good results from Immunoprop and Hepapressin

[Guest guest]

I'm a new member here, have had CFIDS since 1990, also possibly have late-

stage Lyme. Have been getting good results with Immunoprop capsules daily

and Hepapressin injections once a week. Most recent bloodwork shows that

my immune system is bouncing back (slowly, we have to be patient) from

severe HHV-6, cytomegalovirus and Epstein-barr exposures since starting

these two medications more than six months ago. This protocol is prescribed

by my doctor in Manhattan, Enlander, who I recommend for anyone

looking for an internist who UNDERSTANDS the illness. He is the first doctor

I have seen in 15 years who actually is helping me. I ride the train for an hour

and ten minutes, then take the subway 30 blocks to get to his office. This

journey is not easy, but he is worth the trip and worth the price I pay (total

exhaustion) the day after the journey!

I notice that I INSTANTLY feel better after getting a hepapressin injection, and

this feeling of well-being lasts well into the day. Just wanted to put this info

out

there, maybe other CFIDS sufferers can get their own doctors to order these

medications. My insurance pays for the injections but not for the capsules,

which are not that expensive. My husband gives me the shots, it's no big deal.

Good luck to all, please respond if you've had experience with these meds as

well.

Thanks -- tlog55

[Guest guest]

---Yes I am getting good results from this method also.

The injection gives me energy and lasts for five to six days when I

am ready for my next injection. I agree Dr E spends time with me,

seems like he spends time with everyone, how can that be ? I know he

is very busy he treats doormen at 6.45am

In , " tlog55 " <tlog55@y...> wrote:

>

> I'm a new member here, have had CFIDS since 1990, also possibly

have late-

> stage Lyme. Have been getting good results with Immunoprop capsules

daily

> and Hepapressin injections once a week. Most recent bloodwork shows

that

> my immune system is bouncing back (slowly, we have to be patient)

from

> severe HHV-6, cytomegalovirus and Epstein-barr exposures since

starting

> these two medications more than six months ago. This protocol is

prescribed

> by my doctor in Manhattan, Enlander, who I recommend for

anyone

> looking for an internist who UNDERSTANDS the illness. He is the

first doctor

> I have seen in 15 years who actually is helping me. I ride the

train for an hour

> and ten minutes, then take the subway 30 blocks to get to his

office. This

> journey is not easy, but he is worth the trip and worth the price I

pay (total

> exhaustion) the day after the journey!

>

> I notice that I INSTANTLY feel better after getting a hepapressin

injection, and

> this feeling of well-being lasts well into the day. Just wanted to

put this info out

> there, maybe other CFIDS sufferers can get their own doctors to

order these

> medications. My insurance pays for the injections but not for the

capsules,

> which are not that expensive. My husband gives me the shots, it's

no big deal.

> Good luck to all, please respond if you've had experience with

these meds as

> well.

>

> Thanks -- tlog55

>

[Guest guest]

Were does one find capsules of hepapressin? Is this available on line?

Sylvie

>

> ---Yes I am getting good results from this method also.

> The injection gives me energy and lasts for five to six days when I

> am ready for my next injection. I agree Dr E spends time with me,

> seems like he spends time with everyone, how can that be ? I know he

> is very busy he treats doormen at 6.45am

>> I notice that I INSTANTLY feel better after getting a hepapressin

> injection, and

>> this feeling of well-being lasts well into the day. Just wanted to

> put this info out

>> there, maybe other CFIDS sufferers can get their own doctors to

> order these

>> medications. My insurance pays for the injections but not for the

> capsules,

>> which are not that expensive.

[Guest guest]

I second that!

I developed severe unexplained spinal lumbar/sacrum inflammation

overnight last June. No treatment, including two epidural steroid

injections (actually made me sicker), worked. It was so bad that I

couldn't make any movement without excrutiating pains. I was pretty

much an invalid.

Thanks to Dr. Enlander's Hepapressin shots and Immunoprop, my

condition has improved. When pain flares up, a shot makes HUGE

difference in a matter of hour or two. So on really bad weeks, my

body really aches for more frequent shots.

They are life-saver in my case. I don't know about others but my

sed rate is very high, rheumatoid factor and CRP are out-of-this-

worldly high. If spinal inflammation wasn't under control, God knows

what might happen.

Wonder how many people have big time unexplained inflammation

problem and how you deal with it?

Tina

> >

> > I'm a new member here, have had CFIDS since 1990, also possibly

> have late-

> > stage Lyme. Have been getting good results with Immunoprop

capsules

> daily

> > and Hepapressin injections once a week. Most recent bloodwork

shows

> that

> > my immune system is bouncing back (slowly, we have to be

patient)

> from

> > severe HHV-6, cytomegalovirus and Epstein-barr exposures since

> starting

> > these two medications more than six months ago. This protocol is

> prescribed

> > by my doctor in Manhattan, Enlander, who I recommend for

> anyone

> > looking for an internist who UNDERSTANDS the illness. He is the

> first doctor

> > I have seen in 15 years who actually is helping me. I ride the

> train for an hour

> > and ten minutes, then take the subway 30 blocks to get to his

> office. This

> > journey is not easy, but he is worth the trip and worth the

price I

> pay (total

> > exhaustion) the day after the journey!

> >

> > I notice that I INSTANTLY feel better after getting a

hepapressin

> injection, and

> > this feeling of well-being lasts well into the day. Just wanted

to

> put this info out

> > there, maybe other CFIDS sufferers can get their own doctors to

> order these

> > medications. My insurance pays for the injections but not for

the

> capsules,

> > which are not that expensive. My husband gives me the shots,

it's

> no big deal.

> > Good luck to all, please respond if you've had experience with

> these meds as

> > well.

> >

> > Thanks -- tlog55

> >

>