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  <title>disabilities - Attachment Parenting - tribe.net</title>
  <link rel="alternate" href="http://attachedparent.tribe.net/thread/df3cddc2-8744-4961-9063-0f22f3b668ed?format=atom" />
  <subtitle>Tribe.net. Local Connections</subtitle>
  <entry>
    <title>Re: disabilities</title>
    <link rel="alternate" href="http://attachedparent.tribe.net/thread/df3cddc2-8744-4961-9063-0f22f3b668ed#5ea7d334-1e83-4ce3-afc3-ba342f52a5b2" />
    <author>
      <name>MB</name>
    </author>
    <id>http://attachedparent.tribe.net/thread/df3cddc2-8744-4961-9063-0f22f3b668ed#5ea7d334-1e83-4ce3-afc3-ba342f52a5b2</id>
    <updated>2009-03-31T07:13:18Z</updated>
    <published>2009-03-31T07:13:18Z</published>
    <summary type="html">Hi Laurie,&#xD;
I am a right leg above knee amputee. I have a prosthesis but don't use it much. I tend to use crutches more often. I am 22 weeks into my pregnancy, so I can't tell you much yet. But I have heard many good things about the child adapting to the parents disability. I have seen many TV shows on parents with severe disabilities getting along with their children just fine. It just takes patience and a willingness to figure out how to do things differently.&#xD;
&#xD;
Here are two helpful links:&#xD;
&#xD;
1. A good book on pregnancy/childbirth &amp;amp; disability (may have info about raising children too!)&#xD;
http://www.amazon.com/Disabled-Womans-Guide-Pregnancy-Birth/dp/1932603085/ref=sr_1_26?ie=UTF8&amp;amp;s=books&amp;amp;qid=1238483324&amp;amp;sr=8-26&#xD;
&#xD;
2. A place in Berkeley, CA that specializes in helping disabled families adapt:&#xD;
http://lookingglass.org/index.php&#xD;
&#xD;
Hope this helps! Trust me, you're far from alone!!!!</summary>
    <dc:creator>MB</dc:creator>
    <dc:date>2009-03-31T07:13:18Z</dc:date>
  </entry>
  <entry>
    <title>Re: disabilities</title>
    <link rel="alternate" href="http://attachedparent.tribe.net/thread/df3cddc2-8744-4961-9063-0f22f3b668ed#7e7b9e74-f8dd-4263-ae02-905febc95c1d" />
    <author>
      <name>Judith</name>
    </author>
    <id>http://attachedparent.tribe.net/thread/df3cddc2-8744-4961-9063-0f22f3b668ed#7e7b9e74-f8dd-4263-ae02-905febc95c1d</id>
    <updated>2009-03-29T13:41:05Z</updated>
    <published>2009-03-29T13:41:05Z</published>
    <summary type="html">I have friend who se wheelchairs and their children grew up riding on dad's lap or on the back of mom' chair. I heard of a wonderful-sounding woman, never met me, from the nurse practitioner who was her breastfeeding counselor - this mom had serious congenital limb reductions and was a single mother by donor insemination who got the help she needed (she;s from San Luis obispo hwere there is a fantastic movement promoting breastfeeding) to make accommodations so she had a god extended nursing relationship with her baby.&#xD;
&#xD;
i live in berkeley, where the disability rights and respurces movement really startd, and there are a lot of support resources for parents with various disabilities.you might want to find a paretns' group where moms and dads with all kinds of special ways of living can share ideas and friendship for taking care of th wee ones...&#xD;
&#xD;
&#xD;
most babies and toddelrs, and many older kids, loVe being pulled in some kind of a wagon or other wheeled conveyance...is that a possibility with our ankle/  if not, cold both ou you enjoy one of those little cart-scooters and have a good time pushing around on the floor or in a park?  i got introduced to these scooters whenmy aughter was four or five and they plaed all kinds of games on them at the YMca, incldluding a game of :scooter hockey' that as hilariously goo fun for the ougner kids AND the teens.  the carts aren;t expensive.&#xD;
&#xD;
speakaing of the ymCA, does our little gy enjoy swimming and water activities/  most ys and some othe community groups have a warm pool that's emant for tots and for eople who are disabled and those little-kid swim and splash times can be terrific 9and asy on the bones and joints0</summary>
    <dc:creator>Judith</dc:creator>
    <dc:date>2009-03-29T13:41:05Z</dc:date>
  </entry>
  <entry>
    <title>Re: disabilities</title>
    <link rel="alternate" href="http://attachedparent.tribe.net/thread/df3cddc2-8744-4961-9063-0f22f3b668ed#1b76207b-053d-4233-887b-448679796e98" />
    <author>
      <name>Katie</name>
    </author>
    <id>http://attachedparent.tribe.net/thread/df3cddc2-8744-4961-9063-0f22f3b668ed#1b76207b-053d-4233-887b-448679796e98</id>
    <updated>2009-03-29T04:33:35Z</updated>
    <published>2009-03-29T04:33:35Z</published>
    <summary type="html">I don't hide them, just make them more understandable for a child. There have been times where I get frustrated or sad about not being able to run around with him on a bad ankle day. I just tell him why I am sad, even if I am not sure that he understands exactly yet. But I think it is good for kids to see a range of feelings and emotions, as long as they understand it and that it isn't too intense or something. &#xD;
&#xD;
The way I see it, is every parent can offer something unique to their child. I just can't offer anything sporty! And some days are not bad, or my ankle feels ok so we run around, and I just pay for it later! (totally worth it!)&#xD;
&#xD;
And there is a lot of value in having extra story and cuddle time!!</summary>
    <dc:creator>Katie</dc:creator>
    <dc:date>2009-03-29T04:33:35Z</dc:date>
  </entry>
  <entry>
    <title>Re: disabilities</title>
    <link rel="alternate" href="http://attachedparent.tribe.net/thread/df3cddc2-8744-4961-9063-0f22f3b668ed#ab0bcc37-16a0-4e32-b5c9-4955e63ad622" />
    <author>
      <name>$item.owner.firstName</name>
    </author>
    <id>http://attachedparent.tribe.net/thread/df3cddc2-8744-4961-9063-0f22f3b668ed#ab0bcc37-16a0-4e32-b5c9-4955e63ad622</id>
    <updated>2009-03-28T19:54:19Z</updated>
    <published>2009-03-28T19:54:19Z</published>
    <summary type="html">thanks, katie, your post is really helpful and encouraging.  i'm sorry to hear about your arthritis in left ankle.  i'm working on accepting limits more.  it seems when i can do that, i'm not as anxious about not being able to lift bebe, etc... and bebe often responds likewise, more relaxed or more anxious...  i see that bebe is also syncing up with me.... he's learning to be more patient if i'm moving slower.  &#xD;
&#xD;
the hard part is not wanting him to see me in pain or frustrated or sometimes in tears.  do i hide these feelings from him?</summary>
    <dc:creator>$item.owner.firstName</dc:creator>
    <dc:date>2009-03-28T19:54:19Z</dc:date>
  </entry>
  <entry>
    <title>Re: disabilities</title>
    <link rel="alternate" href="http://attachedparent.tribe.net/thread/df3cddc2-8744-4961-9063-0f22f3b668ed#a9aa8aef-6dfd-4bfd-aa9e-021e17eebad2" />
    <author>
      <name>Katie</name>
    </author>
    <id>http://attachedparent.tribe.net/thread/df3cddc2-8744-4961-9063-0f22f3b668ed#a9aa8aef-6dfd-4bfd-aa9e-021e17eebad2</id>
    <updated>2009-03-21T04:35:40Z</updated>
    <published>2009-03-21T04:35:40Z</published>
    <summary type="html">Hi, I am sorry that you have not been well, and that is has been affecting how you are able to be with your child. &#xD;
&#xD;
I have pretty severe arthritis in my left ankle. It makes it hard for me to play with my son, and carry him a lot. I get upset about it often, feeling sad about what it is taking away from me, and my son.&#xD;
&#xD;
But mostly, I try to work with my body. If it is a painful day, I take extra time to sit on the floor and play, or read extra stories. &#xD;
&#xD;
I try to keep positive, and sometimes even push my ankle too far, just to not sacrifice being able to play around the way my son wants me to. But mostly I just learn my limits, and find other fun ways to spend time together, that is less painful for me. &#xD;
&#xD;
I would say we have balance. We don't go to the beach or park as often as he'd like, or I'd like! But it could be worse!&#xD;
&#xD;
I hope you feel better!</summary>
    <dc:creator>Katie</dc:creator>
    <dc:date>2009-03-21T04:35:40Z</dc:date>
  </entry>
  <entry>
    <title>disabilities</title>
    <link rel="alternate" href="http://attachedparent.tribe.net/thread/df3cddc2-8744-4961-9063-0f22f3b668ed#92f6104e-9342-4c03-9231-990fffe83849" />
    <author>
      <name>$item.owner.firstName</name>
    </author>
    <id>http://attachedparent.tribe.net/thread/df3cddc2-8744-4961-9063-0f22f3b668ed#92f6104e-9342-4c03-9231-990fffe83849</id>
    <updated>2009-03-21T02:09:45Z</updated>
    <published>2009-03-21T02:09:45Z</published>
    <summary type="html">i have lyme disease in late stages, and recently symptoms worsened. finding it hard to do things like pick up my four and a half month old bebe, breastfeed, and give him the attention his energized and evergrowing self needs.  wondering if anyone here is coping with an illness or disability...&#xD;
&#xD;
how does this affect parenting for you?&#xD;
how do you cope?&#xD;
how have you and your child found balance (or not)?</summary>
    <dc:creator>$item.owner.firstName</dc:creator>
    <dc:date>2009-03-21T02:09:45Z</dc:date>
  </entry>
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