My First One is Named Sunny Jim
My Second One Is Named Craig Because Dad Means The World To Me.
I Know, It's A Crazy Thing To Do . Haha
Take Care,
Elise xx
I don't think it is crazy I think it is cute! :)
Elise, It shows that you are taking it all in stride. I have a friend with colitis and she named her colon, he is called Larry :D
It makes things easier to deal with is what she tells me. Keeps the sense of humor also through everything.
Thanks for the smile today Elise ;D
Hi there Little One, I think it's wonderful that you are coping with this like you are. I think those names are quite appropriate and loving.
As you know I named my neuropathy "Fred". It's so much easier to put a name to these things and fight with "them" as a person instead of a thing. ;D "Fred" (as in Fred Astaire) is always trying to teach me new dance steps. His newest one is stopping suddenly on the left foot and pitching forward. I don't really like this step, unless he intends to catch me up in mid flight. :( But I always remember, "it could be worse". ;)
Take care dear and say HI to your Dad,
Hugs, Love and God Bless,
Pooh :-*
Elise,
I don't think its a crazy thing to do at all.....and what an honor for your dad...to have your wiggly named after him because you love him so! ;D
You are certainly a special young lady! (http://www.freesmileys.org/smileys/smiley-hug008.gif) (http://www.freesmileys.org/smileys.php)
That is SO cute! If I had a line, I'd name it Piggly Wiggly! I love the idea of naming "symptoms". I'll have to think up something for mine! Good for you all on this positive and humorous aspect of this crazy disease! :D
Elise, That is a great idea. Since you 2 are so close you might as well be on a first name basis. Take care now. Irish ;D
thanks for all the replys in so little time!
nice one, piggly wiggly!! Today i am just having a relaxing day.
BUT tomorrow i have to go to school for a meeting about my wigglys and how they work. Mrs Carter, Liz me and mum and dad will be there. i will just need to show her the end and she will know more then. thats at 12:30AM.
Then we will go home and have some lunch.
THEN we will go to Kingsmill Hospital To see Dr Helen Venning And Jane Ellis About My JDM - Juviniele Dermato Myositis.
And THEN we will go on holiday for the weekend. im going to skegness but i will be taking my laptop so i'll contact you iif i get internet connection.