lyme in Putnam
Frequent Contributor (1K+ posts)
Member # 11561
posted
I'm watching entertainment tonight and am angry about the segment of the stars with ms. Am I being selfish that ms got this publicity outlining their symptoms and Lyme has few or not sure if I believe it's ms and not Lyme. Either way, it's a shame for anyone to go through this. Is it just me being selfish or does your gut tell you practically most disease start as Lyme? How can you tell ms distinctly. Sorry it's just one of those days. I know there is ms, but it's frustrating to be looking at the wrong diagnosis.
-------------------- He took u to it, He'll you through Posts: 2837 | From NE. | Registered: Apr 2007
| IP: Logged |
Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- See the Goldings article - and others - here: ---------------------
posted
I'm interested in this subject a lot. My cousin lived with me in a tick ridden appt. He got sick in 2006 and went through the system before being dx with MS. I got sick in 2009 and went through the system as well, also getting an MS dx.
He has been receiving medical treatment for 5 years now and is gravely ill. He's refused to take my advice of getting correctly tested for lyme. He is 6' 3" and 80some lbs and is fed through a tube while I am in treatment for many TBD's.
I cannot forcibly take him to see an LLMD..Not sure who's to blame, him or the doctors....Ultimately the IDSA.
Cannot say for sure he has lyme but I sure do suspect it. He's on a steroid, painkiller pump that keeps him going...Talk about treating the symptom and not the cause..If/when he dies(in his 30s), I absolutely blame the system.
Theres a point when it is no longer conspiratorial, just fact.
Posts: 109 | From PA | Registered: Feb 2012
| IP: Logged |
Lauralyme
Frequent Contributor (1K+ posts)
Member # 15021
posted
oh wow that is a horrible situation how sad
-------------------- Fall down seven times, get up eight ~Japanese proverb Posts: 1146 | From west coast | Registered: Mar 2008
| IP: Logged |
lpkayak
Honored Contributor (10K+ posts)
Member # 5230
posted
putnam...i think the way you do about it...
lymenow-that is so sad. i am in a similar situation as you. my brother was dx with lyme and treated 3 times . each time it came back. now hes mad at the docs cuz they dont know for sure how to cure him so he is refusing any tx until they have a cure. hes going downhill mentally fast...so fast i dont think he really understands how bad he is. but you're right. you cant force someone. and it hurts.
i think lyme is responsible for more than diseases and syndromes...i think it has a lot to do with aging. for years ppl say..oh my joints are creaky or i forget everything cuz im getting old. but why can there be so many who are in their 80's-90's who are still ok???
-------------------- Lyme? Its complicated. Educate yourself. Posts: 13712 | From new england | Registered: Feb 2004
| IP: Logged |
lpkayak
Honored Contributor (10K+ posts)
Member # 5230
posted
Dr C's Western Blot explanation is discussed here:
-------------------- Lyme? Its complicated. Educate yourself. Posts: 13712 | From new england | Registered: Feb 2004
| IP: Logged |
map1131
Frequent Contributor (5K+ posts)
Member # 2022
posted
I know how you feel Tutu. I've sat back all these years and watched famous people and everyday joe's dx with MS, ALS, etc.
How can I be so aware and the rest of the world seems so unaware? Am I crazy? Is my lyme world so blown up that I think everything is lyme & co?
I don't know why I've been allowed to see the forest for the trees.....but I do. We do. We know these monster(s) and what thye are capable of.
We know we aren't crazy once we see hundreds and thousands post everything we've felt and experienced.
I know when very knowledgable medical doctors like Dr K, Dr B and Dr C etc are seeing the same very high % of these patients with lyme positive WB.... we're not all crazy.
This is for real. When lyme & co is not treated in some form or another for years upon years, people dwindle away and die from MS, ALS, Alz, etc.
Some day it will come to light. I know it.
Pam
oh yeah MS is a symptom. They (the majority) don't look for the cause, the root of these sx. They label it and move on. Sad, so sad.
-------------------- "Never, never, never, never, never give up" Winston Churchill Posts: 6478 | From Louisville, Ky | Registered: Jan 2002
| 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/
UBBFriend: Email this page to someone!
Printer-friendly view of this topic