IM confused with diagnosis

[Mommafirst]

Hey Jennifer -- at the conference this weekend Johns Hopkins announced a new website that they are working on to fully describe all the known mutations. I'm sure they won't have information on your Q one for some time, but they may be able to get you further in understanding what it does and means.
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<br />I know how frustrated you've been and I regularly pray you get the answers and help you need.

 

[JennifersHope]

Thanks Guys, I do know that we consulted John's Hopkins when the second gene was identified and the doctor there, (can't remember his name) was not aware of this gene.....

I am so frustrated, it is beyond words, the emotional roller coaster I was on, now I don't care, I just want to get better. I am going to google about the Nasal PD being normal.

THanks so much....I had the Nasal PD done at UNC....not Mayo.

 

[JennifersHope]

Thanks Guys, I do know that we consulted John's Hopkins when the second gene was identified and the doctor there, (can't remember his name) was not aware of this gene.....

I am so frustrated, it is beyond words, the emotional roller coaster I was on, now I don't care, I just want to get better. I am going to google about the Nasal PD being normal.

THanks so much....I had the Nasal PD done at UNC....not Mayo.

 

[JennifersHope]

Thanks Guys, I do know that we consulted John's Hopkins when the second gene was identified and the doctor there, (can't remember his name) was not aware of this gene.....
<br />
<br />I am so frustrated, it is beyond words, the emotional roller coaster I was on, now I don't care, I just want to get better. I am going to google about the Nasal PD being normal.
<br />
<br />THanks so much....I had the Nasal PD done at UNC....not Mayo.
<br />
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