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Hug Me.. I've got MND.

I guess this is a diary of my thoughts, findings and feelings since being dianosed with MND in December 2011.

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Hug Me.. I've got MND. | nikkiwoodman.blogspot.com Reviews
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I guess this is a diary of my thoughts, findings and feelings since being dianosed with MND in December 2011.
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1 pages
2 eliza writes
3 eliza
4 christina writes
5 hugs chrissie
6 posted by
7 nikki woodman
8 8 comments
9 email this
10 blogthis
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Hug Me.. I've got MND. | nikkiwoodman.blogspot.com Reviews

https://nikkiwoodman.blogspot.com

I guess this is a diary of my thoughts, findings and feelings since being dianosed with MND in December 2011.

INTERNAL PAGES

nikkiwoodman.blogspot.com nikkiwoodman.blogspot.com
1

Hug Me.. I've got MND.: November 2012

http://nikkiwoodman.blogspot.com/2012_11_01_archive.html

Hug Me. I've got MND. I guess this is a diary of my thoughts, findings and feelings since being dianosed with MND in December 2011. Wednesday, 28 November 2012. THIS HAS TO BE MAKE BELIEVE! Once upon a time there was a Princess called Nikki. Sadly she had MND and was confined to a wheelchair. Nikki found this so helpful. She could cook from her wheel chair , stirring and checking each pot and pan. 9:30 she arose , made coffee, got cereal and waited for Princess Laura. her PA. Fearing that the loft ladder...

2

Hug Me.. I've got MND.: PS SOME OF MY PAINTINGS

http://nikkiwoodman.blogspot.com/2013/07/ps-some-of-my-paintings.html

Hug Me. I've got MND. I guess this is a diary of my thoughts, findings and feelings since being dianosed with MND in December 2011. Monday, 29 July 2013. PS SOME OF MY PAINTINGS. Dr in the morning re my funny tummy (was sooo poorly yesterday! So I do hope that Doris is available when I go to Leeds next Monday to see the breathing specialist. Breathing is getting a problem. well you just need to do it don't you! So as a PS, and as I have been asked several times, I will show you some of my work.

3

Hug Me.. I've got MND.: February 2013

http://nikkiwoodman.blogspot.com/2013_02_01_archive.html

Hug Me. I've got MND. I guess this is a diary of my thoughts, findings and feelings since being dianosed with MND in December 2011. Wednesday, 27 February 2013. YOU HAVE TO BE FIT TO BE THIS ILL! So I started a post re carers, 30 hrs ago. As it wasn't complete, ie I got disturbed. I haven't yet published. So I thought I would skip forward to today. I had written a long Blog . And out it has sailed into the ether! Too too tired to re write. And leave you with the life enriching piece of music. It realise ...

4

Hug Me.. I've got MND.: June 2013

http://nikkiwoodman.blogspot.com/2013_06_01_archive.html

Hug Me. I've got MND. I guess this is a diary of my thoughts, findings and feelings since being dianosed with MND in December 2011. Wednesday, 26 June 2013. THE DAY BEFORE I GO TO GLASTO. My friend Laura had borrowed my cases. So I panicked that I didn't have a case! I had given away all other cases when I downsized, realising that I wouldn't be going on any/many? No response. My anxiety rose. Sharon , my support worker, who is very laid back, tried to calm me by saying that we could make a list. I now r...

5

Hug Me.. I've got MND.: January 2013

http://nikkiwoodman.blogspot.com/2013_01_01_archive.html

Hug Me. I've got MND. I guess this is a diary of my thoughts, findings and feelings since being dianosed with MND in December 2011. Thursday, 31 January 2013. It's Thursday at the very end of Jan 2013. I've Blogged for just over a year and as of this moment I have had 20103 hits. Thankyou. Thankyou. I do hope I have helped my family and friends to keep in touch. I do hope I have helped, in some way, others with MND. to keep fighting. Thankyou . Next target 20500 by my birthday on Feb 17th! Thank you Becc...

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My Brother Andrew: April 2012

http://supportingandrew.blogspot.com/2012_04_01_archive.html

Fighting Progressive Bulbar Palsy A type of Lou Gehrig's Disease. MND - Motor Neurone Disease. Working with - www.mndassociation.org. Andrew's Story - Daily Post. Monday, 23 April 2012. Back in June 2010 at a family gathering [ the one pictured above actually ] I remember catching sight of a red wristband Andrew was wearing -turning it over I read " Fighting Lou Gehrig`s Disease " The ALS Association. To anyone thinking of fundraising -please go for it! We made him laugh. Thank you to everyone who su...

supportingandrew.blogspot.com supportingandrew.blogspot.com

My Brother Andrew: Taking a break....

http://supportingandrew.blogspot.com/2012/04/taking-break.html

Fighting Progressive Bulbar Palsy A type of Lou Gehrig's Disease. MND - Motor Neurone Disease. Working with - www.mndassociation.org. Andrew's Story - Daily Post. Monday, 23 April 2012. Back in June 2010 at a family gathering [ the one pictured above actually ] I remember catching sight of a red wristband Andrew was wearing -turning it over I read " Fighting Lou Gehrig`s Disease " The ALS Association. To anyone thinking of fundraising -please go for it! We made him laugh. Thank you to everyone who su...

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Hug Me.. I've got MND.

Hug Me. I've got MND. I guess this is a diary of my thoughts, findings and feelings since being dianosed with MND in December 2011. Tuesday, 17 September 2013. Unfortunately this is Eliza and Christina (Nikki's daughters) here. We are sad to let you know that our mum died, peacefully, on Sunday 8th September 2013 at about 8pm. We may write here again after the funeral, which is to be held on Friday. I know many of you were on twitter with Nikki, but if you do want to comment, please do so here, it would ...

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