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EvansSyndrome · The Evans Syndrome mailing list is for the purpose of sharing information and support to those individuals who have or know som
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Messages 5013 - 5043 of 5091   Oldest  |  < Older  |  Newer >  |  Newest
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5013 lnalou
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Mar 2, 2008
7:17 pm
5014
I think I am supposed to respond to this message to make sure I am still a member of the Evans Syndrome group. I would still like to be included. Thank you....
mnd_sommers
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Mar 7, 2008
4:53 am
5015
what exactly has changed about reaching the group? how is everyone doing? mnd_sommers <mnd_sommers@...> wrote: I think I am...
Shari Miller
sharim61
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Mar 7, 2008
11:28 am
5016
I too would still like to be included in the group, I look to stay up to date with others this way, hope that it still happens Betty Mom to Paul 20 Evans+ ...
bettanmic@...
bettanmic
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Mar 7, 2008
4:18 pm
5017
I also would like to stay abreast of the groups updates. Hope all is well with everyone, Thomas ... From: bettanmic@... To: EvansSyndrome@yahoogroups.com ...
Crimsontyde01@...
crimsontyde01
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Mar 7, 2008
5:58 pm
5018
I'm glad to see people posting to the list again. I have been meaning to send an update on my son for some time now, but never seemed to get to it. When I last...
SAnder823@...
sander823
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Mar 8, 2008
1:03 am
5019
Unfortunately, my dealings with NIH were not as positive... they have NO study available for Evans Syndrome. At separate times, my son had no recordable...
stillermom
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Mar 8, 2008
1:08 pm
5020
Susan, I am so glad to hear everything came out okay with the Lymph nodes. What a relief for all of you. Since Aidan already was transplanted and hopefully no...
Amy Walsh
smlybly
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Mar 8, 2008
4:00 pm
5021
Dear Lou, I hope you are doing well. Micah is currently enrolled in an NIH study. His new doctors in PA are also considering a diagnosis of ALPS. Unphased,...
shelly payson
essbeth3
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Mar 8, 2008
10:31 pm
5022
I too would still like to be included in this group!It is comforting and educational.My daughter is nine and has had this for two years now.She still does well...
dadeslot
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Mar 9, 2008
3:26 pm
5023
I'm glad to be back in the loop. Nick was in crisis in 2001-2002 (Evans and other auto immune issues - including Lupus) and he's doing very well. During that...
Marlene Pritchard
opca@...
Send Email
Mar 9, 2008
8:08 pm
5024
I understand your frustration. I had contacted the NIH about my son in 2000, 2002 and 2004 in the hopes of getting him him evaluated for ALPS - no luck I had...
SAnder823@...
sander823
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Mar 10, 2008
2:54 am
5025
Hi Amy, That is wonderful that Aiden's transplant was successful. I have heard the same thing at ITP conferences - most Evan's cases are something else. An...
SAnder823@...
sander823
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Mar 10, 2008
3:23 am
5026
Marlene, I really appreciate you giving us an update on how your son is doing. I printed your email to show to my 15 year old son. Nick is truly an...
SAnder823@...
sander823
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Mar 10, 2008
4:11 am
5027
Hello, We're new to the group. Our heads are reeling after 6 weeks of blood draws, doctors visits, x-rays and a bone marrow biopsy. Our beautiful, vibrant...
dml0425
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Mar 11, 2008
3:16 am
5029
... blood ... us ... autism.) ... 100.5-- ... have ... enlarged ... heard ... (She ... to ... been ... information, ... that ... has ... light ... was ... ...
rai44260
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Mar 11, 2008
1:31 pm
5030
Denise and Scott, I am so sorry that your daughter has been diagnosed with Evans syndrome. My son Aidan was diagnosed with autoimmune hemolytic anemia at 10...
Amy Walsh
smlybly
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Mar 11, 2008
2:11 pm
5031
Susan & Group, My son now 20 , was diagnosed with Evans at 12. We have had many ups and downs over the years and last year were told he had cancer and then...
bettanmic@...
bettanmic
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Mar 11, 2008
2:26 pm
5032
Dear All, Betty is right - this auto immune ride is a roller coaster! But, thankfully Amy is correct too! There is so much more information and progress for...
Marlene M Pritchard
opca@...
Send Email
Mar 11, 2008
2:55 pm
5033
Hi Marlene, Thank you so much for sharing Nick's accompolishments with us. I don't post very often these days but I monitor the messages and pray for the...
Debra Adamo
sdkkadamo
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Mar 11, 2008
4:59 pm
5034
I also would like to be included in all updates and info with this group. Hope this finds all well. Eileen...
evanswmn
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Mar 11, 2008
6:59 pm
5035
... me too !!!...
jakk5858
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Mar 13, 2008
2:04 am
5036
Hello, I need to know if anyone has anyone has any thoughts on Bone marrow transplants and Evans? I am just a mom trying to understand this whole process I...
jakk5858
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Mar 19, 2008
1:41 pm
5037
Julie, our son, Ben (17) was diagnosed when he was 10. we are lucky that his case is fairly mild and has lived a pretty normal life not withstanding drugs and...
Shari Miller
sharim61
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Mar 19, 2008
1:51 pm
5038
Julie, My son, Aidan, had a bone marrow transplant this past summer. Aidan's disease was a little more complicated than just evans syndrome, basically his...
Amy Walsh
smlybly
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Mar 19, 2008
5:26 pm
5039
Hello, I recently found this wonderful discussion group by searching for medical information that might relate to my own circumstances. I've not been diagnosed...
Nadine Schultz
lnadineschultz
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Mar 24, 2008
1:47 am
5040
How old are you? I am 54 and was diagnosied with evan & ITP 4 years ago. I am going through it right now as I write. This last one was pretty rough. 2...
homesbybev@...
Send Email
Mar 24, 2008
4:35 pm
5041
Hi Bev. Thank you so much for writing. Yes, your experience sounds very scary to me. Hopefully the blood transfusions and medication will get you through it...
Nadine Schultz
lnadineschultz
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Mar 24, 2008
5:43 pm
5042
God Bless you! Remember "By his stripes we were healed." I am amazed at the children that have evans and ITP. I wish everyone healing! Bev Burton Broker...
homesbybev@...
Send Email
Mar 24, 2008
6:03 pm
5043
Hello, Has anyone had any luck with any drugs besides what we have been getting, whole blood,prednisone,ivig.My son has been struggling to maintain his...
jakk5858
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Mar 31, 2008
10:19 pm
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