...Spect scan

[Guest guest]

,

I don't know if you have checked into Dr Uszler yet. If you have not here is

his info.

http://www.drspectscan.com/index12.html

I highly recommend him. I don't know about medicare but it's definitely worth

the effort to call.

Good luck

ita

<xrascott@...> wrote:

AT LAST, I have a prescription from my neurologist for a SPECT scan/

HBOT dive/SPECT scan evaluation. Medicare I am advised will pay for this. I need

advice about where I can get this done. It has to be in the US, I'm sure, to get

Medicare to reimburse, and unless I'm willing to pay extra (which I can't

afford) I need to find someone who accepts Medicare. Any suggestions? Thanks!

Duluth, MN

TBI survivor

Re: [ ] Help about pedi-neuros

> >

> >Dr.s are followers not leaders. The leadership personalities leave the

profession for politics. Neurologists want you to keep needing meds. That way

you will be the bread and butter patients of the practice. Regular small

incoming money!! We used to go to the one in Ga who was fighting Freel's

case for hbot for medicaid. Now I take my daughter to an adult neuro. After the

last 40 last summer, I reduced her meds 33%. She now takes 2 pills per day

instead of 3. Sue

> >

> >Terry Miner <poppatgm (DOT) com> wrote: Hello,

> > I just joined, so I don't know if you (anyone) can help on this subject.

> >

> > My 3mo old g'daughter (Ally) has mild/moderate( ?)HIE. I've been

> > researching HBOT for about 2 wks in hope that there would be a benefit

> > for her. Ally's parents have approached she medical team (thru the

> > pediatrician) as to their position re: HBOT. Her pediatric neurologist

> > just responded with a resounding NO!! He stated that, of the 900

> > members in his association, none of them support the use of HBOT.

> > There is a recent article in their newsletter that evidently sites

> > " numerous " problems, including seizures while undergoing treatment

> > (and not being able to provide aid until decompression is complete).

> > He stated that he has (2) of his patients that have gone thru the

> > treatments (@ the same facility that would provide treatment to ALLY)

> > & haven't shown ANY benefits.

> >

> > Unfortunately, I feel like I'm putting my son-in-law in the middle, as

> > I'm not in direct contact w/the Dr. I've suggested that, since the

> > assoc & this Dr. are pointing out that there is no research supporting

> > the " benefits " and are using these examples (seizures,etc) as

> > potential " risks " , would be kind enough to give me the links

> > supporting these risks?

> >

> > Can anyone offer some support (documents/links, etc), so I can feel

> > confident in pursuing HBOT for ALLY? Ultimatsly, it isn't my call to

> > make. I just want my kids to be as informed as they can be when they

> > decide.

> >

> > Thank you,

> > Terry Miner

> >

> >

> >

> >

> >

> >

> >----------- --------- --------- ----

> >Never miss a thing. Make your homepage.

> >

> >