Guest guest Posted June 17, 1999 Report Share Posted June 17, 1999 Thanks Mish, Thank you all for the b-day emails. What a nice surprise. I turned 27 yesterday. Bobby and I went to an open captioned movie. I found a theater in my area listed at the Tripod web site told us about. A year ago, they didn't have much to offer. But now I see we have these captioned movies showing around here about once a week. We saw The Mummy, I wasn't real impressed with it but the captioning was great! Seeing the words along with feeling the vibrations of sound was cool. The movie wasn't all that hot, the good news is this theater is located inside a big, fancy outlet mall. How could I go wrong? I did learn I can't walk the way I use to. I was worn out before I could even spend money. Mish I don't think they are going to card me anymore, we will see! Check this out for captioned theaters: http://www.tripod.org/ Carla Misha64@... wrote: > From: Misha64@... > > Carla, > Happy birthday girlie!!!!!! I'm sorry I forgot your e-mail address so > this is for everyone's eyes ) I hope that today was good for you, what did > you do??? Another year older huh, well I'll bet you 20 bucks that when we met > in Vegas I won't be the only one that's carded hehee! > Luv ya! > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 17, 1999 Report Share Posted June 17, 1999 ----Original Message Follows---- 27? Dang, you guys are about my age?! So many of you remember wearing your checkered colored Vans to school with your muli-zippered jackets, and parachute pants! Wooo!!!! =D Mark Thanks Mish, Thank you all for the b-day emails. What a nice surprise. I turned 27 yesterday. Bobby and I went to an open captioned movie. _______________________________________________________________ Get Free Email and Do More On The Web. Visit http://www.msn.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 7, 1999 Report Share Posted July 7, 1999 I'm in San Diego, that is fairly close to Sacremeto. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 8, 1999 Report Share Posted July 8, 1999 Rhonda, I live in Vacaville which is west of Sacramento, about 45 minutes away. I will be gone for 3 weeks (Mexico and a deaf camp) but please e-mail about maybe getting together! I don't think anyone knows how fast the tumors grow. Manning tbman@... (no subject) CAN ANYONE TELL ME ANYTHING ABOUT HOW FAST THE TUMORS GROW? ALSO, IS ANYONE IN THE SACRAMENTO, CALI. AREA? THANK'S RHONDA Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 8, 1999 Report Share Posted July 8, 1999 Speedy That was great thanks.You had me sitting in front of my tv like an idiot.I wonder if you fooled " inspector gadget " Jimmy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 1999 Report Share Posted July 23, 1999 RHONDA, MY SON IS 13 AND I AM 35. I WAS 25 WHEN I FIRST DISCOVERED I HAD NF2. I THINK IT IS JUST GREAT THAT YOU ARE TRYING TO FIND OUT ALL THIS INFO FOR YOUR SISTER! BOY, THAT IS LOVE!! :-) I HAVE KNOWN THAT I HAD NF2 FOR 10 YEARS, BUT JUST RECENTLY GOT A COMPUTER SO I AM NEW TO THE CREW! BECAUSE OF MY DIAGNOSIS, THE DOCTORS KNEW WHAT TO LOOK FOR AND WHERE ABLE TO DIAGNOSE MY SON AT AGE 5. HE HAD HIS FIRST TUMOR REMOVAL - A GRAPEFRUIT SIZE TUMOR ON HIS RIGHT OPTIC NERVE - WHEN HE WAS 5!! TALK TO YA LATER! DONNA Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 23, 1999 Report Share Posted July 23, 1999 I thought this was what all parents are asking for? C'mon, there was a letter in 'Dear Abby' a while back when a parent complained that a child returned home because that child had financial problems and had to return home. Yet the parent complained! I thought this was what all parents wanted? Mark ----Original Message Follows---- From: HandsomeJimmy@... Reply-To: NF2_Crewonelist To: NF2_Crewonelist Subject: (no subject) Date: Fri, 23 Jul 1999 07:23:59 -0400 (EDT) From: HandsomeJimmy@... Don't read this if you are feeling a little sentimental without a box of klenex! --- > http://members.tripod.com/~momjkv/oatmeal.html Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 4, 2011 Report Share Posted December 4, 2011 Hi Jodie, As to the best of my knowledge there is not a known spirochete in MS Many cases of MS are lyme.It sounds simply like you herxed but did not do enough things to detox so the neurotoxins from the die off recirculated in your body.Do more to detox and take a binder to absorb the toxins OT - "MS Spirochetes" Posted by: "Jodie Milner" jodjm2@... jodjm2 Date: Sat Dec 3, 2011 9:22 pm ((PST))Hi all,Went to my naturopath guy this past week. I had done a full body coil a week and a half ago as I do on a 4 week basis. I waited a couple of days and hit mycoplasma. Later that day, started going downhill - thought it was a die-off. Can handle a die-off, not fun, but means something is working. But the bizarre thing is that after a few days, I'd feel somewhat better but then the next day, I'd feel worse again (no more coiling), symptoms never went away. They are pretty much my "what is this?" set of symptoms that I had on and off for 3 years before being diagnosed with lyme.So, I go to my naturopath trying to get some direction on what is going on. He can test frequencies and such to see if they will work with your present "top of the pile" problem. He tested for lyme, mycoplasma, babesia, bartonella, etc. He did a scan to see if it was viral or fungal (had dealt with candida earlier this year), possibly parasites, etc. Nothing like that showed up. What did show up was something called "MS Spirochetes". I know I don't have MS, been tested (MRI'd to death since this all started back in 2005) and even had a whole series of MRI's with and without contrast this past year. I know I don't have MS, as no spots and every neurologist I had gone to cleared me of MS as "it would show up on an MRI by now" and the symptoms were strong enough that they would definitely show up on an MRI.So, the naturopath tried explaining that no, I don't have MS (didn't think so) but there is a spirochete that is involved in MS and that is what is the king of the hill right now. The frequencies I have were for lyme and co-infections. He said 2 lyme frequencies were "good for me" (not sure if he meant for lyme or for this particular spirochete?). Of course, I got a naturopath remedy thingy to take twice a day. Just weird - as I had never heard of MS Spirochetes... Are there any frequencies for that? He could only test on frequencies that I came prepared with for the visit.Anyone else out there heard of those? I guess they come along for the ride with lyme, but not sure. And again, it isn't MS, but MS Spirochetes. Thanks much,The "other" Jodie :-)"Im not trying to counsel any of you to do anything really special,except to dare to think, and to dare to go with the truth ,and to dare to love completely." -R. Buckminster Fuller Quote Link to comment Share on other sites More sharing options...
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