Tuesday 22 December 2015

WALKING LIKE A LEGO MAN

A mostly true look at Parkinson’s Disease for those who have less clue than me...

One of the worst things about PD is that it removes some of the things in life that the non-sufferer doesn’t even have to think about, such as smiling, walking and swinging your arms.

The non-sufferer might think that the key signifier of PD is a shaky hand, but it’s not for me.

PD is (in an upside down sort of way) the Swiss Penknife of illnesses, by which I mean it has something to spoil everything you do. It even has the equivalent of a thing for taking boy scouts out of horses’ hooves: crushing fatigue, stiffness, feebleness.


The main signifier of all these things for me is my walk:

· Like a Lego man would walk

· Like a clockwork soldier would march

· Dragging one leg (the right in my case)

· Trudging with feet scraping the floor (both feet)

· Swaying from side to side to try to reduce balance problems (try edging along a row in the cinema)

· Each step tentative, as if the pavement cracks are preparing to trip or swallow me

· Hands clasped behind me, like - God Save Me - Prince Philip

· Exhausted by the effort caused by all of the above
Other physical problems:

· Rising from a low seat or seat without arms

· Rising from a bed

· Tying a shoelace

· Looking up rather than down when walking

· Not smiling

· Getting in and out of small cars; eek!

· Carrying things, especially liquids, while shaking

· Falling asleep in the day (tiredness due to a mix of shaking, efforts to counter shaking, low moods and so on)

· Unable to reach toes to clip nails or put on socks or tie shoes: although I suppose I could get extending nail scissors or Velcro shoes / ties?

· Feeling stiff everywhere else

Etc, etc, etc......

SOLUTION? A PERSONAL TRAINER?

My wife swears by her personal trainer and my daughter bought me 3 sessions with her trainer as a gift, so under their prompting I eventually had to give the idea a try. The trainer’s name is Lee Hicks and he is a Movement Specialist, looking at an individual’s mobility and stability, anywhere from injury through to performance. However, I’m his only PD customer and at 69, I’m his oldest.

First he used my gift sessions to determine the relative success of my movement and stability; looking for potential solutions; and then he started to develop a fight back strategy against this awful PD monster.

My view was that almost a year after diagnosis of PD I was noticeably stiffer, weaker and less capable of conducting the Activities of Daily Living (ADLs) as the experts call them. I was being beaten by PD, was frustrated and short of energy to fight it.

Lee selected a simple set of exercises designed to:

· Increase strength

· Increase stability

· Increase length

· Increase mobility

· Improve balance in motion

· Overall to increase potential ‘pathways to success’

While we have to accept where I am now and that PD might be an inexorable, unbeatable opponent (i.e. it may not be beatable, whatever we do) we can at least assume PD can be defeated and tackle it in a positive frame of mind. The goal is to improve – not just stand still or manage a slow retreat towards morbid or torpid .

At first Lee assessed how I moved to create our strategies for success, gradually focusing on the areas where gains can be made e.g. on my trudging gait and weak right leg, also getting in and out of the car.

Lee also looks at the ADLs and for small gains that can be achieved through small changes and lots of repetition. He also keeps me focused (would I really put myself through all this without him? No!).

Now I’m still not sure of making the team in Rio, but I no longer walk like a Lego man and after a few hesitant steps, particularly first thing in the morning, can be taken for a normal walker. Strain on my hips has reduced and I can put my socks on more easily. I’m still not sure of beating PD, but am at least in with a chance!



THE SWIMMING BATHS

Talk was about the ridiculousness of Donald Trump and his view of Muslims, followed by a critical account of accompanying your wife on Christmas shopping trips. General lack of interest, having to play a role in decision processes being just two of the many negatives.


Then there was having to write individual messages on cards which already had the obvious ‘Merry Christmas’ on them. ‘Bah, humbug, Mr Scrooge’.

5 comments:

  1. Peter still stalking you and yippee for excercise, I had breast cancer 2 yrs ago and all good a low grade treated with a lumpectomy then radiotherapy...curable unlike PD!! Managed to get a GP referral to a health gym annd started eventually last yr 2015 and now with my diagnosis I realise how important it is for strength and balance and although I do not now have 1:1 the trainer is still there for me giving me advice especially with balance

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  2. Greetings, fellow PD advocate here. Below is a link to my latest blog entry about the future of PD therapies, thought you might be interested in taking a look.

    https://tmrwedition.com/2017/03/23/the-future-of-parkinsons-disease-therapies/

    I have recently started collaborating with a number of research labs that are working towards bringing to practice some of the therapies mentioned in that article with the goal of one day bringing an end to this disease.

    I hope that my article might inspire people to keep fighting knowing that there are so many new and exciting therapies coming soon. Feel free to share that information with anyone who you think might benefit from it.

    Looking forward to what the future has in store,
    Benjamin Stecher
    tmrwedition.com

    ReplyDelete

  3. I was suffering from Parkinson's since 2016 & life had become disastrous for me,72 % of my body was covered by Tremors.After taking product from www.ultimateherbalclinic.com under supervision of Dr Ernest Albrecht, I started getting results within 3 weeks of their dosage .One day I got extremely sick, could not keep anything down, difficulty standing, restless sleep,I Started taking this remedies 2 times daily Morning and Evening, I am writing this to inform others that nothing was really working to help my PD other than this product.I went off my previous medications (with the doctor's knowledge) and started on their Parkinson's disease herbal formula.Treatment went very well and tremors are gone.

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  4. My husband was diagnosed with early onset Parkinson's disease at 57.his symptoms were shuffling of feet,slurred speech, low volume speech, degradation of hand writing, horrible driving skills, right arm held at 45 degree angle, things were tough for me, but now he finally free from the disease with the help of total cure ultimate health home, he now walks properly and all symptoms has reversed, he had trouble with balance especially at night, getting into the shower and exiting it is difficult,getting into bed is also another thing he finds impossible.we had to find a better solution for his condition which has really helped him a lot,the biggest helped we had was ultimatehealthhome they walked us through the proper steps,am highly recommended this ultimatehealthhome@gmail.com to anyone who needs help.

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  5. i was diagnosed of parkinson disease 5 years ago,i started azilect,then mirapex as the disease progressed in february last year,and i started on parkinson disease herbal medicine from ultimate life clinic,few months into the treatment i made a significant recovery,almost all my symptoms are gone,great improvement with my movement and balance,it been a year and life has been so good for me,reach them through there website at www.ultimatelifeclinic.com

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