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Re: Help Needed!

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Kathy,

Sorry I do not have any answers to your questions, but you say that this

is his first illness since diagnosis. May I ask what tests were done

and how long did it take you to get a diagnosis?

Thanks for your info,

Barbara

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A good way for me to monitor how sick my daughter is getting is I check her

urine for ketones. The more ketones she spills the sicker she is. When she

is spilling large or moderate amts I add heaping teaspoons of sugar to her

pedialyte and that has kept her out of hospital many times with GI problems.

Also push in as many fluids as you can and keep temperature down. It just

burns up energy. You can purchase ketosticks over the counter at your local

pharmacy. I just take one and mash it into a wet diaper. I'ts best to dip

it in fresh urine. Good luck.

Janelle McGuire

Parent to and

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In a message dated 11/19/99 5:24:01 PM Eastern Standard Time,

KCorley309@... writes:

<<

Okay . . . question is . . . Is there anything more we should be doing for

him right now? This is first illness post-diagnosis (mito complex I and

III). Do we need to run labs? Check for acidosis? Treat with bicarb or

something? What other things should we be doing?

Kathy Corley

>>

Kathy I am sure we would all agree that checking with your docs first is

always the way to go------and I can only give you information that Dr Cohen

gave me for . He told us whenever he is sick to increase fluids like

sportade or gatorade because the increase electrolytes will help your child's

strength in fighting an infection or illness. He also gave me specific

instructions that whenever gets a temp of 101f he is to be

hospitalized with 10% dextrose to give him another sugar boost , IV

antibiotics if necessary to get to the source of the infection, and to have

the lactic and pyruvic ratios checked as well as electrolytes and blood

sugars regularly. he told me that kids with Mito can dehydrate very rapidly

and maintaining proper levels of electrolytes is very important. Oh ya one

more thing he also suggests that you use motrin to reduce fever instead of

tylenol because the tylenol causes too many free radicals in the mitochondria

which is compares to smog in the air. If a person already has a reduced

amount of properly functioning mitochondria then you want to maximize the

ones that work well.

I hope this helps, ---------- and Complex II-III

I remember the first time was sick post dx and I was a basket case and

without experienced parents to talk to I would have gone nuts! I am fortunate

to have 6 right in my home town!

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In a message dated 11/19/99 5:24:01 PM Eastern Standard Time,

KCorley309@... writes:

<<

Okay . . . question is . . . Is there anything more we should be doing for

him right now? This is first illness post-diagnosis (mito complex I and

III). Do we need to run labs? Check for acidosis? Treat with bicarb or

something? What other things should we be doing?

Kathy Corley

>>

Kathy I am sure we would all agree that checking with your docs first is

always the way to go------and I can only give you information that Dr Cohen

gave me for . He told us whenever he is sick to increase fluids like

sportade or gatorade because the increase electrolytes will help your child's

strength in fighting an infection or illness. He also gave me specific

instructions that whenever gets a temp of 101f he is to be

hospitalized with 10% dextrose to give him another sugar boost , IV

antibiotics if necessary to get to the source of the infection, and to have

the lactic and pyruvic ratios checked as well as electrolytes and blood

sugars regularly. he told me that kids with Mito can dehydrate very rapidly

and maintaining proper levels of electrolytes is very important. Oh ya one

more thing he also suggests that you use motrin to reduce fever instead of

tylenol because the tylenol causes too many free radicals in the mitochondria

which is compares to smog in the air. If a person already has a reduced

amount of properly functioning mitochondria then you want to maximize the

ones that work well.

I hope this helps, ---------- and Complex II-III

I remember the first time was sick post dx and I was a basket case and

without experienced parents to talk to I would have gone nuts! I am fortunate

to have 6 right in my home town!

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In a message dated 11/21/99 2:29:40 PM Eastern Standard Time,

Goldenfam4@... writes:

<< Kathy I am sure we would all agree that checking with your docs first is

always the way to go------and I can only give you information that Dr Cohen

gave me for . >>

Hi, -

Thanks for the information! I took to see the pediatrician before I

posted; it's just that she is as much a novice at the mito stuff as I am (or

maybe even moreso according to her . . . I have read more.) We saw Dr. Cohen

recently, but as much information as I left with, I forgot to talk about

acute illness protocols. Actually, though, is doing much better. He

still has a little diarrhea, but is not acting sick at all . . . running

around and laughing and playing like normal! What a relief! Still a little

disconcerting to see him so out one day and then fine the next.

I think (as suggested by several on the list) that his blood sugar must have

taken a nose dive. He wasn't feverish or even acting all that sick. But he

was not taking really any food by mouth, and we ended up going a little

longer than normal before I bolus fed him through his tube . . . between

getting over the stomach bug, an ear infection that was still raging, and not

taking in as much in total calories over the couple of days prior, I think he

just crashed. I will be more careful next time and I will know when to ask

the ped to do labs and IV fluids!!!! I have been mixing a little cornstarch

in his feedings and he is bouncing back nicely!

Thanks to everyone for the help!

Kathy

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Hi Kathy,

I'm glad to hear that is doing so much better.

Could you give me some background info on him. What made you go for all

of the testing? How old is ? From your posts it seems that he is

doing well developmentally. You mention his running around and playing

now that he is felling better. Does this mean he's is not being

affected developmentally by this mitochondrial problem?

I'm asking all of this because my son seems to be fine motor development

wise. He only has a few physical differences that are not obvious. His

tongue protrudes. He has low set ears and I guess that is all. Doctors

have said that this can mean nothing and not to worry about it. His

speech pathologist says he has low tone in his jaw yet overall he is

very muscular. I guess I'm just trying to make sense of all of this and

I hope to find someone out there who has seen the same things.

Thanks for listening,

Barbara

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Hi Kathy,

I'm glad to hear that is doing so much better.

Could you give me some background info on him. What made you go for all

of the testing? How old is ? From your posts it seems that he is

doing well developmentally. You mention his running around and playing

now that he is felling better. Does this mean he's is not being

affected developmentally by this mitochondrial problem?

I'm asking all of this because my son seems to be fine motor development

wise. He only has a few physical differences that are not obvious. His

tongue protrudes. He has low set ears and I guess that is all. Doctors

have said that this can mean nothing and not to worry about it. His

speech pathologist says he has low tone in his jaw yet overall he is

very muscular. I guess I'm just trying to make sense of all of this and

I hope to find someone out there who has seen the same things.

Thanks for listening,

Barbara

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Kathy:

What does the cornstarch do?

Amy

Re: Help Needed!

>From: KCorley309@...

>

>In a message dated 11/21/99 2:29:40 PM Eastern Standard Time,

>Goldenfam4@... writes:

>

><< Kathy I am sure we would all agree that checking with your docs first is

> always the way to go------and I can only give you information that Dr

Cohen

> gave me for . >>

>

>

>Hi, -

>

>Thanks for the information! I took to see the pediatrician before I

>posted; it's just that she is as much a novice at the mito stuff as I am

(or

>maybe even moreso according to her . . . I have read more.) We saw Dr.

Cohen

>recently, but as much information as I left with, I forgot to talk about

>acute illness protocols. Actually, though, is doing much better. He

>still has a little diarrhea, but is not acting sick at all . . . running

>around and laughing and playing like normal! What a relief! Still a

little

>disconcerting to see him so out one day and then fine the next.

>

>I think (as suggested by several on the list) that his blood sugar must

have

>taken a nose dive. He wasn't feverish or even acting all that sick. But

he

>was not taking really any food by mouth, and we ended up going a little

>longer than normal before I bolus fed him through his tube . . . between

>getting over the stomach bug, an ear infection that was still raging, and

not

>taking in as much in total calories over the couple of days prior, I think

he

>just crashed. I will be more careful next time and I will know when to ask

>the ped to do labs and IV fluids!!!! I have been mixing a little

cornstarch

>in his feedings and he is bouncing back nicely!

>

>Thanks to everyone for the help!

>

>Kathy

>

>>Brought to you by www.imdn.org - an on-line support group for those

affected by mitochondrial disease.

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