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Liz/Charlyne

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Hi, Everyone....Liz...glad to hear Tori made it through the sleep studies.

Did you take a camera to get a photo of all them wires?!?!? JFYI....Gareth

had his T & A years before his sleep study and still had the apnea really bad.

Charlyne.....thank you for the cross and papers.

As for Gareth.......well....we're in standby mode, I guess. He saw the ped

rheuma doc today and I was surprised by the visit. A few weeks ago, he

indicated in an e-mail that he felt the ped gastro doc was way off base with

the

Scleroderma possibility. Now.......he's leaning towards it, too, because

that's the only blood work that is coming back positive. I am

sooooooooooooooooo

bummed!!! He wants him to have a whole series of blood work done in 6 weeks

and report back to him the end of Feb. If the results are still positive,

then that is the path we will follow/treatment for. He did say, in his 10

years of practicing that he hasn't seen one case of sine Scleroderma in a

teenager......something to Gareth's good. He still needs the CT scan of the

abdomen to find out what the calcifications are that showed up on his abdominal

X-ray.....nothing to do with the high sed rate or the esophagus!!! He also

needs the MRA of the heart.....something they have to clear with the

radiologist

because he's got the 5 pins in his hip. That will hopefully show what is

bulging in his esophagus. He did say that he felt the esophageal dismotility

was permanent. Thank you so very much for all your prayers.........I really do

appreciate them. Take care,

Everyone.

Margaret

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Man, Margaret! We were all hoping you guys could start off 2007 with some

clarity. Well, we have everything crossed for you and Mr. G and pray 2007 will

bring good health and knowledge of what the heck is going on.

Liz & Family

Liz/Charlyne

Hi, Everyone....Liz...glad to hear Tori made it through the sleep studies.

Did you take a camera to get a photo of all them wires?!?!? JFYI....Gareth

had his T & A years before his sleep study and still had the apnea really bad.

Charlyne.....thank you for the cross and papers.

As for Gareth.......well....we're in standby mode, I guess. He saw the ped

rheuma doc today and I was surprised by the visit. A few weeks ago, he

indicated in an e-mail that he felt the ped gastro doc was way off base with

the

Scleroderma possibility. Now.......he's leaning towards it, too, because

that's the only blood work that is coming back positive. I am

sooooooooooooooooo

bummed!!! He wants him to have a whole series of blood work done in 6 weeks

and report back to him the end of Feb. If the results are still positive,

then that is the path we will follow/treatment for. He did say, in his 10

years of practicing that he hasn't seen one case of sine Scleroderma in a

teenager......something to Gareth's good. He still needs the CT scan of the

abdomen to find out what the calcifications are that showed up on his

abdominal

X-ray.....nothing to do with the high sed rate or the esophagus!!! He also

needs the MRA of the heart.....something they have to clear with the

radiologist

because he's got the 5 pins in his hip. That will hopefully show what is

bulging in his esophagus. He did say that he felt the esophageal dismotility

was permanent. Thank you so very much for all your prayers.........I really do

appreciate them. Take care,

Everyone.

Margaret

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