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ALS For support and discussion of Amyotrophic lateral sclerosis (ALS), also referred to as "Lou Gehrig's Disease." In memory of BobbyB. |
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Member
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Go to Build UK site and say goodbye to Rob, One helluva man
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Yappiest Elder Member
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![]() here is link to the post regarding his passing: http://www.magimedia.co.uk/buildforu...pic.php?t=3253 my deepest sympathy to his wife sharon and their families.
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Community Support Team
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my deepest sympathy to Sharon and all who knew and loved Rob...
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~Chemar~ * . * . These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here. |
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In Remembrance
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![]() http://homepage.ntlworld.com/rob.shaz/home.html Hi, our names are Rob and Sharon. We are both 41 and live in Nottinghamshire,UK. This site is about us and our experiences of living with Motor Neurone Disease/A.L.S. Also known as M.N.D. or Lou Gehrig's Disease,after the famous baseball player who had the disease. Please see the Links Page for more MND/ALS related sites or Rob's Journal to read my own personal experience of living with MND. Please take some time to leave a comment in our Guestbook below: Sign my Guestbook View my Guestbook http://homepage.ntlworld.com/rob.shaz/home.html thank you rob we miss you all ready
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. ALS/MND Registry . |
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Legendary
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Thanks to you all for posting this sad news.
This is Rob who I know from the boards as *Sharob*. I'm so sorry to read of his passing. So young too. ![]() My condolences to his wife and family. |
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In Remembrance
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FROM BUILD UK WEBSITE http://www.magimedia.c...(cropped)3b...f2b25b214867br />Lady_Shaz2005
New Member Joined: 20 Mar 2005 Posts: 21 Posted: Wed Aug 08, 2007 2:21 pm Post subject: -------------------------------------------------------------------------------- Hi everyone I am Rob's daughter Sam and have just read all your lovely messages. I knew my Dad was a great man but I didn't realise how many lives he has touched. My Dad was a great inspiration to me and to a lot of other people and we all feel a huge loss in our lives. I am proud to say that he is my Dad and always will be and his memory will live on through us. All I want to say is live your lives with the determination my Dad had, my Dad won his battle with MND because he never let it beat his determination and sense of humour which made him what he was and now he no longer has MND - he is free. Thanks again to you all for being my Dads friends and keeping him company, I know you all meant a lot to him. All the best to each of you. Sam x Lady_Shaz2005 New Member Joined: 20 Mar 2005 Posts: 21 Posted: Thu Aug 09, 2007 8:51 am Post subject: Balloon for Rob -------------------------------------------------------------------------------- Hi all Its Sam Rob's daughter, me and Sharon understand that all the people that knew my Dad cannot attend his funeral, so in memory of my Dad we are asking for everyone who knew him to release a balloon at 11am on Wednesday 15th August then everyone can be part of his funeral. Thankyou for all your support Sam and Sharon x
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. ALS/MND Registry . |
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