Labradoodle & Goldendoodle Forum
Dr. Doodle
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A group for anyone who deals with or knows someone that deals with chronic, terminal, or long term disease. It is meant to be UPBEAT, to share stories of support to, as well as practical ideas of what to do with our doods when we can't care for them.
Members: 17
Latest Activity: Apr 11, 2016
Discussion Forum
The Spoon Theory...
Started by Jennifer and Jack. Last reply by Sue Ryzdynski Apr 11, 2016. 5 Replies 0 Favorites
I often use this to let others know how I am doing, I simply say I am out of spoons. Or I have plenty of spoons. The Spoon Theoryby Christine Miserandino…Continue
JOB LOSS
Started by Lorraine Bromley. Last reply by Susan and Sasha Nov 10, 2011. 4 Replies 0 Favorites
Well, I have told you all about a month ago I woke up with a sore right hand. That turned into a fiasco of health care trips to my local hospital and my Dr then to the surgeon and in patient…Continue
Need Input.. Being Interveiwed!!!
Started by Jennifer and Jack. Last reply by Jennifer and Jack Jul 3, 2011. 9 Replies 0 Favorites
I was contacted by the Boomer Easionson foundation, which is a foundation formed by Boomer, who has a son with Cystic Fibrosis... Anyway, a great inspiration named Jerry who does pod casts for the…Continue
A day in the life
Started by Jennifer and Jack. Last reply by Tina, Clover, Plus 5 More Apr 4, 2011. 2 Replies 0 Favorites
Since we have such a group of loving people I thought it would be good to continue to get to know each other better, I am not saying people with sickness have it rougher then other people, I just…Continue
Comment Wall
Comment
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Comment by Jena ~ Dublin on April 4, 2011 at 5:18pm
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Hi Lorraine, that is funny. My husband may agree with your husband as well.
Jennifer, Yes, please ask Adina how we can do that. I think we can just right click on the picture, BUT, I think you have to be the creator of the group to do it.....Adina, HELP!!!!!!
Out to see a Movie with my Eldest daughter (12) Soul Surfer~ let you know how it is. Free is a good price otherwise I dont think I would be going....theaters arent my thing, too much vibration and handles (arms) on the chairs which REALLY hurt at any time....appreciate some Doodle prayers!
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Comment by Lorraine Bromley on April 4, 2011 at 5:09pm
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For canadian information on Ehlers try CEDA Canadian Ehlers Danlos website and support group.
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Well my husband might just agree that having Ehlers also means your husband has erectile dysfunction, I am usually too tired or too sore for him to get one!!!! That's just between us he he he he
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Comment by Jennifer and Jack on April 3, 2011 at 7:55pm
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I don't see one, I will have to ask Adina to put a picture in because she is the creator of the group. THanks for the idea though.
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Comment by Nancy, Ned, Clancy, and Charlie on April 3, 2011 at 3:38pm
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Is there a place where you create the group to insert a photo?
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I don't know how to put a picture up next to our group.... I wish I had a picture of a hug or something sweet and loving.. I will have to figure it out, if anyone knows how let me know, you know I am always the last to figure things out
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Now that I have giggled with you all, I am going to google Ehlers-Danlos Syndrome and not EDS.
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That really is funny. I too read up on it and I see that their are varying degrees to the disease. I am glad to hear yours is not life shortening. That doesn't make living with it much easier but at least that is some piece of mind. I have to admit, I never heard of that disease, not even in Nursing school. How does it affect your daily life and the things you can and can not do?
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Tina, that is too funny! Yes, I knew immediatly when you said you googled EDS what came up. My DH and I started laughing too. Yes, you are right, laughs are so far and few between, it's nice to share when you get them, thank you! With EDS though (I mean Ehlers-Danlos Syndrom) I might have wet my pants, all tissue is VERY SOFT.....including bladder!
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Comment by Tina, Clover, Plus 5 More on April 3, 2011 at 1:25pm
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Here's a good laugh for everyone. I'm not familiar with Ehlers Danlos Syndrome and not thinking of this when Jena said she also has EDS. I thought what's EDS, I need to google it. Can anyone guess what comes up at the top of the list? Erectile Dysfunction Syndrome, I started laughing so hard I almost wet my pants. After I'm able to stop laughing maybe I can research Ehlers. Since for me laughs can be few and far between somedays I thought I share.
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