Showing posts with label Anchorage Parkinson's Disease Support Group. Show all posts
Showing posts with label Anchorage Parkinson's Disease Support Group. Show all posts

Thursday, April 18, 2019

No Anchorage Suppport Group Meeting this Saturday, April 20

Hello all, this is a reminder that I am snowbirding in Washington State, so we have no formal meeting this Saturday. The usual space, the Tundra Lounge is still reserved in the Pioneer Home, so if you wish to meet informally and just chew the PD fat, that's fine. I'll be down here through the month of May, so our next official meeting will be the Summer Potluck in June.

Festinate forward,

Peter

Monday, October 5, 2015

October Parkinson's Disease Activities in the Anchorage Area

October means Old Man Winter will soon beat down our doors. But he'll go away after a while, unlike PD. So what choice do you have but to take notice of the Parkinson's events coming to Anchorage in October? There are only two coming, so it shouldn't be too difficult to keep track.
On Monday, October 12, A PDTeleConnection at 1PM (To find the Alaska meeting proceed with all deliberate speed to Providence Hospital West campus on Piper St.  Go to the second floor, walk down the lonnnnnnnng hall that stretches South from the cafe and look for room 2401 pretty much at the end of the hall The speaker will be Deb Fry, Owner and Move Manager of a business that specializes in moving seniors. Topic: Pack with Compassion - A Spokane-area Senior Move Management Business that helps seniors move or helps them stay at home and age-in-place in a compassionate process for either.

​ Our routine support group meeting (insofar as such an extraordinary gathering could be termed "routine) will occur Saturday the 17th in the fifth floor West lounge of the Pioneer Home in downtown Anchorage. Topic: TBA​
Corrections, suggestions and sarcastic remarks are welcome, comment below.
Ploddingly,
Peter

Tuesday, August 18, 2015

Parkinson's and Creativity, an Experiment

Some time ago I came across a story in the news that said people with Parkinson's who were taking Sinemet were more creative than ordinary, generic people. This of course raises many questions about creativity itself, let alone the creativity of those who have this strange and capricious disease. Raised questions, like raised doughnuts, are hard to resist. So at our most recent meeting I ambushed our support group with the following challenge: Write Haiku about Parkinson's disease.

Haiku is a form of Japanese poetry that calls for a three-line poem which is structured to have 5 syllables in the first line, 7 in the second, and 5 in the last line. The lines needn't rhyme, although I think the poetry police will look the other way if they do. Nature is often a topic, but where the form has been appropriated by other cultures the tradition has grown a bit loose.

Where I could detect expression on group members faces as I passed out paper and pens, I thought I saw a certain unwillingness to dive into the murky waters of creative endeavor. To their credit, most people came up with something in the silent quarter hour that passed after the supplies were handed around.

So what do the poems that came out tell us about PD and creativity? Not as much as I'd like. I unscientifically forgot to inquire if there were any people who had PD but were not taking Sinemet, and at least three of the participants were caregivers who did not suffer from Parkinson's themselves. There were no controls, and this is a tiny number of participants that in no way comprises a scientific sample. But we did get some unusual perspectives on the disease, so I hereby declare the experiment a smashing success.

Here, in no particular order are the poems I managed to collect after the meeting.

These first three Are by Pam Dunlap-Shohl.

1
I really care, but
For Parkinson's, not so much.
It saps my patience

2
Two steps forward, and
Three steps back. A halting dance,
bereft of grace

3
"What?" I said, "What?"
"I didn't catch that the first time."
"What did you say?"

Here's one from Bob Rinehart

I shake like the
leaf of Poplar Tremaloides
Sinemet stills me.

Here are mine

1
Drowsily I ask
Wow, do I still have PD?
Let me check... oh, damn.

2
Festination. It's
halts and lurches between you
And your destination.

3
As the rains of Fall
Tumble to the sodden earth
I follow their lead.

Carolyn Rinehart submitted two

1
I don't want PD
In our lives but it has brought
good friends through this group.

2
PD is the pits
But we still can nurture our
Creativity.

And we'll let Susan Wong have the last word

Feels like aliens
Living rent-free in my soul
Who invited you?

If you have a PD haiku you would like to share please submit it as a comment on this post.

Saturday, May 2, 2015

May Parkinson's Disease Events for Southcentral Aalska

Here it is, May already! This is good news for those without PD because it means that it is no longer Parkinson's Disease awareness month. The rest of the country, indeed, the rest of the world, will be free to go back to being unaware of PD. Lucky them. As this is not an option for those who actually have the disease, you will be happy to know that we will have the following blockbuster opportunities to learn more about this affliction, and how to cope with it.
The Telehealth interactive broadcast presentation will be May 11, 2015 at 1:00 p.m. To find the Alaska meeting, proceed with all deliberate speed to Providence Hospital oncology wing on Piper St. ( Go to the second floor, walk down the lonnnnnnnng hall that stretches South from the cafe and look for room 2401 pretty much at the end of the hall on your right. ) Once there, after a certain amount of blundering with the high-tech equipment, we will have a presentation from Caleb Foss, physical Therapist. Topic: Caring for the Caregiver with physical therapy techniques for reducing the chance to getting hurt while caregiving. Tips on how to lift, transfer and move a person with PD.
Our monthly support group meeting May 16th at 3:30, promises to be a humdinger. There will be three different presentations. We will warm up with two short sessions. The first will be on Medicad help for people who have Parkinson's. The second will be from the Alaska representative of the Parkinson's Action Network, outlining the political environment at the federal level for Parkinson's research. These will be followed by the main act, local movement disorder specialist Dr. Alec Glass. Alec will give a talk touching on the current state of PD research, and things that he is hopeful about in the not-too-distant future for the treatment of Parkinson's. There will be time for questions, so if you want to ask a smart and approachable doctor your PD questions, you will never have a better chance.
And don't forget the Regular Tuesday Yoga for PD sessions every Tuesday, 1:30 PM, at the Anchorage Dance Studio, 550 E. 33rd Ave. Anchorage, 99503. Something new is always being presented, so challenge yourself to a safe & uplifting hour of movement and IN-SPIRATION. You will be glad you came!

Your faithful servant,
Peter

Friday, October 3, 2014

Parkinson's Events in Southcentral Alaska for October

With an eerie sense of deja-vu we look into the upcoming PD events and find that once again there will be a Telehealth conference about Parkinson's disease to which you are invited at no charge. Spooky!  The interactive broadcast will take place Monday, October 13, 2014 at 1:00 PM. You can find the Alaska broadcast by going to the Providence Hospital oncology wing on Piper St. Go to the second floor, walk down the lonnnnnnnng hall that stretches South from the cafe and look for room 2401 pretty much at the end of the hall on your right. Presentation Titled: Tools to Aid in Daily Living, especially for those affected by Parkinson’s Disease. -What kind of financial support is available to help pay for needed equipment? For more information contact : center@spokaneparkinsons.org
Our regular support group meeting will follow on the 18th at our usual time, 3:30. Oh, did I say "regular"? My mistake. An extraordinary meeting of the support group will occur on the 18th when Dr. Ryder Gwin, a neurosurgeon will come all the way from Swedish Hospital in Seattle to give us the latest info on how they are handling Deep Brain Stimulation surgery there. He will be joined by Keely Dailey of Medtronic, the maker of the device most commonly used in the procedure. If you are considering this operation, or have always wondered what a brain surgeon looks like, or are just curious about the amazing practice of treating Parkinson's and other neurological problems by inserting electrodes into a person's head you don't want to miss this meeting.
I hope to see you there,
Peter

Thursday, September 4, 2014

September Parkinson's Events in the Anchorage Area

Hello Friends, If anyone knows where August went, could you please notify me? And now, on to September before it gets away! This month's teleconference will be next Monday, September 8. Here is the lowdown, courtesy of the Spokane Parkinson's Resource Center: You are invited to attend the Parkinson’s Education TeleHealth Presentation Monday, September 8, 2014 at 1:00PM. To find the Alaska meeting, proceed with all deliberate speed to  Providence Hospital oncology wing on Piper St. Go to the second floor, walk down the lonnnnnnnng hall that stretches South from the cafe and look for room 2401 pretty much at the end of the hall on your right. Presentation Titled: It’s time to move. What do I do next? Speaker: Holli Korb, General manager Fairwinds Retirement Community Topic: Downsizing, steps and techniques to help reduce the stress of navigating those decisions and finding your new home. Speaker and panel. For more information contact : Parkinson’s Resource Center of Spokane at 509-473-2490 or by email at center@spokaneparkinsons.org  Meetings are free of cost and are also received in several communities over TeleHealth. The Parkinson's TeleHealth Program broadcasts live, interactive educational talks to a network of rural communities in the Northwest. On the SECOND Monday of each month, a guest speaker presents a topic geared toward the interests of Parkinson's families. The information is designed to help participants to improve their knowledge of Parkinson's disease and in turn their quality of life. www.spokaneparkinsons.org

​Our regular support group meeting will be on the 20th of September​
​ . Time is 3:30, Subject TBA. Looking down the road to October, remember we will have a speaker about Deep Brain Stimulation from Swedish Hospital in Seattle. That's all that I know about September Parkinson's news. If you know more, please drop me a line.

Tuesday, July 8, 2014

Parkinson's Events in July around the Anchorage Area

Here is what I know about what is coming up in July ...
MONDAY, JULY 14th Another riveting and interactive teleconference! You are invited to attend the Parkinson’s Education TeleHealth Presentation Monday, July 14, 2014, 1:00 p.m. The topic: Practicing good Nutrition is important for everyone. A practical and useful approach Speakers: Sabrina Gondor, CHHC, AADP, CCWS Certified Holistic Health Coach Danelle Crabtree, CMA-C, Corporate Health Alliance Representative. This seminar gives you basic, practical and useful information about nutrition with a focus about what antioxidants are; why they are important; and how using antioxidants can increase your overall wellness. For more information contact : center@spokaneparkinsons.org

Meetings are free of cost. To find the Anchorage meeting, proceed with all deliberate speed to  Providence Hospital oncology wing on Piper St. (Go to the second floor, walk down the lonnnnnnnng hall that stretches South from the cafe and look for room 2401 pretty much at the end of the hall on your right.) The Parkinson's TeleHealth Program broadcasts live, interactive educational talks to a network of rural communities in the Northwest. On the SECOND Monday of each month, a guest speaker presents a topic eared toward the interests of Parkinson's families. The information is designed to help participants to improve their knowledge of Parkinson's disease and in turn their quality of life.

The regular meeting of the Anchorage Parkinson's Disease Support Group will be held on Saturday, the 19th of July, at 3:30. It's time for our annual picnic potluck. To make this the most festive occasion possible, we will hold the meeting at my house, 9601 Elmore Road. To find the house go to the intersection of Elmore and Abbott Roads, just below Service High School. We are South of Abbott about a quarter mile on Elmore. Our driveway is marked by a green mailbox on your left, halfway up a small hill. Our house has a green metal roof and cedar siding The event is a potluck, so bring something that people will enjoy sharing. We'll see you then!
Peter

Wednesday, November 20, 2013

Here is the Trailer for a New Film About Parkinson's Disease

This looks promising. I backed these guys on Kickstarter, and as a premium, they are supposed to send me a video DVD. When it comes, I plan to share with our support group.  The trailer looks great

Tuesday, November 5, 2013

The Parkinson's Forecast for Anchorage and Vicinity for November


​Hello one and all, here's the Parkinson's Disease roundup for the merry month of November. The word from the Parkinson's​
​ Resource center is that we will not have a telehealth broadcast in November. The program will return on December 9th. The topic for that day will be "laughter MAY be the best medicine". Stay tuned for more as details emerge. For the November meeting on the 16th, I'm trying to get the assistance dog people to come. If they do come, we'll see if we can get them to sit, and speak. So far, they are just playing dead.
And finally, put this bee in your bonnet. I have been the alleged ringleader of the support group for eight years now. It has been a tremendous experience. But I am losing the fire in my belly. It is time for someone else to leap into the breach and lead us to a brighter tomorrow. If you've been thinking to yourself lately that the meetings seem a little flat and that there is more that the group could be doing, that is a sign that you may have what it takes to be the next Parkinson's Poobah here in Anchorage. 

It's not a complicated position. Just a matter of setting up a monthly meeting, getting the word out, and being  resource/liaison to the local community and to the PD world at large. The position comes with some unique privileges. You get to work with some terrific people, and in the course of carrying out the various functions of this office, you will be the person through whom the information flows about the latest developments in the world of PD.
If you have an interest in this, shoot me an email or let me know at the next meeting, which, as noted above, will be November 16.
Thanks,
Peter

Monday, August 6, 2012

Anchorage Parkinson's Disease Support Group August Meeting

OK, so we didn't have much of a Summer. We can still have our Summer Picnic Potluck, darn it! Are we gonna let a little rain stop us from having a good time? (NO!, NO!!!!!) Are we gonna let a whole lot of rain spoil our Summer  plans? (No!!!! NO!!!!) Will massive downpours dampen our spirits? (NO!!!!!NO!!!!!!!!!!!!!!!!) Well alright then, let's meet at our usual digs at the Pioneer Home (We normally have it at my house, but our place is a total wreck as Pam is recovering from a shattered ankle) August 18, 3:30. I'll bring some fancy Italian Soup, you all bring something else.

 That is all,

Chef Pierre

Sunday, July 29, 2012

August Telehealth Conference

Hi folks, I'm back, here is the lowdown on the next telehealth broadcast. This month, it's Lewy Body Dementia and Parkinson’s Disease, the presenters are Helen Whitworth, MS, BSN and Jim Whitworth, LBDA. The program will take place August 13 at room 2401 at 1:00 p.m. in the Providence oncology wing on Piper St.  Go to the second floor walk down the lonnnnnnnng hall that stretches South from the cafe and look for room 2401 pretty much at the end of the hall on your right.


More to come on this month's meeting.
Peter

Wednesday, July 27, 2011

Announcing a New Virtual Gathering Place For Isolated Alaskans With Parkinson' s Disease



It bugs me that there are undoubtedly Alaskans out there with Parkinson's Disease who have no support group nor the ability to travel or live where there is one. As far as I know, the only group is in Anchorage. (Is there some group out there I do not know about? I would love to be corrected about this!)

As an experimental attempt to get at this problem I have created a new facebook page. So you're off in a remote corner of Alaska and dealing with Parkinson's Disease? This is the page for you. Post your questions and we'll try to get answers. Let us know where you are so that you can connect with others in your area. 

Come on in, the stove is warm, and so is the welcome.

Thursday, March 24, 2011

Smiley Crisis




Smiley faces may look innocent, even bland. Don't let the little bastards fool you. That innocuous icon can plunge an unwary soul into startling existential awareness, ripping off the band-aid of denial with a smart sting. One moment you are methodically filling out an online form, the next you are confronted with the unwelcome shock that your relation to reality has significantly shifted without you noticing.

Here's what happened. I have been using the online tool I mentioned a few posts back to track my medications against my on-off cycle. I had run through the process several times and it was becoming familiar. I came to the final step where the program asks you to give a general snapshot of your "wellness" by clicking one of three icons. The choices are a smiley face (feeling good), a non-committal neutral face (feeling average), or a frownie face (feeling bad).

I was about to pick the smiley face when it hit me. Whoa, not so (relatively) fast Parkie boy. You feel good compared to what? The fact is that with PD, I am more likely to aspirate saliva and erupt in a coughing spasm, more apt to have difficulty speaking and being heard, subject to weird involuntary motions if over medicated, and unable to move normally if too far between doses. Yet at that moment, despite whatever symptom I was experiencing, I honestly thought I felt better than average.

That's when I realized how far I had come in incorporating my illness into my self. A different, healthy me who was experiencing the symptoms that I felt would have chosen the frownie face. That is, I would have chosen Mr. Frownie after a quick search for the sheer primordial panic face. But the person that I am, having lived now for more than nine years with various symptoms, has evolved a new scale for quality of life that locates "good" where it's safe to say most healthy people would find the opposite.

Humans are adapters. That's why we're found everywhere on Earth in all seasons, from Point Barrow in January to the Sahara in August. Where adaptation calls for moving we become nomads. Thoreau wrote that he had traveled extensively in Concorde. I've come farther than I ever suspected in Parkinson's Disease.

Monday, January 17, 2011

Jim Kerr and the Amazing Flying APDSG



Anchorage Juggler Jim Kerr visited our support group with tips on balance and stretching. One tip we all agreed to immediately: Avoid stilt walking. We put this into practice right away and not one of us had been on stilts since. Thanks, Jim!

Tuesday, September 14, 2010

Teleheath Conference: That's Entertainment!

A band of die-hard Parkinson's information fanatics were treated to a display of fact-packed, well-thought out answers to questions from around the Northwest fielded by Spokane doctor David Greely. The Q&A was the centerpiece at yesterday's telehealth symposium. The symposium is a monthly interactive broadcast hosted in Anchorage by Providence Hospital. The supporting cast, in the form of small gatherings of attendees from Moses Lake to far-flung Anchorage asked thoughtful questions, and provided a certain amount of sympathetic comic relief as we watched one another struggle with technology using our PD-impaired bodies. (Extra points for the drama provided by the solitary elderly lady who spent several minutes under the table on camera out there somewhere. It was a relief to all of us when you reappeared in your seat and returned to noisily scratching your pencil on what I sure hope was paper.)

While a few questions may have vanished into the haze of the technological Bermuda Triangle, some significant points emerged that were well worth the time and effort of attending. Among the most compelling for me:


Muscle Cramps:
can be treated by proper hydration, metabolic balance and addressing sleep problems, Which is, duh, the way you would treat them in a patient without PD. Sometimes we're not so special.


Eating and Pills:
According to Dr. Greely, nine out of ten people with Parkinson's do not find any difficulty with this. For those that do, he still recommends taking your meds with a small bit of cracker or other non-meat to cue your digestive process to go into action. A pill is not usually enough in itself (unless you are taking some mighty big pills, Chester) to prompt the stomach to empty and push your medicine down the line to your intestines where it can be absorbed into your blood.

Stem Cells: Two thoughts here, relief from this direction is years down the road if it is to come at all, and the problem in the technology is not installing the cells, it's regulating them so that they produce the proper amount of dopamine in the brain. Dr. Greely likened it to the famous "Sorcerer's Apprentice" scene from the Disney Movie Fantasia. First you have one broom, then two, then four, then eight, then chaos.

Exercise I see you rolling your eyes out there. At least that's one part of you that's moving. I know that I harp on this subject ad nauseum. But Dr. Greely made a new point that rang true for me the second he said it. If you exercise, you will get better care from your doctor, from your caregiver and anyone else in your network of care, because you will send the message that you are trying. It doesn't have to be dramatic, start with what you can do and work up. But show those who work to keep you going that you are willing to do your part. They'll love you all the more for it.

Monday, September 13, 2010

As if you were not already busy enough...

OK Parkie Pals, limber up those fingers to mark the following dates on your calendars: TODAY the 13th, 1:00 Telehealth Seminar interactive info session on PD at Providence hospital second floor of the new cancer wing.


Sept 18,Saturday at our regular meeting at the Pioneer Home at 3:30 we will have a presentation on Deep Brain Stimulation (DBS) for Parkinson's Disease from Swedish Hospital in Seattle. Peggy Short, Advanced Nurse Practitioner and DBS programmer will be our main guest. This meeting will also be attended by Keely Daily of Medtronic, the makers of the deep brain stimulator. Unfortunately Dr. Ron Young, a DBS surgeon had to cancel his participation.

Remember our DBS motto, "You need PD like you need a hole in your head." I'll see you there.

Oh, one more thing, I festinated across an excellent blog for those of you who have the exalted, or exhausted, status of PD caregiver. The blog is "Slow and Easy" you can find it here

Must run now, or at least shuffle,

Peter

Saturday, August 14, 2010

Incomi...er, make that Upcoming Anchorage Parkinson's Events

Hello friends, Here's what's coming up in the Anchorage Parkinson's world. August meeting will be held the 21st, Saturday at 3;30in the Anchorage Pioneer home. Betty Berry would be glad to lead a concurrent meeting for caregivers, She asks those interested to please email her at (bberry2205@gci.net). She also writes

"I received a notice in the mail regarding a Senior Housing Fair sponsored by Providence to be held at the Senior Center Thursday, August 19.

Learn about housing options available in Anchorage and Mat-Su for seniors in the areas of : Independent housing - Assisted living - Skilled nursing care and more -(so states the notice.)

Thought this might be of interest to those in the Parkinson Support Group.
Our upcoming meeting will be open phones, sharing tips and experiences."

For the September meeting we will have a group from Swedish Hospital in Seattle including Peggy Short, Advanced Nurse Practitioner and DBS programmer, and Dr Ron Young, a neurosurgeon with nearly 30 years of DBS experience, who is now practicing at Swedish, This meeting will be held the 18th and will also be attended by Keely Daily of Medtronic, the makers of the deep brain stimulator.


If you have a topic you would like to explore at a future meeting please email me

dunlapshohl@gmail.com

A final note, Yoga Instructor Karen Greenwood will soon be offering a Yoga class for the movement impaired through her Anchorage Studio. We will offer to pay class fees for members of the Anchorage Parkison's Support Group. Yoga is recommended for flexibility, strength and balance. Any of you who feel like you are better than average in these important areas, raise your hand. No hands up? Great, I'll see you all there! More details to come.

Pete

Monday, April 12, 2010

OMG! Time for Another Meeting!

Hello friends,

Another month has stormed by like an express subway that doesn't stop at your station. That means it must be meeting time. We will have a guest speaker from the Alzheimer's organization here in town who will tell us about services that they can provide for anyone who has dementia, which of course includes a number of PD sufferers.

The Valiant BETTY BERRY has volunteered to come back with another concurrent session for care partners, so those of you who care for someone with Parkinson's will have a great opportunity to benefit from her experience and generosity.
It all happens at the Swank and sophisticated ANCHORAGE PIONEER HOME this Saturday the 17th of April 3:30 p.m. on the Fifth floor in the West lounge, overlooking scenic Cook Inlet and vibrant downtown Anchorage.

See you there!

Peter

Wednesday, April 22, 2009

Hey Alaska, The Parkinson's specialist will see you now

The wait is over! Alaskans with Parkinson's Disease can now arrange to be seen by a specialist in treatment of this complex condition.

Dr. Alec Glass will soon begin his quarterly visits to Anchorage to provide care to Alaskans who suffer from Parkinson's Disease. His first round here will be the weekend of the 22-24th of May.

Dr. Glass is a fellowship-trained specialist in movement disorders. He practices at the University of California, San Francisco, and with the VA in San Francisco. You can learn more about him here.

To make an appointment to see Dr. Glass, contact


Alaska Neurology Center


3841 Piper Street Suite T345

Anchorage AK 99508

907.565.6000 Phone

1.866.977.2562 Toll Free/Fax

Please help spread the word among people you know who could benefit from this opportunity to better manage the PD beast. This is an excellent chance to move toward better quality of life without having to pass through Seattle or Portland to get there.
Gargantuan thanks to all involved in making this happen, especially Joanne Power, and Dr. Glass.

Festinate forward!

Peter

Monday, September 8, 2008

Patience Pending


We people with Parkinson's are mavericks. We not only march to the beat of a different drummer, sometimes we don't march at all. In fact our theme song should be "I Ain't Marching Anymore" by Phil Ochs. Go with the flow? Not us. No flow, no go.


As members of a culture so manic that it has been forced to slice time into nanoseconds too small for any human to even perceive, we are the dissenting minority. While others multi-task all around us, texting their overfilled to-do lists to their partners while crashing their cars, we struggle to single-task, spending the morning buttoning our shirts or not tying our shoes.


This is role none of us are cut out for these days. Patience cannot be ordered over the Web and then delivered the next day in a brightly-colored Express envelope. Instead, we must learn it. And how do we do that?


Slowly.


Fortunately, we have many opportunities for practice. We spend countless minutes waiting for our meds to kick in. Dopamine brings a rush, but you can't rush dopamine.


Crossing a room can take on the quality of a major expedition, complete with danger. You may be in a hurry, but your feet are on their own schedule, and frankly, they're tired of being ordered around. They will get you there in their own sweet time. Push them too much, and you're going down hard, pal. They'll stick to the floor and you'll topple to their level with a thud that frightens everyone in the vicinity, with the exception of the mutinous extremities themselves. They're already safe on the floor. It won't be them that feels the pain. I don't know a single person with Parkinson's who has injured a foot in a fall.

So you learn not to rush your feet. They have the upper hand.

You want to practice patience? Try removing the cap from the bottle that holds the pills that enable you to take the caps off bottles. Hours of fun. The irony alone will amuse you for eons. Which is how long it will take to get to the pills.

The ultimate exercise for developing patience is the marathon wait for the cure. I remember a friend who bitterly observed that he had been assured that a cure was no more than a decade away. That decade has passed, and so has he. But bitterness sours the present for the sake of an uncertain future. So we need something to do instead of waiting. We have to work in the present to advance the progress toward the day when we can get back in the rat race with everyone else.

I'd love to just stop and smell the flowers, but ever the pranking poltergeist, Parkinson's even takes your sense of smell.