Dear Community of Kingston
Every day in every community across Canada, people are dealing with situations arising from fear, shame, misunderstanding or lack of awareness. Right now, in Kingston whether or not we are part of the LGBTQ community, we are facing action, possibly rooted in hate, certainly rooted in malice, which should be of concern to us all. We have seen a rise in expressions of prejudice, most recently by people, so far protected by anonymity, who are writing malicious and threatening letters to Kingston families.
Many years ago that same situation, and many, many like it, inspired people to form an inclusive and supportive organization for people whose sexual orientation, gender identity or gender appearance caused them or their loved ones discomfort, fear or harm. That organization, PFLAG Canada, has a local Chapter in Kingston.
Our local Chapter, like Chapters all over Canada, has provided safe, peer-based, non-judgmental help and resources to thousands, in situations involving people who need help, from simple listening and the offering of friendship to suicide-prevention. We’ve been here for years when we were needed. We’re here now for anyone who is intimidated, who feels fear or who suffers bullying due to the behaviour of people whose prejudice leads them to unlawful and frightening behaviour.
We know that our city officials take this threat seriously, and that they see it is menacing not just to the letter recipients but to the whole community. Our challenge is in knowing what to do.
If you are concerned for yourself or someone else, call our line at 613 766-1444.
If you are the perpetrator of these or similar threatening actions, know that you are not going to push us back into the closet.
If you want to show support for the LGBTQ community and the families who are the target of these threatening letters, write a note on our PFLAG Kingston Facebook page or tweet your support to pflagcan_king.
In hope for our community,
Stephen Hartley
Always Learning
Tuesday, July 23, 2013
Wednesday, March 27, 2013
Karen's letter_fr
KAREN LAMBERT
Ceci n’est pas la traduction de toute la lettre de Karen, mais
seulement de certaines sections où elle explique pourquoi sa santé l’inquiète et
où elle parle de ce qui, selon elle, peut devenir une pandémie. Pour lire la
lettre de Karen en entier danssa version originale en anglais
« Je souffre du
syndrome de fatigue chronique et dysfonction immunitaire (SFC/SFCDI/EM) et du
sida non dû au VHI ou lymphocytopénie CD4 idiopathique (ICL). Munie de ces deux
diagnostiques cliniques, je pense que le SFC et l’ICL sont essentiellement le
même mystérieux trouble immunitaire. …Peu importe ce à quoi je fais face en ce
moment, cela ressemble fortement à un exemple patent de VIH\SIDA. Mais pour
compliquer mon enquête, je satisfait aussi cliniquement aux critères des CDC
(Centres de contrôle et prévention des maladies) pour le diagnostique du
syndrome de fatigue chronique… »
« De plus en plus, j’ai
l’impression que mon diagnostique systémique est emporté dans les tourbillons perfides
du SFC/EM et du sida. La plupart des personnes affectées par le SFC/EM n’aiment
pas parler des nombreux symptômes et anomalies du système immunitaire qu’elles
partagent avec les personnes qui souffrent du sida. Je pense également que la
plupart des patients préfèreraient qu’on leur annonce qu’ils souffrent du très
mystérieux SFC plutôt que du sida. »
« Je suis titulaire d’une maîtrise.
Dans l’entreprise où je travaille, je suis gestionnaire. Je suis une ancienne
triathlète. Je n’ai jamais pris de drogues injectables. Je n’ai jamais voyagé à
l’étranger. Je peux compter mes partenaires sexuels sur les doigts de mes deux
mains. Du point de vue statistique, je sais que ma maladie, non diagnostiquée
et contagieuse, n’est pas rare…alors, dites-moi, si elles ne tombent pas dans
la catégorie des divers SFC/EM, où
place-t-on toutes ces autres personnes immunodéficientes?.... Pourquoi ne
lit-on rien au sujet des cas de sida qui ne sont pas dus au VIH (et/ou de la
ressemblance du SFC au sida) à la une de tous les journaux du monde?.... »
« Aussi inquiétante qu’est pour moi
ma santé, je suis extrêmement inquiète de la forte possibilité que plus de gens
sont infectés chaque minute, que des cas de sida non liés au VHI (comme le mien)
puissent ne pas être décelés – surtout si on en vient à découvrir que le
virus du SIDA et le SFCDI/ME sont pratiquement la même chose. »
Pour en savoir plus sur le sida d’origine
autre que le VHI et pour découvrir le *nouveau* visage du SIDA, veuillez consulter CFS Straight Talk
Karen's letter
by Karen Lambert
I have Chronic Fatigue Immune
Dysfunction Syndrome (CFS/CFIDS/ME) and HIV-NEGATIVE AIDS, idiopathic CD
lymphocytopenia. With these two clinical diagnoses, I believe that makes
me living proof that the AIDS-like CFS/ME is transmissible, something that
the medical establishment seems unable to admit or to acknowledge. I also
believe it makes me living proof that CFS and HIV-NEGATIVE AIDS are
basically the same mysterious immune disorder.
Three years ago, after a
heterosexual sexual encounter, I became seriously ill with what looks like
the natural disease progression of AIDS. After an “acute infection” and a
“period of asymptomatic
health”, I have fallen extremely ill to an unrelenting, progressively-worsening AIDS-like demise. I can pinpoint exactly when I was infected with my “chronic viral syndrome of unknown etiology”
and because the “acute infection” stage was so distinguishable, I can also pinpoint exactly when my undiagnosed pathogen left my body and infected yet another host.
health”, I have fallen extremely ill to an unrelenting, progressively-worsening AIDS-like demise. I can pinpoint exactly when I was infected with my “chronic viral syndrome of unknown etiology”
and because the “acute infection” stage was so distinguishable, I can also pinpoint exactly when my undiagnosed pathogen left my body and infected yet another host.
Whatever I am currently dealing
with, it strongly resembles classic textbook HIV/AIDS disease. But, to add
to my inquiry, I also clinically satisfy the CDC’s criteria for the diagnosis
of Chronic Fatigue Syndrome.
Increasingly, I have become
concerned that my systemic diagnosis is caught up in the treacherous
politics of CFS/ME and AIDS. Most people with CFS/ME do not like to talk
about the many symptoms and immune abnormalities that they share with AIDS
patients. I also suspect that most ailing patients would rather be told
that they have the very mysterious CFS than to be told that they have
AIDS.
I have a Master’s degree. I am a
director at my firm. I used to be a triathlete. I have never used IV
drugs. I have never traveled abroad. I can count my sexual partners on two
hands. Statistically speaking, I know that my undiagnosed infectious and
communicable disease is not rare…so, you tell me, if they are not in the
miscellaneous CFS/ME category, where are all these other immunosuppressed
people?
Anyone with Chronic Fatigue
Syndrome, who does not consider the possibility that CFS/ME will
eventually progress to a NON-HIV AIDS diagnosis, is very well trumping
their own ability to diagnosis the root cause of their illness.
Why isn’t CFS/ME a reportable
disease overseen by our public health department? Why are ME and CFS
(i.e., the same exact disorder) suspiciously categorized as two separate
illnesses on a worldwide level (i.e., by ICD codes)? Doesn’t anyone else
but me, very clearly see, the catastrophic cover-up going on here?
Why are we not reading about
Non-HIV AIDS cases (and/or the AIDS-like nature of CFS) on the front pages
of every newspaper in the world? And if CFS/ME is Non-HIV AIDS, then,
depending on who you believe, there are anywhere between 500,000 – 14,000,000
Americans out there with a transmissible illness. If that is what it truly
is, our new form of AIDS dwarfs the ‘original’ AIDS epidemic — tenfold!
I want honest answers for myself,
for everyone who is suffering from this hideous illness, and especially
for those who remain uninfected by my undiagnosed infectious and
communicable disease.
As worrisome as my health is to
me, I am extremely troubled by the strong likelihood that more people are
being infected every minute that Non-HIV AIDS cases (like mine) are
allowed to go undetected – especially if it turns out that AIDS and
CFIDS/ME are basically the same disorder.
You can label my AIDS-like
illness whatever you wish. I would even allow you to call it
infectious-CFS, even though it is utterly beyond my realm of comprehension
as to how the medical establishment can generically name an entire disease
paradigm based on just one (of my numerous) symptom(s).
Regardless of how politics may
try to dissuade or delude you, all you need to know is that my idiopathic
immune dysfunction is infectious! It is contagious! And it is spreading,
unleashed, in the world’s population!
I am not afraid to say that I
have AIDS without HIV — idiopathic CD lymphocytopenia — my second official
clinical diagnosis. I am equally as unafraid of saying the most obvious
thing about CFS/ME: it sure does look like AIDS to me.
We talk openly about preparing
for an impending Avian Flu pandemic. Why not talk about the HIV-NEGATIVE
AIDS epidemic that already exists (and is spreading) amongst us?
If it takes courage to think and
to say the things that I do, I hope that there will be a miraculous
outbreak of bravery from coast-to-coast. I stopped fighting for myself a
long, long time ago. I
fight for humanity.
fight for humanity.
I demand a CFS/HIV revolution.
Vive La Revolución.
To learn more about non-HIV AIDS,
and to see the *new* face of AIDS, please visit: CFS Straight Talk
Could I be you?
Karen Lambert
Sunday, July 3, 2011
Powerpoint Presentation: Effective Leadership
With the generous help of RBC and two other donors, and with cooperation from all the PFLAG Canada Region 3 grant recipients, we held a conference at Trent University at the end of May 2011.
This site can be a way for you to benefit from the great experience we had. It was amazing to see how we learned from each other at the regional conference, and how broad and diverse were the skills we all brought to the table.
Other presentations that were made at the Conference will be posted at this site over the next few days. If you would like to be notified when the posts are up, use "Follow" at the upper right of this post and notice of updates will be e-mailed to you. If you were at the conference, you already have copies of these presentations on your flash drives.
Click here for the presentation on Effective Leadership. Please contact me if you'd like clarification or want to discuss any part of the material.
This site can be a way for you to benefit from the great experience we had. It was amazing to see how we learned from each other at the regional conference, and how broad and diverse were the skills we all brought to the table.
Other presentations that were made at the Conference will be posted at this site over the next few days. If you would like to be notified when the posts are up, use "Follow" at the upper right of this post and notice of updates will be e-mailed to you. If you were at the conference, you already have copies of these presentations on your flash drives.
Click here for the presentation on Effective Leadership. Please contact me if you'd like clarification or want to discuss any part of the material.
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