Re: What should be our next step?

January 14, 2011

LDN (low dose naltrexone) might help. We just started it and it's been great here. My kids have a couple high virus titers.

Our biomedical journey began 6 months ago,to date we have started the GFCFSF diet, B12 shots, Mito Support, and mult supplements.We did two months on Nystatin which I think I messed up by giving grape juice during that time to get down the other supplements do so 2 weeks after she got off Nystatin the yeast was back and this time she was put on Diflucan for 30 days, she is almost done with that and the yeast seems to be under control

The last time I spoke with my Dan was in November after I received the lab results for her titers..which makes me sick to my stomach. My daughter has 6 titers that are all high..5 are between 2 and 5 and her Reballa is 385.3. When I pick up the lab results I spoke with Dr Usman who is the head Dan but wasn't my dan, she went over the labs and said that Rublla should never be so high and when I asked if we should do antiviral treatment she said that virus's can be

" tricky " and asked if I have tried the Vitamin A protocol for her measules which was 5.35, I said no and she said that it may help.

Anyway I spoke with my dan who said that she is concerned that my daughter may have a mitochondria dysfunction or a disorder based on some high/low amino acids and also because of something to do with a lactate acid test however because my daughter was on the MCT oil that lab results said to retest once we are off. She started my daughter on a mito support then, added Larix to her supplements and

changed her from B12 drops to B12 Shots.

When I called to schedule my 90 day check up I was told that my dan is turning me over to Dr Usman the head dan.I go in Feb to meet with her. I'm sorry that my post is SO long but my question is what do you think we should be doing next? We know that she has HIGH Viral titers and to be honest with all that we are on I would think I would see some HUGE gains. Since starting biomedical I have been able to get her to make more eye contact, seems to understand alittle bit more

what's going on around her and here and there does show interest books, toys and my other children however she is still doing HER thing most of the time. She has a couple words that she uses from time to time but not everyday,she doesn't commucate in anyway what she wants and the only time she cries is when one of the other kids takes a toy from her. She is still having aproblem completing even a simply task in therapy and most of the time we have a hard time keeping her in the room for therapy.She is 2.5 and I am really struggling with the diet because she is SO picky.

So I guess I'm just wondering what my next step should be? Should I let the dan guide me or should I ask to start antiviral or maybe talk about chelation? I just know that diet and supplements are not going to get her recovered. On my Assessment plan from Novemeber my dan wrote that she would like to do the Vit A protocol, and add BCCA(which I don't now what that is) and also Methione Sl

which I was told because that level is low it makes a person do the same thing over and over.

Any advise on what my next step shoud be? My daghter wasn't tested for heavy metals yet either.Again I'm sorry for the long post...it's just driving me crazy to see her like this and therapy is helping but I know that she has alot of things that are holding her back.

One more thing I don't know if the Vitamin A protocol would be a good thing because she gets a bloated belly from just 5000 iu's of Vit A and I heard that all it does is stur up yeast anyway..her high titers are on the 6 shots from the MMR and DPT.

Thanks for listening

jENNIFER

-- Toni------Mind like a steel trap...Rusty and illegal in 37 states.

January 14, 2011

LDN (low dose naltrexone) might help. We just started it and it's been great here. My kids have a couple high virus titers.

Our biomedical journey began 6 months ago,to date we have started the GFCFSF diet, B12 shots, Mito Support, and mult supplements.We did two months on Nystatin which I think I messed up by giving grape juice during that time to get down the other supplements do so 2 weeks after she got off Nystatin the yeast was back and this time she was put on Diflucan for 30 days, she is almost done with that and the yeast seems to be under control

The last time I spoke with my Dan was in November after I received the lab results for her titers..which makes me sick to my stomach. My daughter has 6 titers that are all high..5 are between 2 and 5 and her Reballa is 385.3. When I pick up the lab results I spoke with Dr Usman who is the head Dan but wasn't my dan, she went over the labs and said that Rublla should never be so high and when I asked if we should do antiviral treatment she said that virus's can be

" tricky " and asked if I have tried the Vitamin A protocol for her measules which was 5.35, I said no and she said that it may help.

Anyway I spoke with my dan who said that she is concerned that my daughter may have a mitochondria dysfunction or a disorder based on some high/low amino acids and also because of something to do with a lactate acid test however because my daughter was on the MCT oil that lab results said to retest once we are off. She started my daughter on a mito support then, added Larix to her supplements and

changed her from B12 drops to B12 Shots.

When I called to schedule my 90 day check up I was told that my dan is turning me over to Dr Usman the head dan.I go in Feb to meet with her. I'm sorry that my post is SO long but my question is what do you think we should be doing next? We know that she has HIGH Viral titers and to be honest with all that we are on I would think I would see some HUGE gains. Since starting biomedical I have been able to get her to make more eye contact, seems to understand alittle bit more

what's going on around her and here and there does show interest books, toys and my other children however she is still doing HER thing most of the time. She has a couple words that she uses from time to time but not everyday,she doesn't commucate in anyway what she wants and the only time she cries is when one of the other kids takes a toy from her. She is still having aproblem completing even a simply task in therapy and most of the time we have a hard time keeping her in the room for therapy.She is 2.5 and I am really struggling with the diet because she is SO picky.

So I guess I'm just wondering what my next step should be? Should I let the dan guide me or should I ask to start antiviral or maybe talk about chelation? I just know that diet and supplements are not going to get her recovered. On my Assessment plan from Novemeber my dan wrote that she would like to do the Vit A protocol, and add BCCA(which I don't now what that is) and also Methione Sl

which I was told because that level is low it makes a person do the same thing over and over.

Any advise on what my next step shoud be? My daghter wasn't tested for heavy metals yet either.Again I'm sorry for the long post...it's just driving me crazy to see her like this and therapy is helping but I know that she has alot of things that are holding her back.

One more thing I don't know if the Vitamin A protocol would be a good thing because she gets a bloated belly from just 5000 iu's of Vit A and I heard that all it does is stur up yeast anyway..her high titers are on the 6 shots from the MMR and DPT.

Thanks for listening

jENNIFER

-- Toni------Mind like a steel trap...Rusty and illegal in 37 states.

January 15, 2011

Thanks for the reply & taken the time to read my Long post LDN is that a natural antiviral? May I ask what kind of changes? I want to be able to offer some options for us to go down instead of my dan just telling me what to do because then it seems like I never get a chance to ask all my questions because of the "money clock". In turn I'm giving my daughter something that I haven't had the time to research.

Thanks again,

To: mb12 valtrex Sent: Sat, January 15, 2011 12:47:41 AMSubject: Re: What should be our next step?

LDN (low dose naltrexone) might help. We just started it and it's been great here. My kids have a couple high virus titers.

Our biomedical journey began 6 months ago,to date we have started the GFCFSF diet, B12 shots, Mito Support, and mult supplements.We did two months on Nystatin which I think I messed up by giving grape juice during that time to get down the other supplements do so 2 weeks after she got off Nystatin the yeast was back and this time she was put on Diflucan for 30 days, she is almost done with that and the yeast seems to be under control :)The last time I spoke with my Dan was in November after I received the lab results for her titers..which makes me sick to my stomach. My daughter has 6 titers that are all high..5 are between 2 and 5 and her Reballa is 385.3. When I pick up the lab results I spoke with Dr Usman who is the head Dan but wasn't my dan, she went over the labs and said that Rublla should never be so high and when I asked if we should do antiviral treatment she said that virus's can be"tricky" and asked if I have tried the Vitamin

A protocol for her measules which was 5.35, I said no and she said that it may help.Anyway I spoke with my dan who said that she is concerned that my daughter may have a mitochondria dysfunction or a disorder based on some high/low amino acids and also because of something to do with a lactate acid test however because my daughter was on the MCT oil that lab results said to retest once we are off. She started my daughter on a mito support then, added Larix to her supplements andchanged her from B12 drops to B12 Shots.When I called to schedule my 90 day check up I was told that my dan is turning me over to Dr Usman the head dan.I go in Feb to meet with her. I'm sorry that my post is SO long but my question is what do you think we should be doing next? We know that she has HIGH Viral titers and to be honest with all that we are on I would think I would see some HUGE gains. Since starting biomedical I have been able to get her to make

more eye contact, seems to understand alittle bit morewhat's going on around her and here and there does show interest books, toys and my other children however she is still doing HER thing most of the time. She has a couple words that she uses from time to time but not everyday,she doesn't commucate in anyway what she wants and the only time she cries is when one of the other kids takes a toy from her. She is still having aproblem completing even a simply task in therapy and most of the time we have a hard time keeping her in the room for therapy.She is 2.5 and I am really struggling with the diet because she is SO picky.So I guess I'm just wondering what my next step should be? Should I let the dan guide me or should I ask to start antiviral or maybe talk about chelation? I just know that diet and supplements are not going to get her recovered. On my Assessment plan from Novemeber my dan wrote that she would like to do the Vit A protocol,

and add BCCA(which I don't now what that is) and also Methione Slwhich I was told because that level is low it makes a person do the same thing over and over.Any advise on what my next step shoud be? My daghter wasn't tested for heavy metals yet either.Again I'm sorry for the long post...it's just driving me crazy to see her like this and therapy is helping but I know that she has alot of things that are holding her back.One more thing I don't know if the Vitamin A protocol would be a good thing because she gets a bloated belly from just 5000 iu's of Vit A and I heard that all it does is stur up yeast anyway..her high titers are on the 6 shots from the MMR and DPT.Thanks for listening jENNIFER

-- Toni------Mind like a steel trap...Rusty and illegal in 37 states.

January 15, 2011

Thanks for the reply & taken the time to read my Long post LDN is that a natural antiviral? May I ask what kind of changes? I want to be able to offer some options for us to go down instead of my dan just telling me what to do because then it seems like I never get a chance to ask all my questions because of the "money clock". In turn I'm giving my daughter something that I haven't had the time to research.

Thanks again,

To: mb12 valtrex Sent: Sat, January 15, 2011 12:47:41 AMSubject: Re: What should be our next step?

LDN (low dose naltrexone) might help. We just started it and it's been great here. My kids have a couple high virus titers.

Our biomedical journey began 6 months ago,to date we have started the GFCFSF diet, B12 shots, Mito Support, and mult supplements.We did two months on Nystatin which I think I messed up by giving grape juice during that time to get down the other supplements do so 2 weeks after she got off Nystatin the yeast was back and this time she was put on Diflucan for 30 days, she is almost done with that and the yeast seems to be under control :)The last time I spoke with my Dan was in November after I received the lab results for her titers..which makes me sick to my stomach. My daughter has 6 titers that are all high..5 are between 2 and 5 and her Reballa is 385.3. When I pick up the lab results I spoke with Dr Usman who is the head Dan but wasn't my dan, she went over the labs and said that Rublla should never be so high and when I asked if we should do antiviral treatment she said that virus's can be"tricky" and asked if I have tried the Vitamin

A protocol for her measules which was 5.35, I said no and she said that it may help.Anyway I spoke with my dan who said that she is concerned that my daughter may have a mitochondria dysfunction or a disorder based on some high/low amino acids and also because of something to do with a lactate acid test however because my daughter was on the MCT oil that lab results said to retest once we are off. She started my daughter on a mito support then, added Larix to her supplements andchanged her from B12 drops to B12 Shots.When I called to schedule my 90 day check up I was told that my dan is turning me over to Dr Usman the head dan.I go in Feb to meet with her. I'm sorry that my post is SO long but my question is what do you think we should be doing next? We know that she has HIGH Viral titers and to be honest with all that we are on I would think I would see some HUGE gains. Since starting biomedical I have been able to get her to make

more eye contact, seems to understand alittle bit morewhat's going on around her and here and there does show interest books, toys and my other children however she is still doing HER thing most of the time. She has a couple words that she uses from time to time but not everyday,she doesn't commucate in anyway what she wants and the only time she cries is when one of the other kids takes a toy from her. She is still having aproblem completing even a simply task in therapy and most of the time we have a hard time keeping her in the room for therapy.She is 2.5 and I am really struggling with the diet because she is SO picky.So I guess I'm just wondering what my next step should be? Should I let the dan guide me or should I ask to start antiviral or maybe talk about chelation? I just know that diet and supplements are not going to get her recovered. On my Assessment plan from Novemeber my dan wrote that she would like to do the Vit A protocol,

and add BCCA(which I don't now what that is) and also Methione Slwhich I was told because that level is low it makes a person do the same thing over and over.Any advise on what my next step shoud be? My daghter wasn't tested for heavy metals yet either.Again I'm sorry for the long post...it's just driving me crazy to see her like this and therapy is helping but I know that she has alot of things that are holding her back.One more thing I don't know if the Vitamin A protocol would be a good thing because she gets a bloated belly from just 5000 iu's of Vit A and I heard that all it does is stur up yeast anyway..her high titers are on the 6 shots from the MMR and DPT.Thanks for listening jENNIFER

-- Toni------Mind like a steel trap...Rusty and illegal in 37 states.

January 15, 2011

Thanks for the reply & taken the time to read my Long post LDN is that a natural antiviral? May I ask what kind of changes? I want to be able to offer some options for us to go down instead of my dan just telling me what to do because then it seems like I never get a chance to ask all my questions because of the "money clock". In turn I'm giving my daughter something that I haven't had the time to research.

Thanks again,

To: mb12 valtrex Sent: Sat, January 15, 2011 12:47:41 AMSubject: Re: What should be our next step?

LDN (low dose naltrexone) might help. We just started it and it's been great here. My kids have a couple high virus titers.

Our biomedical journey began 6 months ago,to date we have started the GFCFSF diet, B12 shots, Mito Support, and mult supplements.We did two months on Nystatin which I think I messed up by giving grape juice during that time to get down the other supplements do so 2 weeks after she got off Nystatin the yeast was back and this time she was put on Diflucan for 30 days, she is almost done with that and the yeast seems to be under control :)The last time I spoke with my Dan was in November after I received the lab results for her titers..which makes me sick to my stomach. My daughter has 6 titers that are all high..5 are between 2 and 5 and her Reballa is 385.3. When I pick up the lab results I spoke with Dr Usman who is the head Dan but wasn't my dan, she went over the labs and said that Rublla should never be so high and when I asked if we should do antiviral treatment she said that virus's can be"tricky" and asked if I have tried the Vitamin

A protocol for her measules which was 5.35, I said no and she said that it may help.Anyway I spoke with my dan who said that she is concerned that my daughter may have a mitochondria dysfunction or a disorder based on some high/low amino acids and also because of something to do with a lactate acid test however because my daughter was on the MCT oil that lab results said to retest once we are off. She started my daughter on a mito support then, added Larix to her supplements andchanged her from B12 drops to B12 Shots.When I called to schedule my 90 day check up I was told that my dan is turning me over to Dr Usman the head dan.I go in Feb to meet with her. I'm sorry that my post is SO long but my question is what do you think we should be doing next? We know that she has HIGH Viral titers and to be honest with all that we are on I would think I would see some HUGE gains. Since starting biomedical I have been able to get her to make

more eye contact, seems to understand alittle bit morewhat's going on around her and here and there does show interest books, toys and my other children however she is still doing HER thing most of the time. She has a couple words that she uses from time to time but not everyday,she doesn't commucate in anyway what she wants and the only time she cries is when one of the other kids takes a toy from her. She is still having aproblem completing even a simply task in therapy and most of the time we have a hard time keeping her in the room for therapy.She is 2.5 and I am really struggling with the diet because she is SO picky.So I guess I'm just wondering what my next step should be? Should I let the dan guide me or should I ask to start antiviral or maybe talk about chelation? I just know that diet and supplements are not going to get her recovered. On my Assessment plan from Novemeber my dan wrote that she would like to do the Vit A protocol,

and add BCCA(which I don't now what that is) and also Methione Slwhich I was told because that level is low it makes a person do the same thing over and over.Any advise on what my next step shoud be? My daghter wasn't tested for heavy metals yet either.Again I'm sorry for the long post...it's just driving me crazy to see her like this and therapy is helping but I know that she has alot of things that are holding her back.One more thing I don't know if the Vitamin A protocol would be a good thing because she gets a bloated belly from just 5000 iu's of Vit A and I heard that all it does is stur up yeast anyway..her high titers are on the 6 shots from the MMR and DPT.Thanks for listening jENNIFER

-- Toni------Mind like a steel trap...Rusty and illegal in 37 states.

January 15, 2011

,

I'm not sure I'd start the Vitamin A protocol w/o the dan because of her bloating on smaller doses - you may have to address possible gut issues first. If it were me, I'd probably find a good enzyme, a good probiotic, get some good antioxidents flowing into her and start a natural antiviral low and slow. The natural may or may not turn out to be enough for her, but between the antioxidants and the natural, it'll get her off to a good start. I'm going to sing 's song here and tell you that getting nutrient-rich foods into her is probably the best thing you can do for her right now. Don't give up. You'll get there!

-Tammy

To: mb12 valtrex Sent: Sat, January 15, 2011 1:11:10 AMSubject: What should be our next step?

Our biomedical journey began 6 months ago,to date we have started the GFCFSF diet, B12 shots, Mito Support, and mult supplements.We did two months on Nystatin which I think I messed up by giving grape juice during that time to get down the other supplements do so 2 weeks after she got off Nystatin the yeast was back and this time she was put on Diflucan for 30 days, she is almost done with that and the yeast seems to be under control :)The last time I spoke with my Dan was in November after I received the lab results for her titers..which makes me sick to my stomach. My daughter has 6 titers that are all high..5 are between 2 and 5 and her Reballa is 385.3. When I pick up the lab results I spoke with Dr Usman who is the head Dan but wasn't my dan, she went over the labs and said that Rublla should never be so high and when I asked if we should do antiviral treatment she said that virus's can be"tricky" and asked if I have tried the Vitamin

A protocol for her measules which was 5.35, I said no and she said that it may help.Anyway I spoke with my dan who said that she is concerned that my daughter may have a mitochondria dysfunction or a disorder based on some high/low amino acids and also because of something to do with a lactate acid test however because my daughter was on the MCT oil that lab results said to retest once we are off. She started my daughter on a mito support then, added Larix to her supplements andchanged her from B12 drops to B12 Shots.When I called to schedule my 90 day check up I was told that my dan is turning me over to Dr Usman the head dan.I go in Feb to meet with her. I'm sorry that my post is SO long but my question is what do you think we should be doing next? We know that she has HIGH Viral titers and to be honest with all that we are on I would think I would see some HUGE gains. Since starting biomedical I have been able to get her to make

more eye contact, seems to understand alittle bit morewhat's going on around her and here and there does show interest books, toys and my other children however she is still doing HER thing most of the time. She has a couple words that she uses from time to time but not everyday,she doesn't commucate in anyway what she wants and the only time she cries is when one of the other kids takes a toy from her. She is still having aproblem completing even a simply task in therapy and most of the time we have a hard time keeping her in the room for therapy.She is 2.5 and I am really struggling with the diet because she is SO picky.So I guess I'm just wondering what my next step should be? Should I let the dan guide me or should I ask to start antiviral or maybe talk about chelation? I just know that diet and supplements are not going to get her recovered. On my Assessment plan from Novemeber my dan wrote that she would like to do the Vit A protocol,

and add BCCA(which I don't now what that is) and also Methione Slwhich I was told because that level is low it makes a person do the same thing over and over.Any advise on what my next step shoud be? My daghter wasn't tested for heavy metals yet either.Again I'm sorry for the long post...it's just driving me crazy to see her like this and therapy is helping but I know that she has alot of things that are holding her back.One more thing I don't know if the Vitamin A protocol would be a good thing because she gets a bloated belly from just 5000 iu's of Vit A and I heard that all it does is stur up yeast anyway..her high titers are on the 6 shots from the MMR and DPT.Thanks for listening jENNIFER

January 15, 2011

,

I'm not sure I'd start the Vitamin A protocol w/o the dan because of her bloating on smaller doses - you may have to address possible gut issues first. If it were me, I'd probably find a good enzyme, a good probiotic, get some good antioxidents flowing into her and start a natural antiviral low and slow. The natural may or may not turn out to be enough for her, but between the antioxidants and the natural, it'll get her off to a good start. I'm going to sing 's song here and tell you that getting nutrient-rich foods into her is probably the best thing you can do for her right now. Don't give up. You'll get there!

-Tammy

To: mb12 valtrex Sent: Sat, January 15, 2011 1:11:10 AMSubject: What should be our next step?

Our biomedical journey began 6 months ago,to date we have started the GFCFSF diet, B12 shots, Mito Support, and mult supplements.We did two months on Nystatin which I think I messed up by giving grape juice during that time to get down the other supplements do so 2 weeks after she got off Nystatin the yeast was back and this time she was put on Diflucan for 30 days, she is almost done with that and the yeast seems to be under control :)The last time I spoke with my Dan was in November after I received the lab results for her titers..which makes me sick to my stomach. My daughter has 6 titers that are all high..5 are between 2 and 5 and her Reballa is 385.3. When I pick up the lab results I spoke with Dr Usman who is the head Dan but wasn't my dan, she went over the labs and said that Rublla should never be so high and when I asked if we should do antiviral treatment she said that virus's can be"tricky" and asked if I have tried the Vitamin

A protocol for her measules which was 5.35, I said no and she said that it may help.Anyway I spoke with my dan who said that she is concerned that my daughter may have a mitochondria dysfunction or a disorder based on some high/low amino acids and also because of something to do with a lactate acid test however because my daughter was on the MCT oil that lab results said to retest once we are off. She started my daughter on a mito support then, added Larix to her supplements andchanged her from B12 drops to B12 Shots.When I called to schedule my 90 day check up I was told that my dan is turning me over to Dr Usman the head dan.I go in Feb to meet with her. I'm sorry that my post is SO long but my question is what do you think we should be doing next? We know that she has HIGH Viral titers and to be honest with all that we are on I would think I would see some HUGE gains. Since starting biomedical I have been able to get her to make

more eye contact, seems to understand alittle bit morewhat's going on around her and here and there does show interest books, toys and my other children however she is still doing HER thing most of the time. She has a couple words that she uses from time to time but not everyday,she doesn't commucate in anyway what she wants and the only time she cries is when one of the other kids takes a toy from her. She is still having aproblem completing even a simply task in therapy and most of the time we have a hard time keeping her in the room for therapy.She is 2.5 and I am really struggling with the diet because she is SO picky.So I guess I'm just wondering what my next step should be? Should I let the dan guide me or should I ask to start antiviral or maybe talk about chelation? I just know that diet and supplements are not going to get her recovered. On my Assessment plan from Novemeber my dan wrote that she would like to do the Vit A protocol,

and add BCCA(which I don't now what that is) and also Methione Slwhich I was told because that level is low it makes a person do the same thing over and over.Any advise on what my next step shoud be? My daghter wasn't tested for heavy metals yet either.Again I'm sorry for the long post...it's just driving me crazy to see her like this and therapy is helping but I know that she has alot of things that are holding her back.One more thing I don't know if the Vitamin A protocol would be a good thing because she gets a bloated belly from just 5000 iu's of Vit A and I heard that all it does is stur up yeast anyway..her high titers are on the 6 shots from the MMR and DPT.Thanks for listening jENNIFER

January 15, 2011

Is all those things getting to the root of the problem? I have to

tell you,I have spent 11 years going doctor to doctor for my

son.Going to ones I thought where the best. Including a Dan doc. for

9 years(he was always in the background).I still thought a Dan

doctor was appropriate along with biomedical.I chose Dr. Usmans

office(they all work together in her office,supposedly).I talked to

2 nurses and they insisted my son was just like the other patients

they have gotten well.My son has extreme reactions to

everything!They still thought he is a perfect fit. So Nov.9,2010 I

drove my son to there office for the appt.. Guess what,I ended up

leaving with 10 different natural therapies.I thought I would give

them the benefit of the doubt ,so I tried there treatment

protocol.Well,my son reacted to everything severely just as I told

the docs would happen.They suggested to start them slower.I did one

every 5 days.The docs where never available.They might call you the

next day or maybe 3 days later.And maybe they had consulted with the

docs and maybe not. It finally came down to my son being so sick

that he needed to be in the hospital.They finaly were convinced that

I needed a phone appt. I waited my week.Had the phone appt..The only

suggested thing to do was to stop everything.They didn't have all

the most important blood work.The appt. was a waste($225.00).They

did not know what to do.And left on vacation(for 2 weeks) and told

me nothing.I received a phone call after that and they said "I can't

help your son.He can't do the naturals we need him on".They had no

referrals for me and no ideas where to go from there. Neadless to

say,$1200.00 later and my son even sicker,I will never refer any one

to that office. I went to Dr. Jan.12,2011. For NIDS

treatment and he seems to understand a lot more on what is going

on.He talks about the root of the problem,not just the symptoms.I

think he is right on.Good luck on your decision. If you would like

to talk please call Tammy F.(785)842-1725.

Our biomedical journey began 6 months ago,to date we have

started the GFCFSF diet, B12 shots, Mito Support, and mult

supplements.We did two months on Nystatin which I think I

messed up by giving grape juice during that time to get

down the other supplements do so 2 weeks after she got off

Nystatin the yeast was back and this time she was put on

Diflucan for 30 days, she is almost done with that and the

yeast seems to be under control

The last time I spoke with my Dan was in November after I

received the lab results for her titers..which makes me

sick to my stomach. My daughter has 6 titers that are all

high..5 are between 2 and 5 and her Reballa is 385.3. When

I pick up the lab results I spoke with Dr Usman who is the

head Dan but wasn't my dan, she went over the labs and

said that Rublla should never be so high and when I asked

if we should do antiviral treatment she said that virus's

can be

"tricky" and asked if I have tried the Vitamin A protocol

for her measules which was 5.35, I said no and she said

that it may help.

Anyway I spoke with my dan who said that she is concerned

that my daughter may have a mitochondria dysfunction or a

disorder based on some high/low amino acids and also

because of something to do with a lactate acid test

however because my daughter was on the MCT oil that lab

results said to retest once we are off. She started my

daughter on a mito support then, added Larix to her

supplements and

changed her from B12 drops to B12 Shots.

When I called to schedule my 90 day check up I was told

that my dan is turning me over to Dr Usman the head dan.I

go in Feb to meet with her. I'm sorry that my post is SO

long but my question is what do you think we should be

doing next? We know that she has HIGH Viral titers and to

be honest with all that we are on I would think I would

see some HUGE gains. Since starting biomedical I have been

able to get her to make more eye contact, seems to

understand alittle bit more

what's going on around her and here and there does show

interest books, toys and my other children however she is

still doing HER thing most of the time. She has a couple

words that she uses from time to time but not everyday,she

doesn't commucate in anyway what she wants and the only

time she cries is when one of the other kids takes a toy

from her. She is still having aproblem completing even a

simply task in therapy and most of the time we have a hard

time keeping her in the room for therapy.She is 2.5 and I

am really struggling with the diet because she is SO

picky.

So I guess I'm just wondering what my next step should be?

Should I let the dan guide me or should I ask to start

antiviral or maybe talk about chelation? I just know that

diet and supplements are not going to get her recovered.

On my Assessment plan from Novemeber my dan wrote that she

would like to do the Vit A protocol, and add BCCA(which I

don't now what that is) and also Methione Sl

which I was told because that level is low it makes a

person do the same thing over and over.

Any advise on what my next step shoud be? My daghter

wasn't tested for heavy metals yet either.Again I'm sorry

for the long post...it's just driving me crazy to see her

like this and therapy is helping but I know that she has

alot of things that are holding her back.

One more thing I don't know if the Vitamin A protocol

would be a good thing because she gets a bloated belly

from just 5000 iu's of Vit A and I heard that all it does

is stur up yeast anyway..her high titers are on the 6

shots from the MMR and DPT.

Thanks for listening

jENNIFER

January 15, 2011