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Hi All

Have not been on in a while and took a while to catch

up. I feel so lucky in that I do not have the extreme

problems some of you have. I do have some of them but

not to the degree you have them. I use to have bowel

problems and a few accidents but after last surgery in

2000 I have not had hardly any problem. I use to have

problem empty my system and some times would have to

go back to bathroom several times. It made it hard to

go places on time and worry about where bathrooms were

on the way. Anyway that I hope is cured.

Now for my question. And hear is some back ground. I

do not think this is related to TCS but want to get

your opion and see if anyone else has this. In 1994 I

had a colonoscopy which showed I had divertuculitous

or at least the pouches. Typically most people do not

have this till they are older. I am 33. In 96 I had

my first flair up. I get pain in my lower left

abnomin. For those of you who do not know what this

is, it is thin areas or bulges in the lower part of

large intestines that get infected. Since the

colonoscopy showed the disease that is the diagnosis

of the pain. I have had about two flair ups a year

and antobotics clear it up. Now I am reading and

having the doctors recomend a colon resection. I

understand that most have great result with this

procedure and keeping this problem from coming back.

What they are recommending is doing it electively so

they can go in and remove diseased part and reconnect.

If I did get a flair up and it burst it would be like

having an apendix burst. Recovering on emergency

surger is about 3 months and elective is 2-3 weeks.

As of now I am going to have it done in March. My

question does anyone else have these symtoms? Has

any one else had a colonresection? Any other thoughts

would be apprieciated.

For you guys I do have problems in bedroom but Having

good luck with Viagra. It was not easy to go to the

doctor on but it was worth it.

someone mentioned the muscle stimulators being

advertised on tv. If anyone starts or are using those

please let me know if they are working. I would love

to find a way to build my leg back up. I do a lot of

walking and standing with work but not sure if I am

gaining any strength in that leg.

Take care

Don

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  • 3 years later...

How about Robitussin pearls/ I have used it but do not recall the warnings.

Also check on the pills that have tuss " in the name. They were recommended

for Liam.

Simmel

>

>Reply-To: LBDcaregivers

>To: " lbdcaregiversegroups " <LBDcaregivers >

>Subject: Question

>Date: Thu, 5 Jan 2006 09:44:56 -0800 (PST)

>

>

>I have seen where Robitussin has been the recommended

>cold/flu medication for congestion, stuffy nose,

>coughing, sneezing for LBD. Jim has a horrible cold,

>so I went to the pharmacy to pick up some Robitussin,

>but every box of Robitussin I looked at had a warning

>not to give to persons with Parkinsons. What is the

>recommended one? Thanks, Jan

>

>

>

>__________________________________________

>Yahoo! DSL – Something to write home about.

>Just $16.99/mo. or less.

>dsl.yahoo.com

>

>

>

>

>Welcome to LBDcaregivers.

>

>

>

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we have not been able to give Mom either the Robitussun type adult syrups or

Sudaphed...the results showed in her mobility / cognizance badly within

hours we have been able to use childrens non - narcotic type cold meds tho

they don't do much....just what happens with Mom......Tom

Question

>

> I have seen where Robitussin has been the recommended

> cold/flu medication for congestion, stuffy nose,

> coughing, sneezing for LBD. Jim has a horrible cold,

> so I went to the pharmacy to pick up some Robitussin,

> but every box of Robitussin I looked at had a warning

> not to give to persons with Parkinsons. What is the

> recommended one? Thanks, Jan

>

>

>

> __________________________________________

> Yahoo! DSL - Something to write home about.

> Just $16.99/mo. or less.

> dsl.yahoo.com

>

>

>

>

> Welcome to LBDcaregivers.

>

>

>

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Jan,

The Robitussin is the one without any other 'letters' on it. It is

only Guaifenesin and no other ingredients. Most drug stores have

their 'house' brand of exactly the same thing, for example,

Walgreens has 'Wal-Tussin'. I'm sure Longs has a similar product.

Jim

Jan wrote:

------------------------------------

Date: Thu, 5 Jan 2006 09:44:56 -0800 (PST)

Subject: Question

I have seen where Robitussin has been the recommended

cold/flu medication for congestion, stuffy nose,

coughing, sneezing for LBD. Jim has a horrible cold,

so I went to the pharmacy to pick up some Robitussin,

but every box of Robitussin I looked at had a warning

not to give to persons with Parkinsons. What is the

recommended one? Thanks, Jan

__________________________________________

Yahoo! DSL – Something to write home about.

Just $16.99/mo. or less.

dsl.yahoo.com

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  • 3 weeks later...

Rhona<

I was going to reply similarly to Courage. My Mum had Seroquel

increased marginally (she started at 12.5 mg x 3 times a day and went

to 25 mg x 2 times a day) when her agitation and hallucinations

increased. That was last April. This month her doctor (on a

suggestion from me) has cut her back down but changed the timing (12.5

mg in the morning and 25 mg at night). This " tweeking " seems to work

quite well.

--- gaat wrote:

---------------------------------

Hi Rhonda,

Since your dad is on a low dose of seroquel 1x a day you might want to

give him the other half tab in the early afternoon and see if this

helps

- it should but again this is just my opinion and Lord knows I am no

doctor. This way the dosing pattern we used for mom and it worked like

a charm for her. Is your dad taking any meds for PD?

Courage

Welcome to LBDcaregivers.

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