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Wellbutrin success (so far) etc   Message List  
Reply | Forward Message #883 of 6214 |
Re: [Peripheral_Neuropathy] Wellbutrin success (so far) etc

Michale,
         For once in my life I am almost at a loss for words. My Anger level ( If I hadnt had so much therapy) LOL would be off the charts t
The knowledge you gave all of these incompetant people ( for lack of a better vulgar word) ,full out there knowing your history on both sides of very close family members and their NEGLECT is unforgiveable. I know ,in order to keep our stress levels low, forgiveness is smart only because we are sick. I wish if there were a better way of allowing someone(like a lawer and a nurse reviewing charts for your case) with out involving you would be just great to sue theirr ass. All that would be needed would be for them to pull the charts. I can't even imagine how they could cover their neglectful asses.
         I am so sorry you werent diagnosed earlier so that you might not have to suffer . I am in the same ballpark but with a misdiagnosed hypothyroidism for years after faithfully doing my part getting checked every 3 mos. Gee now finally the endocrinologists are reading the labs correctly and many are still not doing a darn thing about it. The thyroid effects the entire body and if not balanced correctly can really do a number on us.
            Anyway aside from all that!!  I would like to welcome you . These boards are great for sharing and learning.    Jan S.

Micheal <onagocag55@...> wrote:
Hi
I have not introduced myself yet...
My name is Micheal..I live in Maine along the Canadian border. Diabetes runs in my family big time. My father's Mother was type 1 his father was type 2...also my mother's mother was type 2...what chance did I have. I got cousins who are both insulin dependent and non insulin dependent.
I am now insulin dependent. I never abused alcohol or drugs so my PN is not the results of "bad choices" or excessives.
 
The first signs something was wrong came in 94 I had a bladder infection of unknown reasons (nobody checked my blood). Then later that year I went into the Beth Israel Hospital of Boston complaining on numbness pain, burning and tingling in my right torso in 94 was told I was having "anxiety attack". I said "BUT Doc I don't feel anxious!" He said just go home it will be fine. Its amazing how little understanding and knowledge there is of this disease!
 
In 97 at Mass General I was treated for what was called "Saturday Night Palsy" in my left arm..YET another chance for modern medicine to check my blood sugar yet it never happened despite a man in his mid 40's (at that time) who presents in ER unable to use his left arm with no obvious reason...
 
I have had a lot of major accidents including shattering my left shoulder , shattering my left leg (different accident) and a neck fusion so when this burning tingling pain started in my neck upper arms and face I thought it was due to one of those injuries.
 
Two years ago I broke my left hand while shearing my sheep so when it healed with yet more  burning tingling pain I thought it was due to the fractured bone. Then it began in my right hand of which there is NO preceding incident or accident
 
I was only diagnosed as type 2 Diabetes in 2000 saw my doc regularly had a1c's drawn every 3 months for 6 years. I complained often of the  burning tingling pain but was told it was TOO soon for neuropathy. My Doc now believes I have had untreated Diabetes most of my adult life. It just got missed by poor medical practices and lack of screening.
 
Last October I had to give up a business I had run successfully for 17 years because I just kept getting sicker and sicker..nobody seemed to know what was wrong with me.
I moved out of Boston area so I could buy a house outright no mortgage as I knew Disability was coming.
When I got up here I ended up seeing some quack Nurse Practitioner who even went so far as to take me off glybruide while she was looking directly at classic DPN.
Then it started down my right leg thigh both feet I ended up walking  (if you can call it that) on a cane.
 
FINALLY a new doctor moved to town moved right next door to me..he saw me trying to take my walk..asked me what was wrong with me and I said "I just do not know only that I am diabetic!" He had me make an appointment with him next day...looked me over and said "you have a text book case of classic Diabetic Peripheral Neuropathy." He was surprised nobody had "noticed" it.
 
Now I am on insulin only before meals and I use a slow acting insulin for bedtime. I am also on cymbalta by Lilly which I take once daily..it works INCREDIBLY. I was on twice daily but became TOO jittery. I nearly chewed through my mouth! I have not known a pain free life in years!!!
 
Now mind you folks I AM a Nurse worked Pediatrics' in cardiovascular care and then oncology for my whole life. I of course know about diabetes..I had asked a few times if I was suffering from Neuropathy and was told "NO!".
 
Until I found my new Doctor who is young, just up here from NYC and actually LISTENS to his PT's (novel idea!). I had no idea what was causing me to be so sick!
I have read everything there is on the National Institute of Health (reading this web site was like reading about my life!) as well as a few other qualified Diabetic Sites. There seems to be a lot of new age bs on line about this as well from weird diets etc..not for me!
 
I was suffering for many years without meds..it is so much better now with the Cymbalta!!!!
The pain affects my right side of my head, face. both arms lower arms, wrists, hands, right buttocks, right thigh, right lower leg, both feet. It also affects my whole right chest and torso as well as the left side of my chest (Doc says I may not be able to tell if I am having a heart attack now) also the pain is in both ears right into my ear canals and throat. I have over 75% of my body affected. I also have Gastrophresis (Diabetic Gut) which they knew 5 years ago.
 
I LOVE insulin as it allows me more food choices :) and if someone tried to take my cymbalta away I kill them lol
I joined this list cause I wanted to hear what others were doing trying etc...and to speak of my own success. I am feeling a whole lot better..still can't walk very far without pain though.
 
One good thing is I am now guaranteed my Social Security Disability FINALLY!
They of course are NOT happy..like I gave up my  business that was paying me anywhere from $2000 to $4000 each week for the $1300 I'll get from SSA because $1300 is SO exciting LOL
 
Anyway now that I wrote a novel I'll sign off..looking forward to getting to know everyone. I am sure you all have your own horror stories!
 
Micheal



Thu Aug 10, 2006 1:18 pm

lou_silvestro
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Message #883 of 6214 |
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Hi I have not introduced myself yet... My name is Micheal..I live in Maine along the Canadian border. Diabetes runs in my family big time. My father's Mother...
Micheal
grandfatherstar
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Aug 10, 2006
12:39 pm

Michale, For once in my life I am almost at a loss for words. My Anger level ( If I hadnt had so much therapy) LOL would be off the charts t The knowledge you...
lou silvestro
lou_silvestro
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Aug 10, 2006
1:19 pm

~~~~~~~~~ For once in my life I am almost at a loss for words. My Anger level ( If I hadnt had so much therapy) LOL would be off the charts ~~~~~~~~~~ Hi Jan ...
Micheal
grandfatherstar
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Aug 10, 2006
9:00 pm

I don't think I mentioned I have autonomic PN which affects things like I sweat like a woman in menopause (Yep I have HOT flashes often during a day)..HORRIBLE...
Micheal
grandfatherstar
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Aug 10, 2006
9:08 pm

Michael "after dark", Thats the thing about this disease with me also. For some reason my feet start to itch and it almost feels like the bottoms of my feet...
lou silvestro
lou_silvestro
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Aug 11, 2006
1:53 pm

Hi Jan, Loss of balance and what's called proprioception have been very noticeable. I too, have fallen and have to be very careful about stairs, uneven...
Ken Thorland
ken37917
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Aug 11, 2006
5:00 pm

Ken If I had a cane I'd trip over it LOL Jan S Ken Thorland <ken37917@...> wrote: Hi Jan, Loss of balance and what's called proprioception...
lou silvestro
lou_silvestro
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Aug 11, 2006
9:19 pm

Ken, So very many things go in to appropriate perception of our body parts moving all at the same time, having the body do just what we want it to do. I do...
lou silvestro
lou_silvestro
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Aug 12, 2006
12:12 pm

Hi Jan, no offense taken at all. I haven't been through near the difficulty you or many others have and for that I count myself lucky. Probably the major...
Ken Thorland
ken37917
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Aug 12, 2006
5:50 pm

Ken, THX for the info re: Zetia. Will pass it on to my husband who refuses to take any statins. Jan S. Ken Thorland <ken37917@...> wrote:...
lou silvestro
lou_silvestro
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Aug 13, 2006
11:27 pm

hi back micheal, had to retype your name 3x because my son is michael and fingers had a hard time switching!! lol i was just approved for SSDI. the first...
julianne madsen
jules0223us
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Aug 11, 2006
11:47 am

Hi Julianne, Suicide..thought of that a few times myself with this pain!!! To this day I often ask myself when enough IS enough. I have tied neurontin (HATED...
Micheal
grandfatherstar
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Aug 11, 2006
12:39 pm

~~~~~~~~~~~~ I also have balance and co-ordination issues at times and I just thought it was from the drugs. Thank God I fall into soft objects . ~~~~~~~~ Yep...
Micheal
grandfatherstar
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Aug 11, 2006
4:07 pm
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