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All our hearts go out to you, of course you are welcome to join us. Here is

a place you find hope, from hearing the stories of those who have been

through what you (and I right now) are going through, and have come out the

other side, successfully. There are friends to be made here , and support,

and great advice.

Please do tell us where you live, and what is being done to help your son.

My daughter, , also 12, has been home as well since July, and it is

very difficult both for her and for me. She is not suicidal, but raging out

of control, and we are currently waiting for a psych hospital bed for her to

become available.

ERP (exposure and response therapy) rid of her compulsions, but not

of her obsessions it seems and the pressure of just existing has proven too

much for her. While the walls and doors of my house have suffered greatly,

we don't have a door left on its frame in the house, and I've gotten hurt a

few times from her rage, I am grateful that her rage is outward and not

inward.

There are archives that can be accessed through the OCDparenting main page on

Egroups where you can search for terms such as ERP, and there is a wealth of

information to be found there.

Write soon, and tell us more.

Ellen/NY

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Hi Jenni:

Welcome to this list. I have a 13-year-old son, Steve, who also has OCD

and major depressive disorder (MDD). Being on suicide watch is exhausting

and my heart goes out to you and your family.

Is your son getting any treatment? We found this invaluable in getting the

MDD under control so he could get treatment for the OCD. Steve seems to

have both OCD and MDD as primary diagnoses. In fact now his OCD has been

treated, his relapses are from poop out on meds and his depression comes

back but not so much the OCD.

How are you sleeping? Sleep deprivation is the enemy of coping with NBDs

in our kids. Sometimes our kids have thoughts which are part of violent

obsessions. We also had Steve doing self-injurious behaviors as part of

adjusting to lowering of meds. It can be a real challenge to figure out

what is going on. Good luck, take care, aloha, Kathy (H)

kathyh@...

At 06:35 AM 12/04/2000 +0000, you wrote:

>Hi! I hope you don't mind if I join you, but I've been looking for a

>group like this for ages! I'm the Mom of a 12 year old boy suffering

>from OCD and severe depression. In April of this year he attempted

>suicide, then seemed to improve a lot over the summer, however we are

>back on a suicide watch again, and his school won't allow him to go

>until he can state he has no suicidal thoughts. You can imagine the

>battles starting up round here! When my brain is working better in

>the morning I will try and organize my thoughts and come back here!

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  • 3 years later...

Welcome Terry. I'm glad you found the group.

Lainie

Terry Willoughby <tntw3@...> wrote:

Hello everyone, my name is Terry I am 31 and have SMA T3. I walk with

no aides, although I get " down to earth " a lot but I still get up on

my own. I started having muscular trouble at 8 Yrs old but was

properly diagnosed at 30 after several MIS diagnose before that. I

have a lot of pain from a car wreck I had but other than that all is

well. I wish I knew how long I will be able to walk and Ect. I hope

to learn a lot from all of you. It is very comforting to see so many

others with the same disease getting tougher to share experiences. I

do work and hope to be able to for a while anyway. I am married to a

VERY supportive and wonderful women and we have 4 children. I have 1

brother he is 6'9 and weighs 260 and is very healthy. I am 6' and

weigh 142. so we look a lot alike. Any way I just wanted to say hello

and say I look forward to getting to know all of you. The 1 question

I would like to start with is, are there any meds of any kind that

are helpful vitamin's or what ever. Thank you in advance.

Terry

" I'm not as good as I once was but I'm as good once as I ever was "

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join the list.

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Terry,

Welcome. I live in New York, am 53 and have used a wheelchair since I'm 11. I

don't really know what type I am. I'm a II or III. I did office work for over

20 years, but I no longer work. Unfortunately, I have never married or had

kids. I have just written a book about my life, which will be published next

year.

Napolitano

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  • 4 weeks later...

Welcome !!

Get your mindset ready by re-reading the Body For Life book,

especially focus on Cross the Abyss. And get movin! We're here for

any questions u have!

~Nanci

>

> Hi Everyone,

> I am new to the board but I have done BFL for a about 5 years on

and

> off. I maintained my weight for 3 years and then I have gotten

real

> lazy with the nurtrition side of it and have put on about 15 pounds

> so that is what I am here for. Motivation to get my butt in gear

> and eat right! I am looking forward to getting to know you all

> better and to gleen from your expertise. Hope you all had a very

> merry holiday season. I also am ready to come alive in 2005! Lets

> get this party started!

>

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  • 2 months later...

>

> Hi Everyone,

> My name is Grace and I'm new to this board. Not new to BFL as

I've

> started it a number of times and have NEVER finished it. I

started

> again and AGAIN I feel like I'm falling flat on my fat head!

Welcome. Please try not to feel discouraged. Remember you are not

alone. We have all been there one day or another, one time or

another, one minute or another. One thing that helps me is the

quote: strive for progress not perfection. I'm not perfect, as much

as I'd like to be. When I screw up, I just get back on the wagon and

keep on going.

Colleen

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Guest guest

Hi ,

Thanks for the words of encouragement. I'm printing this out so that I can

see it everyday. I am the worst at beating myself up. Thanks for the links

too, I'm going to go check them out now too.

Grace

>From: Skwigg <skwigg@...>

>Reply-

>

>Subject: Re: New to the board

>Date: Mon, 28 Feb 2005 09:39:00 -0600

>

>We have a little saying around here that goes, " Cheat like hell but

>never quit. " :-) No matter how crazy things get, never consider

>yourself " off " the program. Never entertain the idea that you've

>failed or blown it or that you have to start over. Starting over and

>over and over again will JACK your mind up. It just confirms all those

>nagging doubts that you can't do it, that you're not worth it, that it

>will never work for you, etc.

>

>So, even if you cheat all over the place, keep going the best you can.

>Pay attention to what you're telling yourself. Mentally, there's a

>world of difference between saying " I can't. I've blown it. I quit. "

>and saying " This has been a really rough week but I'm still going and

>nothing will stop me. " See, at least with the second option you feel

>good about yourself and you continue to see results, even though they

>may be slower than if you were going about it all hardcore.

>

>Here are some other posts to check out if you haven't seen them already:

>

>I've Fallen and I Can't Get Up

>http://www.skwigg.com/id63.html

>

>Cheaters Prosper

>http://www.skwigg.com/id28.html

>

>This is Your Brain on Body for Life

>http://www.skwigg.com/id60.html

>

>

>

>

>On Mon, 28 Feb 2005 14:44:44 -0000, Grace <greilly28@...> wrote:

> >

> >

> > Hi Everyone,

> > My name is Grace and I'm new to this board. Not new to BFL as I've

> > started it a number of times and have NEVER finished it. I started

> > again and AGAIN I feel like I'm falling flat on my fat head! I have

> > pretty close to 100 lbs to lose and I'm really discouraged. This is

> > week 4 for me but you wouldn't know it as at the end of week 2 I

> > weighed myself and had only lost a pound so I stopped because I was

> > so down on myself. Well the truth is, I felt pretty good during

> > those 2 weeks and now I'm having a heck of a time starting back up.

> > I feel like such a failure. Although I must say, when I came back to

> > this sight after seeing it a few years ago, the pictures have really

> > helped me. Everyone looks great! I just need to stay focused and

> > that's easier said than done for me. Any words of encouragement or

> > tips would be greatly appreciated.

> > Thanks,

> > Grace

> >

> >

> >

> >

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Guest guest

Hi ,

Thanks for the words of encouragement. I'm printing this out so that I can

see it everyday. I am the worst at beating myself up. Thanks for the links

too, I'm going to go check them out now too.

Grace

>From: Skwigg <skwigg@...>

>Reply-

>

>Subject: Re: New to the board

>Date: Mon, 28 Feb 2005 09:39:00 -0600

>

>We have a little saying around here that goes, " Cheat like hell but

>never quit. " :-) No matter how crazy things get, never consider

>yourself " off " the program. Never entertain the idea that you've

>failed or blown it or that you have to start over. Starting over and

>over and over again will JACK your mind up. It just confirms all those

>nagging doubts that you can't do it, that you're not worth it, that it

>will never work for you, etc.

>

>So, even if you cheat all over the place, keep going the best you can.

>Pay attention to what you're telling yourself. Mentally, there's a

>world of difference between saying " I can't. I've blown it. I quit. "

>and saying " This has been a really rough week but I'm still going and

>nothing will stop me. " See, at least with the second option you feel

>good about yourself and you continue to see results, even though they

>may be slower than if you were going about it all hardcore.

>

>Here are some other posts to check out if you haven't seen them already:

>

>I've Fallen and I Can't Get Up

>http://www.skwigg.com/id63.html

>

>Cheaters Prosper

>http://www.skwigg.com/id28.html

>

>This is Your Brain on Body for Life

>http://www.skwigg.com/id60.html

>

>

>

>

>On Mon, 28 Feb 2005 14:44:44 -0000, Grace <greilly28@...> wrote:

> >

> >

> > Hi Everyone,

> > My name is Grace and I'm new to this board. Not new to BFL as I've

> > started it a number of times and have NEVER finished it. I started

> > again and AGAIN I feel like I'm falling flat on my fat head! I have

> > pretty close to 100 lbs to lose and I'm really discouraged. This is

> > week 4 for me but you wouldn't know it as at the end of week 2 I

> > weighed myself and had only lost a pound so I stopped because I was

> > so down on myself. Well the truth is, I felt pretty good during

> > those 2 weeks and now I'm having a heck of a time starting back up.

> > I feel like such a failure. Although I must say, when I came back to

> > this sight after seeing it a few years ago, the pictures have really

> > helped me. Everyone looks great! I just need to stay focused and

> > that's easier said than done for me. Any words of encouragement or

> > tips would be greatly appreciated.

> > Thanks,

> > Grace

> >

> >

> >

> >

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Guest guest

Thanks for the welcome Colleen!

> >

> > Hi Everyone,

> > My name is Grace and I'm new to this board. Not new to BFL as

> I've

> > started it a number of times and have NEVER finished it. I

> started

> > again and AGAIN I feel like I'm falling flat on my fat head!

>

> Welcome. Please try not to feel discouraged. Remember you are not

> alone. We have all been there one day or another, one time or

> another, one minute or another. One thing that helps me is the

> quote: strive for progress not perfection. I'm not perfect, as

much

> as I'd like to be. When I screw up, I just get back on the wagon

and

> keep on going.

>

> Colleen

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Guest guest

Thanks for the welcome Colleen!

> >

> > Hi Everyone,

> > My name is Grace and I'm new to this board. Not new to BFL as

> I've

> > started it a number of times and have NEVER finished it. I

> started

> > again and AGAIN I feel like I'm falling flat on my fat head!

>

> Welcome. Please try not to feel discouraged. Remember you are not

> alone. We have all been there one day or another, one time or

> another, one minute or another. One thing that helps me is the

> quote: strive for progress not perfection. I'm not perfect, as

much

> as I'd like to be. When I screw up, I just get back on the wagon

and

> keep on going.

>

> Colleen

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  • 1 year later...
Guest guest

You're off to a GREAT start. Keep at it!

>

> I started Body for Life on April 17 and have been going along

nicely.

> I weighed 216 lbs. when I first started and I now weigh 210.5.

I'm

> pretty pleased with that - I am not deceiving myself that this

could

> just be water I'm losing now. I enjoy doing the cardio and upper

body

> work. The lower body exercises is pretty rough on me as my weight

is

> such a problem.

>

> I had a Wheat Thin attack last night but I'm back on track again.

At

> my office, the sweets are kept very close to my desk and I was

> watching one person go through the Little Debbie cakes and the

more I

> watched them the more hungrier I got. I felt like I was suddenly

> starving. Well, I didn't cave in and was sure glad to get home

and

> work out to get my mind off the sweets.

>

> My weakness is Pringles and Pop. I've not had any since I started

> this challenge. I drink flavored water to take the place of pop

and

> fruit to take the place of Pringles. It seems to be working.

>

> I look forward to learning and sharing with all of you.

>

> Cecilia

>

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Guest guest

Welcome - to the board and a great way of eating

n

At 09:32 AM 4/27/2006, you wrote:

>I started Body for Life on April 17 and have been going along nicely.

>I weighed 216 lbs. when I first started and I now weigh 210.5. I'm

>pretty pleased with that - I am not deceiving myself that this could

>just be water I'm losing now. I enjoy doing the cardio and upper body

>work. The lower body exercises is pretty rough on me as my weight is

>such a problem.

>

>I had a Wheat Thin attack last night but I'm back on track again. At

>my office, the sweets are kept very close to my desk and I was

>watching one person go through the Little Debbie cakes and the more I

>watched them the more hungrier I got. I felt like I was suddenly

>starving. Well, I didn't cave in and was sure glad to get home and

>work out to get my mind off the sweets.

>

>My weakness is Pringles and Pop. I've not had any since I started

>this challenge. I drink flavored water to take the place of pop and

>fruit to take the place of Pringles. It seems to be working.

>

>I look forward to learning and sharing with all of you.

>

>Cecilia

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Guest guest

Welcome to the group and to BFL. You are doing a great job! Treats

in the office are killer. It's hard because they are right there,

they don't cost anything (except a broken self-promise) and the guys

eating them (at least in our office) are young and in shape (looks

like it anyway, not that I was looking..).

Flavored water and fruit- YUMMY. Good choices!

Chocolate & sugar.. bad. EXCEPT ON FREE DAY. Gotta love my free days.

Keep up the GREAT work, Cecelia!

>

> I started Body for Life on April 17 and have been going along nicely.

> I weighed 216 lbs. when I first started and I now weigh 210.5. I'm

> pretty pleased with that - I am not deceiving myself that this could

> just be water I'm losing now. I enjoy doing the cardio and upper body

> work. The lower body exercises is pretty rough on me as my weight is

> such a problem.

>

> I had a Wheat Thin attack last night but I'm back on track again. At

> my office, the sweets are kept very close to my desk and I was

> watching one person go through the Little Debbie cakes and the more I

> watched them the more hungrier I got. I felt like I was suddenly

> starving. Well, I didn't cave in and was sure glad to get home and

> work out to get my mind off the sweets.

>

> My weakness is Pringles and Pop. I've not had any since I started

> this challenge. I drink flavored water to take the place of pop and

> fruit to take the place of Pringles. It seems to be working.

>

> I look forward to learning and sharing with all of you.

>

> Cecilia

>

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Guest guest

Very good progress Cecilia! Rest assured that by doing the program you¹re

losing more than water, your losing fat and gaining muscle and before you

know it you¹ll be able to do more of the lower body stuff!

Laurie

> I started Body for Life on April 17 and have been going along nicely.

> I weighed 216 lbs. when I first started and I now weigh 210.5. I'm

> pretty pleased with that - I am not deceiving myself that this could

> just be water I'm losing now. I enjoy doing the cardio and upper body

> work. The lower body exercises is pretty rough on me as my weight is

> such a problem.

>

> I had a Wheat Thin attack last night but I'm back on track again. At

> my office, the sweets are kept very close to my desk and I was

> watching one person go through the Little Debbie cakes and the more I

> watched them the more hungrier I got. I felt like I was suddenly

> starving. Well, I didn't cave in and was sure glad to get home and

> work out to get my mind off the sweets.

>

> My weakness is Pringles and Pop. I've not had any since I started

> this challenge. I drink flavored water to take the place of pop and

> fruit to take the place of Pringles. It seems to be working.

>

> I look forward to learning and sharing with all of you.

>

> Cecilia

>

>

>

>

>

>

>

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  • 2 years later...

Hi, Kristy lyme disease goes away but the damage it causes is with you forever. And yes a muscle rub works for me. Be very careful because it is easier to get again and the side effects get worse. Welcome to the group you will find a lot of good people here I have. LMay

From: mecode4u <mecode4u@...>Subject: New to the board Date: Thursday, September 25, 2008, 10:06 AM

Hello,My name is Kristy. I found out that I have Lymes about 4 years ago. It was found too late, but they still gave me the anti-biotics, which I threw up-BUT I still have every once in a while pain in my elbow. That is what brought me the Dr. in the first place. I felt like I had a severe disease cause it was hard to use my arm. They at first said "it must be your fibromyalgia" . I responded with,"No, I know what that pain feels like". How long does this linger? Am I to suffer forever and what can I do for the pain without asking for drugs? Does an analgesic help?HELPKristy, CMA

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Hi, Kristy lyme disease goes away but the damage it causes is with you forever. And yes a muscle rub works for me. Be very careful because it is easier to get again and the side effects get worse. Welcome to the group you will find a lot of good people here I have. LMay

From: mecode4u <mecode4u@...>Subject: New to the board Date: Thursday, September 25, 2008, 10:06 AM

Hello,My name is Kristy. I found out that I have Lymes about 4 years ago. It was found too late, but they still gave me the anti-biotics, which I threw up-BUT I still have every once in a while pain in my elbow. That is what brought me the Dr. in the first place. I felt like I had a severe disease cause it was hard to use my arm. They at first said "it must be your fibromyalgia" . I responded with,"No, I know what that pain feels like". How long does this linger? Am I to suffer forever and what can I do for the pain without asking for drugs? Does an analgesic help?HELPKristy, CMA

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Hi, Kristy lyme disease goes away but the damage it causes is with you forever. And yes a muscle rub works for me. Be very careful because it is easier to get again and the side effects get worse. Welcome to the group you will find a lot of good people here I have. LMay

From: mecode4u <mecode4u@...>Subject: New to the board Date: Thursday, September 25, 2008, 10:06 AM

Hello,My name is Kristy. I found out that I have Lymes about 4 years ago. It was found too late, but they still gave me the anti-biotics, which I threw up-BUT I still have every once in a while pain in my elbow. That is what brought me the Dr. in the first place. I felt like I had a severe disease cause it was hard to use my arm. They at first said "it must be your fibromyalgia" . I responded with,"No, I know what that pain feels like". How long does this linger? Am I to suffer forever and what can I do for the pain without asking for drugs? Does an analgesic help?HELPKristy, CMA

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Hi Sharon! Welcome!

If it were me, I wouldn't get any of them....here's why:

" Merck warns in its Manual that patients with, or from families with,

B and/or T cell immunodeficiencies should not receive live-virus

vaccines due to the risk of severe or fatal infection. Elsewhere, it

lists features of B and T cell immunodeficiencies as food allergies,

inhalant allergies, eczema, dermatitis, neurological deterioration

and heart disease. To translate, people with these conditions can die

if they receive live-virus vaccines. Their immune systems are simply

not competent enough to guarantee a healthy reaction to the viral

assault from modified live-virus vaccines " .

http://www.dogsadversereactions.com/scienceVaccineDamage.html

My guess is that your doctor's office must purchase by box or case

and they aren't willing to do that though.

http://vaers.hhs.gov/pdf/PackageInserts.pdf

Dawn

http://vaccinesexposed.blogspot.com

>

> Hi All~

> I am new to the board and I wanted to introduce myself. I am the

> mother to 15 month old twins, B/G. We are live in land close

to

> Baltimore. The reason I joined the board is b/c I am in search of

> trying to split up my twins MMR shot. My son has some health

issues

> (egg allergy and prone to seizures) and my gut is telling me not to

> give him the 3 in 1 shot.

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Hi, Sharon. Welcome! You are very smart not to get the MMR all at once. If you

really feel you want to give them separately, it will be worth your while to pay

for the entire box (or three). Much cheaper than therapy for autistic children.

But even then you are not home free with side effects.

I urge you to research more about vaccines before continuing on with any

vaccines. They are not guaranteed to work, let alone for any length of time and

all vaccines carry the risk of death. It is a game of Russian Roulette each and

every time.

Anyway, definitely avoid the 3 in 1.

Winnie

New to the Board

Vaccinations

> Hi All~

> I am new to the board and I wanted to introduce myself. I am

> the

> mother to 15 month old twins, B/G. We are live in land

> close to

> Baltimore. The reason I joined the board is b/c I am in search

> of

> trying to split up my twins MMR shot. My son has some health

> issues

> (egg allergy and prone to seizures) and my gut is telling me not

> to

> give him the 3 in 1 shot. Currently I am doing a alternative

> vaccination schedule. I have made many calls to see about

> splitting

> the shot and either people think I am crazy or I have to order

> 10 of

> each shot. Do you have any suggestions on how I can get my

> twins

> single shots? I looked to see if there was a group in the area

> that

> might buy them and split them but no luck so far. Any info is

> apprecitated!

> TIA

> Sharon

>

>

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Welcome aboard!

I would suggest doing an advanced search using measles as the subject

and Nakken as the author. Just recently the list owner gave us tons

of information about the measles, and come to think of it rubella as

well. I would recommend searching this information out, and seeing

if your gut is maybe telling you not to do any vaccines... The

decision to vaccinate is a personal one, but should only be done once

all the information has been presented. Good luck, if you can't find

the info in the archives let me know and I can email it to you

offlist.

Marci

> >

> > Hi All~

> > I am new to the board and I wanted to introduce myself. I am the

> > mother to 15 month old twins, B/G. We are live in land close

> to

> > Baltimore. The reason I joined the board is b/c I am in search

of

> > trying to split up my twins MMR shot. My son has some health

> issues

> > (egg allergy and prone to seizures) and my gut is telling me not

to

> > give him the 3 in 1 shot.

>

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don't vaccinate, saves a lot of hassle

my last 2 are unvaccinated, now 14 and 12--the 12 year old just went to new

school and did cross country run and she beat her year and the year above, then

they said she had the best time in the whole school.

all vaccines are ineffective and dangerous, I took apart measles one here

http://www.whale.to/vaccines/measles.html

john

New to the Board

Hi All~

I am new to the board and I wanted to introduce myself. I am the

mother to 15 month old twins, B/G. We are live in land close to

Baltimore. The reason I joined the board is b/c I am in search of

trying to split up my twins MMR shot. My son has some health issues

(egg allergy and prone to seizures) and my gut is telling me not to

give him the 3 in 1 shot. Currently I am doing a alternative

vaccination schedule. I have made many calls to see about splitting

the shot and either people think I am crazy or I have to order 10 of

each shot. Do you have any suggestions on how I can get my twins

single shots? I looked to see if there was a group in the area that

might buy them and split them but no luck so far. Any info is

apprecitated!

TIA

Sharon

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

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>

> Hi All~

> I am new to the board and I wanted to introduce myself. I am the

> mother to 15 month old twins, B/G. We are live in land close

to

> Baltimore. The reason I joined the board is b/c I am in search of

> trying to split up my twins MMR shot. My son has some health

issues

> (egg allergy and prone to seizures) and my gut is telling me not to

> give him the 3 in 1 shot. Currently I am doing a alternative

> vaccination schedule. I have made many calls to see about

splitting

> the shot and either people think I am crazy or I have to order 10

of

> each shot. Do you have any suggestions on how I can get my twins

> single shots? I looked to see if there was a group in the area

that

> might buy them and split them but no luck so far. Any info is

> apprecitated!

> TIA

> Sharon

>

Hi Sharon,

Welcome to the group! Please take your time in making this

decision. Don't let anyone pressure you into vaccinating if

something is telling you not to. Trust your instincts! At the very

least, you can delay for as long as necessary while you research

about it. And as for your doctor's office, if they are not willing

to accomodate your wishes, you should really find a new office. Your

doctor should be willing to do whatever you ask as the parent. Good

luck in your research! You may want to do a search on this board for

MMR and reactions for more info. --, Mom to two totally

unvaxxed, very healthy kids!

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  • 3 years later...
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Hi all,

My name is Abigail and I am a 26 year old who was diagnosed with Achalasia

last year in April.

My symptoms started in Nov - Dec 2010 when noticed occasional difficulty

swallowing. I tried chewing more, but it did not seem to help. Then, I started

getting frequent heartburn. I went to see a GI who said these symptoms could be

a number of things and recommended a endoscopy. The endoscopy was normal and he

stretched the LES slightly which he told me shold help with the difficulty

swallowing; it did not.

He then recommended that I have a esophogeal manometry (the worst test EVER!),

which showed that the peristalsis was gone, all the muscles were moving at the

same time. It also showed that my LES was very constricted. At this point my GI

knew I had Achalasia but wanted to do a barium swallow to confirm. He also

ordered a blood test for Chagas disease since I have been to central america 5

times in the past 7 years. The barium swallow showed a delayed release of the

solution and confirmed the diagnosis.

Throughout the months of all of the doctor appointments and tests and things,

I developed a scary new symptom. I would wake up in the middle of the night

coughing up stomach fluid and/or food that had not emptied into my stomach. This

sounds gross, but sometimes the food would come up through my nose. I had to

buy a special pillow and sleep upright. My eating also got worse and I could

only take a couple of bites of each meal. I would be on my second bite, and my

fiance would be finishing his meal. Drinking liquids was just as bad. My weight

dropped dramatically.

I weighed all of my options for treatment and decided to go with the HM with

Dor fundoplication (in Aug). It was done with the Da Vinci robot, which is a

very advanced surgical machine that helps the surgeons to make very precise

incisions and gives them more control. I ended up having to stay in the hospital

for 3 nights rather than the standard 1 due to post operative swelling.Has

anyone else had the HM with DF? If so, how long ago and how are you faring?

Since the surgery I am back up to my normal weight, I can sleep laying down, I

rarely have heartburn, and eating is much better. However, some foods are more

difficult to eat than others. I also occasionally get the spasms and they

usually (and very inconveniently) happen in the middle of the night. I was

taking amitriptyline for this but it did not help too much. What do you guys do

when you have these spasms?

Anyway, I am glad I found a board for Achalasia sufferers. I look forward to

getting to know you all.

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