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Peptizyde is what I use :) Wait a few more weeks before you try this as you

may get quite a dramtic reaction in the form of die off of bugs. Waiting a

while gives some more time for healing to take place and to chip away at any

gut bug issues. Pep will also help with viral issues. Why are you planning on

doing this in particular ?

Mandi in UK

In her book, DeFelice talks about taking proteases between

meals in a smoothie or drink. Would I give the Peptizyde or Zyme

Prime since they have proteases or a seperate protease product. If

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>>>>In her book, DeFelice talks about taking proteases between

> meals in a smoothie or drink. Would I give the Peptizyde or Zyme

> Prime since they have proteases or a seperate protease product.

Peptizyde is the strong all-protease product. Use that one for

between meal protease benefits. I put on in my drink and just sip on

it all day. Usually one drink in the morning and one in the

afternoon. Some products recommend around 4 capsules at a time.

Copious amounts are given for more severe injury or healing. A

fibromylagia group I was in discussed 45 capsules a day as a good

dose. You can play around with it and see what works out best. I just

don't want you to be afraid of going much higher.

>>>>> Also, I am giving Peptizyde and Zyme Prime at the same time

right when he starts eating, is that right?

Absolutely correct. Enzymes themselves can be given together. Sounds

like you are off to a great start.

.

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  • 1 year later...

My son is 3 months old, his birthday is 11/8/05. I noticed his flat

spot at about 5 days old and it has just continued to worsen with

time. At his two month visit my wife had me push to have him seen

by a cranio facial plasic surgen at Children's Boston. The Dr. said

to have our son helmeted for 6-10 weeks as at this early of an age

helmeting is short and very effective. Adding to that my cousin is

the Chief of Plastic Surgery in the Rockville MD area however he

does not do pediatric work. He also recommended the helmeting at an

earlier age rather then later. is now on his 4th day with

his new band and it doing very well with it. We are using

photography to track his progress as the day to day change is going

to be very subtle if you are with the child every day as parents

are...

With regard to the different types of bands, another doctor who is a

personal friend and an ER pediatrition as well as a research doctor

specializing in pediatrics stated that the treatments are all very

similar and one helmet isn't necessarily better then another. So

long as you are seeing results you are doing the right thing.

I can not answer the questions about other complexities as the

plagio/tort are our sons only symtems in addition to minor facial

asymmetry.

I wish you luck in this journey,

Rick

's daddy

--- In Plagiocephaly , " jenna10948 " <jenna10948@...>

wrote:

>

> Hello to Everyone,

>

> My name is Jenna and I am new to this group. My 13 week old son,

> Zachary, has head flattening limited to the back right side of his

> head. He doesn't have any facial asymmetry.

>

> I brought Zach to a craniofacial specialist, who thinks I should

> watch and wait until he's about 5 months old. I don't know what

to

> do. From what I have read, better results and shorter treatment

> durations are seen with earlier intervention. The doctor also

> referred me to Eastern Cranial Affiliates (ECA,)located in

> Arlington, VA, (they also have a location in Garden City Park, NY)

> should I choose to go the route of the helmet.

>

> I have heard lots of different anecdotal stories and they all seem

> to contradict each other. I often hear that this should mostly

> correct on its own, I then hear that it never does. I suppose I

> could wait until Zach is 5 months old, but then I wonder if he

will

> have a better outcome and shorter treatment duration if I take

> action now. Another complicating factor is that Zach has 3

> strawberry hemangionmas on his head.

>

> My questions to the group are:

> 1. Does any part of my story sound like yours and if so, what has

> been your experience?

>

> 2. Does anyone else's child have the complicating factor of the

> hemangiomas?

>

> 3. Did any of you use ECA in either the Virginia or New York

> location and if so, what was your experience?

>

> 4. Any other pearls?

>

> Thank you!

>

> Jenna Steckler

> Rockville, land

>

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My son is 3 months old, his birthday is 11/8/05. I noticed his flat

spot at about 5 days old and it has just continued to worsen with

time. At his two month visit my wife had me push to have him seen

by a cranio facial plasic surgen at Children's Boston. The Dr. said

to have our son helmeted for 6-10 weeks as at this early of an age

helmeting is short and very effective. Adding to that my cousin is

the Chief of Plastic Surgery in the Rockville MD area however he

does not do pediatric work. He also recommended the helmeting at an

earlier age rather then later. is now on his 4th day with

his new band and it doing very well with it. We are using

photography to track his progress as the day to day change is going

to be very subtle if you are with the child every day as parents

are...

With regard to the different types of bands, another doctor who is a

personal friend and an ER pediatrition as well as a research doctor

specializing in pediatrics stated that the treatments are all very

similar and one helmet isn't necessarily better then another. So

long as you are seeing results you are doing the right thing.

I can not answer the questions about other complexities as the

plagio/tort are our sons only symtems in addition to minor facial

asymmetry.

I wish you luck in this journey,

Rick

's daddy

--- In Plagiocephaly , " jenna10948 " <jenna10948@...>

wrote:

>

> Hello to Everyone,

>

> My name is Jenna and I am new to this group. My 13 week old son,

> Zachary, has head flattening limited to the back right side of his

> head. He doesn't have any facial asymmetry.

>

> I brought Zach to a craniofacial specialist, who thinks I should

> watch and wait until he's about 5 months old. I don't know what

to

> do. From what I have read, better results and shorter treatment

> durations are seen with earlier intervention. The doctor also

> referred me to Eastern Cranial Affiliates (ECA,)located in

> Arlington, VA, (they also have a location in Garden City Park, NY)

> should I choose to go the route of the helmet.

>

> I have heard lots of different anecdotal stories and they all seem

> to contradict each other. I often hear that this should mostly

> correct on its own, I then hear that it never does. I suppose I

> could wait until Zach is 5 months old, but then I wonder if he

will

> have a better outcome and shorter treatment duration if I take

> action now. Another complicating factor is that Zach has 3

> strawberry hemangionmas on his head.

>

> My questions to the group are:

> 1. Does any part of my story sound like yours and if so, what has

> been your experience?

>

> 2. Does anyone else's child have the complicating factor of the

> hemangiomas?

>

> 3. Did any of you use ECA in either the Virginia or New York

> location and if so, what was your experience?

>

> 4. Any other pearls?

>

> Thank you!

>

> Jenna Steckler

> Rockville, land

>

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>> With regard to the different types of bands, another doctor who is a > personal friend and an ER pediatrition as well as a research doctor > specializing in pediatrics stated that the treatments are all very > similar and one helmet isn't necessarily better then another.

Rick,

Is this the same doctor you spoke of here who thinks the homemade NOPCO band is better than the STARband? I assume not, but I wanted to clarify.

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>> With regard to the different types of bands, another doctor who is a > personal friend and an ER pediatrition as well as a research doctor > specializing in pediatrics stated that the treatments are all very > similar and one helmet isn't necessarily better then another.

Rick,

Is this the same doctor you spoke of here who thinks the homemade NOPCO band is better than the STARband? I assume not, but I wanted to clarify.

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Different doctor. This doc is/was my parents across the street

neighbor who used to work for Hasbro Childrens in Providence, now

works for Childrens Boston. With all the questions raised here I

called him to get his " inside " scoup on Dr. and NOPCO.

Youv'e already read his comments.

Rick

>

>

>

> --- In Plagiocephaly , " Rick " <richard.clemon@>

wrote:

> >

> > With regard to the different types of bands, another doctor who

is a

> > personal friend and an ER pediatrition as well as a research

doctor

> > specializing in pediatrics stated that the treatments are all

very

> > similar and one helmet isn't necessarily better then another.

>

> Rick,

>

> Is this the same doctor you spoke of here

>

<Plagiocephaly/message/137860>

who

> thinks the homemade NOPCO band is better than the STARband? I

assume

> not, but I wanted to clarify.

>

>

>

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Different doctor. This doc is/was my parents across the street

neighbor who used to work for Hasbro Childrens in Providence, now

works for Childrens Boston. With all the questions raised here I

called him to get his " inside " scoup on Dr. and NOPCO.

Youv'e already read his comments.

Rick

>

>

>

> --- In Plagiocephaly , " Rick " <richard.clemon@>

wrote:

> >

> > With regard to the different types of bands, another doctor who

is a

> > personal friend and an ER pediatrition as well as a research

doctor

> > specializing in pediatrics stated that the treatments are all

very

> > similar and one helmet isn't necessarily better then another.

>

> Rick,

>

> Is this the same doctor you spoke of here

>

<Plagiocephaly/message/137860>

who

> thinks the homemade NOPCO band is better than the STARband? I

assume

> not, but I wanted to clarify.

>

>

>

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  • 1 month later...
Guest guest

Group,

I just recently joined to learn more about LDN. I was diagnosed with

MS over 4 years ago. I started on Avonex and had several

exacerbations, so I recently switched to Rebif. My symptons are

mitigating fortunately. My main question is can I combine LDN with

Rebif? If so, what are the risks, and is anyone currently on this type

of combination therapy? Thanks for any input.

Raleigh

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Guest guest

Hi Raleigh,

No, the two are not OK together. You could use copaxone with LDN, but not

Rebif. Would you like me to send you a copy of the welcome e-mail for LDN?

Welcome to the group

Aletha

[low dose naltrexone] New To Group/Questions

> Group,

>

> I just recently joined to learn more about LDN. I was diagnosed with

> MS over 4 years ago. I started on Avonex and had several

> exacerbations, so I recently switched to Rebif. My symptons are

> mitigating fortunately. My main question is can I combine LDN with

> Rebif? If so, what are the risks, and is anyone currently on this type

> of combination therapy? Thanks for any input.

>

> Raleigh

>

>

>

>

>

>

>

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