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Naturalpathic, Homeopathic, D.O.'s, DAN!

I have learned that we have to take control of our own medical care.

You have to put in the time to study and learn.

>

> So how do you go about finding a doctor familiar with using fish oil

> for apraxia? I am in Pennsylvania (near burg).

>

> Are doctors usually open to using fish oil for apraxia?

> Thanks.

>

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  • 4 months later...
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Larry,

It's similar here in Oz to almost everywhere else in the world - some

docs will and most won't prescribe it. I am lucky that I've had a great

relationship with my General Practitioner since I started seeing her in

1993 not long after I was diagnosed with PLS. In fact she has suggested

other " off label " things to me to try so as I expected she had

absolutely no hesitation in giving me a script for LDN when I presented

her with all the info. She is a seeming rarity for doctors - is willing

to try anything that doesn't involve any/much risk in order to help her

patients get better.

Plenty of compounding pharmacies here too - only problem is beating all

the kangaroos away from the door! :-) The best one I know of is

actually in Adelaide where the original poster was from.

Larry Stahl wrote:

> Hello. This is in response to the post trying to find a Doctor to prescribe

> LDN in Australia. I don't know what Doctors are like there but if you have

> a good relationship with you primary care doctor, you might try showing

> him/her a few pages from the LDN website (http://www.low dose naltrexone.org)

> or others and point out to your doctor that it can't do any harm (and you

> believe it will help).

>

> Do you have compounding pharmacies " Down Under " ? Skip (at Skip's Pharmacy)

> is such a nice guy he might talk to you pharmacist to tell what he does.

>

> Larry

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Great advice Larry. Ill defiantely go armed with more info for my GP and show him the links.

I have found one compounding pharmacy here in Adelaide which is a good sign-I tried calling them today to no avail..so will keep trying and hopefully go about asking them if they have LDN in stock or can point me in the right direction to obtaining some!

Im not giving up!!! ;)

Gemma

low dose naltrexone From: larry@...Date: Sun, 5 Aug 2007 22:25:10 -0600Subject: [low dose naltrexone] Finding a Doctor

Hello. This is in response to the post trying to find a Doctor to prescribe LDN in Australia. I don't know what Doctors are like there but if you have a good relationship with you primary care doctor, you might try showing him/her a few pages from the LDN website (http://www.low dose naltrexone.org) or others and point out to your doctor that it can't do any harm (and you believe it will help).

Do you have compounding pharmacies "Down Under"? Skip (at Skip's Pharmacy) is such a nice guy he might talk to you pharmacist to tell what he does.

Larry

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  • 1 month later...

Connecticut

Derby

Dr. Guarnaccia

(203) 732-1290

Yale/New Haven Medical Dept (Derby Hospital)

Connecticut

???

Dr. Perettes

(203) 445-0614

Here are a list of 2 doctors that have prescribed LDN in the past. I can't say if they are open to it, only that someone reported it to us a long time ago. At least they might know about it. Otherwise you can try your own doctors and let them know it has passed the first Pen State trial with flying colors for Crohn's disease, and they are in the process of trialing it at UCSF for MS.

[low dose naltrexone] finding a doctor

does anybody have any advise on how to find a doctor who will prescribe LDN in Connecticut or surrounding states?

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  • 4 months later...

Hello-

I have had RA since 1988, when it hit me at age 20. I have a severe

case: probably need a hip replacement now, curled hands, etc. etc. I

started the AP in 2000 or 2001, then stopped it within the year for

personal (non-medical) reasons. I'm ready to begin again and want

some opinions regarding doctor selection.

I live in a small SE Kansas town with limited doctor choices. My

local doctor will not prescribe AP, nor will two rheumatologists I

have approached (no surprise). I think an M.D. in a nearby town who

is known to take a more wholistic approach to medicine would prescribe

the AP.

I'm wondering, though: Because I have severe, long-standing RA, would

I be better off making a trip to see Dr. Franco in California? That

would be a convenient choice, because he does all of the testing so I

wouldn't have to find a lab, find someone to send off a blood sample,

and other logistical considerations.

What are your opinions? Would I benefit from seeing Dr. Franco? Or

should I continue looking locally?

I know the choice is ultimately mine. I am not looking for anyone to

make my decisions for me. I'm simply asking for your experiences and

opinions so I can use that information to make an informed decision.

Thanks for your time!

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Personally unless you ran into a problem while taking antibiotics why

see Franco?? Your doctor can do the prescribing and your rheumy can do any

testing you need. And of course we are here <smile>. That's what I did. My

rheumy even told me not to come back unless I wanted her meds and I went

back anyway and she did what I asked for testing and the antinflams I

needed. My FP still won't order the meds so I see a doctor that does more

holistic work. See if you can get a doc to send your blood to be tested for

mycoplasma before you start also.

Hope you get it soon and get better soon.

Cooky

_____

From: rheumatic [mailto:rheumatic ] On Behalf

Of

Sent: Monday, January 21, 2008 2:02 PM

rheumatic

Subject: rheumatic finding a doctor

Hello-

I have had RA since 1988, when it hit me at age 20. I have a severe

case: probably need a hip replacement now, curled hands, etc. etc. I

started the AP in 2000 or 2001, then stopped it within the year for

personal (non-medical) reasons. I'm ready to begin again and want

some opinions regarding doctor selection.

I live in a small SE Kansas town with limited doctor choices. My

local doctor will not prescribe AP, nor will two rheumatologists I

have Year's goals.

..

<http://geo./serv?s=97359714/grpId=93429/grpspId=1705061610/msgId=4

6743/stime=1200942100/nc1=5008808/nc2=3848641/nc3=5170400>

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Hi ,

How are you doing?

Just curious, would you be ope3n to alternative solution? Have you tried

natural supplements? The reason I'm asking is because I have a

cousin who has RA and I asked her to try these 2 strong antioxidants

called OPC-3 and ORAC from Isotonix line. She was a bit hesitate in the

beginning, but she tried it anyway because it's all natural. She

took it the first time on April 2007. She went to doctor in May 2007 and

her C-reactive protein went down from 86 to 68. In August, she went back

to the doctor again and this time her C-reactive protein value went down

drastically to 4.4. Her doctor was surprised. My cousin looks so much

healthier now, less pain, getting better everyday. Not totally cured

yet, but she has a lot of energy now and looks so much healthier. Plus

it's all natural, so no side effect.

Those products were recommended by my friend who is a Nutraceutical

Consultant. I got those products from his website:

www.marketamerica.com/zingo <http://www.marketamerica.com/zingo>

Ok, good luck!

>

> Hello-

>

> I have had RA since 1988, when it hit me at age 20. I have a severe

> case: probably need a hip replacement now, curled hands, etc. etc. I

> started the AP in 2000 or 2001, then stopped it within the year for

> personal (non-medical) reasons. I'm ready to begin again and want

> some opinions regarding doctor selection.

>

> I live in a small SE Kansas town with limited doctor choices. My

> local doctor will not prescribe AP, nor will two rheumatologists I

> have approached (no surprise). I think an M.D. in a nearby town who

> is known to take a more wholistic approach to medicine would prescribe

> the AP.

>

> I'm wondering, though: Because I have severe, long-standing RA, would

> I be better off making a trip to see Dr. Franco in California? That

> would be a convenient choice, because he does all of the testing so I

> wouldn't have to find a lab, find someone to send off a blood sample,

> and other logistical considerations.

>

> What are your opinions? Would I benefit from seeing Dr. Franco? Or

> should I continue looking locally?

>

> I know the choice is ultimately mine. I am not looking for anyone to

> make my decisions for me. I'm simply asking for your experiences and

> opinions so I can use that information to make an informed decision.

>

> Thanks for your time!

>

>

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imel33 <imel33@...> wrote:

Hi ,

How are you doing?

Just curious, would you be ope3n to alternative solution? Have you tried

natural supplements? The reason I'm asking is because I have a

cousin who has RA and I asked her to try these 2 strong antioxidants

called OPC-3 and ORAC from Isotonix line. She was a bit hesitate in the

beginning, but she tried it anyway because it's all natural. She

took it the first time on April 2007. She went to doctor in May 2007 and

her C-reactive protein went down from 86 to 68. In August, she went back

to the doctor again and this time her C-reactive protein value went down

drastically to 4.4. Her doctor was surprised. My cousin looks so much

healthier now, less pain, getting better everyday. Not totally cured

yet, but she has a lot of energy now and looks so much healthier. Plus

it's all natural, so no side effect.

Those products were recommended by my friend who is a Nutraceutical

Consultant. I got those products from his website:

www.marketamerica.com/zingo <http://www.marketamerica.com/zingo>

Ok, good luck!

>

> Hello-

>

> I have had RA since 1988, when it hit me at age 20. I have a severe

> case: probably need a hip replacement now, curled hands, etc. etc. I

> started the AP in 2000 or 2001, then stopped it within the year for

> personal (non-medical) reasons. I'm ready to begin again and want

> some opinions regarding doctor selection.

>

> I live in a small SE Kansas town with limited doctor choices. My

> local doctor will not prescribe AP, nor will two rheumatologists I

> have approached (no surprise). I think an M.D. in a nearby town who

> is known to take a more wholistic approach to medicine would prescribe

> the AP.

>

> I'm wondering, though: Because I have severe, long-standing RA, would

> I be better off making a trip to see Dr. Franco in California? That

> would be a convenient choice, because he does all of the testing so I

> wouldn't have to find a lab, find someone to send off a blood sample,

> and other logistical considerations.

>

> What are your opinions? Would I benefit from seeing Dr. Franco? Or

> should I continue looking locally?

>

> I know the choice is ultimately mine. I am not looking for anyone to

> make my decisions for me. I'm simply asking for your experiences and

> opinions so I can use that information to make an informed decision.

>

> Thanks for your time!

>

>

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  • 1 year later...
Guest guest

How To Obtain Low Dose Naltrexone (LDN)

http://www.webspawner.com/users/howtoobtainldn/index.html

International Antiaging Systems Naltrexone

http://www.antiaging-systems.com/iasstore/acatalog/naltrexone.html

Doctors Who Prescribe LDN

http://www.ldners.org/resources.htm

FIND A DOCTOR

http://www.thecompounder.com/homedoctor.php

The preferred compounding pharmacy for Low-Dose Naltrexone for Dr Bihari.

http://www.irmatpharmacy.com/

Skip's Pharmacy, the one I use

http://skipspharmacy.com/ldn.php

My MS/LDN story/1988 - 2009

http://tinyurl.com/mejs2t

>

> How can you find a doctor that will prescribe LDN? I'm exhausted trying to

find one to help. They are very eager to do surgery and chemo though.

>

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You can find doctors who prescribe LDN by going to this site:

http://crystalangel6267.webs.com/contactcrystal.htm

>

> My name is a. I am recently diagnosed PPMS. I live in

> Chattanooga and have a neurologist here. I also have a neurologist at

> the Vanderbilt University MS Research Center. I was put on Cellcept

> (which I couldn't tolerate). I want to start LDN after reading a LOT

> about it. If my docs aren't willing to write a rx for it, who can I

> talk to (phone consultation) to get the right med?

>

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