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LDN & Lupis?

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Dear Friends,Are any of you using LDN for Lupis? A friend of my daughter's is interested in looking intot it.Thank you for your help,Destiny

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Are you seeing a doc that specializes in auto-immune illnesses? A specialist like this might be better able to help you with testing,diagnosis and treatment in addition to LDN. Lupus/auto-immune issues are not a specialty of neurologists.

I am fortunate in that my rheumatologist also specializes in autoimmune diseases and osteoporosis.

Hope this helps, mjh

Then about 2 years ago all my testfor lupus came back negative. and when I went to seemy neurologist, he told me the liklihood of me having2 autoimmune illnesses was slim to none and that I hadMS. I still have the raynaulds and the rash across myface periodically, so who really knows for sure, all Iknow is the LDN is helping and I am very pleased sofar. I hope this helps you going forward. Good Luck. All the best.Start the year off right. Easy ways to stay in shape in the new year.

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Hi Destiny:

I was originally told 10 years ago that I had Lupus,

the symptoms I displayed with that was numbness in my

hands, the rash across my face and nose and raynaulds

phenomenon. All my blood work came back positive for

Lupus for a good many years. I also was told that I

had a clotting problem so the doctor put me on low

dose baby aspirin. Then about 2 years ago all my test

for lupus came back negative. and when I went to see

my neurologist, he told me the liklihood of me having

2 autoimmune illnesses was slim to none and that I had

MS. I still have the raynaulds and the rash across my

face periodically, so who really knows for sure, all I

know is the LDN is helping and I am very pleased so

far. I hope this helps you going forward.

Good Luck. All the best.

--- Destiny <destinyellen@...> wrote:

> Dear Friends,

>

> Are any of you using LDN for Lupis? A friend of my

> daughter's is interested in looking intot it.

>

> Thank you for your help,

>

> Destiny

>

________________________________________________________________________________\

____

Be a better friend, newshound, and

know-it-all with Mobile. Try it now.

http://mobile./;_ylt=Ahu06i62sR8HDtDypao8Wcj9tAcJ

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Hello:

Yes, I was followed by a Rheumatologist for a good

many years but stopped going when I learned that I had

the MS, and my bloodwork came back negative for Lupus.

The only symptoms I have with lupus is the rash and

the raynaulds. Not sure about the anti coagualant

factor but I periodically get my blood work done

anyways. So, hopefully that is no longer an issue as

well.

Thanks,

--- foxhillers@... wrote:

>

>

> Are you seeing a doc that specializes in

> auto-immune illnesses? A

> specialist like this might be better able to help

> you with testing,diagnosis and

> treatment in addition to LDN. Lupus/auto-immune

> issues are not a specialty of

> neurologists.

>

> I am fortunate in that my rheumatologist also

> specializes in autoimmune

> diseases and osteoporosis.

>

> Hope this helps, mjh

>

> Then about 2 years ago all my test

> for lupus came back negative. and when I went to

> see

> my neurologist, he told me the liklihood of me

> having

> 2 autoimmune illnesses was slim to none and that I

> had

> MS. I still have the raynaulds and the rash across

> my

> face periodically, so who really knows for sure,

> all I

> know is the LDN is helping and I am very pleased so

> far. I hope this helps you going forward.

> Good Luck. All the best.

>

>

>

>

>

>

> **************Start the year off right. Easy ways

> to stay in shape.

>

http://body.aol.com/fitness/winter-exercise?NCID=aolcmp00300000002489

>

________________________________________________________________________________\

____

Looking for last minute shopping deals?

Find them fast with Search.

http://tools.search./newsearch/category.php?category=shopping

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Guest guest

I have a dear friend who has Lupis. She knows that my son is taking

LDN for MS and has inquired about it. She would like for me to get

information for her regarding the taking LDN for Lupis. Since she

isn't computer literate I told her I would ask on this site. Can any

of you direct me to information regarding this subject or if you have

lupis and are taking LDN would you e-mail me? She has an appointment

in March with her Rheumatologist. Thanks everyone. Gloria

>

> >

> >

> > Are you seeing a doc that specializes in

> > auto-immune illnesses? A

> > specialist like this might be better able to help

> > you with testing,diagnosis and

> > treatment in addition to LDN. Lupus/auto-immune

> > issues are not a specialty of

> > neurologists.

> >

> > I am fortunate in that my rheumatologist also

> > specializes in autoimmune

> > diseases and osteoporosis.

> >

> > Hope this helps, mjh

> >

> > Then about 2 years ago all my test

> > for lupus came back negative. and when I went to

> > see

> > my neurologist, he told me the liklihood of me

> > having

> > 2 autoimmune illnesses was slim to none and that I

> > had

> > MS. I still have the raynaulds and the rash across

> > my

> > face periodically, so who really knows for sure,

> > all I

> > know is the LDN is helping and I am very pleased so

> > far. I hope this helps you going forward.

> > Good Luck. All the best.

> >

> >

> >

> >

> >

> >

> > **************Start the year off right. Easy ways

> > to stay in shape.

> >

> http://body.aol.com/fitness/winter-exercise?

NCID=aolcmp00300000002489

> >

>

>

>

>

______________________________________________________________________

______________

> Looking for last minute shopping deals?

> Find them fast with Search.

http://tools.search./newsearch/category.php?category=shopping

>

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