
I like things that move fast, I enjoy seeing progress, growth excites me.
However, today I’m thankful for things that move slow, mostly the progress of Motor Neurone Disease (or commonly called Lou Gehrig’s Disease/ALS) in my body.
I know I can’t walk the same, my hands are weaker and I need more help getting around, but in light of where I was expected to be by now, this disease is moving slowly by MND / ALS standards.
I am living in days of grace – and aren’t we all?
Some would say my slow progress is a miracle. I believe that. Others would say it’s due to the practical things I have done and choices I have made. I believe that too. Daily, I pray, I meditate, I rest. Daily, I concentrate on minimising stress, a known accelerant of MND / ALS, and follow a strict vitamin regime.
You see, the medical world has no traditional way to fight MND / ALS at this time. There is no surgery, no treatment that I can have to remove the disease or kill it. In fact, what looks like surrender to the disease is actually the most effective way of fighting the disease: rest, peace and hope!
It’s strange to fight with rest, to agitate with peace, to move forward with hope – but as is the case with life, you have to do what you can do and leave the rest to God.
I wonder if in your life, in what you face right now and the season you are in, if you’ve been trying to fight with force, energy and speed when instead, you should be resting.
There’s a lot to be said for rest. For one, it’s how God designed us to operate, with work and rest, rhythmically, infused by Sabbaths. Not only that, but He also leads us to rest if we follow Him there. So, how do you rest? Do you take a walk by the beach, work out, hang out with family, worship, read?
When you rest, you put yourself in a position to receive the peace of God. It’s a peace that supersedes your experience and sustains you through your day. Ultimately, that you would put your hope unswervingly in God, the one who can do more than we could ever hope, dream or imagine.
And that’s exactly what I am doing. I’m resting in the truth that today is a gift and I’m thankful for it. I’m living with peace in the face of death and disability. I have a hope that what I see as a future dream, a cure for anyone who is ever diagnosed with MND / ALS, will one day become a present day reality.
I pray rest, peace and hope for you today too.
Phil
October 31, 2014 at 6:48 am
Amen, Phil.
Just about everyone I know that has been diagnosed with ALS/MND was/is a Type A personality, including myself and I’m guessing you also. Type A’s generally don’t know what the rest you’re referring to is until something like this horrible disease teaches them. It’s a tough lesson, but I get it now – I wish I would have figured it out before ALS.
Glad you enjoyed your trip.
October 31, 2014 at 8:27 am
How true you are Bill. If only we had lets hope others can learn from our lessons. Peace to you and your family my friend.
October 31, 2014 at 6:57 am
Phil, as laways – you bring beautiful, costly wisdom & grace to us all – how generous are you … to find something in this battle – to share with us all. thankyou. greater peace, rest and strength to you & Lenore.
October 31, 2014 at 8:35 am
Thanks so much Donna for your encouragement. Yes the battlefield is filled with lessons for us all. Love to you and the family.
October 31, 2014 at 7:21 am
Phil, you never cease to inspire! You always have but do even more now. Thank you!
October 31, 2014 at 8:36 am
Thanks mate appreciate you presence through the blog. It does make a difference.
October 31, 2014 at 7:44 am
Bless you Ps Phil!! I praise God for the slow progression of this insidious disease you are inspirational to others sufferers and those who care for them. Thanks for sharing all your lovely pics of the family, beautiful!!
Sent from my iPad
October 31, 2014 at 8:40 am
Hi Hazel, thanks again. I know you know only so well. Its a comfort to have people who know first hand that sometimes life’s beautiful lessons are learned in life’s ugliest places.
October 31, 2014 at 6:18 pm
Thanks for the pearls of wisdom Phil. Great perspective!
God bless!
November 6, 2014 at 2:51 pm
Thanks Dave. Appreciate you reading and taking the time to reply.
October 31, 2014 at 9:18 pm
beautiful wisdom
November 6, 2014 at 2:51 pm
Thanks Tania
November 1, 2014 at 11:04 am
Hi Phil, I have been looking on the MND site NZ, and found this and thought it rather beautiful. I am enjoying your Fridays with Phil, and am encouraged by your faith. Take care, Claire
The blue cornflower
The blue cornflower is the international flower of hope for motor neurone disease. The Cornflower symbolizes courage. It can withstand both frost and drought and its strong blue colour never fades, no matter what it faces. Like the cornflower people with MND show tremendous courage and strength of character to cope with this most challenging of diseases.
Helping people living with motor neurone disease
E āwhina ana i te hunga e taumaha ana i te mate taki uaua a ngā pūtau io
November 6, 2014 at 2:52 pm
Thanks Claire really appreciate.
June 20, 2015 at 6:59 pm
Hi Phil I am indeed being blessed with your Friday blog. The last Friday”s one on the choices we make blessed me as well
June 22, 2015 at 7:04 am
Hi John. Thank you. I hope you and your family are well.