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Hi Bonnie,

A very warm welcome to you! I am glad you found this group. There are a

couple of us who have done Cellcept. I just got off of it after a three month

try. Unfortunately, it did not work for me, but Rita is having more success

with it than I did.

Please keep us informed on how it is going for you. Do you know what dose of

Cellcept you will be on? I really pray you will get good results.

Welcome again Bonnie,

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Hi Bonnie,

A very warm welcome to you! I am glad you found this group. There are a

couple of us who have done Cellcept. I just got off of it after a three month

try. Unfortunately, it did not work for me, but Rita is having more success

with it than I did.

Please keep us informed on how it is going for you. Do you know what dose of

Cellcept you will be on? I really pray you will get good results.

Welcome again Bonnie,

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my Neph used the Mayo clinic research to make up the treatment plan, but I

was not an official part of the study.

I had severe problems with nausea on the higher dose, and it was still a

problem, although less of a problem, on the lower dose. I stayed on the higher

dose for a month and a half, then the lower dose the second month and a half.

My anemia also got worse on the Cellcept leaving me feeling pretty wiped out.

Exercise was SO hard, harder than it has been all these years with IgAN.

I hesitate to tell you all this because I don't want to discourage you from

something that may work well for you, but it is the honest truth since you

asked. About all I could do was get through work every day, but I persevered

and

made it through. It had been helping me, I would have continued on it beyond

the three months (which just ended June 2nd), but since my creatinine was just

rising, it was not worth the side effects to stay on it.

I really hope it helps you though! I just seem to be very sensitive to side

effects of medications.

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Hi Bonnie, Welcome to the group, I'm happy you found us. I don't know

anything about the Mayo Clinic study but good luck with getting into it. I

know studies like that can help many once completed. Welcome again!

Amy

New to you

> Hello everyone, I was recently diagnosed with Ig A. Am now doing quite

well. Creat. and protein stable as well as B/P (finally). Was wondering if

anyone out there is enrolled in the Ig A study with Cellcept through Mayo

Clinic etc. If so, how are things going? I am in the preliminary phase

currently. Will change from my usual dose of Altace (20mg/day) to

Lisinopril (uncertain dose) within the week. Then continue on for 3 months

and if proteinuria goes down enough (<0.6 grams/24 hours) will stay on that

regime (with Avapro, HCTZ, and 12.5 grams of fish oil/day. I don't look

forward to changing to Lisinopril because I am doing so well on Altace, but

that is part of the study protocol. Please give me a holler if you have

been involved with the study, or know anyone who is participating. Thanks!

Anyother words of wisdom would be helpful as well. Bonnie

>

>

>

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Hi Bonnie, Welcome to the group, I'm happy you found us. I don't know

anything about the Mayo Clinic study but good luck with getting into it. I

know studies like that can help many once completed. Welcome again!

Amy

New to you

> Hello everyone, I was recently diagnosed with Ig A. Am now doing quite

well. Creat. and protein stable as well as B/P (finally). Was wondering if

anyone out there is enrolled in the Ig A study with Cellcept through Mayo

Clinic etc. If so, how are things going? I am in the preliminary phase

currently. Will change from my usual dose of Altace (20mg/day) to

Lisinopril (uncertain dose) within the week. Then continue on for 3 months

and if proteinuria goes down enough (<0.6 grams/24 hours) will stay on that

regime (with Avapro, HCTZ, and 12.5 grams of fish oil/day. I don't look

forward to changing to Lisinopril because I am doing so well on Altace, but

that is part of the study protocol. Please give me a holler if you have

been involved with the study, or know anyone who is participating. Thanks!

Anyother words of wisdom would be helpful as well. Bonnie

>

>

>

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Hi Bonnie, Welcome to the group, I'm happy you found us. I don't know

anything about the Mayo Clinic study but good luck with getting into it. I

know studies like that can help many once completed. Welcome again!

Amy

New to you

> Hello everyone, I was recently diagnosed with Ig A. Am now doing quite

well. Creat. and protein stable as well as B/P (finally). Was wondering if

anyone out there is enrolled in the Ig A study with Cellcept through Mayo

Clinic etc. If so, how are things going? I am in the preliminary phase

currently. Will change from my usual dose of Altace (20mg/day) to

Lisinopril (uncertain dose) within the week. Then continue on for 3 months

and if proteinuria goes down enough (<0.6 grams/24 hours) will stay on that

regime (with Avapro, HCTZ, and 12.5 grams of fish oil/day. I don't look

forward to changing to Lisinopril because I am doing so well on Altace, but

that is part of the study protocol. Please give me a holler if you have

been involved with the study, or know anyone who is participating. Thanks!

Anyother words of wisdom would be helpful as well. Bonnie

>

>

>

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, thanks for your very quick response. I'm curious what type of problems

did you have with the Cellcept? Was it associated with the Mayo study, or did

your nephrol. prescribe it? Thanks Bonnie

W4JC@... wrote:Hi Bonnie,

A very warm welcome to you! I am glad you found this group. There are a

couple of us who have done Cellcept. I just got off of it after a three month

try. Unfortunately, it did not work for me, but Rita is having more success

with it than I did.

Please keep us informed on how it is going for you. Do you know what dose of

Cellcept you will be on? I really pray you will get good results.

Welcome again Bonnie,

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, thanks for your very quick response. I'm curious what type of problems

did you have with the Cellcept? Was it associated with the Mayo study, or did

your nephrol. prescribe it? Thanks Bonnie

W4JC@... wrote:Hi Bonnie,

A very warm welcome to you! I am glad you found this group. There are a

couple of us who have done Cellcept. I just got off of it after a three month

try. Unfortunately, it did not work for me, but Rita is having more success

with it than I did.

Please keep us informed on how it is going for you. Do you know what dose of

Cellcept you will be on? I really pray you will get good results.

Welcome again Bonnie,

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Guest guest

, thanks for your very quick response. I'm curious what type of problems

did you have with the Cellcept? Was it associated with the Mayo study, or did

your nephrol. prescribe it? Thanks Bonnie

W4JC@... wrote:Hi Bonnie,

A very warm welcome to you! I am glad you found this group. There are a

couple of us who have done Cellcept. I just got off of it after a three month

try. Unfortunately, it did not work for me, but Rita is having more success

with it than I did.

Please keep us informed on how it is going for you. Do you know what dose of

Cellcept you will be on? I really pray you will get good results.

Welcome again Bonnie,

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Welcome to the group. I hope you find it as comforting as I do to

have such a wonderful group of people supporting you.

I am not on a " study " but I have been taking Cyclosporine, which I

think is the same as cellcept? I have been on it for 4 months. I

have very high proteinuria 6000+ and so far it hasn't seemed to work

for me. I hope you have better success.

Jill

> Hello everyone, I was recently diagnosed with Ig A. Am now doing

quite well. Creat. and protein stable as well as B/P (finally).

Was wondering if anyone out there is enrolled in the Ig A study with

Cellcept through Mayo Clinic etc. If so, how are things going? I

am in the preliminary phase currently. Will change from my usual

dose of Altace (20mg/day) to Lisinopril (uncertain dose) within the

week. Then continue on for 3 months and if proteinuria goes down

enough (<0.6 grams/24 hours) will stay on that regime (with Avapro,

HCTZ, and 12.5 grams of fish oil/day. I don't look forward to

changing to Lisinopril because I am doing so well on Altace, but

that is part of the study protocol. Please give me a holler if you

have been involved with the study, or know anyone who is

participating. Thanks! Anyother words of wisdom would be helpful

as well. Bonnie

>

>

>

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Guest guest

Oops, my bad, I thought they were the same, it sounded familiar to

me for some reason. Sorry for the confusion!

> Hi Jill,

>

> Cyclosporin and Cellcept are two different drugs. I have not ever

been on

> Cyclosporin though and don't know too much about it.

>

>

>

>

>

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Guest guest

Oops, my bad, I thought they were the same, it sounded familiar to

me for some reason. Sorry for the confusion!

> Hi Jill,

>

> Cyclosporin and Cellcept are two different drugs. I have not ever

been on

> Cyclosporin though and don't know too much about it.

>

>

>

>

>

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Guest guest

Oops, my bad, I thought they were the same, it sounded familiar to

me for some reason. Sorry for the confusion!

> Hi Jill,

>

> Cyclosporin and Cellcept are two different drugs. I have not ever

been on

> Cyclosporin though and don't know too much about it.

>

>

>

>

>

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Bonnie,

Just curious - who is your neph. in Colorado?

Betsy

> Hi Rita, Thank you for your quick response.  I am beginning to love

> this site more and more every day.  To access information at Mayo: 

> www.mayoclinic.org   then go to Rochester,  then Clinical Trials, then

> Kidney and Urology.  There's a lot more information within this site. 

> Kinda fun to " tour " around and see what's happening in the world of

> nephrology as well as research.  Mayo at Rochester has 37

> nephrologists, and I absolutely think my Neph is great (Dr.

> Fernenza).  I am so grateful to be referred to the " best in the

> world. "   (Although I really believe my Neph in Colorado is the best in

> the area as well)  I have been to Mayo 3 times in the past 5 weeks,

> but don't have to go back for a month now.  Hope to hear from you

> periodically.  Thanks again for responding, especially so quickly. 

> Bonnie

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Bonnie,

Just curious - who is your neph. in Colorado?

Betsy

> Hi Rita, Thank you for your quick response.  I am beginning to love

> this site more and more every day.  To access information at Mayo: 

> www.mayoclinic.org   then go to Rochester,  then Clinical Trials, then

> Kidney and Urology.  There's a lot more information within this site. 

> Kinda fun to " tour " around and see what's happening in the world of

> nephrology as well as research.  Mayo at Rochester has 37

> nephrologists, and I absolutely think my Neph is great (Dr.

> Fernenza).  I am so grateful to be referred to the " best in the

> world. "   (Although I really believe my Neph in Colorado is the best in

> the area as well)  I have been to Mayo 3 times in the past 5 weeks,

> but don't have to go back for a month now.  Hope to hear from you

> periodically.  Thanks again for responding, especially so quickly. 

> Bonnie

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Bonnie,

Just curious - who is your neph. in Colorado?

Betsy

> Hi Rita, Thank you for your quick response.  I am beginning to love

> this site more and more every day.  To access information at Mayo: 

> www.mayoclinic.org   then go to Rochester,  then Clinical Trials, then

> Kidney and Urology.  There's a lot more information within this site. 

> Kinda fun to " tour " around and see what's happening in the world of

> nephrology as well as research.  Mayo at Rochester has 37

> nephrologists, and I absolutely think my Neph is great (Dr.

> Fernenza).  I am so grateful to be referred to the " best in the

> world. "   (Although I really believe my Neph in Colorado is the best in

> the area as well)  I have been to Mayo 3 times in the past 5 weeks,

> but don't have to go back for a month now.  Hope to hear from you

> periodically.  Thanks again for responding, especially so quickly. 

> Bonnie

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Betsy, I have Dr. Harberts, and Dr. Stanley Sicher. Are you from Colorado

too?

Betsy Cabell wrote:Bonnie,

Just curious - who is your neph. in Colorado?

Betsy

> Hi Rita, Thank you for your quick response. I am beginning to love

> this site more and more every day. To access information at Mayo:

> www.mayoclinic.org then go to Rochester, then Clinical Trials, then

> Kidney and Urology. There's a lot more information within this site..

> Kinda fun to " tour " around and see what's happening in the world of

> nephrology as well as research. Mayo at Rochester has 37

> nephrologists, and I absolutely think my Neph is great (Dr.

> Fernenza). I am so grateful to be referred to the " best in the

> world. " (Although I really believe my Neph in Colorado is the best in

> the area as well) I have been to Mayo 3 times in the past 5 weeks,

> but don't have to go back for a month now. Hope to hear from you

> periodically. Thanks again for responding, especially so quickly.

> Bonnie

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I feel silly, in that I spelled Dr. Fervenza's name incorrectly below. Sorry to

all. Big OOPS, I get thinking and typing and make mistakes and forget to spell

check. Bonnie

Betsy Cabell wrote:Bonnie,

Just curious - who is your neph. in Colorado?

Betsy

> Hi Rita, Thank you for your quick response. I am beginning to love

> this site more and more every day. To access information at Mayo:

> www.mayoclinic.org then go to Rochester, then Clinical Trials, then

> Kidney and Urology. There's a lot more information within this site..

> Kinda fun to " tour " around and see what's happening in the world of

> nephrology as well as research. Mayo at Rochester has 37

> nephrologists, and I absolutely think my Neph is great (Dr.

> Fernenza). I am so grateful to be referred to the " best in the

> world. " (Although I really believe my Neph in Colorado is the best in

> the area as well) I have been to Mayo 3 times in the past 5 weeks,

> but don't have to go back for a month now. Hope to hear from you

> periodically. Thanks again for responding, especially so quickly.

> Bonnie

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I feel silly, in that I spelled Dr. Fervenza's name incorrectly below. Sorry to

all. Big OOPS, I get thinking and typing and make mistakes and forget to spell

check. Bonnie

Betsy Cabell wrote:Bonnie,

Just curious - who is your neph. in Colorado?

Betsy

> Hi Rita, Thank you for your quick response. I am beginning to love

> this site more and more every day. To access information at Mayo:

> www.mayoclinic.org then go to Rochester, then Clinical Trials, then

> Kidney and Urology. There's a lot more information within this site..

> Kinda fun to " tour " around and see what's happening in the world of

> nephrology as well as research. Mayo at Rochester has 37

> nephrologists, and I absolutely think my Neph is great (Dr.

> Fernenza). I am so grateful to be referred to the " best in the

> world. " (Although I really believe my Neph in Colorado is the best in

> the area as well) I have been to Mayo 3 times in the past 5 weeks,

> but don't have to go back for a month now. Hope to hear from you

> periodically. Thanks again for responding, especially so quickly.

> Bonnie

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I feel silly, in that I spelled Dr. Fervenza's name incorrectly below. Sorry to

all. Big OOPS, I get thinking and typing and make mistakes and forget to spell

check. Bonnie

Betsy Cabell wrote:Bonnie,

Just curious - who is your neph. in Colorado?

Betsy

> Hi Rita, Thank you for your quick response. I am beginning to love

> this site more and more every day. To access information at Mayo:

> www.mayoclinic.org then go to Rochester, then Clinical Trials, then

> Kidney and Urology. There's a lot more information within this site..

> Kinda fun to " tour " around and see what's happening in the world of

> nephrology as well as research. Mayo at Rochester has 37

> nephrologists, and I absolutely think my Neph is great (Dr.

> Fernenza). I am so grateful to be referred to the " best in the

> world. " (Although I really believe my Neph in Colorado is the best in

> the area as well) I have been to Mayo 3 times in the past 5 weeks,

> but don't have to go back for a month now. Hope to hear from you

> periodically. Thanks again for responding, especially so quickly.

> Bonnie

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Hey Bonnie I'm in Colorado too, just East of Colorado Springs. :o) I see

Dr. Brad Yuan, great guy and great with my kids which is a big plus for me.

I love his support staff too. If there is one thing that will turn me off

of a good doctor it's a rude or insensitive support staff.

Amy

Re: New to you

> Betsy, I have Dr. Harberts, and Dr. Stanley Sicher. Are you from

Colorado too?

>

> Betsy Cabell wrote:Bonnie,

> Just curious - who is your neph. in Colorado?

>

> Betsy

>

>

>

> > Hi Rita, Thank you for your quick response. I am beginning to love

> > this site more and more every day. To access information at Mayo:

> > www.mayoclinic.org then go to Rochester, then Clinical Trials, then

> > Kidney and Urology. There's a lot more information within this site..

> > Kinda fun to " tour " around and see what's happening in the world of

> > nephrology as well as research. Mayo at Rochester has 37

> > nephrologists, and I absolutely think my Neph is great (Dr.

> > Fernenza). I am so grateful to be referred to the " best in the

> > world. " (Although I really believe my Neph in Colorado is the best in

> > the area as well) I have been to Mayo 3 times in the past 5 weeks,

> > but don't have to go back for a month now. Hope to hear from you

> > periodically. Thanks again for responding, especially so quickly.

> > Bonnie

>

>

>

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Hey Bonnie I'm in Colorado too, just East of Colorado Springs. :o) I see

Dr. Brad Yuan, great guy and great with my kids which is a big plus for me.

I love his support staff too. If there is one thing that will turn me off

of a good doctor it's a rude or insensitive support staff.

Amy

Re: New to you

> Betsy, I have Dr. Harberts, and Dr. Stanley Sicher. Are you from

Colorado too?

>

> Betsy Cabell wrote:Bonnie,

> Just curious - who is your neph. in Colorado?

>

> Betsy

>

>

>

> > Hi Rita, Thank you for your quick response. I am beginning to love

> > this site more and more every day. To access information at Mayo:

> > www.mayoclinic.org then go to Rochester, then Clinical Trials, then

> > Kidney and Urology. There's a lot more information within this site..

> > Kinda fun to " tour " around and see what's happening in the world of

> > nephrology as well as research. Mayo at Rochester has 37

> > nephrologists, and I absolutely think my Neph is great (Dr.

> > Fernenza). I am so grateful to be referred to the " best in the

> > world. " (Although I really believe my Neph in Colorado is the best in

> > the area as well) I have been to Mayo 3 times in the past 5 weeks,

> > but don't have to go back for a month now. Hope to hear from you

> > periodically. Thanks again for responding, especially so quickly.

> > Bonnie

>

>

>

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Guest guest

Hey Bonnie I'm in Colorado too, just East of Colorado Springs. :o) I see

Dr. Brad Yuan, great guy and great with my kids which is a big plus for me.

I love his support staff too. If there is one thing that will turn me off

of a good doctor it's a rude or insensitive support staff.

Amy

Re: New to you

> Betsy, I have Dr. Harberts, and Dr. Stanley Sicher. Are you from

Colorado too?

>

> Betsy Cabell wrote:Bonnie,

> Just curious - who is your neph. in Colorado?

>

> Betsy

>

>

>

> > Hi Rita, Thank you for your quick response. I am beginning to love

> > this site more and more every day. To access information at Mayo:

> > www.mayoclinic.org then go to Rochester, then Clinical Trials, then

> > Kidney and Urology. There's a lot more information within this site..

> > Kinda fun to " tour " around and see what's happening in the world of

> > nephrology as well as research. Mayo at Rochester has 37

> > nephrologists, and I absolutely think my Neph is great (Dr.

> > Fernenza). I am so grateful to be referred to the " best in the

> > world. " (Although I really believe my Neph in Colorado is the best in

> > the area as well) I have been to Mayo 3 times in the past 5 weeks,

> > but don't have to go back for a month now. Hope to hear from you

> > periodically. Thanks again for responding, especially so quickly.

> > Bonnie

>

>

>

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Guest guest

We are in the Denver area (Centennial). My son has IgAN and goes to the

Renal Transplant Clinic at University Hospital. Where are you located?

Amy is just east of Colorado Springs.

Betsy

> Betsy, I have Dr. Harberts, and Dr. Stanley Sicher.  Are you

> from Colorado too?

>

> Betsy Cabell wrote:Bonnie,

> Just curious - who is your neph. in Colorado?

>

> Betsy

>

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We are in the Denver area (Centennial). My son has IgAN and goes to the

Renal Transplant Clinic at University Hospital. Where are you located?

Amy is just east of Colorado Springs.

Betsy

> Betsy, I have Dr. Harberts, and Dr. Stanley Sicher.  Are you

> from Colorado too?

>

> Betsy Cabell wrote:Bonnie,

> Just curious - who is your neph. in Colorado?

>

> Betsy

>

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