Fellowship in Life - Comfort Food for the Soul!

Fellowship in Life is a fun place where friends (Christians and non-believers alike) come to share their life experiences with one another. Do you have a need for prayer? A desire for fun, fellowship and a healthy dose of silliness? Do you enjoy discussing current events and a wide variety of other subjects? Or perhaps you just want to have a good conversation with someone who has a comforting shoulder and an understanding heart? If so, Fellowship in Life is the place for you! There is a great deal to see and do. So won't you take a few moments to sit back, relax and enjoy a nice warm cup of fellowship with us?

Join us at Fellowship in Life . . . where you can always find healthy servings of comfort food for the soul!

 

The symbol of MND is the cornflower.

 

This is my candle of hope.  To me it is eternal.

 

 

 

 

 

This is me, auntym, the manager of "Memory Lane @ Home."  I enjoy my "time-out" on the internet and was told it's the best thing for me.

 

I've created my own recipe website and I have included a page for MND/ALS patients, of all stages, for anyone to add to or just peruse.  I hope to get more recipes from the PALS network so I can have a really good page, but I don't know quite what to feed anyone with MND.

 

Remember "Memory Lane @ Home;" it's not just my site, it's yours as well!

 

My partner has passed on, but the work will carry on.  So to honor his memory please our community and add your recipes. Otherwise my husband's life was in vain.  That is what he wanted and to succumb to MND so quickly is not what we wanted or something his family can understand.  A brave man in the face of adversity; he knew so little about MND, but faced the truth of it.

 

AuntyM

 

Hi, my name is Joe Harris. Welcome to my site, I hope you find the information provided to be helpful. It is my hope to ease the burden of life for those living with ALS by addressing quality of life issues, financial concerns, and current advocacy efforts. With the advent of modern technology, ALS survivors can live meaningful and productive lives. However, there continues to be issues with respite care and other advocacy concerns that need to be addressed. This site will be tailored to Idaho residents but will provide useful information for all.

http://www.joesalsadvocacy.com/

 

hi to everyone!

 

i am a new member to the ALS group a/o 12/25/2004. 

 

i am listing my webpage, with a section that i had written in honor of my dad, who passed away from ALS in 1978.

 

 

please feel free to view my dedication to him.  i loved him, miss him and will always keep his memory alive in my heart.

 

best wishes and happy holidays to all ~

 

java

 

p.s., in order for the music on my pages to load quickly, click on the little arrows in the popup from geocities that appear on each of my pages in the top right hand corner and not the X.  this will allow the music to play, while minimizing the popup window.  when you view my pages, click on the link that says - for my dad.

 

webpage : the java hut  http://www.geocities.com/java4me2.geo/index.html

 

 

 Welcome to the
Fargo-Moorhead MDA/ALS Support Group

If you or someone you love
would like to share concerns and ideas
about living with A.L.S.,
please feel welcome to join our monthly support group.

 

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See my web page on how I am dealing with MND/ALS

 

http://robertmnd.blogspot.com 

 

Robert     New Zealand

Hello Friends,

 

  My name is Jim and I have Amyotrophic Lateral Sclerosis (ALS), otherwise known as Lou Gehrig’s disease. I have started a new stem cell action group. Traditionally people do not like to discuss religion and politics; however, it makes no sense to avoid these subjects when they adversely affect medical research--which is the only hope for many. People’s lives may be at stake, others spend a lifetime in wheelchairs unnecessarily and some have to choose between life on a ventilator or certain death within days or weeks, also needlessly. With so much at stake, we must forget about traditions and discuss these subjects openly.

  I am a <st1:place w:st="on"><st1:State w:st="on">Missouri</st1:State></st1:place> Synod Lutheran. My synod is against embryonic stem cell research (ESCR). Did I join another church because of their position? No, I write to them explaining why they are wrong. Nancy Pelosi and Ted Kennedy belong to the Roman Catholic Church. They do not adhere to their Church’s stance on ESCR. Have they left the Catholic Church? No, and they support ESCR as publicly as anyone could.

  This group is for discussing the religious and political opposition to stem cell research. It is for activists who do not hold their tongue when something wrong—they expose rather than condone! People who want to counter lies with truthful information and take aggressive action against politicians who oppose the Stem Cell Enhancement Act. If you are religiously or politically sensitive, this is not the group for you. Individuals opposed to stem cell research are welcome; however, you should join seeking the truth--apostatizing is not acceptable. This group will also publish advancements in embryonic stem cell research.
  Why is this group different? Censorship is not a primary concern here! You are free to express your opinion—this group practices “Freedom of Speech!” Everyone is expected keep a civil tongue, be factual not theoretical, and you must not berate fellow members because of a difference of opinions.<o:p></o:p>

  If you are interested in joining this new group the following is a link:  Click to join stem cell advocates.

Be well,<o:p></o:p>

<o:p> </o:p>

Jim  AKA- pigiron308@yahoo.com<o:p></o:p>

http://groups.yahoo.com/group/stemcelladvocates