Re: IVIG; yes it has worked great for me.

[Guest guest]

, how expensive is it for you in the U.S.?

To: <mscured >

Cc:

Date: 10/26/2010 09:56 PM

Subject: IVIG; yes it has worked great for me.

Has anyone undergone IVIG treatments?

Intra Venous Immune Globulin?

Yes, I currently receive IVIG treatments every 3 weeks for the past year.

IVIG was previously used at times of severe relapse for me. I do not

tolerate any of the CRAB medicines, novantrone, tysabri, or prednisone. I

was on LDN for 2.5 years but continued to have very debilitating relapses.

I receive gamma globulin IVIG infusion through a specialty pharmacy nurse.

Everyone has been amazed at what my doctors thought was rapidly

progressive MS. I have had no relapses in a year for the first time since

2003. After 2 years in wheelchair and then migrating and dependence on

walker, I gave that up as well as my cane. I otherwise follow a BBD

profile and avoid a number of food allergies and eat all organic foods.

BTW anyone know what to do with an electric wheelchair; willing to donate.

I kept a hold of it for the past 2 years constantly recharging the battery

because my docs kept guessing I’d be back in it….but it is obvious now

that it will no longer be needed. I’m in North Carolina.

IVIG is also being used in my case to address other autoimmune diseases as

well which are now in remission as well including systemic scleroderma,

sjogrens, antiphospholipid syndrome.

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[Guest guest]

, how expensive is it for you in the U.S.?

To: <mscured >

Cc:

Date: 10/26/2010 09:56 PM

Subject: IVIG; yes it has worked great for me.

Has anyone undergone IVIG treatments?

Intra Venous Immune Globulin?

Yes, I currently receive IVIG treatments every 3 weeks for the past year.

IVIG was previously used at times of severe relapse for me. I do not

tolerate any of the CRAB medicines, novantrone, tysabri, or prednisone. I

was on LDN for 2.5 years but continued to have very debilitating relapses.

I receive gamma globulin IVIG infusion through a specialty pharmacy nurse.

Everyone has been amazed at what my doctors thought was rapidly

progressive MS. I have had no relapses in a year for the first time since

2003. After 2 years in wheelchair and then migrating and dependence on

walker, I gave that up as well as my cane. I otherwise follow a BBD

profile and avoid a number of food allergies and eat all organic foods.

BTW anyone know what to do with an electric wheelchair; willing to donate.

I kept a hold of it for the past 2 years constantly recharging the battery

because my docs kept guessing I’d be back in it….but it is obvious now

that it will no longer be needed. I’m in North Carolina.

IVIG is also being used in my case to address other autoimmune diseases as

well which are now in remission as well including systemic scleroderma,

sjogrens, antiphospholipid syndrome.

This message is intended only for the addressee and may contain information that

is confidential or privileged. Unauthorized use is strictly prohibited and may

be unlawful. If you are not the intended recipient, or the person responsible

for delivering to the intended recipient, you should not read, copy, disclose or

otherwise use this message, except for the purpose of delivery to the addressee.

If you have received this email in error, please delete and advise the IT

Security department at infosec@... immediately.

Please consider the environment before printing this e-mail.