Thursday, September 23, 2010

Warm Fuzzies

 


THURSDAY, SEPTEMBER 23, 2010

Warm Fuzzies




Last year when I was diagnosed with breast cancer, it didn't take long for the word to spread. We were inundated with cards, letters, flowers, and gifts from neighbors, family, and friends. I tried so hard to keep up with thank you cards but realized before too long that there was no way I would be able to thank everyone. It's been almost a year since my mastectomy; it was the week before General Conference, which is always the 1st weekend in October. The surgeon came into my room 2 days after my surgery and told me that the VILLAIN had spread and that I would need another surgery; I remember looking at Eric with tears in both of our eyes. I asked if it would be ok if I went home for the weekend and came back, and she agreed that it would be good for me to go home for a few days. That weekend I watched every session of the Conference from my bed in my bedroom. One of the talks that touched me and also was an answer to prayers was a talk given by Thomas S. Monson. He showed a picture of a jar much like the one I have here on my blog; he explained about a Primary President who had sent this to him; the jar was filled with warm fuzzies. The primary children collected the warm fuzzies in her ward every week. When they came to primary, if they had done a service for someone, they were allowed to put a warm fuzzy in the jar. After one year, the jar was full. I loved that idea so much that I decided to start putting a warm fuzzy in my own jar every time someone did a service for our family. I didn't tell anyone about it; I just did it. It is a year later, and my jar is full in more ways than one. We have been blessed with friends, neighbors, and family members who have served us. I say, "Thank You" I keep this jar on my dresser in my bedroom where I can see it every day and never forget it. We have some really good doorbell ditchers in our neighborhood; so often, we would open the door to see a jar of salsa and chips or some type of treat, but no one to claim the service... I could see children running down the street, hoping not to get caught... parents are teaching their children to serve others without recognition; I love it.
This jar of warm fuzzies represents all of the people who have given un-selfishly this past year as they have served our family; our family loves you and will never forget; we feel your love.

Wednesday, September 22, 2010

He's Been

 

WEDNESDAY, SEPTEMBER 22, 2010

He's been out ONE year ♥




I love hearing from my missionary son; he entered the MTC one year ago today. So that means he will be home in one year yay !!!


Oh, I miss his smiling face and cute sense of humor; he always has a good attitude and never talks badly about others. I love those qualities in him. He is serving in Santiago now; he loves the area and the people. 

I can see how the Lord is refining him and molding him into a great missionary. I get emotionally overwhelmed when I think about how much Blake and our family have been blessed. 

Unless something surprising happens with my health next year at this time I will be gettin' the best hug ever from Elder Williams


Thursday, September 16, 2010

Then the Guilt took over


 Tuesday, September 16, 2010

Then the Guilt took over...



Okay, today I got productive and made like a million Pumpkin Chocolate Chip Cookies, click here and scroll down for the recipe. I got all the ingredients from Walmart and got them all out and ready while Recker took a nap this morning. When I pulled out the oil, it smelled rancid..... wow that was disgusting. I have not baked anything for so long. The oil smelled awful, and I had to run to Walmart again and get cooking oil. It's a little frustrating to have everything you need but one ingredient. I told Eric (who was laying with Recker... so cute) that I needed to go get oil. Then he said to me, "are you going to eat any of these cookies?" of course, I said, "no," he quickly replied, "Then why bother to bake them?" I thought about that question while I was running through Walmart. I think I want to bake something for my family; just because I am not eating sugar and flour does not mean they need to go without it. RIGHT? Besides, I love to bake, and I feel like it's that time of year; I missed out on it last year. They smelled so good baking in the oven, I could not resist ..... I did eat one, and it tasted so good to me. Then the guilt took over, and I was done. I have this love/hate relationship with the NO SUGAR NO FLOUR thing. I love that my body feels clean and renewed; I hate that I love the delicious combinations you can create with sugar and flour; I am such a baked goods girl. Pastries, cookies, cakes, I love them all.

It wore me out making all those cookies, my body is not what it used to be, and I wonder if it ever will be again.

Oh yeah, and some people have asked about my recipes ..... when you open my blog, if you click on the button that says cookbook, it will take you to my recipes. I now have almost 1,000 recipes on there. I love that my girls can get a recipe whenever they need one; it's been fun.

2 COMMENTS 

Tuesday, September 14, 2010

Hip Pain

 

TUESDAY, SEPTEMBER 14, 2010

Hip Pain

This week my hips are really in pain. It hurts to walk up and down the stairs at my house. I don't like taking the pain medicine because it makes me feel like I am giving in to it.
Also, this week I have been receiving emails from the American Cancer Society, the last email that came asked me if I was ready to purchase a wig or look at their catalog for hats and beanies..... WHAT? Been there, done that, there should be some kind of filter that lets A.C.S know we are done with chemo and moving on with our lives. I have had a bit of a bad attitude this past week, can you tell? I really don't mind getting the emails. Still, when I opened the TLC catalog, it brought back a wave of emotions and memories, Tamy and I looked at that catalog a year ago, and I considered purchasing some hats from them but decided against it. Then when I did decide to buy one, I got a prescription from my oncologist and bought one at a store close to Mayo Clinic. I never wore it, never, not even once. I think my kids and all their friends have more fun wearing that wig; even Recker wore it one day.

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Monday, September 13, 2010

Happy Birthday Elder Williams

 

MONDAY, SEPTEMBER 13, 2010

Happy Birthday, Elder Williams

Today is Blakes's Birthday .... huge shout out to him ......woo hoo.

Dear Elder Williams
I love you, son. Happy Birthday. You are 22 today, so hard to believe. I remember the day you were born like it was yesterday, dad was so excited to finally have a boy, and I was overjoyed to hold you in my arms. You weighed 9 lbs 8 oz. and 21 inches long

Thank you for so many memories over the years; dad and I love you more than words can say. You are on your mission now and will probably not read this until you get home or later in your life, but today I want you to know I love being your mom, and I am so proud of the man you are becoming. I pray every day that you will be blessed and watched over, that the Lord will comfort you in times you need it and push you on the days you think you can't go anymore. We are truly blessed to have you in our family. xoxo Mom

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Saturday, September 11, 2010

Dog Bite in the Dominican Republic

 

SATURDAY, SEPTEMBER 11, 2010

Dog Bite in the DR

This week I got these pictures from my cute missionary son and an email telling me he had been bit by a dog. As a result of the bite, he has been extremely sick. Sometimes I think it's better for mom's not to know everything; we just sit and worry too much. I know the Lord can take better care of him than I can, so today, I just turn it over to the Lord. Oh, and by the way, it was not the dog in these pictures that bit him. It was a Rottweiler.
















Friday, September 10, 2010

Recker Loves BONBON

 

TUESDAY, SEPTEMBER 21, 2010

Recker ♥'s BONBON



So my house is a mess, the floors need to be vacuumed and cleaned, the kitchen is .... actually not too bad the family room has toys everywhere, clothes are in the washing machine and dryer, my bedroom .... let's just say the bed is not made. My bathroom needs some serious cleaning, however........ I get to spend all day with Recker. He demands my every minute, and I love it. I have finally learned how to put everything aside and enjoy the moments I know I will never get back, the kitchen will always be there, but I may not, so I want to enjoy every second I have with this little guy. Today he had his first PLUOT (PLUM), and this is what it looked like..... what a mess; then he had a fun bath, splashing water everywhere and laughing the whole time.

Tuesday, September 7, 2010

DAMN VILLIAN

 


TUESDAY, SEPTEMBER 7, 2010

DANG VILLAIN

Today, my oncologist diagnosed me with the 1st stages of Osteoporosis and arthritis in my lower back. WOW, I did not see that one coming; I should have; it seems that everything they have told me I "might" get, I have gotten. I really don't know whether to scream or cry...... well actually, I did allow myself to call a little tonight on my way to work, and it felt good. Eric is out of town, so I don't have anyone to cry with....haha ok, enough of the pity party; I'm good now its been a few hours, and I can breathe.

I was excited to see the doctor today because I wanted to see if the labs would show how hard I have been working on not eating sugar, flour, or processed foods ... the surprise is he didn't say one thing about that except that "oh you've lost some weight" I thought "seriously? .... that's it? that's all he has to say about that? who cares about my weight what about the fact that I have been in deprivation of sugar for 4 months?" (except for that little trip to Paris .... I didn't tell him about that)
I knew right away that things were not going good when he said, "so, young lady, really, how have you been feeling?" it really wasn't about what he said but more of how he said it that made me feel like some bad news was coming down the pike. I told him the usual stuff, my lower back sometimes hurts, that my legs and hips hurt all the time, making it difficult to exercise and that my fingers go numb once in a while. Also, my lymphodema acts up. My arm swells up, especially now that I am on the computer at work for long periods, and let's not forget about Mr. Hotflash. Dr. Northfelt said in his low doctor voice, "we need to go over your labs"  I just knew the bad news was on the tip of his tongue, and it finally did. He showed me the x-rays, which are now clear and precise pictures of my spine, back, and bones. He explains that the pain in my hips and legs is partly because of the neuropathy I got during chemo. Still, we have a new problem, Osteoporosis caused by the Arimidex I'm taking, something I was told today I will be on indefinitely for the rest of my life. The Arthritis in my lower back was caused by the Chemo Treatments I received. DANG DANG DANG VILLAIN, I seriously don't despise you!!!!

He told me how sorry he was to tell me this because he knows I am working so hard to do everything possible to not recurrence and be such a good patient. He told me about a patient he had just met with who is diabetic and has cancer but who refuses to know her insulin counts. "I will probably be stuck with this patient for 30 years, continuing to tell her what to do to save her life, and she won't take one suggestion. I have you who do more than I suggest you do, and you are faced with another hurdle. I wanted to say, "you're right, so what do we do about it?" but I didn't. I just stared at him with some stupid look on my face.... he was sitting right in front of me, and I was seriously tempted to kick him.... hard.

Just once, I want to go to Mayo Clinic and get some good news ..... it will come, right? I can't tell if the VILLAIN is winning or if I am winning anymore. The Arimidex blocks estrogen and is precisely what stage 3 CANCER patients take to HELP them survive for many years, but on the flip side, I guess patients have to live with the sometimes consequences. Damn, VILLAIN, I hope this does not keep me from being able to do everything on my bucket list... Dr. Northfelt said within 10 years, I will be IN FULL BLOOM of OSTEOPOROSIS ..... I want to serve a mission with Eric; I want to run a marathon. How can I do these things if I am crippled? It just testifies to me more that I need to get everything done in my life that I want to do as fast as possible to create memories for those I love. I'm still planning on training for that marathon next year. Blessings will come; I just have to remember, if not in this life, they will come in the next as long as I embrace the Gospel of Jesus Christ.

2 COMMENTS 

Monday, September 6, 2010

Love This

moNDAY, SEPTEMBER 6, 2010

Love This

I found this quote while I was reading today and Loved it

.....some blessings come soon,
some come late and some
don't come until HEAVEN;
but for those who embrace
the Gospel of Jesus Christ
they will come.
- Jeffrey R Holland

4 COMMENTS 

Friday, September 3, 2010

Mayo Madness

 

FRIDAY, SEPTEMBER 3, 2010

Mayo Madness











This morning I needed to be at Mayo Clinic by 7am. When I arrived, the underground parking lot was empty, no one was playing the piano, and there was no greeter to say "welcome to Mayo Clinic." No one else riding in the elevator. Even the gift shop was not open yet. Today the halls of Mayo Clinic were empty and unusually quiet.
I love the cute lady that checked me in. She is from Russia, and she usually checks me in. She remembers me because my name is Russian and is quite popular. Whenever I see her, she always says, "good morning Monya" today, she even told me my hair looked so cute. 

After checking in and registering for my procedures, I sat down in the chemo lab waiting room. I listened as a man talked to his wife sitting right in front of me (he was pretty loud). He was talking to her about FAITH. He commented that he is not buying the whole "faith as a mustard seed." Suppose we have faith you will be healed. In that case, he was telling her, "we have shown our faith, we have prayed day and night with a pure heart asking the Lord to help us, we read from the Bible every day, but yet here we sit at Mayo Clinic getting ready for you to go into chemo treatment and you are dying" ... he continued to say "Jesus Christ had faith, and he still died. His daddy could have saved him, but he didn't. Instead, he let him die" (the man was of African American heritage, and I loved his southern baptist accent). At this point, I was thinking, "Is this man trying to give his wife a pep talk? Because it's not quite coming out that way." Then he turned to her, gave her a hug, and said the sweetest things. It made me tear up. "I just love you so much, and I hate to see you going through this." He continued to say they had done all the doctors had asked of them.  WOW, I could not believe what I had heard of all days for me to come to Mayo Clinic. I needed to be reminded about FAITH. The Lord could take all this away if he wanted to. He could have taken away the pain of his only son, but he didn't because he had a plan for him.  

Gog has a plan for all of us; it doesn't make it easier to accept life's bumps and bruises, but when I really think about what plan He has for me, I realize how special I am in his eyes. I love that the Lord put this man in my path today, and I needed to hear what he was saying.
Three women came in and were sitting in the waiting room. All of them are bald, and all receive chemo treatment today. They all looked very ill; a sudden attack came over me. Seeing them triggered something within me. The reality of what I have been through flooded my brain like a Tsunami. They looked so sick, and I wondered if I looked like that? 

I remember how I felt; oh my goodness, I just wanted to get out of there--seeing all this brought back some horrible memories. I couldn't breathe. My chest felt like a weight was on top of it. I stood up and began to pace. I knew people were looking at me. I could hear them saying, "Do you think she's OK?" I can listen to them, but I just want them to disappear. I wish Tamy was here. Suddenly when they called my name, I could snap out of it long enough to walk over to the nurse. She introduced herself, and I am usually pretty good about remembering their names but not today. I just wanted to get this over with. We walked into the chemo lab, and I was still a little dazed but able to fake my way through it...when she accessed my port, I had to ask her to put on a face mask. She forgot to do it; this made her have to start all over with the sterilization process, but I remember Tamy telling me to never let anyone access my port without a mask and gloves on. Honestly, I have never had to ask a nurse at Mayo. This was the 1st time. Finally, when she did get the port accessed, it was excruciating this time. An immediate medicinal taste hit my taste buds when she flushed it, and my face quinced. She asked if I was ok; I said, "Yeah, I never get used to that taste." She took 6 vials of blood, put a band-aid over my port, and scooted me out to my next appointment. I hate the smell of the chemo suites, so I was ok with leaving quickly.

My next appointment was not for 1.5 hours, so I decided to go visit my favorite people in radiology/oncology; none of them were at work yet, and they don't start until after 8 am. That was a disappointment, and I really wanted to see some cute cheerful faces to help me get through the rest of the tests I have today. Oh, Well, back to the concourse level to check-in and wait.
At least this floor is not ALL VILLAIN patients; some of them have heart problems and other sicknesses, its hard to tell. At least with VILLAIN patients, I can tell by the "no hair" and the fact that I can look in their eyes and know what they are thinking and how they are feeling. Whenever I enter the Mayo Building, all of my senses are activated.

I SEE everyone and everything around me so clearly now, not foggy like it was a year ago.
I HEAR the sounds of loving husbands and wives giving support and encouragement where it is needed.
I TASTE the chemicals, the ones that are supposed to help me.
I SMELL the sickness in the air and want to throw up.

I sit back, close my eyes and try to go to Paris, riding on a bike in the mountains, yes finally I'm at my happy place with my happy husband Frenchie and we are smiling, and picking wild berries ..... then suddenly I hear "MONYA WILLIAMS" over the loudspeaker, it's my turn for my bone test. I had to get dressed in the Lovely Hospital Attire for this one; after the bone density test, I also had the bone mineral test done, back to chemo lab to reaccess the port.....This has indeed been an emotionally draining day, I can hardly stay awake as I blog, but I wanted to get it all blogged to remember it.
I return to see Dr Northfelt next Tuesday, I am crossing my fingers that not eating sugar, flour or processed foods for 3 months has paid off. The labs will tell ..... I just want Dr Northfelt to walk in the room and say "you are cancer free, or at least say I'm in remission" I don't think based on our last conversation that, that is going to happen any time soon, but a girl can dream right? I always have that .....dreaming, hoping and praying

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