- Mom, I posted what you wrote here instead of in comments - thanks for posting. Tell more fun stories! The picture here is of Norma and Mom.
- Janet writes: My daughter Twila started this and I think it's great. Now I guess I will have to share with everyone some of the other "goofy" things I have done. A few years back my friend Norma Linkhart and I drove to Memphis, TN to see everything related to Elvis of course. While we were driving, Twila was flying into Memphis. On the way, Norma and I were to busy talking to pay attention to signs and ended up going many, many mile out of the way. It took us 14 hours to get there, approximately 9 to get home, so that gives you an idea. While there I of course took my crazy glasses and Billy Bob teeth. Naturally I wore them everywhere up and down the street and even in stores, buying items and acting like nothing was unusual. In the meantime Twila and Norma are standing out side of the store laughing like crazy at absolutely nothing; at least that is how it would have appeared to others. I also danced with a guy dresses like Elvis, again with the glasses and teeth. There are many other stories, this is just one.
- November 27, 2011 5:45 PM
My marvelous Mom, Janet Marlene, was diagnosed with multiple myeloma in May 2010. I decided to write this blog to share my Mom's experience with fighting MM all the while keeping her smile & incredible sense of humor. She continues to be an inspiration, & I love her very much! I'm hoping she will join me in writing this.
Monday, November 28, 2011
Sunday, November 27, 2011
Catching Up... and Thanksgiving
Thanks Mom for posting your funny story (above). So, I am finally catching up on our blog. Pete and I just returned home to Virginia from Xenia, Ohio, after a great holiday with Mom. We spent Thanksgiving with Sheri and family. Sheri is the daughter of one of Mom's best friends ever, Pat Felton. She loaded us up with all kinds of leftovers and sent us off feeling well loved. We missed seeing my cousin Cathie, as her husband Dale has a flu bug. My husband Pete and Petunia-Mom visited with her forever friend from Bowersville (school days), Jane, who was visiting Ohio from Delaware with her husband Bob. They visited with Jane's sister, Lois, and her family, Sue and Roger, while I was catching up with friends from high school with whom I've reconnected with on Facebook. We also spent a day with my brother Tony and his sparkling wife, Anna, seeing their beautiful home, meeting their snuffle bugs, JT (James Taylor, of course) and Coco (Chanel) - Yorkshire Terriers - and connecting even more.
Before this Thanksgiving visit, I spent a couple weeks with Mom in Xenia (though I had to work from there). With her diligence and motivation, she found a new oncologist, Dr. Gordon, who we both loved. He totally "got" Mom and her wishes for quality of life and understands her sensitivity to medications. He is not of the "my way or the highway" mentality of her last oncologist. A blessing indeed. Even better, we connected with some really special folks at a MM support group at Miami Valley Hospital in Dayton - what a great group of people. At this meeting, there were some tears, lots of stories shared and so many nods of agreement and understanding and support, and so, so much hope! Every story told there included dire prognoses - months, a few years, five years, one year. Amazingly, every. single. person. (no matter what stage) was well beyond - often by many many years - their prognosis. Mom and I left feeling connected and lifted by these wonderful people sharing their hope and experience.
So, tomorrow Mom embarks on a low dose round of chemo. She's not thrilled... but she's staying Petunia-Frog-Eyes positive. She has the support of us all, I know that, and she welcomes hearing from you (funny face pictures are always a bonus!). She has much love behind her, and I have no doubt she will be in remission quicker than the blink of an eye.
Before this Thanksgiving visit, I spent a couple weeks with Mom in Xenia (though I had to work from there). With her diligence and motivation, she found a new oncologist, Dr. Gordon, who we both loved. He totally "got" Mom and her wishes for quality of life and understands her sensitivity to medications. He is not of the "my way or the highway" mentality of her last oncologist. A blessing indeed. Even better, we connected with some really special folks at a MM support group at Miami Valley Hospital in Dayton - what a great group of people. At this meeting, there were some tears, lots of stories shared and so many nods of agreement and understanding and support, and so, so much hope! Every story told there included dire prognoses - months, a few years, five years, one year. Amazingly, every. single. person. (no matter what stage) was well beyond - often by many many years - their prognosis. Mom and I left feeling connected and lifted by these wonderful people sharing their hope and experience.
So, tomorrow Mom embarks on a low dose round of chemo. She's not thrilled... but she's staying Petunia-Frog-Eyes positive. She has the support of us all, I know that, and she welcomes hearing from you (funny face pictures are always a bonus!). She has much love behind her, and I have no doubt she will be in remission quicker than the blink of an eye.
The Why's of Petunia's Blog
I thought I would share what motivated me to start this blog. The bottom line was that I realized that writing about my Mom's experience - and eventually allowing the blog to reach a wider audience - might actually encourage or inspire, give courage or hope to, or in some way help someone else who has multiple myeloma or other cancer, or help someone who loves someone with MM or cancer.
All of us know of or hear of or meet someone with cancer - it seems like it's everywhere. In the space of a week, I had so many emails or talks with friends related to cancer. It was weird. What really got me thinking about blogging (hoping that my Mom would write too) - was when two friends asked me to send them my Mom's multiple myeloma protocol - the supplements and things she is doing that have led to her remission of MM.
There was my friend whose coworker's daughter was diagnosed with breast cancer; our friend who was diagnosed at age 46 (same age as me) with non-Hodgkin lymphoma and had started chemotherapy; another friend who has a coworker who is facing, at age 36, a recurrence of her colon cancer. There's my niece who was fighting cancer and lost the battle. The last motivating straw was hearing about a dear friend's brother being diagnosed with multiple myeloma, the same supposedly "rare" cancer as my Mom. He was 49 at diagnosis and started chemotherapy for his MM (an update on him is that he is responding great to the treatment!).
What is going on?
When faced with cancer - or disease of any kind - we all have to make our own difficult decisions, taking in all that we can to decide the best course. In this last year, we've learned so much about multiple myeloma, cancer in general, the billion dollar cancer industry, nutrition and supplements and the part they play in our health, and how to help the body fight cancer... the list is endless.
I have some questions to pose: What do you think about an adult's right to refuse treatment for cancer (or any disease) and to try alternative therapies, or to try nothing? Is it an easy answer? Have you ever contemplated this for yourself?
What's Up?
This blog hasn't received the attention from me that I hoped it would. As with many new undertakings - life intervenes! It was a busy summer with gardening. Mom has been doing great. We spent her 72nd birthday in June at Bethany Beach with family (thanks to my in-laws having a wonderful place that they share), and we made a repeat trip back in September to celebrate my 47th birthday with more family. Mom's markers (the classic "to watch" MM markers of beta 2 microglobulin, M protein, the IgG level, and the kappa serum light free chain) went up the last few months, out of the normal range. This is when the oncologists usually recommend starting a new or different combination of treatment - chemo, that is. We are in the process of revamping Mom's supplement MM protocol... and she is in the process of considering having a very low dose and short round of chemo to get those numbers back into the range. She also started taking curcumin a few months ago. Curcumin is the active ingredient in the spice turmeric. It has lots of indications in helping multiple myeloma with no side effects. I've "met" some awesome folks on Facebook, on the Multiple Myeloma Support Group (nonprofit) as well as on the forums at The Myeloma Beacon. I will be adding some website links related to these items.
Tuesday, July 5, 2011
From Whence Came the Name of Petunia Frog Eyes
My Mom's nieces & nephews & other kids have long called her Aunt Funny Face... and Petunia Frog Eyes. I've known of the Petunia Frog Eyes nickname since I can remember. I was hoping my Mom would write about the origins of this nickname. In the meantime, she tells the story about when she was a cheerleader back in her home town of Bowersville, Ohio. Whenever there was a basketball game and all of the cheerleaders would go over to meet the opposing team, shaking hands with each other, sharing their names, my Mom always said "Hi, I'm Petunia Frog Eyes!" with a smile... and never batted an eye. I love this story. There are so many funny stories like this one that my Mom tells. I want her to tell some of those stories here! (come on Mom!!). I was a pretty humorless teenager - which probably made her wonder from whence I came! Thank goodness her Humor Gene did express itself in me as I swam out of the angst of teen years. Laughing and being silly is one of my most favorite things to do, especially with my Mom.
Saturday, May 28, 2011
Memorial Day Weekend 2011
Hope everyone is having a fun holiday weekend.
Every Memorial Day weekend as long as I can remember, my Mom attends her alumni banquet. What's always fascinated me is that this is alumni from the entire history of the school. The number of attendees is around 114 this year - yes, a very small & close-knit school. She has been on the committee that does all of the planning, arranging the food, keeping up with addresses, who will attend, etc. So, today, as I type, my Mom is spending time with lifelong friends and her sisters and family: Connecting, renewing the bonds, laughing, & telling stories. I love this about my Mom - her numerous connections with so many special people. Even better is to know she feels well enough to do all that she did in preparation to help make this event a success. In the recent week, her back was aching more than usual... Dr. Soin, her pain specialist, helped her with an injection. Taking her pillow with her makes any seat more comfortable. Anyway, I can't wait to hear all the details of the banquet.
Next up: Petunia's Plane Trip into Dulles International Airport on June 11! We'll be driving to the beach to celebrate her 72nd birthday with family. Lots of west and wewaxation and soaking up the negative oceanic ions and howling at the full moon. Can't wait.
Oh, and the MM labs... we are waiting on one more, the beta-2. All of the others are just a teensy bit higher... but these fluctuations are normal even for those on constant conventional chemo. The other labs that matter are so normal - she has a lipid panel (cholesterol) that many would envy!
(Added later, pics from our trip to the beach to celebrate Mom's 72nd birthday!)
Every Memorial Day weekend as long as I can remember, my Mom attends her alumni banquet. What's always fascinated me is that this is alumni from the entire history of the school. The number of attendees is around 114 this year - yes, a very small & close-knit school. She has been on the committee that does all of the planning, arranging the food, keeping up with addresses, who will attend, etc. So, today, as I type, my Mom is spending time with lifelong friends and her sisters and family: Connecting, renewing the bonds, laughing, & telling stories. I love this about my Mom - her numerous connections with so many special people. Even better is to know she feels well enough to do all that she did in preparation to help make this event a success. In the recent week, her back was aching more than usual... Dr. Soin, her pain specialist, helped her with an injection. Taking her pillow with her makes any seat more comfortable. Anyway, I can't wait to hear all the details of the banquet.
Next up: Petunia's Plane Trip into Dulles International Airport on June 11! We'll be driving to the beach to celebrate her 72nd birthday with family. Lots of west and wewaxation and soaking up the negative oceanic ions and howling at the full moon. Can't wait.
Oh, and the MM labs... we are waiting on one more, the beta-2. All of the others are just a teensy bit higher... but these fluctuations are normal even for those on constant conventional chemo. The other labs that matter are so normal - she has a lipid panel (cholesterol) that many would envy!
(Added later, pics from our trip to the beach to celebrate Mom's 72nd birthday!)
Mom and Jane, best friends since high school, June 2011 |
Mom celebrating her 72nd birthday on Bethany Beach! June 18, 2011 |
Artsy fartsy but cool pic of Mom enjoying the beach. |
Monday, May 16, 2011
Here we go!
Well, I'm brand new to blogging and surprised I've gotten this far. I'm making this post to see if, well, I can make a post. I'm hoping my Mom will join me here on this blog... to bring her unique viewpoint & sense of humor and goofaliciousness to this blog... and because, well, it is for her and about her. Not sure what this blog will evolve to be, but hopefully you will join us on the this blogging journey. Currently, we are watching the labs roll in online on Ohio State University's My Chart. My Mom sees Dr. Glen Aukerman (his brother, Norm, was a coach/teacher at Xenia High School back when I was in high school... many moons ago, circa 1982!). Dr. A is the head of the Integrative Medicine Department and has a great sense of humor. Okay, here we go...
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