the getting better list. please please forgive me
i didnt know there was such a list! ________________________________ From: Janice Nichols <[email protected]> To: Dalton Garis <[email protected]>; Robert Pall <[email protected]>; [email protected] Sent: Tuesday, December 6, 2011 6:08 PM Subject: Re: [TMIC] Losing my mind! Dalton, I thought you were on the “getting better” list - what happened? Any changes in stress levels, medications, physical activity? Janice From: Dalton Garis Sent: Tuesday, December 06, 2011 9:31 AM To: Robert Pall ; [email protected] Subject: Re: [TMIC] Losing my mind! I would agree with you completely; I need help with TM. Now, my attacks are returning and I get these contractions all over my body when I try to do things. They were at bay and now have returned; and all I did was to address some envelopes the previous day. Yes; can we keep on the subject? But I have made many friends here and would love to continue a more general conversation with them. Use our email addresses to form your own "friend" group, gleaned from the TMIC, and you will contact those who want to chat, without disturbing others. Kindest regards to all, and I need to discuss the return of those debilitating seizures. Dalton Garis (718) 838-0437 From: Robert Pall <[email protected]> Date: Tue, 6 Dec 2011 10:24:03 -0500 (EST) To: <[email protected]> Subject: [TMIC] Losing my mind! Resent-From: <[email protected]> Resent-Date: Tue, 6 Dec 2011 07:26:56 -0800 I really need help. Everyday I end up with 100 emails from "people living with TM", TM Folks and a little bit of the original TM group. >I do not want to chat about everything....I want to talk about TM and TM only. >I realize I am lucky that I am not totally disabled (I can walk and drive)and >I understand where some of the TM'rs are in front of their computer all day >long. I end up deleting almost all of my mail due to the volume....this does >not help me nor the originators of the emails. >Maybe it is just me ...but wouldn't it be better to have just one TM site as >well as far less confusing? >I have had TM for more than 14 years and I head up the New Jersey TM support >group.....this original TM site has given me more good advice than I could >have possibly hoped for.....but now when I go on the other sites I no longer >know the history of the tm patient which does not allow me to answer most of >the questions put forth. >I am probably just venting ....I just want to know what others feel and what >we should if anything do about it! >All the best! > >Rob in New Jersey
