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 » blood draws

 - UBBFriend: Email this page to someone!    
Author Topic: blood draws
Cobweb
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Just wanted to know what to expect-I always go to the same labcorp for bloodwork.

Today the tech told me my left arm was no good for blood draws anymore-too much scar tissue from previous draws-so she took it from right arm.(which has also had many blood draws )

I asked her what happens when my right arm is kaput-she said then we'll try the feet!

Where are all the places on the body used for routine blood draws?? [Eek!]

Carol B

IP: Logged | Report this post to a Moderator
seibertneurolyme
Frequent Contributor (5K+ posts)
Member # 6416

Icon 1 posted      Profile for seibertneurolyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hubby usually has them use a butterfly needle and take blood from his hands. He has had IV drips infused in his feet before a couple of times in doctor's offices.

I think the thigh is another area I have heard mentioned before.

Bea Seibert

Posts: 7306 | From Martinsville,VA,USA | Registered: Oct 2004  |  IP: Logged | Report this post to a Moderator
Cobweb
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Thanks Bea- I think I would rather the thigh than the hand.
Carol

IP: Logged | Report this post to a Moderator
serendipity
LymeNet Contributor
Member # 8474

Icon 1 posted      Profile for serendipity     Send New Private Message       Edit/Delete Post   Reply With Quote 
Carol,
I have scar tissues built up in the veins in my arms.
So the techs use the veins in my hands, it is a slightly more painful procedure - I try to get someone experienced to do it. No one has mentioned the feet yet. And the thigh us extremely painful, at that point I would refuse bloodwork.

I hate this disease.
Sorry I just felt like venting.
I had "great veins" for blood draws two years ago.

[ 05. December 2006, 12:36 AM: Message edited by: serendipity ]

Posts: 628 | From the south | Registered: Dec 2005  |  IP: Logged | Report this post to a Moderator
Cobweb
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Serendipity-I think you posted on this topic before- but I was too lazy to search it back up.

HMmmmm-thighs? Hands? guess I'll just have to cross that bridge when I come to it. I'm thinking maybe I will be well enough, soon enough, to do without blood draws before it becomes an issue. How's that for wishful thinking!

I feel badly because last Monday my daughter had eight vials of blood drawn for her primary Duck-so I reassured her that yesterday they wouldn't be taking nearly so much blood-but what do I know- they took another eight vials yesterdy,too for the LLMD. Kind of undermines a mother's crediblility. [Frown]

Anybody feel like a voodoo doll?
Carol B

IP: Logged | Report this post to a Moderator
notcrazykate
LymeNet Contributor
Member # 10458

Icon 1 posted      Profile for notcrazykate     Send New Private Message       Edit/Delete Post   Reply With Quote 
Every time I go to my LLMD I leave half wondering if they're vampires [Wink]
Posts: 106 | From Michigan | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
lou
Frequent Contributor (5K+ posts)
Member # 81

Icon 1 posted      Profile for lou     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am also at the point of having butterfly needles in my hands. Helps to drink a lot of water beforehand and stay very warm, especially extremities. I bundle up, take a hot shower, wear gloves, look like a total goof.
Posts: 8430 | From Not available | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
Lioness
LymeNet Contributor
Member # 10655

Icon 1 posted      Profile for Lioness     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have had SO much blood drawn it is a wonder I have any blood left!

It is funny b/c they always say "you can look away" but it does not bother me when they take blood.

They would have to go all over b/c I was being stuck so much and they could not take (or inject) in the same place they had recently done.

Between the blood draws, IV's, injections. I am ammune to it!

But I HATE having things put in my veins! (ABX, vitamins, minerals, vaccines, anesthesia, etc...)

One key to having the veins poked... BE SURE YOU ARE WELL HYDRATED! It helps puff up the veins!

Posts: 240 | From MA | Registered: Nov 2006  |  IP: Logged | Report this post to a Moderator
Cobweb
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Thanks all-maybe I should switch draw times from early AM-when it's cold and I haven't had much to drink yet, to afternoon-warmest part of the day with plenty of time to drink before hand.

If they go for the hands though I am going to have to remind myself to breathe, just breathe- and I never ever look.

IP: Logged | Report this post to a Moderator
schnuddelka
LymeNet Contributor
Member # 8031

Icon 9 posted      Profile for schnuddelka   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
I actually have lots of problems with this. My veins are REALLY small and they can never find them, so I get poked 1-5 times per draw.

Feet - sounds awful, but since my arms don't work anymore, and "old faithful" in both hands are too scarred up, they've resorted to this.

The doctor has to order it specifically from the foot, but I find that the veins on my ankles are much less sensitive than my hands were.

eventually, there's always the juggular [lol]

--------------------
When given lyme make lymeade!
A tick check a day keeps lyme away! [email protected]
Raising awareness by creating as many lymebassadors as possible!

Posts: 158 | From Northern Wisconsin | Registered: Oct 2005  |  IP: Logged | Report this post to a Moderator
Cobweb
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Thanks Schnukums- I have actually refused to let them use my hands-it hurts so much-glad to hear the foot/ankle isn't as bad. Again- I haven't had to cross that bridge yet.

I think we should go for Wormsers jugular. [cussing]

IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 4 posted            Edit/Delete Post   Reply With Quote 
Carol, I like my hands; one that I don't write with. 1-2 months ago, I had problems and my hand swelled up; but generally no problems.

I'd hate to do feet; mine are so sensitive plus heel pain. [cussing]

IP: Logged | Report this post to a Moderator
pab
Frequent Contributor (1K+ posts)
Member # 904

Icon 1 posted      Profile for pab     Send New Private Message       Edit/Delete Post   Reply With Quote 
Jordan had a hard time with blood draws. He now puts on a Thermacare wrap before we leave home. It keeps his arm really warm and the blood draws are much easier.

--------------------
Peggy

~ ~ Hope is a powerful medicine. ~ ~

Posts: 2775 | From MN | Registered: Apr 2001  |  IP: Logged | Report this post to a Moderator
imanurse
LymeNet Contributor
Member # 7022

Icon 1 posted      Profile for imanurse     Send New Private Message       Edit/Delete Post   Reply With Quote 
I can no longer have draws on the left ever since my MRI last year. After they injected contrast it infiltrated and I had a large lump in my antecub area for 6 months. They tried recently to draw from that side and guess what... too much scar tissue.

My daughter always passes out when they take her blood. Friday we went in for routine labs and a cot wasn't available so we had to draw in the chair. I recognized the spacy stare and told the technician she is going to pass out now. The tech without a brain immediately left to get some juice. Duh. As I quickly grabbed my daughter to support her body she went limp, did the shaking jerking thing all over. I was supporting her head and body but the chair was right next to the wall and when she jerked her head hit the wall. Not hard, but enough to make a good noise.

The lab tech finally comes back and says here's your juice and I glared at her and said, "Don't you know you should never leave a patient if they are going to pass out?" She opens the door to the lab and screams, "I NEED HELP!!" Everyone came running freaking out and I just chuckled and I said, "I told the tech she was going to pass out and she did. At that point getting juice is not going to help if she can't drink it. She did hit her head on the wall. Please make a note of this somewhere that we must have her lie down." My daughter just then came to and puked all over the floor. Hopefully that tech won't ever leave a patient again if they say they are going to faint!!

--------------------
**Eat Chocolate**

Posts: 942 | From USA | Registered: Mar 2005  |  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.