kidsgotlyme
Frequent Contributor (1K+ posts)
Member # 23691
posted
I just got my daughter's medical records dating back to '00 when all of this started. I can't go back in time, but boy do I wish I could!!
The signs and symptoms were there all along. Even things I didn't remember. I feel so bad for not putting it together sooner.
I know I can't beat myself up, and it's not really my fault. I really trusted that the doctors were more intelligent than me and knew what was best for my child.
Life could be so different right now if I had known the true cause of her many symptoms.
I'm just rambling here. Nobody could understand how I feel except here. So sad!
-------------------- symptoms since 1993 that I can remember. 9/2018 diagnosed with Borellia, Babesia Duncani, and Bartonella Hensalae thru DNA Connections. Posts: 1470 | From Tennessee | Registered: Dec 2009
| IP: Logged |
We cannot go back. Thankfully, you now know and are taking action.
That thought gives me a lot of peace because I know so many kids are out there suffering and their parents have no clue. (I was one of them just a few months ago)
Also, thankfully, your daughter won't have to grow up still sick and have to figure it out for herself. She has you advocating for her!
-------------------- aperture Posts: 551 | From Louisville, KY | Registered: Nov 2011
| IP: Logged |
poppy
Frequent Contributor (1K+ posts)
Member # 5355
posted
Yes, I have had that feeling too. If only I had persisted in trying find out the reason for my swollen knee, had seen the tick and associated the red mark with lyme disease. Had access to more info about lyme disease. Accurate info! Then I would not have given up in disgust at the doc who told me my knee wasn't swollen, take a diuretic.
Fast forward almost three years, roof falls in on me....seizures, myriad symptoms.
Posts: 2888 | From USA | Registered: Mar 2004
| IP: Logged |
randibear
Honored Contributor (10K+ posts)
Member # 11290
posted
it's not what you did in the past that counts, it's that you are doing it now, helping her all you can.
some never see the light.
-------------------- do not look back when the only course is forward Posts: 12262 | From texas | Registered: Mar 2007
| IP: Logged |
lpkayak
Honored Contributor (10K+ posts)
Member # 5230
posted
i feel that way about my mom...and how she suffered and died...without real dx and tx...but i have to let it go and do the best i can today
its not our fault...hopefully what we all go thru will help those to come
maybe our grand kids and and great grand kids wont have to deal with this
-------------------- Lyme? Its complicated. Educate yourself. Posts: 13712 | From new england | Registered: Feb 2004
| IP: Logged |
jackie51
Frequent Contributor (1K+ posts)
Member # 14233
posted
I didn't know either. What is so obvious to us on Lymenet now other folks never get or get too late. If I hadn't been sick all those years, my children might not have suffered as long.
Mine are getting better, one is ready to get off meds. The other one is definitely on her way. I felt good today without the weight of their world on my shoulders.
It's a learning journey and we do our best. And, yes, the folks here really understand. My lyme doc understands too, thank God for that.
Posts: 1374 | From Crazy Town | Registered: Dec 2007
| IP: Logged |
kidsgotlyme
Frequent Contributor (1K+ posts)
Member # 23691
posted
I don't know what we would do without each other
-------------------- symptoms since 1993 that I can remember. 9/2018 diagnosed with Borellia, Babesia Duncani, and Bartonella Hensalae thru DNA Connections. Posts: 1470 | From Tennessee | Registered: Dec 2009
| IP: Logged |
I can't BELIEVE I took so long to realize something was wrong- I was falling asleep at work, sleeping 18 hours a day, forgetting people I'd known for a year...and I wrote it off as just stress and fatigue from school!!
second-guessing does nothing. Now you know you can fix. Your daughter is lucky you figured this out and are supporting her. I imagine with the lack of info about Lyme disease many children are undiagnosed for many, many years or possibly their whole life.
Posts: 503 | From Alberta, Canada | Registered: Jun 2009
| IP: Logged |
kidsgotlyme
Frequent Contributor (1K+ posts)
Member # 23691
posted
I was just so surprised at a lot of things I had forgotten about. When you read it all at once, it's really shocking!! I had been wanting to get her records for a long time now so I could share it with her LLMD.
-------------------- symptoms since 1993 that I can remember. 9/2018 diagnosed with Borellia, Babesia Duncani, and Bartonella Hensalae thru DNA Connections. Posts: 1470 | From Tennessee | Registered: Dec 2009
| IP: Logged |
kidsgotlyme
Frequent Contributor (1K+ posts)
Member # 23691
posted
We really did have a great pediatrician. I'm quite sure that if he had known anything at all about lyme disease, he would have helped us.
-------------------- symptoms since 1993 that I can remember. 9/2018 diagnosed with Borellia, Babesia Duncani, and Bartonella Hensalae thru DNA Connections. Posts: 1470 | From Tennessee | Registered: Dec 2009
| IP: Logged |
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,
NJ08534USA http://www.lymenet.org/