LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » General Support » 2nd week on meds for lyme life sucks pitty party

 - UBBFriend: Email this page to someone!    
Author Topic: 2nd week on meds for lyme life sucks pitty party
shorty31
Junior Member
Member # 21903

Icon 1 posted      Profile for shorty31     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have been on the meds for 1 week and 1 day or is it 1 week and 1 day?

I feel worse with each & every day!!! Is that normal?

I only remember ever having a tick on me being when I was 19 or 20 some where around there. I'm 31 nowI have have hospitalizing migrains since I was 20.

I could go on with all the issues but u all know them.

Any how I'm having ha hard time dealing with "treatment" and I m bearly being treated!!

I have found a few Drs. and I have a few appts coming up but untill then the "treatment" is just 100 mg 2x per day doxy. LOL

Any how I having a hard time dealing my whole body hurts, my joints, my arms my legs my head my neck my back my hips my head my head my head my fingers.

I can't sleep but I'm so tiered all I want to do is sleep. I sleep all day and Im awach all night.

I still go to work but I work on my feet & every step is like a knife stabing in so part of my body.

I want to cry but it hurts.

I have to be strong.

My Husband lost his job in Jan (on my B-Day) by the way.

My kidneys are failing becoue of bad stone due to my addrenal gland not working right that started 4 years ago.

When I told the dr to to test 4 other things she told me the kidney thing was genetic

Im 31 I have 2 kids great kids boys both. The dr. wants both of my boys to be tested they might have it also.

I'm poor becouse I didn't go to collage right after high school. I took a few years off....


When I tryed to go back my brain didn't work the same.

I failed out becouse I started having stones and migrains by know one could fix me there was nothing wrong with me.

It was all In my head.

Now I finally have a job I love and I don't think I'm going to be able to keep it....

My head hurts.

I can't make it go away I can't sleep

Got to tell you I would give up if it wern't 4 my boys.

I have to teach them to be strong

I wish the people closest to me could have even an bit of compassion instead

I hear about how hard there lives r

You know how they have more money then they know what 2 do with & how their bigest health issue is they r haveing a hard time having a baby

Know 1 eles I know has any health issues other then the baby thing


Ok so what it comes down 2 Is Im angry & sad. I didn't do anything wrong I shouldn't be sick

I hate that people have a hard time reading I don't hit entter alot.

I hate that I can't spell to save my life (never could)but I still hate it and it is worse now.

I hate that I'm one of those people that can't read understand if I don't hit enter alot.

I'm depressed.

I want to die

I don't want to be sick

I was happy 2 find out I had Lyme (until I found out what that ment) I though ya I have Lyme now I can take some pills and get better

I just fell like I'm going to die . But I won't b that lucky!!

Ill have to be turchered

I know It gets worse before it gets better blablabla la lalalalala

OK so now It is your turn

Your turn to vent or maybe cheer me up.

I got to tell you letting this all out where the whole world could read it is liberating

Posts: 9 | From lansdale pa | Registered: Aug 2009  |  IP: Logged | Report this post to a Moderator
KGK
Member
Member # 21845

Icon 1 posted      Profile for KGK     Send New Private Message       Edit/Delete Post   Reply With Quote 
I'm sorry you feel so bad. I'm in a similar situation-- been sick a long time and just started clarithromycin and plaquenil.

It is all very sad and frustrating. My doctor and family keep reminding me how important it is to try to stop being angry.

Easier said than done, but I know they're right.

I'm not sure I can cheer you up, but you are certainly not alone!!

--------------------
Kirsten, NH

+Lyme 2000, 10 days abx
RA, sero- 2002
Heart murmur 2006
Narcolepsy 2008
current: LLMD since 8/09

Posts: 11 | From NH | Registered: Aug 2009  |  IP: Logged | Report this post to a Moderator
Geneal
Frequent Contributor (5K+ posts)
Member # 10375

Icon 1 posted      Profile for Geneal     Send New Private Message       Edit/Delete Post   Reply With Quote 
Without my two young children (who tested positive too for Lyme)

I wouldn't be here doing okay.

I couldn't work for over two years.

Off meds now, but symptoms are slowly creeping back.

I've been where you are.

Had just lost my house to Katrina (4 years ago yesterday)

Then got so sick. Couldn't walk, couldn't talk.

Me...a Speech Pathologist who couldn't get a whole sentence out.

No "blablabla's", but wishing to send you some hope.

Prayers of hope and comfort coming your way.

I treated for over 2.5 years to get where I am.

More to go.

Family issues here too.

Only my Mom has taken the time to really listen and learn.

No one else and I have a nurse in the family.

Anger was one emotion I didn't have.

I didn't have the energy.

My children kept me going...I had to for them.

This is the right place to vent and the right place for support.

BTW, the first five weeks on doxy were like a scene from a horror movie.

Be kind to yourself. Watch your diet.

Rest when you can. If you get to feeling too sick,

Call your LLMD and let them know.

Herxing isn't fun.

My LLMD doesn't advocate pushing through bad ones.

Drink lots of water too.


Hugs,

Geneal

Posts: 6250 | From Louisiana | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
joalo
Frequent Contributor (1K+ posts)
Member # 12752

Icon 1 posted      Profile for joalo     Send New Private Message       Edit/Delete Post   Reply With Quote 
I don't have any words of wisdom but I just wanted to tell you things will get better. It took two straight years of treatment for me to start to feel better. [Eek!]

I would not be here either if I didn't have my children. I got sick when I was pregnant with my first child and he will be 24 on Monday. My kids are both adults now and I was so sick that I barely remember their childhoods. [Frown]

My kids turned out to be very caring, self-sufficient adults because of my illness and I thank God now that I didn't end my life years ago. [Smile]

I was sick a looong time before I started treatment so it's taking me longer to get well.

You are not alone. We all understand what you are going through. Feel free to "vent" here anytime you feel like it! [kiss]

JoAnne

--------------------
Sick since January 1985. Misdiagnosed for 20 years. Tested CDC positive October 2005. Treating since April 2006.

Posts: 3228 | From Somewhere west of the Mississippi | Registered: Aug 2007  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.