Re: Questions for Spokesperson from GSK about PSSD

[Guest guest]

>

> Seroxat is Paxil, right?

>

> yeah paxil is called seroxat in england.

[Guest guest]

About half of the people in the group are still taking SSRIs. So

although they don't have PSSD, I think it's good that they are aware of

it.

Paxil definitely seems to be the worst.

Vornan

I have noted that our poll

> shows it has caused more PSSD than any of the other SSRI`s (22%).

>

> Also is there a known number of people within the group who have PSSD

> because i know that some group members are still taking ssri`s.

>

[Guest guest]

I was on Paxil for only 3 months, 1st month 10mg a day, and the next two months, 5mg a day. This is well below minimum dosage at many Drs did not believe at what state I was in. I was a complete vegetable, no sex drive. After quiting, problem with erection and no sex drive. went on for two years.

I feel If get off my clomid, the ED and lax of sex drive will come back. I have no doubt in my mind, Paxil is worst.

-Steve

About half of the people in the group are still taking SSRIs. So although they don't have PSSD, I think it's good that they are aware of it.Paxil definitely seems to be the worst.Vornan

I have noted that our poll > shows it has caused more PSSD than any of the other SSRI`s (22%).> > Also is there a known number of people within the group who have PSSD

> because i know that some group members are still taking ssri`s.>

[Guest guest]

To all members who are still taking SSRI,

This might sound corny but it really hurts me to see people still

taking SSRI after all the evidence that SSRIs are harmful especially

in this group. Not to discourage any of you guys but I really think

you have to make a choice between taking SSRI for the rest of your

life or getting off of it, if you are young enough to recover. It

is a totally different life afterwards and really unimaginably

painful and sad. So if you have any doubt about not continuing the

SSRI for the rest of your life in the future, I would recommend to

taper off very very very slowly for your health ASAP. So you can get

over the painful stage early and start the road of recovery. Just my

honest opinion for people who still have a long way to go in life

like me.

>

> About half of the people in the group are still taking SSRIs. So

> although they don't have PSSD, I think it's good that they are

aware of

> it.

>

> Paxil definitely seems to be the worst.

>

> Vornan

>

> I have noted that our poll

> > shows it has caused more PSSD than any of the other SSRI`s (22%).

> >

> > Also is there a known number of people within the group who have

PSSD

> > because i know that some group members are still taking ssri`s.

> >

>

[Guest guest]

Ive just spoken on the phone to the moderator of the seroxat user

group and told her about our group and PSSD.As it happens she is

supported in the running of her group by a doctor who has PSSD

himself. He has been impotent for around 5 years since discontinuing

seroxat (paxil) and has tried various alternative medicine sources to

reverse it.He had expressed interest in conducting studies into PSSD

among his patients and writing an article on it himself before

learning of our group last night.

She told me that many of the people in her group have described not

being the same for a long time after discontinuing seroxat (paxil)

and feeling as if their " brains had changed " .Many of them have

complained of agression and low moods caused by the SSRI thats last

long after discontinuing it.

Shes met with the Medicines and Healthcare Products Regulatory Agency

(MHRA) the english equivalent of the FDA and has questioned them

about the number of side effects reported to them.She has stressed

the need to report any adverse side effects to them using the yellow

card scheme thats available at doctors surgeries or can be completed

online -

http://www.mhra.gov.uk/home/idcplg?IdcService=SS_GET_PAGE & nodeId=287

Her meeting with the spokesperson from GSK has been postponed and she

is due to visit Dr Benbow now on 30th of this month.

[Guest guest]

Good for you, .

What's your current email? I have two of yours but neither is

working.

V

>

>

>

> Ive just spoken on the phone to the moderator of the seroxat

user

> group and told her about our group and PSSD.As it happens she is

> supported in the running of her group by a doctor who has PSSD

> himself. He has been impotent for around 5 years since

discontinuing

> seroxat (paxil) and has tried various alternative medicine sources

to

> reverse it.He had expressed interest in conducting studies into

PSSD

> among his patients and writing an article on it himself before

> learning of our group last night.

>

> She told me that many of the people in her group have described

not

> being the same for a long time after discontinuing seroxat (paxil)

> and feeling as if their " brains had changed " .Many of them have

> complained of agression and low moods caused by the SSRI thats

last

> long after discontinuing it.

>

>

> Shes met with the Medicines and Healthcare Products Regulatory

Agency

> (MHRA) the english equivalent of the FDA and has questioned them

> about the number of side effects reported to them.She has stressed

> the need to report any adverse side effects to them using the

yellow

> card scheme thats available at doctors surgeries or can be

completed

> online -

>

>

>

> http://www.mhra.gov.uk/home/idcplg?

IdcService=SS_GET_PAGE & nodeId=287

>

>

> Her meeting with the spokesperson from GSK has been postponed and

she

> is due to visit Dr Benbow now on 30th of this month.

>

[Guest guest]

Hi Vornan

my email address is kevinbennett23us@... .I wasnt

aware that emails werent getting to me on it but ive emailed you from

that address hopefully youll receive it.

[Guest guest]

It is very ironic that the doctor cant cure himself of PSSD and

looking elsewhere for help. If only more doctors like that exist

here in the US. It is great to know something is being done over

there.

>

>

>

> Ive just spoken on the phone to the moderator of the seroxat

user

> group and told her about our group and PSSD.As it happens she is

> supported in the running of her group by a doctor who has PSSD

> himself. He has been impotent for around 5 years since

discontinuing

> seroxat (paxil) and has tried various alternative medicine sources

to

> reverse it.He had expressed interest in conducting studies into

PSSD

> among his patients and writing an article on it himself before

> learning of our group last night.

>

> She told me that many of the people in her group have described

not

> being the same for a long time after discontinuing seroxat (paxil)

> and feeling as if their " brains had changed " .Many of them have

> complained of agression and low moods caused by the SSRI thats

last

> long after discontinuing it.

>

>

> Shes met with the Medicines and Healthcare Products Regulatory

Agency

> (MHRA) the english equivalent of the FDA and has questioned them

> about the number of side effects reported to them.She has stressed

> the need to report any adverse side effects to them using the

yellow

> card scheme thats available at doctors surgeries or can be

completed

> online -

>

>

>

> http://www.mhra.gov.uk/home/idcplg?

IdcService=SS_GET_PAGE & nodeId=287

>

>

> Her meeting with the spokesperson from GSK has been postponed and

she

> is due to visit Dr Benbow now on 30th of this month.

>

[Guest guest]

I know two doctors here who had/have PSSD. Statistically there must

be thousands.

> >

> >

> >

> > Ive just spoken on the phone to the moderator of the seroxat

> user

> > group and told her about our group and PSSD.As it happens she is

> > supported in the running of her group by a doctor who has PSSD

> > himself. He has been impotent for around 5 years since

> discontinuing

> > seroxat (paxil) and has tried various alternative medicine

sources

> to

> > reverse it.He had expressed interest in conducting studies into

> PSSD

> > among his patients and writing an article on it himself before

> > learning of our group last night.

> >

> > She told me that many of the people in her group have described

> not

> > being the same for a long time after discontinuing seroxat

(paxil)

> > and feeling as if their " brains had changed " .Many of them have

> > complained of agression and low moods caused by the SSRI thats

> last

> > long after discontinuing it.

> >

> >

> > Shes met with the Medicines and Healthcare Products Regulatory

> Agency

> > (MHRA) the english equivalent of the FDA and has questioned them

> > about the number of side effects reported to them.She has

stressed

> > the need to report any adverse side effects to them using the

> yellow

> > card scheme thats available at doctors surgeries or can be

> completed

> > online -

> >

> >

> >

> > http://www.mhra.gov.uk/home/idcplg?

> IdcService=SS_GET_PAGE & nodeId=287

> >

> >

> > Her meeting with the spokesperson from GSK has been postponed

and

> she

> > is due to visit Dr Benbow now on 30th of this month.

> >

>

[Guest guest]

assuming you cant get in touch with me on that email address which is

my permanent one im able to receive mail on doctorskill2006@...

probably for the next week or so before aol censorship again favours

the pharmaceutical industry and they kick me offline.