in our house.

I called to order.  Hung up…I don’t need them.  I redialed, hung up again and the third time I dialed, I placed the order.  I chose to allow myself to be “ok” with my decision.  I normally wouldn’t do something like that.  I talk myself out of purchases out all the time.  This particular purchase, two days after my mother’s angel-versary, seemed “right”.  I was happy.  The money will work itself out.

Now, I am anxiously awaiting my new set.  The best part is, I got the set in this brilliant purple color.  That’s right:  purple!   Had you been here, you’d have just heard my giddy joy of having cookware in my favorite color.  Can’t wait to make some more amazing meals.

New cookware warrants new recipes, no?

Picture This

Published March 13, 2015 by lynn k scott

I’ve never been a fan of having my picture taken.  I actually despised it at one point.  It wasn’t until almost two years ago, when I responsible for planning my mother’s funeral and we were trying to find pictures of her, that I realized, I was becoming my mother.  I was leaving no trace of my existence because I was worried I looked fat or the camera didn’t add just 10 lbs but more like 40 lbs in its rendition of me.

After that, I promised, I would begin taking more pictures of myself, having them printed and keeping them accessible.  I would allow my picture to be taken by others.  I would be ok with it.  I admit, I’ve had a drink or four over that decision, but I’ve steadily grown to accept the fact that it’s ok.

I didn’t say I wouldn’t take 15 selfies to get one acceptable shot, but I’m a work in progress.  I can say that, honestly, because I know me.  Others who know me, would agree.  I want my children and friends to have something to remember me by.  I see pictures of before I dropped 40 lbs in one year.  No wonder I get surprised reactions from those who haven’t seen me in quite awhile.  I literally shed four 10-lb bags of potatoes off my body.

I won’t promise I won’t delete this post somewhere down the line, but I was doing a comparison picture today and I found this one that I really do like.  Heck, I even took it, which makes it even better.  I captured “me”.  So enjoy a rare glimpse of me. Future followers of my blog may not get this opportunity.

Life is too precious and too short to not be accepting of yourself.  Learn to live for now, because tomorrow isn’t promised to anyone.  Life made sure I was well aware of that fact.  Without further adieu….


A recounting of a life

Published March 11, 2015 by lynn k scott

I wrote this paper in December as part of my final report which had to be on death and dying.  I literally finished it at 11:00 p.m. the night before it was due.  I could not bring myself to write this paper, prior to that moment in time.  It was an excruciating process.  Part of the assignment was to interview someone who is dying or the someone dealing with someone who has died.  I was given special permission to write about my sister as well as permission to interview my mother.

Our papers were graded while we took our final.  My professor actually gave me a hug when she returned my paper.  She finally understood why my classmate said my picture should be near “resilience” in the dictionary after one of our “interview” exercises. I actually think I should be on some campaign about not turning into an alcoholic within the last six years; considering I’ve buried my father, sister and mother in that time-frame.

Names have been changed or omitted for privacy reasons.  Here is my “final” paper.


Kathi was born in Upstate  NY in the summer of 1974.  She grew up with in a nuclear family; a mother, father, and two sisters.  Lynn was the oldest, then Kathi and then came Robyn.  While growing up, Kathi was educationally gifted but despised school and dropped out when she was 16 years old.  She was the “wild child” of the family.  Whether it was school fights, breaking curfew, or refusing to do homework because she knew the answers already so why should she prove it, she definitely followed the beat of her own drum.  Having a mother who survived non-lymphoma Hodgkin’s Disease, losing a father to stomach cancer a few year’s prior, the diagnosis that Kathi received when she was 37 years old changed everything:  Stage-4 breast cancer.

Kathi remained in her small, country hometown.  In fact, the entire family was there, except for Lynn.  After her father passed in 2007, Kathi moved back to her childhood home with her daughter and lived with her mother.  Years later, she married and had two more children; both girls.  Shortly after her youngest’s birth, Kathi’s husband and Lynn’s oldest son, entered the Army together and Kathi became an Army wife.  While her husband and nephew headed to the mid-west for Basic training, Kathi settled into being a single mom.  She was lucky to have the support of her mother to help with the children.  As her mother was retired, Kathi was able to work and not have to worry about paying for daycare.

When her husband graduated from Basic training and then A.I.T. (Advanced Individualized Training), Lynn had a chance to meet her brother-in-law, as she attended the A.I.T. graduation ceremony.  It was the first time she’d meet her brother-in-law.  It was a defining moment, as he spoke so highly of his wife, it gave Lynn something to think about.  Lynn decided to reach out to Kathi.  The two sisters had been estranged and hadn’t spoken in over 10 years.

It turned out Kathi had wanted to reconnect with Lynn as well.  The two spent a lot of time on Facebook, calling each other and texting to catch up.  While Lynn was involved in supporting deployed troops, Kathi was involved with supporting the veterans.  The two never knew that about each other.  Kathi became one of Lynn’s biggest supporters.  Frequently, Kathi would have her two youngest daughters draw pictures and then she would send them to Lynn, along with other care package supplies and Lynn would make sure deployed soldiers received them.  This was a bond the two shared, community support of the military.  While their bond grew, Kathi and Robyn’s relationship all but deteriorated.  They had very different views on life in general and they parted separate ways, so to speak.

The reunion turned out to be short-lived.  Within months of the sisters finding each other again, Kathi’s chiropractor had found a lump near her breast.  He didn’t think it was anything but suggested she get it looked at.  Kathi was very nervous.  She called Lynn, before posting the test results on FaceBook.  Several lumps were found in her right breast and the lymph nodes surrounding the breast.  More tests came back.  There was cancer in the lungs.  Further testing showed it was breast cancer and not lung cancer.  If breast cancer is present in the lungs, that means the cancer has metastasized and that wasn’t good.  Kathi’s prognosis was just as bleak.  She was given six months to a year to live.  Her family was devastated.  Kathi took it hard.  She had a teenage daughter and two very small children to think about.  She didn’t want to die.

August 24, 2011, Kathi posted on her Facebook account, “Today is Day 1 of kick this cancer in the butt”.  She was very positive, upbeat and energetic.  She had a fight ahead of her.  A fight that would claim her life if she didn’t win.  To cheer Kathi on, a friend, who was a professional artist, created the “It will all get better bear”.  This bear featured a plush brown teddy bear, like the kind a small child would have, with a band-aid over its heart”.  Kathi was touched.  The family was moved.  Kathi had support and it helped her knowing that.

The All Will Get Better Bear

While Kathi loved nature, gardened, very hands on and do it yourself, type of person, she did have a bad habit:  smoking.  Her oncologist insisted she quit smoking.  Kathi made several attempts.  She would go days and sometimes weeks, before the cigarettes tightened their grip on her.  She eventually gave up and just continued to smoke, although she did cut down.

While Kathi started chemotherapy, the long-distance marriage wasn’t working out as planned.  It was strained at best and was leading toward divorce.  That was Kathi’s goal, beat the cancer, get a divorce and visit her sister in California.  Sadly, Kathi had to stay married while she was sick, because she needed the free healthcare coverage.  Ironically, the closest doctor that accepted her insurance was an hour away.  On top of having to fight for her life, the ­stressors just kept coming.

As Kathi was unable to drive, friends and family stepped in either watch her daughters or drive her to treatments and appointments.  Church members and a local division of the Girl Scouts dropped off food.  The Girl Scout troop  were dropping off food every week, on the same day.  Kathi and her mother appreciated it.  Sometimes, with the treatment schedule, it was hard to cook or get time to shop.  Having homemade meals that could just be reheated was a huge help to the family.

By December 2011, Kathi was excited as an MRI showed necrosis (death) in the core of the largest tumor.  It renewed her hope that she was getting better and she would fight this.  She was losing her hair by this point, and was in a wig by January.  The victory would be short-lived.

In February 2012, Kathi began losing feeling in her right hand.  Just another development is was Kathi thought.  Turns out Kathi had lesions on her brain.  There was a treatment available.  A one-shot treatment that would require her to go to the hospital every day for a week.  More volunteers helped make that possible.  Kathi’s oldest daughter took on the role of a surrogate parent to her younger siblings.  She was old enough to watch them, cook for them and take care of them, if need be.

Kathi was hospitalized in February and came home in March.  Even though chemotherapy and radiation were progressing, Kathi’s mother wanted her to think ahead, just in case the doctors were right about the timeline for her life.  Legal papers needed to be filed.  Her oldest daughter was her husband’s step-child and he would be legally able to take her if Kathi didn’t appoint a guardian for her.  Kathi appointed my mother as the guardian and also of her two youngest girls.  Her husband was an absentee parent, so Kathi’s mother could fight for custody, should the worst happen.

Kathi gave her aunt, a nurse who lived near them, medical power of attorney, which would allow her aunt to make decisions about her medical care if she was unable to communicate.  Kathi  knew her mother wouldn’t make the appropriate choices regarding her health care.  She knew her aunt was familiar enough with medical terminology that she would respond logically.

Kathi’s mother and Lynn spoke often.  They were facing reality, while praying for a miracle.  Lynn was advised to come home, especially after the treatment for the brain lesions.  In March 2012, Lynn, her husband and daughter flew to New York.  Kathi and Lynn had not seen each other in 14 years.  Her husband and daughter had never met her side of the family.  Lynn resumed her role as the oldest child.  While visiting with her sister, when Kathi felt good enough to stay up and visit, Lynn resumed cleaning and cooking.  Lynn was the cook of the family, knew how to prepare food from scratch versus using prepared food.  Kathi used to cook like that, but with being sick, their mother reverted back to premade food.  The week went quickly and Lynn and her family had to return to California.  Lynn and Kathi gave each other a long hug.  It meant a lot, that hug, as they just didn’t do that.  They rarely showed physical affection for each other.  Neither would say goodbye because Kathi knew that would be admitting the cancer was winning.

The end of April proved to be another indication this fight was taking its toll.  Kathi stood up one day, and her legs gave out.  She could not stand, walk or support herself.  A trip to the local emergency room proved frustrating.  The staff didn’t believe her as they couldn’t immediately find anything wrong.  They wanted to discharge her as they didn’t believe there was any treatment to be given.  After Kathi’s family reiterated she had cancer and something wass wrong, they reluctantly ordered some more scans and found a mass on her spine.  She was admitted and later transferred to the hospital, an hour away from her home, where her oncologist treated her.

A lumbar puncture was done.  Hematology came back and said Kathi didn’t have transverse myelitis, which was suspected.  Transverse myelitis was a rare, inflammatory disease of the spinal cord.  Kathi was referred back to neurology.  Neurology said since it wasn’t transverse myelitis, that they weren’t able to help and referred her back to oncology.  This proverbial passing the buck took place a few times and she eventually ended up with oncology.  Sadly, neither department wanted to take credit for Kathi, yet now she’s been diagnosed with paralysis from the waist down and was still in the hospital.

The cancer was robbing this once feisty, independent woman of her ability to care for herself, much less her children.  Kathi’s middle daughter was beginning to develop behavioral issues.  She was five years old, knew her mom was sick, but didn’t fully understand.  The younger girls were being passed around as the need to tend to Kathi increased.

The problem now became what to do with Kathi.  She had no use of her legs and couldn’t care for herself.  While her home did have a ramp to get into the house, it wasn’t wheelchair ready.    Surgery couldn’t be done on the lump on her spine.  She stayed in the hospital for the time being.  Kathi’s mother and Robyn (who re-entered Kathi’s life) drove the girls to see their mom as often as possible.

Kathi was using Facebook to keep in touch with friends, track her battle and continuing her military support and keeping in touch with her sister Lynn.  Mid-April, Kathi posted that she and her family were being bombarded with the, “how can we help” question from friends.  She reluctantly, posted a list of items the family used.  It gave those who wanted to help and opportunity to do so.  Kathi’s pride had prevented her from asking for help.  She grew up fiercely independent and the cancer wouldn’t allow her to maintain that status.

On May 6, 2012, Kathi’s oldest daughter and her prom date, dressed up in their prom clothing and headed off to the hospital to show Kathi.  Kathi was able to see her daughter, in a beautiful prom dress and her friend in a tux.  She never knew her daughter missed the prom.  Her daughter just wasn’t up for it.  Kathi posted pictures on Facebook of her daughter.  She frequently made posts about her status, received support from online friends and it helped her not feel so isolated while stuck in the hospital.

Within a week after seeing her daughter all dressed up, a frank conversation took place.  The doctor said she wasn’t going to be able to stay in the hospital just because she was paralyzed.  Options were discussed as to what options would be in her best interest.  The only options were to return home on Hospice or to try to find a nursing home and go there on Hospice.  Kathi wasn’t getting better and there were no further treatments to be done.  This was when Kathi was forced to accept reality.  Her mother stated that this was when Kathi lost hope and gave in to cancer.  She now was face to face with her own mortality.  Kathi had reached the final stage of dying:  acceptance.

Kathi and Lynn each had a military Facebook page.  That was their family bond and had several mutual friends in common.  Kathi asked Lynn to keep her page updated when she couldn’t.  Lynn agreed.  Starting mid-May, Lynn updated Kathi’s page as she was no longer able to.

Kathi would not be returning home.  Her mother had several animals, Kathi’s kids to take care of and they couldn’t afford a full-time nurse.  Luckily, they found a nursing home that would take her and it was only three miles from her home.  This meant her daughters could see her every day.  In May of 2012, Kathi was transferred to the nursing home.  Her mother reported she was very confused.  She was hoping the medication and the move were the reason.

Kathi was able to visit with her daughters often.  Some days it was only for 15 minutes, other days it was an hour.  She was beginning to refuse food.  Sometimes it was days before she’d want to eat.  The nurse told the family that it was a natural progression and indication of declining health.  Lynn reported this on Kathi’s Facebook page.  One of Kathi’s friends wanted to know why they just didn’t sedate her and give her a feeding tube.  Lynn had to explain would be a life-sustaining treatment.  She couldn’t receive artificial nutrition or hydration while on Hospice.

Lynn continued to update Kathi’s page.  The news was bleak.  She had nothing good to report other than the girls and Kathi’s family were able to be with her more now that she was placed locally.  On June 11, 2012, Lynn had to report that Kathi was unresponsive and her pupils were dilated.  The family was told to “expect the call” at any time.  June 12, 2012 is when Lynn made the final status update tracking Kathi’s battle with breast cancer.  Lynn reported her Robyns had called her about 15 minutes prior to the post.  Kathi had lost her battle with breast cancer.  Kathi died within nine months of her initial diagnosis.  She fought with everything she had.  Kathi’s cancer was extremely aggressive and behaved in manners which no one, including herself, her family or the medical field expected.  In the end, Kathi opted for passive euthanasia.  She wanted to die naturally, without medical intervention..

On June 17, 2012, Kathi’s friends and family were in ­mourning as they said their farewells at a small ceremony at a local funeral pallor.  Kathi had conveyed her wish to be cremated and that wish was honored.  While it was only nine months from diagnosis to death, the cancer stripped her of who she was and left a medicated shell in its stead.  They chose to remember Kathi the way Dillion Thomas stated:   “Do not go gentle into that good night.  Rage, rage against the dying of the light”.  She did too.  She fought breast cancer with all her might.

I chose to interview my mother, so to speak.  I was originally going to use my sister’s conversations, emails and Facebook status, yet I knew that wouldn’t work, especially toward the end.  What I meant regarding my mother’s interview is that I did use her conversations and emails as she died June 25, 2013, suddenly.  I barely was able to write this paper while I completed the “interview” portion.   I did learn that I am not as far in the grieving process as I thought.  I convinced myself I was closer to acceptance when I’m still very angry.  Couple that with survivor’s guilt that my younger sister died before me, which I don’t find natural, and I’ve got a much longer road to acceptance than I originally thought.  While death is the inevitable conclusion of life, some deaths affect you differently.  You never quite grasp how deeply affected you will be until it happens.

QOTD: Topic – Worry (by the Dalai Lama)

Published February 16, 2015 by lynn k scott

I heard this quote again last night and it really hit home.  I’ve been working on letting things be as they are.  Perhaps this is why I have a connection with this quote.

If you have fear of some pain or suffering, you should examine whether there is anything you can do about it. If you can, there is no need to worry about it; if you cannot do anything, then there is also no need to worry. (by the Dalai Lama)

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