Yes Jeannie, I have had an endoscopy....NO problem...at least for me. Twilight
meds, remember nothing....not even a sore throat afterwards....I've had two of
them. several years apart. Hope yours goes as well as mine. Easier on the body
than a colonoscopy. Good luck with the bone marrow biopsy Friday. glad they
will take a good look at what is going on and can reset from there...So sorry
you are so nauseated.....Take good care...and jeannie, if you feel at all like
talking, happy to listen. Feel free to email me at personal email and I can
give you phone number.
Beth
-----Original Message-----
From: 'Icandoallttc' via CMLHope <cmlhope@googlegroups.com>
To: cmlhope <cmlhope@googlegroups.com>
Sent: Wed, Jan 14, 2015 4:23 pm
Subject: Re: [CMLHope] Hi all finally going in for an endoscopy next week.
Anyone have an endoscopy ? Jeanie
Sent from my iPhone
On Jan 14, 2015, at 2:14 PM, "'Icandoallttc' via CMLHope"
<cmlhope@googlegroups.com> wrote:
Maybe they can find out why my side is hurting.
Blessing everyone
Jeanie
Sent from my iPhone
On Jan 14, 2015, at 10:57 AM, "'Icandoallttc' via CMLHope"
<cmlhope@googlegroups.com> wrote:
They put you to sleep for Bma.
Sent from my iPhone
On Jan 14, 2015, at 10:56 AM, "'Icandoallttc' via CMLHope"
<cmlhope@googlegroups.com> wrote:
Hi it's not me who lost their dad-- I lost mine many years ago.
I am still so nauseas.
Hanging in there.
Doing Bma fri.
Blessings
Jeanie
Sent from my iPhone
On Jan 13, 2015, at 4:06 AM, sherri swanson <swanson.sherri...@gmail.com> wrote:
Jeanie,
I'm so sorry for your loss. You will always have them in your heart.
I lost my parent a long time ago but I miss them as if it were yesterday. When
I read your message, I looked at their photo and asked them to take good care
of your dad.
L'chaim,
Sherri
On Mon, Jan 12, 2015 at 1:14 PM, 'Icandoallttc' via CMLHope
<cmlhope@googlegroups.com> wrote:
Thank you Greenie
I need that.
Blessings
Jeanie
Sent from my iPhone
On Jan 12, 2015, at 1:30 PM, Myvety2k via CMLHope <cmlhope@googlegroups.com>
wrote:
Hi Jeanie, hang in their, I'm thinking good thoughts and passing them on to
you.
greenie
In a message dated 1/12/2015 1:08:27 P.M. Eastern Standard Time,
cmlhope@googlegroups.com writes:
Thanks Susan.
I'm hanging in there!!!
Blessings.
Jeanie<emoji_u1f41f.png><emoji_u1f41f.png><emoji_u1f41f.png>
Sent from my iPhone
On Jan 11, 2015, at 11:17 PM, "'Susan Zimmerman' via CMLHope"
<cmlhope@googlegroups.com> wrote:
Awwwww Marcie!
I am so sorry for your loss, dear one. I know you've been being a good
caregiver for several years to your dad. You will be rewarded some day for
that. My heart hurts for you, so will surely be lifting you in prayer. No
matter what the age, the loss is huge when we are the ones left behind. It
was so kind of your rabbi to mention your CML battle. I pray you stop
having those horrible cramps, too. Traveling mercies for you all.
And Jeanie, also know what it's like to have a bad day from hydrea. Many
(including me) felt like they have the flu with the nausea, and I pray this
will not last long at all. A new day is coming, and I sure do hope your
doc puts you on something that works! (maybe bosulif?) Here's wishing you
the best, dear one.
Love and 18's,
Susan
-----Original Message-----
From: 'Marcie Goodman' via CMLHope <cmlhope@googlegroups.com>
To: cmlhope <cmlhope@googlegroups.com>
Sent: Sun, Jan 11, 2015 10:59 pm
Subject: Re: [CMLHope] Jeanie's relapse
Hi Jeanie,
So sorry you are having a tough time. I'm praying for you to have good test
results and a much better week.
My 94 year old father passed away on Friday, funeral was today. During
evening prayers our rabbi asked that everyone pray for not only my father
and our family but for our group struggling with the impact of CML. My dad
hated the fact that I had this illness and knew that I had such a wonderful
online support family.
So lots of prayers for you and all of us headed out from Baltimore all week!
Much love,
Marcie
Sent from my iPhone
On Jan 11, 2015, at 9:33 AM, 'Icandoallttc' via CMLHope
<cmlhope@googlegroups.com> wrote:
Hi Marty.
I feel so bad today!!!
Thinks it's from the hydrea.
I will print that out and keep it close.
I love psalms also.
Keep praying.
Jeanie 18's
Sent from my iPhone
On Jan 11, 2015, at 8:05 AM, Marty Gartenberg <wa2...@gmail.com> wrote:
Jeanie, I know that your feeling low right now but things will work out
for you. You must have this in your heart and I know that you do.
FOCUS.
This was something that was given to me by one of my close friends when
I had to live in that plastic bubble for all of those many months. I
would read it all the time and I am now passing it on to you, and it is
being sent to you from my heart because I remember my doubts but then
again I also remember my strengths.
EXPECT THE BEST, MIND OVER MATTER. SUCCESS IS A FUNCTION OF SELF
CONFIDENCE. TO HAVE SUCCESS AT ANYTHING YOU MUST FIRST LEARN TO BELIEVE
IN YOURSELF. IF YOU EXPECT THE WORSE THEN THAT IS EXACTLY WHAT YOU WILL
GET (MIND OVER MATTER) IF YOU EXPECT THE BEST THEN THAT IS WHAT YOU
WILL GET.
WHAT WE HAVE TO LEARN TO DO IS TO CHANGE OUR MENTAL HABITS, OUR STATES
OF MIND. LEARN TO EXPECT AND NOT TO DOUBT. BY DOING THIS YOU BRING
EVERYTHING INTO THE REALM OF POSSIBILITY. WHEN YOU LEARN TO BELIEVE
THEN WHAT YOU THOUGHT TO BE IMPOSSIBLE THEN MOVES INTO THE AREA OF
POSSIBILITY.
EVERY GREAT THING EVENTUALLY BECOMES POSSIBLE FOR YOU. MY BELIEF AT THE
BEGINNING OF A DOUBTFUL UNDERTAKING IS THE ONE THING THAT INSURES THE
SUCCESSFUL OUTCOME...
FOCUS...
Yes Jeanie you just keep on focusing because you are much more powerful
then you think.
Now you know why I keep on sending 18's.
18's,
Marty
On Sat, Jan 10, 2015 at 10:38 AM, 'Icandoallttc' via CMLHope
<cmlhope@googlegroups.com> wrote:
Hi Marty
Thanks for you uplifting message.
I am back to square one with my counts--
700 thousand platelets
163.28 WBC
ANC high
Creatine high
Potassium high
Took me off sprycel.
Allipurinoll 2 pills
Hydrea 3 twice a day
Yes I will fight!!!
Just so tired.
I think dr will put me on new drug mon.
Got to see if there is a mutant.
Prays and love to all.
18's. <emoji_u1f41f.png>
Jeanie
Sent from my iPhone
On Jan 10, 2015, at 4:31 AM, sherri swanson <swanson.sherri...@gmail.com>
wrote:
Hi Richard,
If it's one thing I got, It's Attitude! At least that's what my mom
would tell me when I was a teenager. LOL
Sorry to hear about the car. This cold weather can be brutal on a
car's battery. Glad you were able to get a new and now you’re good
to go.
Uor wind chills have been bad too. And we have some open fields so
there is nothing to block that wind. The other morning it was so
cold that the water froze in our community and none of had any
water for awhile. It's a good thing I'm an early raiser and I took
my shower while we had water.
Currently, it is -7 with a wind chill of -25 where I live and it
isn't going to be above zero until 9 am. That's cold.
Stay warm Richard and think spring!
L'chaim,
Sherri
On Fri, Jan 9, 2015 at 11:29 PM, Marty Gartenberg
<wa2...@gmail.com> wrote:
Hi Jeanie,
So many things effect your kidneys. The simple ageing factor is
just one of them. Some medicines will also contribute to kidney
function probably some of these TKI's. Mine finally gave out from
all of the chemotherapy and radiation I had more then 25 years
ago.
I can make a suggestion: If you are not diabetic try drinking
cranberry juice. Not the ones that are mixed up with juices like
grape juice. Ocean Spray has pure cranberry juice so you might
want to try it. Even if you are diabetic they also make a light
cranberry juice.
You know what? You have been through so much that this is only a
bump in the road for you, and so it is for me.
We have two choices. One, continue to fight and the other is not
an option for me or you.
That is why I always end any of my posts with 18's. You just hang
in there sweetie.
Marty
On Fri, Jan 9, 2015 at 7:55 AM, ICANDOALLTTC via CMLHope
<cmlhope@googlegroups.com> wrote:
Hi Sherri,
I think the tki's contribute to kidney disease. I think that I
am in the beginning of the disease and I have been on tki's for
11 years now.
Hang in in there; blessings
Jeanie<3
In a message dated 1/9/2015 3:21:09 A.M. Eastern Standard Time,
swanson.sherri...@gmail.com writes:
Hi Marty,
Thanks for the prayers and right back at ya.
I've been struggling with my kidney disease for many years
and didn't know it, and then one day voilà the doctors found
that there was a problem and that I'd been fighting it for
years hence the diagnoses of Chronic Kidney Disease. And the
funny thing is, I'm the only one in my entire family that has
any of these diseases. My family had its share of health
issues from heart disease to diabetes. But never anything
like what I have. All my doctors just shake their heads. I
tell them that I like to keep things interesting. And what
they like is that I have a sense of humor. And at this point,
it is much better to joke and laugh than to worry and cry.
While I still take what I have seriously, I'm just happy to
be here.
I would be a lot happier if the weather here would warm up.
For crying out loud it was -5 here yesterday and I was out in
it. Now that is one hearty person or a very foolish one. The
jury is still out on that one. Today it is going to be a
balmy 8. Woohoo! A heat wave. And, again I'll be out in it
as I have to go and get a Rx that I need.
L'chaim,
Sherri
On Thu, Jan 8, 2015 at 10:40 PM, Marty Gartenberg
<wa2...@gmail.com> wrote:
Dear Sherri,
Yes, you are a fighter and it takes one to know one. I pray
that everything turns out well for you.
And you are correct that all of the radiation and
chemotherapy did destroy both of my kidneys. It has been
over 25 years that I had my BMT. It took many years for my
kidneys to fail and that is probably why most transplant
centers will usually not use total body radiation any more
unless it is really needed.
18's,
Marty
On Thu, Jan 8, 2015 at 1:31 PM, sherri swanson
<swanson.sherri...@gmail.com> wrote:
Hi Marty,
The doctors are trying to treat the different illnesses
that are included in my condition. There are so many and
they do so many different things, that I am happy just to
to be here. I agree that as we get older there are some
unusual things that that find us. But in the long run, we
all got something. I'm a survivor. It's what I do. So
when I found out on Monday that I have a large mass on my
thyroid, I told my doctor I guess we're going to be busy
this winter. At least I'm not an alarmist.
<35C.png>
I too have trouble with my kidneys. Not to the extend
that you do, I'm working to keep myself at the current
level of stage III Kidney Disease. Some days, I'm good
others, not so much. Lately I've not been doing so good
and I've had to go and buy new shoes as my feet have been
so swollen that my current size no longer fit. I wear
compression socks all the time as well.
My Nephrologist ran some blood work and found that my
sodium was very low and and so was a bunch of other
levels. Now, he is an alarmist. If I even look like I'm
getting a cold he freaks out. I love him dearly, and I do
what he says, but I can't sneeze without him making me go
see my GP or the Oncologist or whatever doctor he thinks
I need to see.
I've heard that when you have a BMT and have to have
radiation and chemo, sometimes kidney failure is
possible. How long have you been on the list for
transplant?
Well, I'm glad that you are here and that you are strong.
You're an inspiration to all of us. Thanks for all you do
Marty.
L'chaim
Sherri
On Thu, Jan 8, 2015 at 10:07 AM, Marty Gartenberg
<wa2...@gmail.com> wrote:
Hi again Sherri,
Hopefully you will be able to be treated for this
condition. It seems that as most of us get older we
start suffering from some very unusual things, but that
is the price we must pay to remain alive. We just have
to do whatever we can to keep on going because we have
no other choice.
My kidneys failed four years ago and I must be on
dialysis because it is keeping me alive until I can
hopefully receive a kidney transplant.
This happened because when I received a bone marrow
transplant more then 25 years all of the radiation and
chemotherapy started to destroy my kidneys, but i'm
still alive today because of it. We all have our own
battles in life and that is just the way it is.
I wish you much health and happiness in this New Year.
18's,
Marty
On Thu, Jan 8, 2015 at 5:19 AM, sherri swanson
<swanson.sherri...@gmail.com> wrote:
Hi Marty,
Happy New Year. I hope you are well. Thanks for the
research I enjoyed article. I could only wish it was
as simple as being as side effect of my TKI. In my
case, nothing is ever simple LOL. What I have is
called Autonomic Neuropathy. Basically, my Autonomic
Nervous System has malfunctioned. Here is a link for
you to read if you would like to.
http://en.wikipedia.org/wiki/Dysautonomia
In a nutshell, Autonomic Neuropathy is a nerve
disorder that affects involuntary body functions,
including heart rate, blood pressure, perspiration
and digestion.
It isn't a specific disease. Autonomic Neuropathy
refers to damage to the autonomic nerves. This damage
disrupts signals between the brain and portions of
the autonomic nervous system, such as the heart,
blood vessels and sweat glands. This can cause
decreased or abnormal performance of one or more
involuntary body functions.
Autonomic Neuropathy can be a complication of a
number of diseases and conditions. And some
medications can cause autonomic neuropathy as a side
effect. Signs, symptoms and treatment of autonomic
neuropathy vary depending on the cause, and on which
nerves are affected.
L'Chaim,
Sherri
On Wed, Jan 7, 2015 at 7:02 PM, Marty Gartenberg
<wa2...@gmail.com> wrote:
Hi Sherri,
I did a little research on your no sweating
problem, and it is probably a side effect of your
TKI treatment.
I also ran across an article which you can read
here. It does mention something about the lack of
sweating. It probably has nothing to do with your
problem but maybe you should read it anyway.
http://en.wikipedia.org/wiki/Fabry_disease
18's,
Marty
On Wed, Jan 7, 2015 at 5:29 AM, sherri swanson
<swanson.sherri...@gmail.com> wrote:
Hello,
I've had CML for 12 years and I've taken Gleevec
for those 12 years. I've also experienced night
sweats for many years. At first I was told that
it was due to menopause because of my age at the
time. Go figure. When that was no longer an
option, the only thing left was the Gleevec.
Since being dx'd with the CML in 2003, I've been
dx'd with other chronic illnesses that are just
as serious.
With these new illnesses came a new problem. I no
longer sweat at all. So now I have the complete
opposite problem. No matter how hot it is, I
never sweat. I a way, it's nice because I'm
always cold and I long for very hot days so I can
go out side in the heat. But my oncologist has
warned me to not do it for very long as I have no
way to control my body temperature.
Unfortunately, it works the same way with the
cold. My body temperature is a constant 95
degrees.
So, in answer to your question, yes, the Gleevec
does cause night sweats. It is one of its side
effects. Unfortunately, I was not able to find a
remedy for my night sweats other than going to
the extreme which I do not recommend.
<332.png>
I hope everyone has a good New Year and is
healthy. Keep my posted as to what you find out.
Even thought I no long have this issue, I would
still like to be kept in the
loop.
L'chaim
Sherri
On Tue, Jan 6, 2015 at 4:19 PM, 'Marcie Goodman'
via CMLHope <cmlhope@googlegroups.com> wrote:
Hello, Susan. Gosh, we are just sweating
through this it seems. I will see what may be
available naturally, as I don't want hormones
either. Sorry you are experiencing this same
problem which I hope to solve.
Best wishes to you, Roy and your beautiful
family for a blessed New Year.
Marcie
Sent from my iPad
On Jan 5, 2015, at 10:17 PM, "'Susan Zimmerman'
via CMLHope" <cmlhope@googlegroups.com> wrote:
Dear Marcie,
I have had night sweats for years, intensifying
after my dx in 2005. I have day sweats, too.
When I stand up for more than five minutes to
do anything at all I start profusely sweating
from weakness. I think part of this is from
the bosulif, but most is from the stroke
weakness and need for hormones. I will not
take artificial hormones and have not gotten
the good kind that are specially made for each
person. I totally sympathize with you Marcie.
You might want to go to a naturalist doctor
about getting a test for hormones and then they
will make a compound for you of cream that
usually works. Regular md's only know to
prescribe the synthetic or horse hormones which
do cause cancer. That's my take on it, hope
you find some relief!!!
Thanks for your always uplifting posts! Happy
New Year to you, too!
Susan F. Zimmerman
-----Original Message-----
From: 'Marcie Goodman' via CMLHope
<cmlhope@googlegroups.com>
To: cmlhope <cmlhope@googlegroups.com>
Sent: Mon, Jan 5, 2015 8:41 am
Subject: [CMLHope] Night Sweats
Happy New Year, dear friends. I'm wondering if any of you suffer with night
sweats as a side effect of your TKI. I do, and have, over the years of my
treatment. I don't know that it is happening more frequently but the sweats
seem
to be more intense. Is there anything that you know of that will help?
Many thanks for always being there to offer encouragement and assistance.
Marcie
Sent from my iPad
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You received this message because you are subscribed to the Google
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For more options, visit this group at
http://groups.google.com/group/CMLHope
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You received this message because you are subscribed to the Google
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[CMLHope]
A support group of http://cmlhope.com
-------------------------------------------------
You received this message because you are subscribed to the Google
Groups "CMLHope" group.
To post to this group, send email to CMLHope@googlegroups.com
To unsubscribe from this group, send email to
cmlhope-unsubscr...@googlegroups.com
For more options, visit this group at
http://groups.google.com/group/CMLHope
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You received this message because you are subscribed to the Google
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an email to cmlhope+unsubscr...@googlegroups.com.
For more options, visit https://groups.google.com/d/optout.
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[CMLHope]
A support group of http://cmlhope.com
-------------------------------------------------
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
To post to this group, send email to CMLHope@googlegroups.com
To unsubscribe from this group, send email to
cmlhope-unsubscr...@googlegroups.com
For more options, visit this group at
http://groups.google.com/group/CMLHope
---
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
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email to cmlhope+unsubscr...@googlegroups.com.
For more options, visit https://groups.google.com/d/optout.
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[CMLHope]
A support group of http://cmlhope.com
-------------------------------------------------
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
To post to this group, send email to CMLHope@googlegroups.com
To unsubscribe from this group, send email to
cmlhope-unsubscr...@googlegroups.com
For more options, visit this group at http://groups.google.com/group/CMLHope
---
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
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email to cmlhope+unsubscr...@googlegroups.com.
For more options, visit https://groups.google.com/d/optout.
--
--
[CMLHope]
A support group of http://cmlhope.com
-------------------------------------------------
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
To post to this group, send email to CMLHope@googlegroups.com
To unsubscribe from this group, send email to
cmlhope-unsubscr...@googlegroups.com
For more options, visit this group at http://groups.google.com/group/CMLHope
---
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
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email to cmlhope+unsubscr...@googlegroups.com.
For more options, visit https://groups.google.com/d/optout.
--
--
[CMLHope]
A support group of http://cmlhope.com
-------------------------------------------------
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
To post to this group, send email to CMLHope@googlegroups.com
To unsubscribe from this group, send email to
cmlhope-unsubscr...@googlegroups.com
For more options, visit this group at http://groups.google.com/group/CMLHope
---
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
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email to cmlhope+unsubscr...@googlegroups.com.
For more options, visit https://groups.google.com/d/optout.
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--
[CMLHope]
A support group of http://cmlhope.com
-------------------------------------------------
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
To post to this group, send email to CMLHope@googlegroups.com
To unsubscribe from this group, send email to
cmlhope-unsubscr...@googlegroups.com
For more options, visit this group at http://groups.google.com/group/CMLHope
---
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
To unsubscribe from this group and stop receiving emails from it, send an email
to cmlhope+unsubscr...@googlegroups.com.
For more options, visit https://groups.google.com/d/optout.
--
--
[CMLHope]
A support group of http://cmlhope.com
-------------------------------------------------
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
To post to this group, send email to CMLHope@googlegroups.com
To unsubscribe from this group, send email to
cmlhope-unsubscr...@googlegroups.com
For more options, visit this group at http://groups.google.com/group/CMLHope
---
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
To unsubscribe from this group and stop receiving emails from it, send an email
to cmlhope+unsubscr...@googlegroups.com.
For more options, visit https://groups.google.com/d/optout.
--
--
[CMLHope]
A support group of http://cmlhope.com
-------------------------------------------------
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
To post to this group, send email to CMLHope@googlegroups.com
To unsubscribe from this group, send email to
cmlhope-unsubscr...@googlegroups.com
For more options, visit this group at http://groups.google.com/group/CMLHope
---
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
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to cmlhope+unsubscr...@googlegroups.com.
For more options, visit https://groups.google.com/d/optout.
--
--
[CMLHope]
A support group of http://cmlhope.com
-------------------------------------------------
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
To post to this group, send email to CMLHope@googlegroups.com
To unsubscribe from this group, send email to
cmlhope-unsubscr...@googlegroups.com
For more options, visit this group at http://groups.google.com/group/CMLHope
---
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
To unsubscribe from this group and stop receiving emails from it, send an email
to cmlhope+unsubscr...@googlegroups.com.
For more options, visit https://groups.google.com/d/optout.
--
--
[CMLHope]
A support group of http://cmlhope.com
-------------------------------------------------
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
To post to this group, send email to CMLHope@googlegroups.com
To unsubscribe from this group, send email to
cmlhope-unsubscr...@googlegroups.com
For more options, visit this group at http://groups.google.com/group/CMLHope
---
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
To unsubscribe from this group and stop receiving emails from it, send an email
to cmlhope+unsubscr...@googlegroups.com.
For more options, visit https://groups.google.com/d/optout.
--
--
[CMLHope]
A support group of http://cmlhope.com
-------------------------------------------------
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
To post to this group, send email to CMLHope@googlegroups.com
To unsubscribe from this group, send email to
cmlhope-unsubscr...@googlegroups.com
For more options, visit this group at http://groups.google.com/group/CMLHope
---
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
To unsubscribe from this group and stop receiving emails from it, send an email
to cmlhope+unsubscr...@googlegroups.com.
For more options, visit https://groups.google.com/d/optout.
--
--
[CMLHope]
A support group of http://cmlhope.com
-------------------------------------------------
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
To post to this group, send email to CMLHope@googlegroups.com
To unsubscribe from this group, send email to
cmlhope-unsubscr...@googlegroups.com
For more options, visit this group at http://groups.google.com/group/CMLHope
---
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
To unsubscribe from this group and stop receiving emails from it, send an email
to cmlhope+unsubscr...@googlegroups.com.
For more options, visit https://groups.google.com/d/optout.
--
--
[CMLHope]
A support group of http://cmlhope.com
-------------------------------------------------
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
To post to this group, send email to CMLHope@googlegroups.com
To unsubscribe from this group, send email to
cmlhope-unsubscr...@googlegroups.com
For more options, visit this group at http://groups.google.com/group/CMLHope
---
You received this message because you are subscribed to the Google Groups
"CMLHope" group.
To unsubscribe from this group and stop receiving emails from it, send an email
to cmlhope+unsubscr...@googlegroups.com.
For more options, visit https://groups.google.com/d/optout.
