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Never Give Up.......Motor Neurone Disease.

Never Give Up.Motor Neurone Disease. Saturday, August 09, 2008. As was before, so will be. Greetings to those who knew Robert personally, Greetings to those who's lives he touched in some way, Greetings to those who found strength and gained a insight into a life shared by family and reluctantly shared by a cruel Mistress known as Motor Neurone Disease. This is a short post, I am somewhat a simple man, not eloquent with words, but I will say this;. Cattle die, kindred die;. Every man is mortal;. The fina...

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Never Give Up.......Motor Neurone Disease. | robertmnd.blogspot.com Reviews

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Never Give Up.Motor Neurone Disease. Saturday, August 09, 2008. As was before, so will be. Greetings to those who knew Robert personally, Greetings to those who's lives he touched in some way, Greetings to those who found strength and gained a insight into a life shared by family and reluctantly shared by a cruel Mistress known as Motor Neurone Disease. This is a short post, I am somewhat a simple man, not eloquent with words, but I will say this;. Cattle die, kindred die;. Every man is mortal;. The fina...

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7 to be continued

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Never Give Up.......Motor Neurone Disease. | robertmnd.blogspot.com Reviews

https://robertmnd.blogspot.com

Never Give Up.Motor Neurone Disease. Saturday, August 09, 2008. As was before, so will be. Greetings to those who knew Robert personally, Greetings to those who's lives he touched in some way, Greetings to those who found strength and gained a insight into a life shared by family and reluctantly shared by a cruel Mistress known as Motor Neurone Disease. This is a short post, I am somewhat a simple man, not eloquent with words, but I will say this;. Cattle die, kindred die;. Every man is mortal;. The fina...

INTERNAL PAGES

robertmnd.blogspot.com

1

Never Give Up.......Motor Neurone Disease.: Grandchildren

http://robertmnd.blogspot.com/2008/05/grandchildren.html

Never Give Up.Motor Neurone Disease. Friday, May 30, 2008. Photo of the three boys busy with cardboard boxes.who needs expensive toys. It is only a short while later and the lounge floor has become a disaster area with boys, toys and empty cardboard boxes. Books are found in quick succession for Nana to read to the two oldest boys while baby has decided to investigate the drawer handles of the china cabinet. Children the world over can in many instances regardless of where they live bring stability to a ...

2

Never Give Up.......Motor Neurone Disease.: Sixty six years and still going

http://robertmnd.blogspot.com/2008/03/sixty-six-years-and-still-going.html

Never Give Up.Motor Neurone Disease. Tuesday, March 25, 2008. Sixty six years and still going. Well, here I am on a slightly overcast day in sunny New Plymouth. I am sitting propped up on the bed with my laptop on a tray deciding what to say. On the 24th I turned 66 ( wow, that's really old ) and was shouted out to an evening meal with my wife, son John and family. Oh if only I could I said with a smile. Posted by Robert at 2:13 PM. Subscribe to Post Comments [ Atom. May you find the Strength to face tom...

3

Never Give Up.......Motor Neurone Disease.: The "PEG"

http://robertmnd.blogspot.com/2007/12/peg.html

Never Give Up.Motor Neurone Disease. Tuesday, December 04, 2007. A new stage in my life starts. Wheeled into the operating theatre about 11am Tuesday morning 27th November. Twenty minutes later its all over and with Jan walking beside me I am taken up to the medical ward where as it turns out I am to spend the next two and a half days . A shot of Morphine soon had that under control. And again that night some more pain. Do I have any regrets about having the peg put in. Posted by Robert at 11:06 PM.

4

Never Give Up.......Motor Neurone Disease.: Christmas wishes....

http://robertmnd.blogspot.com/2007/12/christmas-wishes.html

Never Give Up.Motor Neurone Disease. Monday, December 17, 2007. Christmas comes but once a year. This is a time for peace, friendship, harmony, companionship and also a time to be able to spend it with family and friends. Christmas is celebrated right round the world and has the ability to bring together people of different races and religions. It is a time to smile, laugh, sing and remember times gone past. A time to look back and think of all those who have helped you. I wish you all a Merry Christmas.

5

Never Give Up.......Motor Neurone Disease.: Bonus

http://robertmnd.blogspot.com/2008/05/bonus.html

Never Give Up.Motor Neurone Disease. Wednesday, May 28, 2008. When we approach the cross road of life some of us are in the position of knowing, all be it approximately, of when that time will be. The two and a half years that I was given will be the middle of next month and I fully intend to exceed that period of time. To anyone diagnosed with ALS/MND you ask why! I have every reason to feel sorry for myself, but my disability, condition, call it what you will, is minor. There are other people out t...

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gobeyondals.wordpress.com

برای آنکه يادم باشد | زندگی، ALS و خيلی چيزهای ديگر

https://gobeyondals.wordpress.com/2011/02/26/برای-آنکه-يادم-باشد

زندگی، ALS و خيلی چيزهای ديگر. پس نتیجه بگیریم که این ALS نیست؟ امروز نه آغاز و نه انجام جهان است ←. برای آنکه يادم باشد. فوریه 26, 2011. شهریور امسال، مادر بزرگ با واکر راه می رفت، کتاب می خواند و مثل همیشه اش بود، آنطور که می شناسمش. دیدن همه نوشتهها بر اساس چیستا ←. این نوشته در ALS. ارسال شده. این نوشته را نشانهگذاری. پس نتیجه بگیریم که این ALS نیست؟ امروز نه آغاز و نه انجام جهان است ←. پاسخی بگذارید لغو پاسخ. دیدگاهتان را اینجا وارد نمایید. نشانی هرگز عمومی نمیشود). درحال اتصال به %s. ای ال اس چیست؟

gobeyondals.wordpress.com

اينطوری شروع شد | زندگی، ALS و خيلی چيزهای ديگر

https://gobeyondals.wordpress.com/2011/02/02/اينطوری-شروع-شد

زندگی، ALS و خيلی چيزهای ديگر. از آخر به اول ←. فوریه 2, 2011. فیزیوتراپی هم در کنارش شروع شد. تا بهار 89 قدرت پاها کمی بهتر شد اما بلند شدن از حالت نشسته سخت تر شده بود. یک وقتهایی مثلا موقع بلند شدن از روی توالت فرنگی این موضوع دردسر ساز بود. برای حمام قبلش به دیوار دسته های متعدد کوبیده بودند، اما کافی نبود. یک صندلی بلند دسته دار مخصوص دستشویی روی توالت فرنگی گذاشتند. پريروز رفتند پیش نورولوژیست پنجم. در یک کلینیک شلوغ در یک بیمارستان دانشگاهی. به شرح معاینات توسط رزیدنتش گوش داده بود، نوار ع...الآن،...

gobeyondals.wordpress.com

چیستا | زندگی، ALS و خيلی چيزهای ديگر

https://gobeyondals.wordpress.com/author/gobeyondals

زندگی، ALS و خيلی چيزهای ديگر. يكى كه گريه و خنده اش با هم است، يكى كه كفر و ايمانش با هم است، يكى كه در هم است، يكى كه مى خواست پيامبرى باشد بى منت و مزد، كه راه برود و مثل تيستو سبز انگشتى، انگشت سبزش را بكشد اينطرف و آنطرف، و هرجا شدتى مى بيند، فرجى از آستينش در آورد. بعد فهميد دير رسيده است، سالهاست كه ديگر هيچكس به يقينى پيامبرانه نائل نيامده است. اوت 25, 2011. امروز نه آغاز و نه انجام جهان است. آوریل 3, 2011. برای آنکه يادم باشد. فوریه 26, 2011. پس نتیجه بگیریم که این ALS نیست؟ فوریه 24, 2011.

jeannie-world.blogspot.com

Jeannie's World: August 2006

http://jeannie-world.blogspot.com/2006_08_01_archive.html

My name is Jeannie I am 33 years old, this blog is about me and my fight against Motor neurone disease. I started showing signs of Motor neurone disease (MND) also known as Amyotrophic lateral sclerosis (ALS) in June 2000. Symptoms started in my left foot with stiffness and progressed slowly to my legs, hands, and speech. I was diagnosed in July 2001. Tuesday, August 08, 2006. This is my life. Me with girls (2004 I think). Posted by Jeannie at 4:13 PM. Sunday, August 06, 2006. Posted by Jeannie at 4:16 PM.

jeannie-world.blogspot.com

Jeannie's World: April 2007

http://jeannie-world.blogspot.com/2007_04_01_archive.html

My name is Jeannie I am 33 years old, this blog is about me and my fight against Motor neurone disease. I started showing signs of Motor neurone disease (MND) also known as Amyotrophic lateral sclerosis (ALS) in June 2000. Symptoms started in my left foot with stiffness and progressed slowly to my legs, hands, and speech. I was diagnosed in July 2001. Thursday, April 12, 2007. My power chair has just been collected for repair, know doubt it is the batteries and they claim If there is two or so months war...

jeannie-world.blogspot.com

Jeannie's World: May 2007

http://jeannie-world.blogspot.com/2007_05_01_archive.html

My name is Jeannie I am 33 years old, this blog is about me and my fight against Motor neurone disease. I started showing signs of Motor neurone disease (MND) also known as Amyotrophic lateral sclerosis (ALS) in June 2000. Symptoms started in my left foot with stiffness and progressed slowly to my legs, hands, and speech. I was diagnosed in July 2001. Thursday, May 31, 2007. Pictures of our back garden. Posted by Jeannie at 11:27 AM. Bethany's School sports day. Posted by Jeannie at 11:14 AM. Ive purchas...

jeannie-world.blogspot.com

Jeannie's World: January 2007

http://jeannie-world.blogspot.com/2007_01_01_archive.html

My name is Jeannie I am 33 years old, this blog is about me and my fight against Motor neurone disease. I started showing signs of Motor neurone disease (MND) also known as Amyotrophic lateral sclerosis (ALS) in June 2000. Symptoms started in my left foot with stiffness and progressed slowly to my legs, hands, and speech. I was diagnosed in July 2001. Tuesday, January 30, 2007. We are all doing good. Well until next time here are a few photo's of my new style xxx. Posted by Jeannie at 2:06 PM. I'm feelin...

gobeyondals.wordpress.com

امروز نه آغاز و نه انجام جهان است | زندگی، ALS و خيلی چيزهای ديگر

https://gobeyondals.wordpress.com/2011/04/03/امروز-نه-آغاز-و-نه-انجام-جهان-است

زندگی، ALS و خيلی چيزهای ديگر. برای آنکه يادم باشد. امروز نه آغاز و نه انجام جهان است. آوریل 3, 2011. مادربزرگ چهارشنبه شب در منزل نبضش رفت، نفسش سخت شد و از هوش رفت، اهل خانه قلبش را ماساژ دادند، به اورژانس زنگ زدند و تمام شب بر بالین مادربزرگ در اورژانس بیمارستان، قطرات دوپامین را تنظیم کردند. چرا این اراجیف را می نویسم؟ پی نوشت، عکس را ببینید:. دیدن همه نوشتهها بر اساس چیستا ←. این نوشته در ALS. ارسال شده و با ALS. برچسبگذاری شده. این نوشته را نشانهگذاری. برای آنکه يادم باشد. پاسخی بگذارید لغو پاسخ.

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Never Give Up.......Motor Neurone Disease.

Never Give Up.Motor Neurone Disease. Saturday, August 09, 2008. As was before, so will be. Greetings to those who knew Robert personally, Greetings to those who's lives he touched in some way, Greetings to those who found strength and gained a insight into a life shared by family and reluctantly shared by a cruel Mistress known as Motor Neurone Disease. This is a short post, I am somewhat a simple man, not eloquent with words, but I will say this;. Cattle die, kindred die;. Every man is mortal;. The fina...

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