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	<title>Comments on: Let Your Parenting Journey Begin&#8230;</title>
	<atom:link href="http://www.disabledparents.net/?feed=rss2&#038;page_id=12" rel="self" type="application/rss+xml" />
	<link>http://www.disabledparents.net</link>
	<description>...the internet&#039;s one-stop resource for parents with disabilities</description>
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		<title>By: janine colon</title>
		<link>http://www.disabledparents.net/#comment-494</link>
		<dc:creator>janine colon</dc:creator>
		<pubDate>Wed, 04 Jan 2012 23:23:03 +0000</pubDate>
		<guid isPermaLink="false">http://www.disabledparents.net/?page_id=12#comment-494</guid>
		<description>hey mariah i completely understand what you are going thru fight now as hard as you can cps teriminated my rights due to lack of of services and my health having cerebral palsy and a seizure disorder i am appealling this and suing the state of ma dcf</description>
		<content:encoded><![CDATA[<p>hey mariah i completely understand what you are going thru fight now as hard as you can cps teriminated my rights due to lack of of services and my health having cerebral palsy and a seizure disorder i am appealling this and suing the state of ma dcf</p>
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		<title>By: mariah carter</title>
		<link>http://www.disabledparents.net/#comment-435</link>
		<dc:creator>mariah carter</dc:creator>
		<pubDate>Wed, 21 Dec 2011 00:50:20 +0000</pubDate>
		<guid isPermaLink="false">http://www.disabledparents.net/?page_id=12#comment-435</guid>
		<description>hi my name is mariah and iam 20 and i am 32 weeks prego an i have mild cerbral palsy and am a single mom with no help from my family an now i have cps on my butt saying that they can take her cause they think that i cant take of her she is the only baby i can have what can i do i dont wanna lose her?</description>
		<content:encoded><![CDATA[<p>hi my name is mariah and iam 20 and i am 32 weeks prego an i have mild cerbral palsy and am a single mom with no help from my family an now i have cps on my butt saying that they can take her cause they think that i cant take of her she is the only baby i can have what can i do i dont wanna lose her?</p>
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	<item>
		<title>By: Ableize Disabled Pregnancy and Parenthood</title>
		<link>http://www.disabledparents.net/#comment-381</link>
		<dc:creator>Ableize Disabled Pregnancy and Parenthood</dc:creator>
		<pubDate>Mon, 12 Dec 2011 17:33:29 +0000</pubDate>
		<guid isPermaLink="false">http://www.disabledparents.net/?page_id=12#comment-381</guid>
		<description>Hi
I just came across your site after realising that Ableize, the U.K.&#039;s largest disability resource was not covering disabled pregnancy and parenting issues of disabled, we are now working rectify this building are respectable resource of reliable sites such as yours and have indeed included you within that section.

The Ableize disabled pregnancy and parenting section can be seen at http://www.ableize.com/health-and-fitness/Pregnancy-and-Parenthood/ and I hope your inclusion in this helps drive traffic to your very informative and much sought after information site.

Keep up the good work.

Robin
www.ableize.com</description>
		<content:encoded><![CDATA[<p>Hi<br />
I just came across your site after realising that Ableize, the U.K.&#8217;s largest disability resource was not covering disabled pregnancy and parenting issues of disabled, we are now working rectify this building are respectable resource of reliable sites such as yours and have indeed included you within that section.</p>
<p>The Ableize disabled pregnancy and parenting section can be seen at <a href="http://www.ableize.com/health-and-fitness/Pregnancy-and-Parenthood/" rel="nofollow">http://www.ableize.com/health-and-fitness/Pregnancy-and-Parenthood/</a> and I hope your inclusion in this helps drive traffic to your very informative and much sought after information site.</p>
<p>Keep up the good work.</p>
<p>Robin<br />
<a href="http://www.ableize.com" rel="nofollow">http://www.ableize.com</a></p>
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	<item>
		<title>By: janine colon</title>
		<link>http://www.disabledparents.net/#comment-352</link>
		<dc:creator>janine colon</dc:creator>
		<pubDate>Wed, 07 Dec 2011 15:41:17 +0000</pubDate>
		<guid isPermaLink="false">http://www.disabledparents.net/?page_id=12#comment-352</guid>
		<description>good mourning,
                               i am still waiting to hear from the court regarding my parental rights recently i was told that my son  has autism so i would like to know if there are services that would help both me and my son i live in massassachusetts please contact me at ccljani@aol.com or 774-365-0536
                                                                                                                                   janine</description>
		<content:encoded><![CDATA[<p>good mourning,<br />
                               i am still waiting to hear from the court regarding my parental rights recently i was told that my son  has autism so i would like to know if there are services that would help both me and my son i live in massassachusetts please contact me at <a href="mailto:ccljani@aol.com">ccljani@aol.com</a> or 774-365-0536<br />
                                                                                                                                   janine</p>
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		<title>By: Elaine</title>
		<link>http://www.disabledparents.net/#comment-317</link>
		<dc:creator>Elaine</dc:creator>
		<pubDate>Wed, 30 Nov 2011 16:56:19 +0000</pubDate>
		<guid isPermaLink="false">http://www.disabledparents.net/?page_id=12#comment-317</guid>
		<description>My husband and I are expecting our first child and he is in a wheelchair.  Can any of you recommend cribs that are w/c accessible?</description>
		<content:encoded><![CDATA[<p>My husband and I are expecting our first child and he is in a wheelchair.  Can any of you recommend cribs that are w/c accessible?</p>
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		<title>By: John Heckbert</title>
		<link>http://www.disabledparents.net/#comment-257</link>
		<dc:creator>John Heckbert</dc:creator>
		<pubDate>Wed, 23 Nov 2011 21:09:18 +0000</pubDate>
		<guid isPermaLink="false">http://www.disabledparents.net/?page_id=12#comment-257</guid>
		<description>Interesting website and I hope you do well with it because it is a much needed resource to a community often under-serviced by the professionals. It was my 32 year old daughter that reminded me how unique her situation was, and that triggered my search today. 

A bit of background for everyone - Karin was born with C7 Spina Bifida in August of 1957 in Oberhausen, Germany. She had surgery at 6 days old to protect the spinal cord that protruded outside her body, a tonsilectomy at age 8 in Toronto, Ontario, Canada at the Hospital for Sick Children, a Harrington rod implanted at age 13 in Toronto, Ontario, Canada at the Hospital for Sick Children and a skin graft done at age 16 in Welland, Ontario, Canada to correct a pressure ulcer. She was permanently confined to a manual wheelchair, and when we met on a blind date in October, 1976, all 6&#039;6&quot; of me fell head over heels for this 4&#039;10&quot; angel. 

In September of 1978, we were married (in a Catholic Church) despite the reservations of my family, her family and the church. We were among the first group in Canada to take a mandatory marriage preparation course, which only added to our resolve to make our marriage work. 

Shortly after we were married, we found out Karin was pregnant! Karin was in heaven, and in May of 1979 our darling daughter - all 7 pounds, 1 ounce - was born. A mere nine weeks later, we found out she was pregnant again (more concern this time) and in April of 1980, our son - a hefty 8 pounds, 5 ounces - was born. And if that wasn&#039;t enough, Karin became pregnant with our third - another daughter - 7 pounds, 13 ounces - a whole lot more concern with pregnancy. There were no traces of any disability in our children - unless you consider lactose intolerance (from their father&#039;s side) a disability. 

Karin passed away this past January of squamous cell bladder cancer at the age of 54, having survived long enough to see all three of her children married to absolutely beautiful people, and celebrated the birth of two grandsons. It was Karin&#039;s hope that she would be able to help disabled teenaged girls and women struggling with their fertility and sexuality - and maybe she still can. 

The trigger that started this search - my oldest daughter mentioned that she and her siblings were the only children from a disabled parent that she ever met. And she also mentioned that Karin and I were active in the disabled community in Toronto as program directors and volunteers for different agencies in the City, so she grew up around a lot of disabled people. 

So here is my shout out to the adult, natural born children of a parent who was disabled at the time of their birth. I believe these people have different issues than those adopted by a disabled parent, or a parent who became disabled sometime after their birth, because their parents were different. I&#039;d love to connect with you here on this board to share experiences with me and my children as well. 

If you are a disabled parent of a child and want help, please don&#039;t hesitate to put the call out. I&#039;m not sure I&#039;ll be any help to you (because I&#039;m not disabled myself) but I will try to share Karin&#039;s wisdom with you. Maybe it&#039;ll help and Karin&#039;s legacy will live on.

May God bless everyone who participates on this site because we all know God doesn&#039;t make junk. 

John</description>
		<content:encoded><![CDATA[<p>Interesting website and I hope you do well with it because it is a much needed resource to a community often under-serviced by the professionals. It was my 32 year old daughter that reminded me how unique her situation was, and that triggered my search today. </p>
<p>A bit of background for everyone &#8211; Karin was born with C7 Spina Bifida in August of 1957 in Oberhausen, Germany. She had surgery at 6 days old to protect the spinal cord that protruded outside her body, a tonsilectomy at age 8 in Toronto, Ontario, Canada at the Hospital for Sick Children, a Harrington rod implanted at age 13 in Toronto, Ontario, Canada at the Hospital for Sick Children and a skin graft done at age 16 in Welland, Ontario, Canada to correct a pressure ulcer. She was permanently confined to a manual wheelchair, and when we met on a blind date in October, 1976, all 6&#8217;6&#8243; of me fell head over heels for this 4&#8217;10&#8243; angel. </p>
<p>In September of 1978, we were married (in a Catholic Church) despite the reservations of my family, her family and the church. We were among the first group in Canada to take a mandatory marriage preparation course, which only added to our resolve to make our marriage work. </p>
<p>Shortly after we were married, we found out Karin was pregnant! Karin was in heaven, and in May of 1979 our darling daughter &#8211; all 7 pounds, 1 ounce &#8211; was born. A mere nine weeks later, we found out she was pregnant again (more concern this time) and in April of 1980, our son &#8211; a hefty 8 pounds, 5 ounces &#8211; was born. And if that wasn&#8217;t enough, Karin became pregnant with our third &#8211; another daughter &#8211; 7 pounds, 13 ounces &#8211; a whole lot more concern with pregnancy. There were no traces of any disability in our children &#8211; unless you consider lactose intolerance (from their father&#8217;s side) a disability. </p>
<p>Karin passed away this past January of squamous cell bladder cancer at the age of 54, having survived long enough to see all three of her children married to absolutely beautiful people, and celebrated the birth of two grandsons. It was Karin&#8217;s hope that she would be able to help disabled teenaged girls and women struggling with their fertility and sexuality &#8211; and maybe she still can. </p>
<p>The trigger that started this search &#8211; my oldest daughter mentioned that she and her siblings were the only children from a disabled parent that she ever met. And she also mentioned that Karin and I were active in the disabled community in Toronto as program directors and volunteers for different agencies in the City, so she grew up around a lot of disabled people. </p>
<p>So here is my shout out to the adult, natural born children of a parent who was disabled at the time of their birth. I believe these people have different issues than those adopted by a disabled parent, or a parent who became disabled sometime after their birth, because their parents were different. I&#8217;d love to connect with you here on this board to share experiences with me and my children as well. </p>
<p>If you are a disabled parent of a child and want help, please don&#8217;t hesitate to put the call out. I&#8217;m not sure I&#8217;ll be any help to you (because I&#8217;m not disabled myself) but I will try to share Karin&#8217;s wisdom with you. Maybe it&#8217;ll help and Karin&#8217;s legacy will live on.</p>
<p>May God bless everyone who participates on this site because we all know God doesn&#8217;t make junk. </p>
<p>John</p>
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		<title>By: Mara</title>
		<link>http://www.disabledparents.net/#comment-245</link>
		<dc:creator>Mara</dc:creator>
		<pubDate>Tue, 22 Nov 2011 23:42:35 +0000</pubDate>
		<guid isPermaLink="false">http://www.disabledparents.net/?page_id=12#comment-245</guid>
		<description>Hi.  I&#039;m Mara.  My husband is a polio survivor.  I&#039;m looking for a crib (to order, not build) that is easily accessible.  I saw a few online that open towards you, like 2 doors.  It seems like a lot of the disability websites for baby furniture are shut down.  Any suggestions?

Thank you!</description>
		<content:encoded><![CDATA[<p>Hi.  I&#8217;m Mara.  My husband is a polio survivor.  I&#8217;m looking for a crib (to order, not build) that is easily accessible.  I saw a few online that open towards you, like 2 doors.  It seems like a lot of the disability websites for baby furniture are shut down.  Any suggestions?</p>
<p>Thank you!</p>
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		<title>By: Heather Mathews</title>
		<link>http://www.disabledparents.net/#comment-224</link>
		<dc:creator>Heather Mathews</dc:creator>
		<pubDate>Sun, 20 Nov 2011 23:01:50 +0000</pubDate>
		<guid isPermaLink="false">http://www.disabledparents.net/?page_id=12#comment-224</guid>
		<description>WHat happened to the page with all the equipment listed, specifically the crib?</description>
		<content:encoded><![CDATA[<p>WHat happened to the page with all the equipment listed, specifically the crib?</p>
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		<title>By: milagros lopez</title>
		<link>http://www.disabledparents.net/#comment-204</link>
		<dc:creator>milagros lopez</dc:creator>
		<pubDate>Thu, 17 Nov 2011 23:43:32 +0000</pubDate>
		<guid isPermaLink="false">http://www.disabledparents.net/?page_id=12#comment-204</guid>
		<description>My name is Milagros but everyone calls me Nini., I&#039;m 28 years old and I&#039;m 7 seven months pregnant, I live with my fiance&#039; in an apartment. I have C.P, but it doesnt slow me down. I&#039;m determined to be the best mommy I can be for my daughter. I&#039;m going to name her, Jullaniesse. I get lots of help from my friends and family, they&#039;re all very supportive of my pregnancy.For years my doctor told me I could never have a baby, but look at me now. I&#039;m due in Febuary and I cant to meet my beautiful daughter. :) My doctor recommended this website and it&#039;s opening my eyes to being a disabled parent. It tells me how easy it is for a disabled parent to do everything that Non-disabled parents can do. I&#039;m very excited for Febuary, because when that month rolls along, me and fiance&#039; are going to be a family &lt;3</description>
		<content:encoded><![CDATA[<p>My name is Milagros but everyone calls me Nini., I&#8217;m 28 years old and I&#8217;m 7 seven months pregnant, I live with my fiance&#8217; in an apartment. I have C.P, but it doesnt slow me down. I&#8217;m determined to be the best mommy I can be for my daughter. I&#8217;m going to name her, Jullaniesse. I get lots of help from my friends and family, they&#8217;re all very supportive of my pregnancy.For years my doctor told me I could never have a baby, but look at me now. I&#8217;m due in Febuary and I cant to meet my beautiful daughter. <img src='http://www.disabledparents.net/wp-includes/images/smilies/icon_smile.gif' alt=':)' class='wp-smiley' />  My doctor recommended this website and it&#8217;s opening my eyes to being a disabled parent. It tells me how easy it is for a disabled parent to do everything that Non-disabled parents can do. I&#8217;m very excited for Febuary, because when that month rolls along, me and fiance&#8217; are going to be a family &lt;3</p>
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		<title>By: Sue Timpson</title>
		<link>http://www.disabledparents.net/#comment-203</link>
		<dc:creator>Sue Timpson</dc:creator>
		<pubDate>Thu, 17 Nov 2011 21:56:29 +0000</pubDate>
		<guid isPermaLink="false">http://www.disabledparents.net/?page_id=12#comment-203</guid>
		<description>Hi all,
It&#039;s be awhile since there was any mail from anybody.  Just wanted to let my fellow Northern Californians know that at the Abilities Expo that starts tomorrow in downtown San Jose@ the convention center.  I am going and Janette is coming up from So Cal.  If anyone else from the list is coming it would be nice to know and meet up if we could.
Please post to the list</description>
		<content:encoded><![CDATA[<p>Hi all,<br />
It&#8217;s be awhile since there was any mail from anybody.  Just wanted to let my fellow Northern Californians know that at the Abilities Expo that starts tomorrow in downtown San Jose@ the convention center.  I am going and Janette is coming up from So Cal.  If anyone else from the list is coming it would be nice to know and meet up if we could.<br />
Please post to the list</p>
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