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I know, late so Mom Sharon can send me to the corner. We had a nice time visiting my daughter and took a few days to come home ... every day was supposed to rain with heavy Tstorms but nary a one.

It was nice to get away for a bit but I'm finding that driving for 6 hours straight is getting too much for me. When we finally stop, I'm exhausted. Add to that dehydrated because I don't drink enough. Drink means many many pee stops where there's mainly bush.

Sharon, hope your bladder is okay and if it's still bad go to the dr please. Because I was too afraid to try the pill the dr gave me for the GERD or whatever I have, all I drank in 4 days was a big flat bottle of gingerale and a couple of glasses of water. Now I'm paying for it :(. One positive is I worked up the courage to try the pills and I've had 3 nights and days of NO acid reflux. Now I'm a bit worried because I've lost 15 pounds which is great. But I definitely want to lose some more, not put on.

Anyway I've been just lying under the fan ... bedroom close to bathroom and drinking H2O. Also had a disagreement with the Canadian MS Society who called to ask me to provide stamps and send letters to friends and family asking for donations. I said until they recognize the possible potential of CCSVI, I won't help them raise a dime. The co-ordinator of blah blah blah called me back and feigned ignorance which is laughable since she's also involved with their website. Which has blocked any discussion of the subject including results from those who've had the treatment.

She then asked if my local society had offered me much help and I told her when I was first diagnosed, frightened and feeling very much alone I contacted them. It took over a week for someone to get back to me and the convo was cut short when "well what CRAB are you on? Reply-None. "Well then what is it you want from us or are you asking for money?" Reply-EXPLETIVE.

Oops, sorry didn't mean to ramble on so .... hugs, Cait

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I'm glad to hear you are home from your visit, Cait. That's great about the pill helping the acid reflux! Three nights of sleep is wonderful. My son and my granddaughter have acid reflux too. big hugs SharonThis email is a natural hand made product. The slight variations in spelling and grammar enhance its individual character and beauty and in no way are to be considered flaws or defects. To: MSersLife Sent: Sat, July 31, 2010 7:47:51 PMSubject: Checking in

I know, late so Mom Sharon can send me to the corner. We had a nice time visiting my daughter and took a few days to come home ... every day was supposed to rain with heavy Tstorms but nary a one.

It was nice to get away for a bit but I'm finding that driving for 6 hours straight is getting too much for me. When we finally stop, I'm exhausted. Add to that dehydrated because I don't drink enough. Drink means many many pee stops where there's mainly bush.

Sharon, hope your bladder is okay and if it's still bad go to the dr please. Because I was too afraid to try the pill the dr gave me for the GERD or whatever I have, all I drank in 4 days was a big flat bottle of gingerale and a couple of glasses of water. Now I'm paying for it :(. One positive is I worked up the courage to try the pills and I've had 3 nights and days of NO acid reflux. Now I'm a bit worried because I've lost 15 pounds which is great. But I definitely want to lose some more, not put on.

Anyway I've been just lying under the fan ... bedroom close to bathroom and drinking H2O. Also had a disagreement with the Canadian MS Society who called to ask me to provide stamps and send letters to friends and family asking for donations. I said until they recognize the possible potential of CCSVI, I won't help them raise a dime. The co-ordinator of blah blah blah called me back and feigned ignorance which is laughable since she's also involved with their website. Which has blocked any discussion of the subject including results from those who've had the treatment.

She then asked if my local society had offered me much help and I told her when I was first diagnosed, frightened and feeling very much alone I contacted them. It took over a week for someone to get back to me and the convo was cut short when "well what CRAB are you on? Reply-None. "Well then what is it you want from us or are you asking for money?" Reply-EXPLETIVE.

Oops, sorry didn't mean to ramble on so .... hugs, Cait

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Hey Cait,I can relate to the bladder/travel situation. We were 6people in a car for 12 hours, and it was tough to geteveryone in 'sync' with their bathroom needs! My husbandhates to stop, so it made it all the more challenging!Stay cool, and keep drinking!love, Kate Checking inTo: MSersLife > I know, late so Mom Sharon can send me to the corner. We had a > nice time visiting my daughter and took a few days to come home > ... every day was supposed to rain with heavy Tstorms but nary a > one. > > It was nice to get away for a bit but I'm finding that driving > for 6 hours straight is getting too much for me. When we > finally stop, I'm exhausted. Add to that dehydrated because I > don't drink enough. Drink means many many pee stops where > there's mainly bush.> > Sharon, hope your bladder is okay and if it's still bad go to > the dr please. Because I was too afraid to try the pill the dr > gave me for the GERD or whatever I have, all I drank in 4 days > was a big flat bottle of gingerale and a couple of glasses of > water. Now I'm paying for it :(. One positive is I worked up > the courage to try the pills and I've had 3 nights and days of > NO acid reflux. Now I'm a bit worried because I've lost 15 > pounds which is great. But I definitely want to lose some more, > not put on.> > Anyway I've been just lying under the fan ... bedroom close to > bathroom and drinking H2O. Also had a disagreement with the > Canadian MS Society who called to ask me to provide stamps and > send letters to friends and family asking for donations. I said > until they recognize the possible potential of CCSVI, I won't > help them raise a dime. The co-ordinator of blah blah blah > called me back and feigned ignorance which is laughable since > she's also involved with their website. Which has blocked any > discussion of the subject including results from those who've > had the treatment.> > She then asked if my local society had offered me much help and > I told her when I was first diagnosed, frightened and feeling > very much alone I contacted them. It took over a week for > someone to get back to me and the convo was cut short when "well > what CRAB are you on? Reply-None. "Well then what is it you > want from us or are you asking for money?" Reply-EXPLETIVE.> > Oops, sorry didn't mean to ramble on so .... hugs, Cait> love and blessings,Kate

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