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Hi Pam,

I also have problems with EBV and have for over 20 years.

http://www.netdoctor.co.uk/medicines/100001328.html

There is a drug called Imunivor that helps me with this.

You are really lucky of you are still able to exercise. What you could consider

is cutting this

right down and giving your body a chance to recover. I speak as a survivor of 2

graded exercise

programs that made me much worse.

Kindest regards,

Annette

___________________________________________________________

Answers - Got a question? Someone out there knows the answer. Try it

now.

http://uk.answers./

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1. A multitude of different kinds of Antioxidants to mop up the many kinds of

free radicals

which are being produced in your body and weakening your immune system. You will

be

amazed at the results.

2. Transfer Factor for specific viral infections. Boosts NK cells. An excellent

treatment.

3. GHS by ProHealth

4. Stay away from high EMR environments: i.e. Cell phones, WiFi, WiMax,

computers!

5. Chelation therapy if you have heavy metal (e.g. lead, aluminum, mercury)

toxicity.

6. Acupuncture

7. Chinese Medicine

8. Qi Gong

>

> Hello,

>

> I was recently confirmed by blood test as positive for EBV as a

> recurrence. I would guess I've dealt with EBV/CFS for about 4 years,

> not having any idea what I was dealing with. Although I'm active,

> professional, and a single parent who exercises regularly and eats

> well, I'm still dealing with this horrid fatigue plus other classic

> symptoms. It is hell!

>

> I am taking Neem, and drinking Mangosteen.

>

> What other alternative treatments are recommended?

>

> Pam

>

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  • 1 year later...
Guest guest

It didn't do anything for me, kind of gave me a brain buzz, didn't sleep better and not less pain.

Deb Halvorson

From: lisacole641 <lisacole641@...> Sent: Friday, May 22, 2009 3:38:05 PMSubject: Recently diagnosedHello grp! I have been recently diagnosed with FM. I have so many questions, but my first one is does anything help with the pain? My Dr started me on gabapentin today. Does anyone have any experience with this drug?------------------------------------

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Hi there,

Gababentin was a huge help for me. I started taking it to help with sleep. In the beginning I had alot of dizziness and that dizziness did decrease over time but I would still be dizzy in the mornings.

I took it for about five years. I had to stop because I had so much memory loss with it. I also take Topomax for migraines and that drug causes lots of memory issues. So I had to decide which one to take off the menu. It was the Gabapentin. After a very, very difficult detox I began to REALLY realize how much it had been helping. I don't take any pain meds now. I bare the pain and use only Homeopathic and herbal remedies. I don't want to get into the cycle of pain meds.

hugs,

Sue

From: Debbie Halvorson <djh_50fab@...>Subject: Re: Recently diagnosed Date: Friday, May 22, 2009, 7:01 PM

It didn't do anything for me, kind of gave me a brain buzz, didn't sleep better and not less pain.

Deb Halvorson

From: lisacole641 <lisacole641@...> Sent: Friday, May 22, 2009 3:38:05 PMSubject: Recently diagnosedHello grp! I have been recently diagnosed with FM. I have so many questions, but my first one is does anything help with the pain? My Dr started me on gabapentin today. Does anyone have any experience with this drug?------------------------------------

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  • 3 months later...

Generally, when people ask for surgeons, go to the websites and click on the

thoracic surgical director or minimally invasive surgical director. There's

your surgeon, usually. In Texas, I'd start w/ MD branch and find the

top surgeon. Many sugeons are extremely fortunate if they trained there.

Almost always we end up at the closest MAJOR teaching facility and with the top

surgical director. They use us to train others, and usually they do the surgery

themselves. They aren't hidden away.

Sandy

>

> I have had dysphagia for 30 years, have seen numerous doctors and done

numerous tests. I have FINALLY been diagnosed with classic achalasia in

conjunction with hypertensive LES. I live in Texas but went to UNC Chapel Hill

to see Dr. Shaheen. He has referred me to a GI by the name of

Tarnasky. I have to have a Heller Myotomy. I am trying to find a surgeon in

Texas if possible. I would appreciate it if anyone knows the names of any

surgeons with a vast experience in this surgery located in Texas.

>

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  • 7 months later...
Guest guest

My hubby went to usf health/tampa general group of Dr. Ross and Rosemurgy.

Number is 813-259-0929/813-844-4006. They say they have 'pioneered' the

laproscopic way of the myotomy surgery and do partial wraps. They have done 521

of them I think they said. Consultation first obviously. They are good

surgeons. Good luck! Steph

achalasia

From: floridagators@...

Date: Tue, 6 Apr 2010 18:20:09 -0700

Subject: Recently diagnosed

I was recently diagnosed with Achalasia. I do not see to have severe symptoms

yet, I can still eat and swallow normally half of the time. The other half

there is some definite slowness at the LES area. I have regurgitated 3 times so

far and wake up choking almost every night...

I was wondering if anyone has the name of a good surgeon in the South Florida

area. If not, anyone good in the state of Florida?

Thanks so much!

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Guest guest

Hi, my name is and my son was diagnosed when he was 11 with Achalasia. He

had surgery that same year, by Dr. Rosemurgy> He had a Heller myotomy with

fundiplication laproscopically. that was 5 years ago> I highly recommend him> We

seem him as needed> If you have any question or concerns please feel free to

email me @ devincentisg@...

D

>

> I was recently diagnosed with Achalasia.  I do not see to have severe symptoms

yet, I can still eat and swallow normally half of the time.  The other half

there is some definite slowness at the LES area.  I have regurgitated 3 times so

far and wake up choking almost every night...

>

> I was wondering if anyone has the name of a good surgeon in the South Florida

area.  If not, anyone good in the state of Florida?

>

> Thanks so much!

>

>

>

>

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Guest guest

WOW, I hate being 38 years old with Achalasia I can't imagine what it would be

like to only be 11 and have it! It was pretty scary not knowing what was wrong

with me when symptoms first started ... your kid sounds quite brave! Has he had

any reoccurrence? Hopefully he is one of the lucky ones who have excellent

results (I wasn't)

> >

> > I was recently diagnosed with Achalasia.  I do not see to have severe

symptoms yet, I can still eat and swallow normally half of the time.  The other

half there is some definite slowness at the LES area.  I have regurgitated 3

times so far and wake up choking almost every night...

> >

> > I was wondering if anyone has the name of a good surgeon in the South

Florida area.  If not, anyone good in the state of Florida?

> >

> > Thanks so much!

> >

> >

> >

> >

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Guest guest

Yes, he has had some recurrences< such as food getting stuck or severe chest

spasms. However, he has been on prevacid 30mg 2x a day since the surgery and we

notice these problems occur when he doesnt take the prevacid everyday twice a

day. Of course, he's a kid, but I think he finally is seeing the differnce

between compliance and non-compliance!

> > >

> > > I was recently diagnosed with Achalasia.  I do not see to have severe

symptoms yet, I can still eat and swallow normally half of the time.  The other

half there is some definite slowness at the LES area.  I have regurgitated 3

times so far and wake up choking almost every night...

> > >

> > > I was wondering if anyone has the name of a good surgeon in the South

Florida area.  If not, anyone good in the state of Florida?

> > >

> > > Thanks so much!

> > >

> > >

> > >

> > >

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  • 9 months later...

I have been recently diagnosed with ear canal cholesteatoma, after one primary

Doc, 3 ENT's and an ear specialist. It has been a long haul. I have had this

earache now for 9 months. The last visit to my doctor was very painful and since

then, as of the last 2 weeks, the pain in my right ear has gotten worse, the

fullness and pressure I feel near my right ear going down into my jaw area has

increased by double, at least, the ringing in my ear has went from now and then

to constantly in just the last week... the dizziness (vertigo) has also gotten

worse in severity and longer in duration. They have scheduled surgery for Feb.

24th, I have already had 2 ct scans, and some other stuff done in prep for the

operation. I am nervous to say the least about what to expect, and now that it

seems to be progressing, I am worried what the real damage is going to be once

they get in there. This ringng is really starting to get to me, as of today. It

is louder and more bothersome than ever. And the pain is worse too. I am

allergic to many pain meds so all I can take is something that I only take at

night because it is so strong. During the day I have just been dealing with it

but today it hurts worse than ever. Also, I am 45 years old and worried that my

recovery time is going to be longer because of my age. I don't have much help

and I have a seven year old. This is debillitating sometimes, putting me in bed

or on the couch whether I like it or not. Any women out there my age, or anybody

out there my age, that is going or has went through this? Any advice would be

appreciated.

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