Guest guest Posted February 19, 2006 Report Posted February 19, 2006 Hi Pat, That's me. I live about 25 miles south east of there - haven't been in that area for ages. Yep, definitely summer here - got to 110+ not long ago though today a very pleasant mid to high 70s. Cheers, Gove wrote: > or Akiba, > > Which of you live in Melbourne, > Australia? My daughter in law, > Muenchen, mother is Jane > Spiteri, 211 Heath St., Port > Melbourne, , is there now > visiting from Colorado Springs, CO, USA. > Stop by and tell Jane and (whose husband > -who is my son, an M. D.) " Hello from > Cincinnati, OH from her mother in law, > Pat the Hat. Wish I were there-I heard it's > summer in Australia. Thanks. Pat Gove Quote
Guest guest Posted February 20, 2006 Report Posted February 20, 2006 , Thanks for replying. Stay out of the heat - bad for MS. Warm regards, Pat Gove >From: C <covo@...> >Reply-low dose naltrexone >low dose naltrexone >Subject: Re: [low dose naltrexone] Melbourne, Australia >Date: Sun, 19 Feb 2006 16:31:19 +1100 > >Hi Pat, > >That's me. I live about 25 miles south east of there - haven't been in >that area for ages. Yep, definitely summer here - got to 110+ not long >ago though today a very pleasant mid to high 70s. > >Cheers, > > > Gove wrote: > > > or Akiba, > > > > Which of you live in Melbourne, > > Australia? My daughter in law, > > Muenchen, mother is Jane > > Spiteri, 211 Heath St., Port > > Melbourne, , is there now > > visiting from Colorado Springs, CO, USA. > > Stop by and tell Jane and (whose husband > > -who is my son, an M. D.) " Hello from > > Cincinnati, OH from her mother in law, > > Pat the Hat. Wish I were there-I heard it's > > summer in Australia. Thanks. Pat Gove > > Quote
Guest guest Posted February 21, 2006 Report Posted February 21, 2006 Pat, Lucky??? for me I don't have MS. I have PLS (Primary Lateral Sclerosis) and the heat doesn't affect me any more than a 'normal' person. However, if I get cold I can't move - I just go rigid. Gove wrote: > , > > Thanks for replying. Stay out of the heat - bad for MS. > Warm regards, Pat Gove Every day I beat my own previous record for number of consecutive days I've stayed alive. . ,-._|\ Covington / Oz \ \_,--.x/ v Quote
Guest guest Posted February 21, 2006 Report Posted February 21, 2006 Has anyone with MS had body aches when starting ldn ? How long till you see results? Thank you On 2/21/06 6:59 AM, " C " <covo@...> wrote: > Pat, > > Lucky??? for me I don't have MS. I have PLS (Primary Lateral Sclerosis) > and the heat doesn't affect me any more than a 'normal' person. > However, if I get cold I can't move - I just go rigid. > > > > Gove wrote: > >> , >> >> Thanks for replying. Stay out of the heat - bad for MS. >> Warm regards, Pat Gove > > > > Every day I beat my own previous record for number of consecutive days I've > stayed alive. > . > ,-._|\ Covington > / Oz \ > \_,--.x/ > v > > > > > > Quote
Guest guest Posted February 22, 2006 Report Posted February 22, 2006 > > > >> , > >> > >> Thanks for replying. Stay out of the heat - bad for MS. > >> Warm regards, Pat Gove > > > > > > > > Every day I beat my own previous record for number of consecutive days I've > > stayed alive. > > . > > ,-._|\ Covington > > / Oz \ > > \_,--.x/ > > v > > > > > > > > > > > > Quote
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