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I'm still wiped out but that is to be expected after being put through the

mill and being inpatient for a week at CCF.

I'm on my first 12 hr day of TPN today. I was discharged by the home health

nurse this morning on her first visit. I took charge and did what I knew how

to do. I think I shocked the nurse. hehe It was a requirement of CCF that

home health at least come even though I didn't need any assistance. I had an

allergic reaction the first night of TPN in the hospital. The Lipids and Pepcid

were removed and so far I've done well since.

I saw Dr. Cohen and he was excellent and personable.He was very excited that

a brand new gene test is available for me. It's the OCTN2 gene-carnitine

transporter gene. Thats the one I've been needing for so long. It's going to

Horizon labs but it may be a long time to get the results. He also had me get

the MNGIE and Creatine test done as well. He invited me to come back over lunch

and be a guest for the neuro residents conference training. It was flattered

and obliged. I was seated in the front of the room with all these doc's

infront of me. It was done really well in a teaching/diagnosing fashion. Dr.

Cohen called on one resident to do the medical history and another to do the

physical exam. I wasn't to tell them anything that they didn't ask me or tell

my

Dx. The purpose was to see if they could diagnose a patient in 30 mins. It

led to a very interesting conversation which I believe would have gone on for

some time had I not had to leave for my gastro testing.

The gastro testing was very painful. Let's just say I was too small for the

equipment normally used. :( The pending results are very abnormal according

for my colonic transit study. I was given a pseudo obstruction Dx.

The sleep study was terrible. I wasn't able to lay down until 11:30 due to

delays with getting me ready and all the equipment put on. It was an abnormal

study showing REM obstructive sleep apnea.I only slept 49 %. It's not the

type where you snore but I won't know the details until this next week when Dr.

Cohen is back from vacation.

I was trained on how to self administer Forteo shots as well. I did ok but

have site reactions and some bleeding afterwards which nobody can really

explain. I've spoken with my doc. and the company that makes Forteo.

I think thats pretty much the highlights. Thanks for all your prayers!

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Guest guest

Wow, that sounds like quite the visit at CCF. I had a thought as to the

Forteo reaction you had. It may very well have been an additive or

preservative that caused the problem, not the med itself. I can't use

novacaine with epi in it and Laurie has a problem with a preserviative.

Marcaine comes to mind for some reason, but Laurie can't tell us for

sure until next week since she will be off line until Tuesday.

I'm very proud of you and your being able to tell the home care nurse

what needed to be done instead of the other way around. Good luck with

the test results and let us know what you find out.

Hugs,

LILQT4U1984@... wrote:

>I'm still wiped out but that is to be expected after being put through the

>mill and being inpatient for a week at CCF.

>I'm on my first 12 hr day of TPN today. I was discharged by the home health

>nurse this morning on her first visit. I took charge and did what I knew how

>to do. I think I shocked the nurse. hehe It was a requirement of CCF that

>home health at least come even though I didn't need any assistance. I had an

>allergic reaction the first night of TPN in the hospital. The Lipids and

Pepcid

>were removed and so far I've done well since.

>I saw Dr. Cohen and he was excellent and personable.He was very excited that

>a brand new gene test is available for me. It's the OCTN2 gene-carnitine

>transporter gene. Thats the one I've been needing for so long. It's going to

>Horizon labs but it may be a long time to get the results. He also had me get

>the MNGIE and Creatine test done as well. He invited me to come back over

lunch

>and be a guest for the neuro residents conference training. It was flattered

>and obliged. I was seated in the front of the room with all these doc's

>infront of me. It was done really well in a teaching/diagnosing fashion. Dr.

>Cohen called on one resident to do the medical history and another to do the

>physical exam. I wasn't to tell them anything that they didn't ask me or tell

my

>Dx. The purpose was to see if they could diagnose a patient in 30 mins. It

>led to a very interesting conversation which I believe would have gone on for

>some time had I not had to leave for my gastro testing.

>The gastro testing was very painful. Let's just say I was too small for the

>equipment normally used. :( The pending results are very abnormal according

>for my colonic transit study. I was given a pseudo obstruction Dx.

>The sleep study was terrible. I wasn't able to lay down until 11:30 due to

>delays with getting me ready and all the equipment put on. It was an abnormal

>study showing REM obstructive sleep apnea.I only slept 49 %. It's not the

>type where you snore but I won't know the details until this next week when

Dr.

>Cohen is back from vacation.

>I was trained on how to self administer Forteo shots as well. I did ok but

>have site reactions and some bleeding afterwards which nobody can really

>explain. I've spoken with my doc. and the company that makes Forteo.

>I think thats pretty much the highlights. Thanks for all your prayers!

>

>

>

>

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Guest guest

,

Sounds like you had an exciting visit there. And very interesting.

(well, you may have a different description for the gastric testing -

and it's probably not " interesting " ).

I was interested in the carnitine transport gene (OCTN2). As I have

a carnitine deficiency also - I would imagine this is one of the

genes that I should have tested when I have my biopsy. How recently

did they start testing on this gene?

And... just curious - were any of the residents able to diagnose you

within the thirty minutes?

Maggie

> I'm still wiped out but that is to be expected after being put

through the

> mill and being inpatient for a week at CCF.

> I'm on my first 12 hr day of TPN today. I was discharged by the

home health

> nurse this morning on her first visit. I took charge and did what

I knew how

> to do. I think I shocked the nurse. hehe It was a requirement of

CCF that

> home health at least come even though I didn't need any

assistance. I had an

> allergic reaction the first night of TPN in the hospital. The

Lipids and Pepcid

> were removed and so far I've done well since.

> I saw Dr. Cohen and he was excellent and personable.He was very

excited that

> a brand new gene test is available for me. It's the OCTN2 gene-

carnitine

> transporter gene. Thats the one I've been needing for so long.

It's going to

> Horizon labs but it may be a long time to get the results. He

also had me get

> the MNGIE and Creatine test done as well. He invited me to come

back over lunch

> and be a guest for the neuro residents conference training. It

was flattered

> and obliged. I was seated in the front of the room with all these

doc's

> infront of me. It was done really well in a teaching/diagnosing

fashion. Dr.

> Cohen called on one resident to do the medical history and

another to do the

> physical exam. I wasn't to tell them anything that they didn't

ask me or tell my

> Dx. The purpose was to see if they could diagnose a patient in 30

mins. It

> led to a very interesting conversation which I believe would have

gone on for

> some time had I not had to leave for my gastro testing.

> The gastro testing was very painful. Let's just say I was too

small for the

> equipment normally used. :( The pending results are very abnormal

according

> for my colonic transit study. I was given a pseudo obstruction Dx.

> The sleep study was terrible. I wasn't able to lay down until

11:30 due to

> delays with getting me ready and all the equipment put on. It was

an abnormal

> study showing REM obstructive sleep apnea.I only slept 49 %. It's

not the

> type where you snore but I won't know the details until this next

week when Dr.

> Cohen is back from vacation.

> I was trained on how to self administer Forteo shots as well. I

did ok but

> have site reactions and some bleeding afterwards which nobody can

really

> explain. I've spoken with my doc. and the company that makes

Forteo.

> I think thats pretty much the highlights. Thanks for all your

prayers!

>

>

>

>

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Guest guest

What a trip ! I'm curious too about whether or not they were able

to dx you. That's very cool that you were asked to participate and

I bet you were just dying to tell them...or laugh out loud ! It's

like hands on sherades.

Sorry to hear about your GI experiences. I have a lot of GI

problems too and there are few things in life worse than that. No

one knows unless they've been through it for months or years on

end. Hope things start to improve for you soon. I'll be praying

for ya :)

bug

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Guest guest

Maggie,

I believe the test just became available last week. It is very cutting edge.

I would inquire if it's something you should look into.

The residents did a pretty good job. They got in the general area, and then

with a little prodding figured it out. Dr. Cohen told them that they did well

because I was a very difficult case.

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