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Inga, You live in in an extraordinary beautiful place in Italy, Lake of Garda. We visited the place several years ago and noticed almost a tropical climate. It was very humid and hot as it was summer.However, just not far north from there towards Austria, the climate was very refreshing while the area was still breathtaking.I wander if the location change within Italy would be helpful to you. However, by going to Iceland in July and August, you have the best of the both worlds. I want to mention that after my husband was placed on small amounts of agonist Permax, his intolerance towards heat has almost disappeared.Inga, it was a pleasure, hearing from that part of the world. This List offers beneficial information on all aspect of PD. Take care. Emily ----- Original Message ----- From: "IngibjörgStefánsdóttir" <[log in to unmask]> To: <[log in to unmask]> Sent: Thursday, June 27, 2002 2:10 AM Subject: Re: PARKINSN Digest - 26 Jun 2002 (#2002-318) > Hello, I am Inga, Icelandic, living in Italy by the Lake of Garda and there is a lot if humidity. June has been tremenously warm so far or up to 40°C (104°F) some days. I was diagnosed 94 but started 92, on medicine since 94. Today I take 4x0,7 mg of Mirapex, 2x5mg of Selegerlin and 1x62,5 mg of Madopar in the morning to get started. In these warm days i have an excessive sweat, never ecsperienced anything like this before. Even though I take a shower after few minutes I am all sweat again .... like I was just stepping out from it. I have contacted other PWP in italy about this matter and they all exsperience the same. I go to Iceland every year in July - August and I noticed as soon as I am out of the warm in Italy and into the fresh air of my country the sweat stops and the dizziness goes away too.. I noticed also that some days I sweat less and I checked every day the humidity levels which is very variable in this area and the outcome was:: more sweat = more humidity. I hope this will be some help. > Inga > > > ATTACHMENT part 6 message/rfc822 Date: Wed, 26 Jun 2002 20:14:12 -0700 > From: charlotte A mancuso > Subject: Re: Symptoms > > Hi, > > Re: sweating: it can be both--my mother had PD and was on only > Cogentin--that's all there was--it's for tremor like Artane. Although > she was only 88 lbs and 5'4" and was a size 12 just to fit her big bones, > she perspired profusely. She really suffered in the heat, and in every > other way. And I've heard this from others who say that the PD will do > it--heat regulation is one of those autonomic systems that can get out of > wack from PD. > > But, read the full text for excessive sweating under known side effects > of PD drugs as well as many other drugs, like some antidepressants, > especially SSRIs for example--I know some of those are known to cause > excessive sweating in some people. > > I live in Northern Calif, where it is usually only moderately warm, and > low humidity by day, and a glorious 25-30 degrees cooler at night when > the fog comes in and brings down the temp and raises the humidity--you > guessed it--I'm sweating like a pig unless it's December! After a > shower, by the time I've struggled to dress and fuss to get ready, I'm > all sweaty again and too tired to be bothered, but I go on anyway, and > turn on the "air" in my car full blast--even often in cool weather. > > BTW, I'm taking 12-14 mg of requip, and have been as high as 16mg. But > then, there was too much edema. I also take every other thing for PD and > more. I was diagnosed in 98 (should have been 96 or even earlier), and > I'm thinking DBS in the STN. I can't stand the trade-offs of symptoms vs > side effects--it's a merry-go-round, and I'm already dizzy from the meds > and PD! I wanna get off! sigh... > > Charlotte > > On Wed, 26 Jun 2002 16:29:57 EDT cwatts > writes: > > Charlotte You are correct in saying that 6mg of Requip > > is not a therapeutic dose. I had such a bad experience with Mirapex > > (sleeping) that we are increasing the dose of Requip slowly. The > > dosage has just been increased to 2mg 3times daily along with > > Selegiline 5mg 2times daily. I am starting to have a little more > > energy but I am still very slow! > > I was wondering if > > anyone else on the list has noticed an intolerance to heat. I live > > in Illinois and it has been really warm (90's) and if I am outside > > only a short time, I sweat profusely. I am wondering if it is the > > disease or the meds. Thanks Cathy > > > > ---------------------------------------------------------------------- > > To sign-off Parkinsn send a message to: > > mailto:[log in to unmask] > > In the body of the message put: signoff parkinsn > > ATTACHMENT part 7 message/rfc822 Date: Wed, 26 Jun 2002 20:09:05 -0700 > From: Tony Schoonenberg > > Subject: > > Hi my name is Tony Schoonenberg for the past 16 years I have had parkinsons. > For the past 10 years > i have been Dr. Iaconos assint I have written 7 papers with him I have had 3 > pallidotomys and a > vp shunt now i have devloped dystona in my right foot witch has conifed my > to a wheel chair. Unforently i have had to retire so i have joined > this list i hope i can be of help. > > > > > --------------------------------- > Do You Yahoo!? > Sign-up for Video Highlights of 2002 FIFA World Cup > > ---------------------------------------------------------------------- > To sign-off Parkinsn send a message to: mailto:[log in to unmask] > In the body of the message put: signoff parkinsn ---------------------------------------------------------------------- To sign-off Parkinsn send a message to: mailto:[log in to unmask] In the body of the message put: signoff parkinsn