Wednesday, June 11, 2014
Del Immune's Top 60 Cancer Blogs
Well paint me surprised! I was notified last month that Ramblings of a Cancer Kid Mom has been named in the top 60 cancer blogs on the web. It was a pleasant surprise, and very validating. I'm so pleased and humbled to be able to offer help, hope, or inspiration to others. If you would like to find other cancer blogs (about pediatric cancer, or other types of cancer) you can visit the Del Immune blog post on the subject. I hope you will find an extra snippet of hope within their virtual pages!
Wednesday, May 14, 2014
More Life Lessons 101 with Teacher Katie: complaints
You may not have a child with cancer, but surely you are busy. We all are. You have your own storms: they may be physical, mental, or emotional. We all have problems, and I'd bet we can all agree that all of them suck.
I grew up with a saying (that is likely and hopefully untrue, but still) that says, "90% of the people you tell your troubles to, don't care. The other 10% are glad you've got them." While I don't think EVERYONE is that callous, I do think there is a lesson to learn from the saying. While your problems are most important to you, my problems are most important to me. So the next time I feel like complaining, I'm going to take my own advice and keep my big mouth shut! Do you ever feel like complaining (I know the answer to that!)? How do you deal?
Wednesday, April 16, 2014
Losing Weight [of the emotional kind]
A few years ago, when we were staying in the Ronald McDonald House of Memphis, our little family was playing in the "game room". A teen boy and his father came in to hang out. They were waiting for the shuttle to pick them up and take them to the grocery store.
At some point, the conversations turned to the fact that we had a car. You see, we don't live far enough away that it warrants flying to Memphis, so we have to drive. This particular family's situation was the opposite--which meant they had flown into town and were without a car. The father began telling us how terrible it was to rely on the hospital shuttle for things like going to the grocery store. Both I and my husband got the distinct impression he was asking for a ride...without actually asking.
For whatever reason, neither of us offered said ride. The man eventually got a little huffy and puffy, and left the game room.
Looking back, this moment fills me with guilt and shame. Oh sure, we had lots of reasons to NOT help. What if we needed our car? What if Emma needed to go to the hospital for something (and this was a legitimate concern, as these kids can literally be A-OK one minute and extremely sick the next)? We couldn't offer a ride...could we?
Do you have any "silly" regrets like this? Any resolve to not let it happen again? Share them here and we can help each other learn :).
At some point, the conversations turned to the fact that we had a car. You see, we don't live far enough away that it warrants flying to Memphis, so we have to drive. This particular family's situation was the opposite--which meant they had flown into town and were without a car. The father began telling us how terrible it was to rely on the hospital shuttle for things like going to the grocery store. Both I and my husband got the distinct impression he was asking for a ride...without actually asking.
For whatever reason, neither of us offered said ride. The man eventually got a little huffy and puffy, and left the game room.
Looking back, this moment fills me with guilt and shame. Oh sure, we had lots of reasons to NOT help. What if we needed our car? What if Emma needed to go to the hospital for something (and this was a legitimate concern, as these kids can literally be A-OK one minute and extremely sick the next)? We couldn't offer a ride...could we?
We talked about this man recently, remembering how we had the means to help but didn't. We decided that if we were ever in the same situation again, we would definitely help. The Bible tells us to not withhold good when it is in our power to give it. I had to let go of my guilt over the situation--truthfully, it wasn't that big of an issue. He got his ride to the grocery store and all was well. But.Do you have any "silly" regrets like this? Any resolve to not let it happen again? Share them here and we can help each other learn :).
Wednesday, March 12, 2014
Post Traumatic Stress Disorder...or something like it
Once upon a time there was a girl. She was a happy girl. A brave girl. A silly girl. Unfortunately, this girl hit a roadblock, and it sent her to a not-so-happy place. Doctors now think Emma has a mild form of post traumatic stress disorder--more specifically, Pediatric Medical Trauma Stress.
Several studies have been done now which link children with cancer, and their caregivers, to PTSD.
Here is one description:
HYPER-AROUSAL (Taken from After the Injury in regard to children with PTSD)
Hyper-arousal also starts with a natural and normal response to danger – the “fight or flight response.” After an injury or accident, this “fight or flight” response might not turn off, even when you are safe.
- Your heart keeps pounding and you start sweating.
- Your body is still on the lookout for danger.
Another great site on the subject is the Children's Hospital of Philadelphia site. They talk about the symptoms preventing a child from performing every day tasks. This, in particular, seems to be Emma's issue.
Still, I am astounded daily by this child's strength. She recognizes that she has a "problem", and you can literally see it in her face as she fights it. I have no doubt she will overcome, and it inspires me to keep going. Really and truly.
Have you ever witnessed this type of strength in someone else? Did it inspire you to do a little better? Try a little harder? Become a little greater?
I ask for prayers for Emma, as well as any child (or any person in general, really) who faces this. It is heartbreaking, to say the least.
Wednesday, February 12, 2014
Carla Rossi's The Living End of Cancer
Hello, Katie!
Thank you for letting me stop by your blog to
celebrate the release of The Living End of Cancer,
my personal memoir about my journey through non-Hodgkin lymphoma.
There’s no need to explain to anyone hanging out
around here how catastrophic that “day you get the diagnosis” day really
is. So I will just share with you one of
the things that happened shortly thereafter that enabled me to get battle-ready.
As I sat dumbstruck, a scripture dropped into my
head and heart. “I will not die, but
live, and declare the works of the Lord.”
At the time I couldn’t even remember where it was in the Bible or if I
had it right, but soon I was reading the powerful declarations from Psalm 118
and realized this would be my mantra.
When
someone asked me how I was doing, I didn’t admit to how bad I felt
or gush about the horrors of chemo, I simply stood tall and said, “I will not
die, but live, and declare the works of the Lord.”
Now in complete remission, that’s what I’ve tried to
do with my cancer memoir – declare the works of the Lord. I had the right medicine at the right time
with the right team of medical professionals and caregivers – and I had my
faith and God’s healing hand to get me through.
The
Living End of Cancer is honest and sometimes raw, but
it’s also full of scripture, humor, and hope.
My intent in getting my journey on paper has always been to encourage
others. The cancer fight is not pretty,
but we are not alone.
I
shall not die but live, and declare the words of the Lord. Psalm 118:17 KJV
Connect
with Carla:
Twitter:
@carlarossiwrite
Wednesday, January 15, 2014
Cartwheels and Neuropathy
Yes, I realize that is an odd title. But in our world, the two have merged. You see, the first one is helping the second one.
Emma was diagnosed with neuropathy a few months ago. It is in her hands, and it basically means she has zero strength in that area. For instance, on the physical therapist's little "squeeze machine", most girls Emma's age can squeeze 27 lbs. of pressure. Emma could squeeze 5. This was concerning for several reason, though obviously only for quality of life purposes. (I am going somewhere with this, so hang on!)
The neuropathy isn't a new thing. She had it throughout most of her treatment, especially in her feet. She did overcome the foot issue with physical therapy long ago. The hand issue is something we all assumed was getting better, but realized recently that it wasn't. So she did a little physical therapy, mostly at home but in a PT facility as well.
This week she got it in her head that she was going to do a cartwheel. I smiled and nodded my encouragement, but truthfully, inside, I had my doubts. Emma is weak, I told myself. Emma doesn't have any hand/arm strength or any core strength. Emma is going to fail.
And do you know what happened? She did not fail. Oh, she did the first twenty times. But that kid...she just didn't give up, bless her. She kept on, and on, and on. She is still keeping on, and it's been three days now. She is almost 100% there. She can launch herself forward, and she gets her feet almost all the way up now.
What a lesson for me. While I know she couldn't have done that a couple months ago, with the PT we've been doing every single day for at least 90 days, she has developed the strength to do something she couldn't have done back then.
Facing something hard? Feel free to tell me about it.
And don't. Give. Up. Keep. Trying. Keep. Trying. Keep. Trying.
Emma was diagnosed with neuropathy a few months ago. It is in her hands, and it basically means she has zero strength in that area. For instance, on the physical therapist's little "squeeze machine", most girls Emma's age can squeeze 27 lbs. of pressure. Emma could squeeze 5. This was concerning for several reason, though obviously only for quality of life purposes. (I am going somewhere with this, so hang on!)
The neuropathy isn't a new thing. She had it throughout most of her treatment, especially in her feet. She did overcome the foot issue with physical therapy long ago. The hand issue is something we all assumed was getting better, but realized recently that it wasn't. So she did a little physical therapy, mostly at home but in a PT facility as well.
This week she got it in her head that she was going to do a cartwheel. I smiled and nodded my encouragement, but truthfully, inside, I had my doubts. Emma is weak, I told myself. Emma doesn't have any hand/arm strength or any core strength. Emma is going to fail.
What a lesson for me. While I know she couldn't have done that a couple months ago, with the PT we've been doing every single day for at least 90 days, she has developed the strength to do something she couldn't have done back then.
Facing something hard? Feel free to tell me about it.
And don't. Give. Up. Keep. Trying. Keep. Trying. Keep. Trying.
Tuesday, December 31, 2013
New Year's Resolutions
___ ___ Check Yes or No
Determination. That is the way to get it done. Just as I am determining to post more here.
While Emma's cancer journey is over, life after cancer continues, and that stinking cancer has definitely left its effects on Emma. I have a few things to say about that, so stay tuned. And thank you for stopping in.
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