# My baby girl has Spinal Muscular Atrophy (SMA)

**URL:** <https://boards.straightdope.com/t/my-baby-girl-has-spinal-muscular-atrophy-sma/547126>\
**Category:** Miscellaneous and Personal Stuff I Must Share\
**Created:** [July 18, 2010, 3:17pm UTC](https://boards.straightdope.com/t/my-baby-girl-has-spinal-muscular-atrophy-sma/547126 "2010-07-18T15:17:44Z")\
**Posts on this page:** 20\
**Page:** 41

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**Author:** ![janis\_and\_c0](https://sea3.discourse-cdn.com/straightdope/user_avatar/boards.straightdope.com/janis_and_c0/32/21_2.png) [@janis\_and\_c0](https://boards.straightdope.com/u/janis_and_c0)\
**Post date:** [August 13, 2011, 6:06am UTC](https://boards.straightdope.com/t/my-baby-girl-has-spinal-muscular-atrophy-sma/547126/801 "2011-08-13T06:06:01Z")

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Here is what I have posted on my FB feel free to repost, modify, etc.

HOOT HOOT!! (o)^(o) This little owl is being posted to raise awareness about Spinal Muscular Atrophy, or SMA. SMA is an inherited disease that causes progressive muscle weakness that eventually becomes severe., inluding problems with breathing & swallowing. There is no cure or treatment for SMA. The lifespan with SMA is seldom longer than 2 – 3 years. SMA is the #1 genetic killer of young childen, and yet, few have even heard of it. August is SMA Awareness Month! Please spread the word and raise awareness by re-posting!!!  
(I included a link in comments to GOF)

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**Author:** ![janis\_and\_c0](https://sea3.discourse-cdn.com/straightdope/user_avatar/boards.straightdope.com/janis_and_c0/32/21_2.png) [@janis\_and\_c0](https://boards.straightdope.com/u/janis_and_c0)\
**Post date:** [August 13, 2011, 6:17am UTC](https://boards.straightdope.com/t/my-baby-girl-has-spinal-muscular-atrophy-sma/547126/802 "2011-08-13T06:17:21Z")

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Sorry about the Double post, but I had to modify my original facebook post, it now says:

HOOT HOOT!! (o)^(o) This little owl is being posted to raise awareness about Spinal Muscular Atrophy, or SMA. SMA is an inherited disease that causes progressive muscle weakness. There is no cure or treatment for SMA. The lifespan with SMA is seldom longer than 2 – 3 years. SMA is the #1 genetic killer of young childen, and yet, few have even heard of it. August is SMA Awareness Month! Please spread the word and raise awareness by re-posting!!!

(Sorry I couldn’t include all the info… Stoopid FB character limit!!!)

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**Author:** ![Bearflag70](https://avatars.discourse-cdn.com/v4/letter/b/8e7dd6/32.png) [@Bearflag70](https://boards.straightdope.com/u/Bearflag70)\
**Post date:** [August 13, 2011, 8:43am UTC](https://boards.straightdope.com/t/my-baby-girl-has-spinal-muscular-atrophy-sma/547126/803 "2011-08-13T08:43:16Z")

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Perfect! Trying to squeeze too much info in can backfire because no one will read it, so the character limit is a good thing.

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**Author:** ![jjimm](https://avatars.discourse-cdn.com/v4/letter/j/ba8739/32.png) [@jjimm](https://boards.straightdope.com/u/jjimm)\
**Post date:** [August 13, 2011, 10:00am UTC](https://boards.straightdope.com/t/my-baby-girl-has-spinal-muscular-atrophy-sma/547126/804 "2011-08-13T10:00:53Z")

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**Bearflag70** , you probably don’t remember this, but a year ago, back at the start of this thread I [mentioned someone](http://boards.straightdope.com/sdmb/showpost.php?p=12755049&postcount=177) I knew and went to school with who had SMA.

I’ve finally found details of her (she changed her name hence not finding her). She died last year. But she was AGED 40!!! She achieved so, so much despite her disability. She was an inspiration to humanity, disabled people, and people with SMA, in that order. And in answer to your question, she had the Type 1 severe form of SMA - but defied the odds.

Please read her story: [Rowen Jade](http://www.guardian.co.uk/society/2010/oct/03/rowen-jade-obituary).

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**Author:** ![Bearflag70](https://avatars.discourse-cdn.com/v4/letter/b/8e7dd6/32.png) [@Bearflag70](https://boards.straightdope.com/u/Bearflag70)\
**Post date:** [August 13, 2011, 11:59pm UTC](https://boards.straightdope.com/t/my-baby-girl-has-spinal-muscular-atrophy-sma/547126/805 "2011-08-13T23:59:57Z")

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What an inspiration!

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**Author:** ![Clockwork\_Jackal](https://avatars.discourse-cdn.com/v4/letter/c/b5e925/32.png) [@Clockwork\_Jackal](https://boards.straightdope.com/u/Clockwork_Jackal)\
**Post date:** [August 14, 2011, 6:15pm UTC](https://boards.straightdope.com/t/my-baby-girl-has-spinal-muscular-atrophy-sma/547126/806 "2011-08-14T18:15:19Z")

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> [@janis\_and\_c0](#):
>
> Sorry about the Double post, but I had to modify my original facebook post, it now says:
> 
> HOOT HOOT!! (o)^(o) This little owl is being posted to raise awareness about Spinal Muscular Atrophy, or SMA. SMA is an inherited disease that causes progressive muscle weakness. There is no cure or treatment for SMA. The lifespan with SMA is seldom longer than 2 – 3 years. SMA is the #1 genetic killer of young childen, and yet, few have even heard of it. August is SMA Awareness Month! Please spread the word and raise awareness by re-posting!!!
> 
> (Sorry I couldn’t include all the info.. Stoopid FB character limit!!!)

I will totally post that to my facebook page too!

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**Author:** ![Bearflag70](https://avatars.discourse-cdn.com/v4/letter/b/8e7dd6/32.png) [@Bearflag70](https://boards.straightdope.com/u/Bearflag70)\
**Post date:** [August 14, 2011, 6:26pm UTC](https://boards.straightdope.com/t/my-baby-girl-has-spinal-muscular-atrophy-sma/547126/807 "2011-08-14T18:26:56Z")

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Hey SDMB SMA Warriors, please [go to this site](http://mom.babble.com/mom/mominations/mominees/charity/morgan-shanahan) and click “like” for Morgan. She’s a blogger mom and supporter of [Getty Owl Foundation](http://gettyowl.com/gof/).

If she wins, GOF gets $5k to help fight SMA!

Tell your friends!

[The rankings](http://mom.babble.com/mom/mominations/leading-mominees/).

Thanks!

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**Author:** ![rocking\_chair](https://sea3.discourse-cdn.com/straightdope/user_avatar/boards.straightdope.com/rocking_chair/32/2918_2.png) [@rocking\_chair](https://boards.straightdope.com/u/rocking_chair)\
**Post date:** [August 23, 2011, 10:35pm UTC](https://boards.straightdope.com/t/my-baby-girl-has-spinal-muscular-atrophy-sma/547126/808 "2011-08-23T22:35:55Z")

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i’m voting for my favourite hooting blog. is there a prize that goes with this? or is it mostly for getting out the message and having the m. v. b.?

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**Author:** ![lisiate](https://avatars.discourse-cdn.com/v4/letter/l/f05b48/32.png) [@lisiate](https://boards.straightdope.com/u/lisiate)\
**Post date:** [August 24, 2011, 5:52am UTC](https://boards.straightdope.com/t/my-baby-girl-has-spinal-muscular-atrophy-sma/547126/809 "2011-08-24T05:52:56Z")

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**Bearflag70** I have an eight month old daughter so I can sort of imagine what you’ve been through as a father over the last year. I’d like to think I’d be as strong and positive as you have been and be able to carry on as well as you have if I were in your situation. I’d like to think that but to be honest I can’t. You sir, are an inspiration.

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**Author:** ![Bearflag70](https://avatars.discourse-cdn.com/v4/letter/b/8e7dd6/32.png) [@Bearflag70](https://boards.straightdope.com/u/Bearflag70)\
**Post date:** [August 24, 2011, 6:47am UTC](https://boards.straightdope.com/t/my-baby-girl-has-spinal-muscular-atrophy-sma/547126/810 "2011-08-24T06:47:33Z")

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> [@rocking\_chair](#):
>
> i’m voting for my favourite hooting blog. is there a prize that goes with this? or is it mostly for getting out the message and having the m. v. b.?

$50 gift card, bragging rights, and momentum in the Sacramento community for SMA awareness.

Personally, I imagine using the blog award as part of our Getty Owl resume to help drum up sponsorships for our local events. We are in the process of seeking sponsorships for our big even, Getty Owl Run, in February 2012.

We initially thought of the August SMA Awareness campaign as not only raising awareness but also a springboard for marketing the Run. The Art Auction was an afterthought and we didn’t originally plan on August being a fundraiser at all. That worked out nicely, I think.

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**Author:** ![Bearflag70](https://avatars.discourse-cdn.com/v4/letter/b/8e7dd6/32.png) [@Bearflag70](https://boards.straightdope.com/u/Bearflag70)\
**Post date:** [August 24, 2011, 7:07am UTC](https://boards.straightdope.com/t/my-baby-girl-has-spinal-muscular-atrophy-sma/547126/811 "2011-08-24T07:07:32Z")

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> [@lisiate](#):
>
> **Bearflag70** I have an eight month old daughter so I can sort of imagine what you’ve been through as a father over the last year. I’d like to think I’d be as strong and positive as you have been and be able to carry on as well as you have if I were in your situation. I’d like to think that but to be honest I can’t. You sir, are an inspiration.

Thank you so much. I appreciate it truly.

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**Author:** ![Bearflag70](https://avatars.discourse-cdn.com/v4/letter/b/8e7dd6/32.png) [@Bearflag70](https://boards.straightdope.com/u/Bearflag70)\
**Post date:** [August 24, 2011, 7:51am UTC](https://boards.straightdope.com/t/my-baby-girl-has-spinal-muscular-atrophy-sma/547126/812 "2011-08-24T07:51:28Z")

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> [@Bearflag70](#):
>
> $50 gift card, bragging rights, and momentum in the Sacramento community for SMA awareness.
> 
> Personally, I imagine using the blog award as part of our Getty Owl resume to help drum up sponsorships for our local events. We are in the process of seeking sponsorships for our big even, Getty Owl Run, in February 2012.

Expanding on this point, what we have learned since venturing into the nonprofit world is that businesses just don’t sponsor nonprofits for the hell of it; they buy sponsorships as a marketing investment. When purchasing a nonprofit sponsorship, they want a return in the form of a name on the shirt, a name on the website, a name on the flyers, access to whatever captive audience the Foundation can drum up, etc.

When we go looking for sponsorships, we have an uphill battle right now because we are in our first year as a nonprofit and this is our first Run. We need to be able to convince businesses their sponsorship dollars will be a good investment for them. Part of that pitch includes us trying to convince them that “we mean business” and we can perform. Hence, we need to build our “resume” and our standing in the community as a cause that is able to grab public attention.

The more successful our events are, the more SMA awareness we raise. That, in turn, helps get sponsorships, which means we can do bigger and better events in the future… raising even more SMA awareness and raising even more sponsorships in an upward spiral.

Since this is our first year, we need as many feathers in our cap as we can get.

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**Author:** ![Nava](https://avatars.discourse-cdn.com/v4/letter/n/da6949/32.png) [@Nava](https://boards.straightdope.com/u/Nava)\
**Post date:** [August 24, 2011, 9:18am UTC](https://boards.straightdope.com/t/my-baby-girl-has-spinal-muscular-atrophy-sma/547126/813 "2011-08-24T09:18:49Z")

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> [@Bearflag70](#):
>
> Hey SDMB SMA Warriors, please [go to this site](http://mom.babble.com/mom/mominations/mominees/charity/morgan-shanahan) and click “like” for Morgan. She’s a blogger mom and supporter of [Getty Owl Foundation](http://gettyowl.com/gof/).

_shaking a fist at **Bearflag70** _ Damnit! You made me reactivate my facebook account! :mad:

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**Author:** ![twickster](https://avatars.discourse-cdn.com/v4/letter/t/ec9cab/32.png) [@twickster](https://boards.straightdope.com/u/twickster)\
**Post date:** [August 24, 2011, 2:11pm UTC](https://boards.straightdope.com/t/my-baby-girl-has-spinal-muscular-atrophy-sma/547126/814 "2011-08-24T14:11:03Z")

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> [@Bearflag70](#):
>
> Hey SDMB SMA Warriors, please [go to this site](http://mom.babble.com/mom/mominations/mominees/charity/morgan-shanahan) and click “like” for Morgan. She’s a blogger mom and supporter of [Getty Owl Foundation](http://gettyowl.com/gof/).
> 
> If she wins, GOF gets $5k to help fight SMA!
> 
> Tell your friends!
> 
> [The rankings](http://mom.babble.com/mom/mominations/leading-mominees/).
> 
> Thanks!

Just saw this – done, and I made a note on my FB page, so hopefully a few people there who are no longer as active here will see it as well.

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**Author:** ![SciFiSam](https://avatars.discourse-cdn.com/v4/letter/s/47e85d/32.png) [@SciFiSam](https://boards.straightdope.com/u/SciFiSam)\
**Post date:** [August 24, 2011, 2:35pm UTC](https://boards.straightdope.com/t/my-baby-girl-has-spinal-muscular-atrophy-sma/547126/815 "2011-08-24T14:35:40Z")

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> [@jjimm](#):
>
> **Bearflag70** , you probably don’t remember this, but a year ago, back at the start of this thread I [mentioned someone](http://boards.straightdope.com/sdmb/showpost.php?p=12755049&postcount=177) I knew and went to school with who had SMA.
> 
> I’ve finally found details of her (she changed her name hence not finding her). She died last year. But she was AGED 40!!! She achieved so, so much despite her disability. She was an inspiration to humanity, disabled people, and people with SMA, in that order. And in answer to your question, she had the Type 1 severe form of SMA - but defied the odds.
> 
> Please read her story: [Rowen Jade](http://www.guardian.co.uk/society/2010/oct/03/rowen-jade-obituary).

I think I met her, many years ago under her original name. 40 years is too short, but she had a good life in that time.

Beaflag, I ‘liked’ that post. And your wife looks like a film star in that picture.

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**Author:** ![rocking\_chair](https://sea3.discourse-cdn.com/straightdope/user_avatar/boards.straightdope.com/rocking_chair/32/2918_2.png) [@rocking\_chair](https://boards.straightdope.com/u/rocking_chair)\
**Post date:** [September 7, 2011, 11:50pm UTC](https://boards.straightdope.com/t/my-baby-girl-has-spinal-muscular-atrophy-sma/547126/816 "2011-09-07T23:50:06Z")

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hopefully things went well in august for sma awareness.

i see there has been a new addition to the household… little furry kitty rich is just adorable and the pic. with getty and her furry brothers is just too adorable! i’m glad they are all getting along.

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**Author:** ![Bearflag70](https://avatars.discourse-cdn.com/v4/letter/b/8e7dd6/32.png) [@Bearflag70](https://boards.straightdope.com/u/Bearflag70)\
**Post date:** [September 8, 2011, 6:35am UTC](https://boards.straightdope.com/t/my-baby-girl-has-spinal-muscular-atrophy-sma/547126/817 "2011-09-08T06:35:57Z")

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SMA Awareness Month went well for Getty Owl, thanks.

We got a resolution through Sacramento City Council  
We had a successful SMA Awareness walk  
We had a successful SMA Art Auction fundraiser  
We had a “Tell 5” campaign where people told 5 people about SMA  
The blog was nominated by a local TV station for the Most Valuable Blogger  
We helped an SMA family navigate a lengthy stay in the Pediatric ICU  
We provided an SMA family with some needed equipment  
We assisted a newly diagnosed family better understand SMA  
We got a great article in the Sacramento Bee newspaper  
Probably some other things I’m not remembering at the moment

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**Author:** ![rocking\_chair](https://sea3.discourse-cdn.com/straightdope/user_avatar/boards.straightdope.com/rocking_chair/32/2918_2.png) [@rocking\_chair](https://boards.straightdope.com/u/rocking_chair)\
**Post date:** [September 8, 2011, 12:54pm UTC](https://boards.straightdope.com/t/my-baby-girl-has-spinal-muscular-atrophy-sma/547126/818 "2011-09-08T12:54:01Z")

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wow! that is fantastic.

one little girl can make a very big difference.

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**Author:** ![Elysium](https://avatars.discourse-cdn.com/v4/letter/e/3be4f8/32.png) [@Elysium](https://boards.straightdope.com/u/Elysium)\
**Post date:** [September 8, 2011, 1:10pm UTC](https://boards.straightdope.com/t/my-baby-girl-has-spinal-muscular-atrophy-sma/547126/819 "2011-09-08T13:10:03Z")

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That’s awesome! I participated in the Tell 5, and the little placard is still on my office door here at work 🙂

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**Author:** ![rocking\_chair](https://sea3.discourse-cdn.com/straightdope/user_avatar/boards.straightdope.com/rocking_chair/32/2918_2.png) [@rocking\_chair](https://boards.straightdope.com/u/rocking_chair)\
**Post date:** [September 15, 2011, 12:45am UTC](https://boards.straightdope.com/t/my-baby-girl-has-spinal-muscular-atrophy-sma/547126/820 "2011-09-15T00:45:33Z")

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whoot! hoot! hoot! finest number one blogger! congratulations, getty owl!

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