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michellemalkin's profile
Michelle Malkin
Michelle Malkin
Michelle Malkin
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@michellemalkin

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Michelle MalkinVerified account

@michellemalkin

Little brown woman. Big mouth. Wife. Mom. Entrepreneur. Geek. #StillAThing #ManitouIncline Host of #michellemalkininvestigates on CRTV. #freedanielholtzclaw

USA
michellemalkin.com
Joined August 2008

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    Michelle Malkin‏Verified account @michellemalkin 14 May 2015

    If any of you have experience with Ehlers-Danlos Syndrome, I'm interested in hearing from you. #momtweets

    6:13 PM - 14 May 2015
    • 32 Retweets
    • 25 Likes
    • Goaliegeorge Mark Flesner Alex Bravobabe THE _ NATIONALIST steve lowe 😁Joe...😍❤F❤😍 Chelskii Jay Hostetler
    51 replies 32 retweets 25 likes
      1. New conversation
      2. ToniMitrovic‏ @MitroT 14 May 2015
        Replying to @michellemalkin

        @michellemalkin My daughter. She's autistic. They monitor her heart valves. Then double jointed/headaches

        1 reply 0 retweets 2 likes
      3. Michelle Malkin‏Verified account @michellemalkin 14 May 2015
        Replying to @MitroT

        @MitroT thank you for your feedback. are your daughter's headaches migraines? any signs of "dysautonomia?" breathing problems?

        7 replies 0 retweets 1 like
      4. Jennine‏ @jenninejones 14 May 2015
        Replying to @michellemalkin

        @michellemalkin She has kept folder on all medical care. Was extremely to find diagnosis and might help you with that & coping techniques.

        0 replies 0 retweets 1 like
      5. End of conversation
      1. New conversation
      2. Sarah‏ @sarah_wxtx 14 May 2015
        Replying to @michellemalkin

        @michellemalkin I believe I have it. Mitral valve prolapse, double jointed, etc.

        2 replies 0 retweets 0 likes
      3. Michelle Malkin‏Verified account @michellemalkin 14 May 2015
        Replying to @sarah_wxtx

        @sarahrstevenson any breathing problems?

        2 replies 0 retweets 0 likes
      4. Sarah‏ @sarah_wxtx 14 May 2015
        Replying to @michellemalkin

        @michellemalkin no, other than during anxiety attacks

        1 reply 0 retweets 0 likes
      5. Michelle Malkin‏Verified account @michellemalkin 14 May 2015
        Replying to @sarah_wxtx

        @sarahrstevenson do they take a long time to resolve? thank you!

        1 reply 0 retweets 0 likes
      6. Sarah‏ @sarah_wxtx 14 May 2015
        Replying to @michellemalkin

        @michellemalkin no, usually around 15 min. I think I get anxious when my heart beats weird and have some shortness of breath.

        3 replies 0 retweets 0 likes
      7. Taryn‏ @TarynOnthenews 14 May 2015
        Replying to @sarah_wxtx

        @sarahrstevenson Sorry to jump in, but I occasionally get that heart beating weirdly with shortness of breath. Is that anything tolook into?

        1 reply 0 retweets 0 likes
      8. Sarah‏ @sarah_wxtx 14 May 2015
        Replying to @TarynOnthenews

        @TarynOnthenews ask your dr. Mine has me get an echocardiogram every 3 years to monitor my MVP.

        1 reply 0 retweets 2 likes
      9. Taryn‏ @TarynOnthenews 14 May 2015
        Replying to @sarah_wxtx

        @sarahrstevenson thank you

        1 reply 0 retweets 0 likes
      10. 2 more replies
      1. New conversation
      2. Denise Vanderbroeck‏ @DACVanderbroeck 20 May 2015
        Replying to @michellemalkin

        @michellemalkin made an awareness video about #eds hope you like it!http://youtu.be/_w4OkwLbNs4 

        1 reply 0 retweets 1 like
      3. Michelle Malkin‏Verified account @michellemalkin 20 May 2015
        Replying to @DACVanderbroeck

        @DACVanderbroeck thank you so much. the EDS community has been amazing.

        1 reply 0 retweets 0 likes
      4. Denise Vanderbroeck‏ @DACVanderbroeck 20 May 2015
        Replying to @michellemalkin

        @michellemalkin thank you for sharing! #loveyourself

        0 replies 0 retweets 0 likes
      5. End of conversation
      1. Alex‏ @alexjreaves 14 May 2015
        Replying to @michellemalkin

        @michellemalkin I have EDS type 2! Mild classical

        0 replies 1 retweet 2 likes
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      1. Bravobabe‏ @debbravobabe 14 May 2015
        Replying to @michellemalkin

        @michellemalkin my 15 year old daughter suffered horribly. Sigh. I've turned your post over to my Mn group

        0 replies 1 retweet 2 likes
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      1. BuildTheWall‏ @changeisneeded_ 14 May 2015
        Replying to @michellemalkin

        @michellemalkin Many of those with EDS also have POTS.

        0 replies 0 retweets 2 likes
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      1. Jennine‏ @jenninejones 14 May 2015
        Replying to @michellemalkin

        @michellemalkin Neice diagnosed with this approx 10 yrs ago. Rare disorder, took a long time to get diagnosed. #momtweets

        0 replies 0 retweets 2 likes
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      1. New conversation
      2. NicoleKimberlin‏ @NicoleKimberlin 14 May 2015
        Replying to @michellemalkin

        @michellemalkin I have EDS type 3.

        1 reply 0 retweets 0 likes
      3. tina‏ @SaltOnMySpoon 15 Sep 2015
        Replying to @NicoleKimberlin

        @NicoleKimberlin @michellemalkin So do I and I'm worried that if I had kids they would get it. Do your children have it or dysautonomia? ❤️

        1 reply 0 retweets 0 likes
      4. NicoleKimberlin‏ @NicoleKimberlin 15 Sep 2015
        Replying to @SaltOnMySpoon

        @SaltOnMySpoon @michellemalkin My kids do not have any signs of dysautonomia. I had a bad spinal fluid leak, that most likely is to blame.

        1 reply 0 retweets 0 likes
      5. tina‏ @SaltOnMySpoon 15 Sep 2015
        Replying to @NicoleKimberlin

        @NicoleKimberlin oh no! I'm sorry. You have POTS?

        1 reply 0 retweets 0 likes
      6. NicoleKimberlin‏ @NicoleKimberlin 15 Sep 2015
        Replying to @SaltOnMySpoon

        @SaltOnMySpoon Nope, no POTS. I have neurallly mediated syncope. It's under the dysautonomia umbrella.

        2 replies 0 retweets 0 likes
      7. tina‏ @SaltOnMySpoon 15 Sep 2015
        Replying to @NicoleKimberlin

        @NicoleKimberlin ugh. awful. Do your children have eds? (Sorry for all the questions!) lol

        1 reply 0 retweets 0 likes
      8. NicoleKimberlin‏ @NicoleKimberlin 15 Sep 2015
        Replying to @SaltOnMySpoon

        @SaltOnMySpoon Nope no EDS diagnoses for them yet thank goodness. I'm hoping they didn't get my bad genes, just my looks lol!

        1 reply 0 retweets 1 like
      9. tina‏ @SaltOnMySpoon 15 Sep 2015
        Replying to @NicoleKimberlin

        @NicoleKimberlin Lol yes you are so pretty!

        1 reply 0 retweets 1 like
      10. 2 more replies

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