Parkinson’s Awareness Month, Day 22 – 25: The Miracle of Metamorphosis

I truly believe God laid this on my heart to share. As I wrote it, several people who also have YOParkinson’s disease (or are a caregiver to PWP or selflessly fighting hard for a cure) came to mind and I would like to dedicate this post to them, as they have been an inspiration, an encouragement and a support to me in quiet and loud, obvious and not so obvious ways, but in just the right ways and at just the right times when I needed a laugh or a shoulder to cry on or listening ear… Thank you Judy Hensley and her mom Becky, Jeanette Hoffman, Karen Fernandez, Marian Bulama, Ardyce Glessing, Tom Intili, Becky Green, Carol Meenan, Michael Johnston, Karin Norgardt, Cherie Mann, Enzo Simone, Ideliza Hernandez, Jodi Mara, Kari Marrs, Lori saviers, Ken Glowienke, Mary Kellerman, Nicole Freeman, Peggy Willocks, Terrie Starr, ‘Parky’ Wetherall, Rob Bristol, Eileen Bencivengo, Tina Lagonegro, and… my family. You are all butterflies to me.

The Miracle of Metamorphosis…

Class, today we are going to learn about… Metamorphosis.

Now, the word metamorphosis means to change and/or transform. This word is used to describe the life and transformation of a little caterpillar. The part we will focus on today is the chrysalis stage, when the spunky little critter forms a cocoon and undergoes miraculous changes in secret and emerges… a beautiful, soft butterfly

Let’s look at the process. Here he comes, little Clyde, a short, chunky, furry sort, lumbering along on the branch of transformation. He’s pretty tuckered out already, having shed his skin several times already in his lifetime (depending on what kind of little guy he is), having become stronger and stronger, bigger and bigger with each turn he makes. A regular body builder among the caterpillar clan.

Now, Clyde has an agenda. He has a job to do and eventually he finds the perfect spot for his work to begin. He doesn’t know how to explain why he’s about to do what he’s about to do, after all, we all know that caterpillar’s can’t talk. However, he just has this ‘feeling’ that he must find the perfect leaf on which to do what he’s about to do. And for Clyde, this truly is the first day of the rest of his life.

No more will he be trying to hide from inquisitive children who find him fascinating and hold him much too tight. No more will he barely miss the soles of heavy feet as he tries to cross the sidewalks. For today is the beginning of a new life. For today, Clyde is going to begin to be transformed.

As Clyde decides on the large maple leaf tucked near the curve of a branch beyond the reach of a large child, a teacher looking for examples of nature’s miracles, or gusty afternoon winds, he makes himself comfortable. Quite talented, Clyde hangs upside down on the leaf and begins to spin himself an amazing cocoon, in which he will hide for the next two weeks or so.

Now, Clyde the caterpillar isn’t aware of all the mumbo jumbo, but now inside his comfy, cozy and protective cubby, known as the pupa or chrysalis – Clyde will transforms into something amazing.

Clyde will lose his stubby little legs and trade them in for two long and slender ones. His bulging biceps will somehow become delicate wings that will enable him to float and flitter about, taking him to unimaginable new heights among his familiar world. He will develop a long tongue that drinks of a flower’s nectar – flowers of plants he use to chew up one side and then down the other. Two antennae from which to smell will emerge from his head where before there were two microscopic smellers, instead.

***

It has been almost two weeks. The cocoon shakes. Clyde has finished his work and is ready to reappear.

His muscles have disappeared and he is soft and weak. Only by repeatedly beating his newfound wings will he become stronger. As he flaps and flutters his wings in a flurry of excitement, his senses acclimatize themselves to the surroundings where he has reappeared and blood and oxygen begin to fill his system so that he is able to function properly. Clyde keeps at this ritual for about an hour, when he is then ready to leave his little cocoon and begin his new life.

What does all that have to do with Parkinson’s disease?

Sometimes it seems there has to be more to this life than living and dying. A popular Christian recording artist, Steven Curtis Chapman, wrote a song based on that idea…

“And there’s more to this life, than living and dying

More than just trying to make it through the day.

More to this life, more than these eyes alone can see

And there’s more than this life alone can be.”

And truly, there is. So often, we who struggle with different aspects of having a chronic disease, can often wonder what that ‘more’ is. Some days it’s all we can do to make it through this day and on to the next one. Maybe it’s the physical aspect – the slowing down, the falling, the intense pain, the shaking. Maybe it’s the mental – the forgetfulness, the slurred speech, the effects of the medication on the other parts of our brain. Or maybe it’s the emotional – the ups and downs, the what-ifs and the fears.

There is more. While we flounder in our faith, we hold onto hope. A hope that says a cure is coming. And while we wonder when that cure will get here, through the days, months, and perhaps even years of waiting for that day, we trust in a mighty God who keeps His promises. Promises that claim constant companionship…

Be strong and courageous. Do not be afraid or terrified because of them, for the LORD your God goes with you; he will never leave you nor forsake you.” Deut 31:6

Promises that claim His sovereignty in a chaotic world…

“For I know the plans I have for you,” declares the Lord, “plans to prosper you and not to harm you, plans to give you hope and a future.” Jer. 29:11

Promises that claim His strength in our weakness…

That is why, for Christ’s sake, I delight in weaknesses… in difficulties. For when I am weak, then I am strong. 2 Cor 12:10

You see, it is in the waiting – in the chrysalis stages of living – where we are changed. In the pain and through it. In the heartache over having this disease (or some other one). It is in the stage where we realize how fragile, frail, weak, and weary we are where we are made strong. It is when we don’t give up hope and we fight to live. We flap our wings and while we may not fly to new heights physically, mentally we can…

…those who hope in the LORD will renew their strength. They will soar on wings like eagles; they will run and not grow weary, they will walk and not be faint. Is 40:31

When we start out in life, we are much like Clyde, just lumbering along, minding our own business and then poof! Someone squashes us (not literally). Being ‘squashed’ can be…. we get bad news, someone we love passes away, we’re told we have Parkinson’s disease or a loved one has Alzheimer’s.

That is the perfect place in which to wrap up in the Lord’s cocoon – his protection – and rest in Him. When we stay close and allow Him to protect and cover us, He transforms us into something much, much more beautiful. The result is worth the wait, even if the twelve days turn into twelve months that might turn into twelve years. During the process, we can come out of the other side perfected if we will choose to trust during the transformation.

I see it every day among PWP (people with Parkinson’s) and I know it exists in people with other chronic and or terminal diseases, other illnesses and… let’s not forget – caregivers.

PWP’s and the like…

Don’t give up. Don’t give in. There is more to this life than living and feeling as if you’re dying. You have a large part in the living. You may not believe it, you may not feel it – but you do. A very important part. As you walk through this time of ‘chrysalis-ness’, a time of transformation, of trusting Him to be there, to guide, to carry and hold you – just hang in there – like Clyde did. It won’t be long before this transformation is complete and you will have emerged a beautiful and strong new creation, flitting about with new wings. I know. I’ve seen it happen.

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An Open Letter to Enzo Simone from Judy

Dear Enzo, my friend,

I write this to you but many parts also apply to all The Regulars. The hand written copy of this note on the back may be hard to read but it is done with a purpose. The effort and time it takes me with PD to write this note takes a significant effort. But I compare it to the efforts of you and your members who climb mountains, and see how small my effort is!

I want to try and say ‘Thank You’, for not only what you and the Regulars do today, but what you have done, and what we will do in the future!

Even if a small benefit comes from your efforts in the world’s eyes, DO NOT let others define your successes or failures. I tell you this because in the hearts and lives of many living with ALZ and PD you have made a HUGE difference!!

For example, many days it may seem PD has turned my life up-side-down and I look around and I am reminded of one who encourages others just by having these two words as his motto/nickname/etc: “WORLD UP!” It is then I tell myself–”do not let PD turn your world into a mess, but do what you can to make the best of it!”

Thank you all so much for showing us each a simple but profound truth of hope for our illnesses: “Together is One!” Thank you for bringing two communities together and allowing us to find new friends, touch new lives, and see new hope.

I could go on but I want you to know this:

I could call you my HEROES but that would not impress you, so I hope thanking you for being my friend and advocate for a cure will be enough to let you know just how much you and The Regulars and all those who support the ‘quest for a cure” mean to me!

I will endure for a cure..and may climb a mountain while I wait!

Much respect and admiration,

Judy “IN10CITY” Hensley
Johnson City TN
47 yrs old, diagnosed with PD 7 yrs ago
Note: If you are not familiar with Enzo and the Regulars, you owe it to yourself to visit their website at www.10mountains10years.blogspot.com. You will be amazed and blessed.

Awareness for Parkinson’s and Alzheimer’s Disease for Facebookers

RF245634…Breast Cancer awareness has been popular the past few weeks… many of us wanting the same awareness for Parkinson’s and Alzheimer’s disease… We thought of adding something different to our status for the next few days.

Ex: Day 1 (Wednesday 13th): round off the number of people you know that have PD/Alzheimer’s (1-100). For those who ask what it means, say ‘Stay tuned!’

Day 2 (the 14th): Put the name(s) of family, friend, or self who have the disease and for those who ask again, ‘Stay tuned’

Day 3 (Fri/15th), final day: Everyone lists a symptom (tremble, shake, memory) – anything that pertains to the illness. That evening post your status with the results and what they refer to, such as, “I know ‘3’ people (or whatever your # was) that have PD/ALZ, their names are ____, and _____ is a symptom of PD/ALZ.

Let’s promote awareness for PD and ALZ. Thank you for your support! And, thanks for Focus On A Cure for an ingenious idea!