Looking Forward to 2016

The cures we want aren’t going to fall from the sky. We have to get ladders and climb up and get them.

— Michael J. Fox

As 2015 comes to a close, those of us in the Parkinson’s community are excited about the many new  research discoveries regarding the causes and treatments for Parkinson’s Disease.  It seems that every week in the past few months, another discovery, whether it is a drug or therapy,  has shown to be effective in either slowing the progression of the disease or in some cases, even reversing it.  In the 7 years since I was diagnosed, I have never been so hopeful that maybe this year will bring the big breakthrough.

This is exciting news, especially since some of those drugs that show a positive effect in PD patients have already been approved for other diseases, thus reducing the time for FDA approval for persons with Parkinson’s.  Even salicylic acid, the main ingredient in aspirin, which we all have in our medicine cabinets, has proven to be effective for reducing the cell-death that leads to Parkinson’s.  Today there was even more good news.  Researchers at Scripps Clinic and Scripps Research Institute in San Diego are beginning trials on humans using stem-cells taken from the patient’s own skin.  Watch this video on KUSI News  Once the pilot project is approved by the FDA, the clinical trials should open up to multi-national research centers.  Researchers expect this to be a long term treatment for the movement disorders associated with PD.    FDA approval could be made in the next 24-36 months.

For me, 2015 brought about many changes.  My second grandchild was born in May, followed two weeks later by the passing of my mother.  It was a very tumultuous, emotional time for me.  I began writing shortly before my mother’s death, which eventually led to this blog.  This was one of the things that helped me to get through that very difficult time.  Thank you to all of my followers around the world.  It has been a very gratifying experience to share my “adventures with Parkinson’s” with all of you, making new friends because of our common bond.  I have almost 100 followers, so if you have not yet followed “Twitchy Woman” either here or on Facebook, please follow now so that we can get to 100 by December 31.

So looking forward to 2016:

A cure, perhaps?  Or at least a treatment that reverses the progression of PD.  Michael J. Fox said that the Michael J Fox Foundation has one mission – to find a cure – and once that cure is found, he will shut down his Foundation.  Let’s hope that 2016 is the year that he will close up shop.

For me, I plan to continue writing, enjoying this new-found creative outlet that I discovered after PD diagnosis.   Maybe I will end up like every other Parkinson’s patient with a blog and write a book.  OK, maybe a pamphlet.

Speaking of books, I hope to review a few more in the coming months, including the just published “Goodbye Parkinson’s, Hello Life!” by Alex Kerten, whose Gyro-Kinetics Center in Herzliya, Israel is a leader worldwide in treating clients with Parkinson’s and other movement disorders.  I have just started reading this and want to try some of his exercises for relieving PD symptoms.  Stay tuned.

I have become a PD Advocate for the Parkinson’s Disease Foundation after having spent a wonderful weekend with 25 other women with PD at the PDF’s Women & Parkinson’s Initiative conference last September.   I am looking forward to engaging with other women with PD living in Los Angeles.   On January 17, I will be hosting a meeting for women with PD to learn about the Women & Parkinson’s Initiative and to hear from a local PDF Research Advocate about getting involved in clinical research for PD.   If you are interested in this or future events for Women & PD in LA, please contact me directly.

IMG_0387I will continue to work on my boxing skills with Rock Steady Boxing NY/LA.  It is very hard work and great exercise.  Boxing has improved my balance and reflexes, and most importantly, my tennis game.   Besides, the men way outnumber the women in boxing classes, which makes it even more fun.  (Just don’t tell my husband).

Ommmmmmmmmmm……..yoga is the one calming activity that I regularly participate in.    It keeps me aware of my body, my balance and stretches my muscles.  I can still do a tree pose successfully most days, no worse than the others in the classes I attend.   Shavasana, Corpse Pose, at the end is better than a nap.  When I am done with class I am ready to take on the day.

Finally, I am looking forward to a year of new adventures with my husband, and not allowing Parkinson’s to take charge of me.  I will be in charge of my Parkinson’s and continue to enjoy life with my family and friends.

Wishing all of you a happy holiday and wonderful, healthy New Year.


Hanukkah-And-Christmas-3  hdallpictures.com

7 responses to “Looking Forward to 2016”

  1. Great post!!! Go stem cells!

  2. Thanks for the info about Gyro-Kinetics I want to try that!! Best wishes and happy new year. Moving forward!!

  3. Reblogged this on defeatparkinsons and commented:
    This for a very happy and blessed new year 2016 & a very lovely holiday season …may the Lords blessings be with you all year round…if you have faith like a little mustard seed anything is possible YES even a cure…,there are new treatments on the way…in meantime enjoy life..color outside the lines, sing at the top of your lungs, do something good for you everyday like exercise- biking, wLking, swimming, taichi, yoga, dancing, boxing ( but get doctors approval first not everyone is medically stable or capable to do this – sometimes you can hurt yourself more unknowingly) for instance if you had multiple back surgeries this is not medically recommended …
    Do something meaningful for others – this is the secret of a happy..long life! Get involved in your community in whatever you can ..as little or as much lend an ear, be a friend, be a mentor to other women. With Pd or other caregivers etc…feed your souls …meditate..pray, and read good books…
    Don’t forget to eat a little dark chocolate keeps your brain and heart healthy and Parkinson’s symptoms improved because dopamine and other happy chemicals 🎄🎄🎄🎄🎄🎄🎄

  4. Hi Sharon,

    I met you at the boxing gym a few weeks ago and have been following twitchy woman posts ever sense. I live in a pretty remote town and so being evolved in a. Group is a little difficult, but am very interested in the January 17th meeting you are hosting. I am willing to travel to Southern California and am looking forward to receiving more information.

    Thank you so much for the twitchy woman posts hope you have a happy new year.


    Sent from my iPhone


    1. Hi Phyllis
      Are you the one from Mammoth? I heard the snow is great, but we stopped skiing 15 years ago because of my husbands knee. I can’t tolerate the cold anyway so we have no plans to start again.

      I am glad you are enjoying the blog and you are definitely welcome to join us on Jan 17. We are probably going to meet once every other month, which might make it easier for you to come more than once. Maybe you can stay and go to boxing too.

      Have a great holiday and a happy new year


  5. Hello Sharon, As always, I deeply enjoy whatever you and others write. So sorry to hear your mother passed in 2015. That is a heavy! I still miss my mom more than I ever dreamed I would, even though she was 88, & sharp as a tack, when she died of cancer in l991, I was so lucky that we were truly friends, & she loved my two adopted children so very much. But there are days when I miss her with
    all my heart, and I talk to her and tell her how we are all doing. I was in such denial of her illness, and was busy planning her 90th birthday party when she passed. I think losing a mom or dad is so heart-wrenching. myrnaspecktor @att.net

    1. Thanks for keeping us educated, informed, optimistic and hopeful. Many blessings to you and your family in the new year.

Leave a Reply to skrischer Cancel reply

Please log in using one of these methods to post your comment:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. Log Out /  Change )

Connecting to %s

This site uses Akismet to reduce spam. Learn how your comment data is processed.

A Note To My Readers

I love to see your comments and get your emails as we share our collective experiences. But based on a couple of private questions from some of you, remember, I am just a lay person and a patient like the rest of you. For medical and similar advice, you need to talk to your own doctor

Twitchy Woman

Twitchy Women partners with the Parkinson’s Wellness Fund to ensure we have the resources to offer peer support for women with Parkinson’s.