Help witth travel info.......

[Guest guest]

I was wondering if anyone could tell me if they know of any help

that airlines offer for travel. Our latest neurologist want us to

start planning on having a muscle biopsy done and we need to find

the cheapest way to get from TX to Atlanta. Any info that anyone

has will help. I know we can probably stay in the RM house when we

get there, but it's getting there that will be expensive. Thanks in

advance!

Vicki~ mom to Caden (almost 12 mo.) possible mito

[Guest guest]

Vicki,

Here is a website that has a lot of different resources,as far as flights

go.Angel Flight,CHildrens flight of hope,Delta Air sky wish,,etc. I think you

should be able to find one that would work,for you. BTW,,where in Tx are you ?

We are in Denton,about 60 miles north of Dallas.

Kim mom to Meaghan 15 ~~Katelyn 12 Bipolar,and OCD ~~ Logan 7 Autism,congenital

myopathy,possible mitochondrial disease,and JRA ~~ and Ethan 5 and 100 % BOY

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[Guest guest]

Southwest Airlines was great when I asked for tickets to send a little friend who has Leigh's, along with his Dad and his Grandmother from Oklahoma to San Diego for evaluation. They provided round trip tickets for everyone and even let us change the scheduling at the last minute when the Doctor released him earlier than we expected! I cannot find the name of the person with whom I talked, but I know that I obtained the information through their website. If you have no luck, let me know and I will try to find the letter that I received from them -- I think it is at the office and I am at home right now! Good luck!!

Sue

I was wondering if anyone could tell me if they know of any help that airlines offer for travel.

[Guest guest]

We are in San Angelo, TX. My sister lives in ville though. We are seeing neurologists at Cooks in Ft. Worth ( Dr. Saleem Malik & Warner?) and we had Caden's ERG done at the Retina Foundation of the SW in Dallas. We have also seen a metabolicist at TX Children's in Dallas. We are scheduled to be admitted to Cooks in the next 2 weeks to have more tests done. So we will be back up there soon. They also want us to have a muscle bio. done, so we can have it done there, or go to Atlanta. I think we will go on and go to Shoffner in Atlanta. We are also waiting to see if the ish Rites Hospital will accept Caden so we can see the neurologist there in the CP clinic. I almost went to run track in college at North TX!! Stayed here at Angelo State U to run instead. It's a small world! Where are your doctors? Any info on the Dallas area docs would help. Thanks for the info. I will look into the sites.

Vicki~mom to Caden (almost 12 months) possible mito

Re: Help witth travel info.......

Vicki, Here is a website that has a lot of different resources,as far as flights go.Angel Flight,CHildrens flight of hope,Delta Air sky wish,,etc. I think you should be able to find one that would work,for you. BTW,,where in Tx are you ? We are in Denton,about 60 miles north of Dallas.Kim mom to Meaghan 15 ~~Katelyn 12 Bipolar,and OCD ~~ Logan 7 Autism,congenital myopathy,possible mitochondrial disease,and JRA ~~ and Ethan 5 and 100 % BOY________________________________________________________________Get your name as your email address.Includes spam protection, 1GB storage, no ads and moreOnly $1.99/ month - visit http://www.mysite.com/name today!Please contact mito-owner with any problems or questions.