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In a message dated 6/15/06 5:27:59 P.M. Eastern Daylight Time,

richvank@... writes:

I have been on the prescription wheel for a long time.

I

> live in Delaware and can't seem to find a doctor here that has a

clue.

> I seen one and after telling him NO DRUGS, he wrote more scripts.

I

> threw them out.

> I take 400 mgs of Mag in the morning and 400 about 1pm but the

> exhaustion hits me so hard by 2 I'm done. I got to lay down. Can

> anyone help ??

>

>

> J>>

Hi J,

Not that there are any guarantees, but have you tried accupuncture? If you

live in nothern DE you can contact Wiper at (302) 994-6838. In

addition, I believe his wife, Dianne Newman is doing some herbal and

nutritional

work with CFIDS/Fibro people.

Good luck,

Maxine

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I don't know if this will help, but Jill wrote about a doc in Georgia that has a

clinic that doesn't use drugs of any kind. You might want to give them a call.

I myself am going to work with him on Lyme and see where it goes. I, too, have

developed severe allergies to most drugs and dyes over the past couple of years.

Very strange to have systems break down so. Anyway the # for the clinic is

678-990-5401. I'm in California and will be working with them long distance.

Maybe that would work for you. Good Luck!

Mercuria <mercuria@...> wrote:

On Jun 15, 2006, at 7:13 AM, Jay wrote:

> I'm too the end of my rope and hope someone in here may help. I know I

> have CFIDS and Fibro. I have walked away from the medical community

> alltogether. I'm severly allergic to all prescription drugs now. I

> live in chronic pain not only from the Fibro and CF but I survived a

> car accident 3 years ago.

> It has all been a guessing game to keep me from being so suicidal and

> why. All the doctors wanted to was prescribe more. What I did figure

> out was not only use my Cpap but use magnesium 2xs a day. Without it I

> get nuts, really nuts. I went off all meds 2 months ago after weaning

> for weeks. I have been on the prescription wheel for a long time. I

> live in Delaware and can't seem to find a doctor here that has a clue.

> I seen one and after telling him NO DRUGS, he wrote more scripts. I

> threw them out.

> I take 400 mgs of Mag in the morning and 400 about 1pm but the

> exhaustion hits me so hard by 2 I'm done. I got to lay down. Can

> anyone help ??

Magnesium's co-factor is Vitamin B6. If you take each of your mag

doses with 100 mg of B6, you might get even better effect from it. B6

will help your muscle and nerve tissue begin to repair. Methyl B12 is

another important nutrient for this. Fortunately, neither is expensive.

I also had good results with CPAP and mag. But my fibro also

responded to two other things: getting my silent thyroid disorder

treated (this will involve another prescription drug -- possibly

Armour thyroid or cytomel), and discovering that I had a food allergy

to soy. A LOT of fibro patients have food sensitivities: there are

elimination diets all over the web that will guide you in identifying

possible culprits in your own diet. Wheat, eggs, nightshades

(tomatoes, potatoes, peppers) and soy are all common allergens that

can cause joint inflammation. I eat soy and just seize up for about

24-48 hours.

The odds that you have a messed-up thyroid are high -- and higher

since the car accident, especially if you had whiplash. Car accidents

are notorious fibro triggers, and whiplash damage to the thyroid is

one of the major reasons. If you can't find a doctor who will treat

silent thyroid (they're hard to find), a possible interim home

solution might be virgin coconut oil, which contains various EFAs

that support thyroid performance. The best stuff is at

www.tropicaltraditions.com.

We talk a lot about glutathione on this list, too. You might get a

small bottle of oral glutathione and start taking a bit each day. It

will help with inflammation, detox, and tissue healing; and many of

us have had much-improved energy from it. Another form of glutathione

is a whey powder called RenewPro. I put this and a fat spoonful of

coconut oil in my breakfast smoothie every morning.

There's a lot of stuff to try. Not all of it will work, of course,

but the key is to keep on keeping on. I'm in my third decade with

this monster, and have been just as miserable as you describe. And I

got better -- mostly by just trying everything that made sense, and

quite a few things that didn't.

Sara

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I'm also using HBOT and the clinic I mentioned uses them, too. Thanks Jill.

Kent MacLaughlin <mac@...> wrote: Have you checked into Hyper Baric

Oxygen therapy?

___________________________________

Kent

- É×ÈÕÓ

____________________________________

Good Morning

I'm too the end of my rope and hope someone in here may help. I know I

have CFIDS and Fibro. I have walked away from the medical community

alltogether. I'm severly allergic to all prescription drugs now. I

live in chronic pain not only from the Fibro and CF but I survived a

car accident 3 years ago.

It has all been a guessing game to keep me from being so suicidal and

why. All the doctors wanted to was prescribe more. What I did figure

out was not only use my Cpap but use magnesium 2xs a day. Without it I

get nuts, really nuts. I went off all meds 2 months ago after weaning

for weeks. I have been on the prescription wheel for a long time. I

live in Delaware and can't seem to find a doctor here that has a clue.

I seen one and after telling him NO DRUGS, he wrote more scripts. I

threw them out.

I take 400 mgs of Mag in the morning and 400 about 1pm but the

exhaustion hits me so hard by 2 I'm done. I got to lay down. Can

anyone help ??

J

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Hi Jay,

I am so sorry to hear what you have been put through.

So many scummy doctors just slap a CFS label on you and chuck drugs

at you and they think that is all they have to do, its disgusting!

But dont worry, you have come to a very good place.

Its a disgrace that too many arrogant doctors choose think that this

illness is a mental illness even in the face of all the scientific

proof otherwise, but they are wrong it is not psychological, its

entirely physical and organic.

I know this type of illness can have emotional and mental

consequences, but these symptoms only come secondarily, in other

words you get them as a result of what ails you, but they are not the

cause of it.

There are lots of things to be done to help you that dont involve

drugs, activity management is the first one that comes to mind seeing

as you are suffering from post-exertional illness and exercise

intolerance; just type 'Pacing CFS' into your search engine you will

start to get some good websites coming up with any luck, pacing

really helps and its free and healthy.

I would suggest that to begin with you could just keep reading some

of the posts here and all will become much clearer to you soon.

Then when you find something that interests you in particular, type

the word in the search box above the page, and it will bring up all

the posts on that subject.

This site is a goldmine of information about experimental and

alternative ways to treat what is causing your symptoms.

good luck and good health to you

best wishes

..

>

> I'm too the end of my rope and hope someone in here may help. I

know I

> have CFIDS and Fibro. I have walked away from the medical community

> alltogether. I'm severly allergic to all prescription drugs now. I

> live in chronic pain not only from the Fibro and CF but I survived

a

> car accident 3 years ago.

> It has all been a guessing game to keep me from being so suicidal

and

> why. All the doctors wanted to was prescribe more. What I did

figure

> out was not only use my Cpap but use magnesium 2xs a day. Without

it I

> get nuts, really nuts. I went off all meds 2 months ago after

weaning

> for weeks. I have been on the prescription wheel for a long time. I

> live in Delaware and can't seem to find a doctor here that has a

clue.

> I seen one and after telling him NO DRUGS, he wrote more scripts. I

> threw them out.

> I take 400 mgs of Mag in the morning and 400 about 1pm but the

> exhaustion hits me so hard by 2 I'm done. I got to lay down. Can

> anyone help ??

>

>

> J

>

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Hi, Jay.

I wonder if you have tried Epsom salt baths for your pain. That may

help. A couple of cups of Epsom salts in water as warm as you can

tolerate, for 20 minutes or so. Some of the magnesium sulfate will

pass through your skin. The sulfate is good for the cartilage in

your joints, and the magnesium is good for muscles and nerves.

Rich

>

> I'm too the end of my rope and hope someone in here may help. I

know I

> have CFIDS and Fibro. I have walked away from the medical

community

> alltogether. I'm severly allergic to all prescription drugs now. I

> live in chronic pain not only from the Fibro and CF but I survived

a

> car accident 3 years ago.

> It has all been a guessing game to keep me from being so suicidal

and

> why. All the doctors wanted to was prescribe more. What I did

figure

> out was not only use my Cpap but use magnesium 2xs a day. Without

it I

> get nuts, really nuts. I went off all meds 2 months ago after

weaning

> for weeks. I have been on the prescription wheel for a long time.

I

> live in Delaware and can't seem to find a doctor here that has a

clue.

> I seen one and after telling him NO DRUGS, he wrote more scripts.

I

> threw them out.

> I take 400 mgs of Mag in the morning and 400 about 1pm but the

> exhaustion hits me so hard by 2 I'm done. I got to lay down. Can

> anyone help ??

>

>

> J

>

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Guest guest

Hi Jay,

If you want to avoid the drug route you could try chiropractic and

acupuncture. Especially with a car accident and whiplash it may provide

significant relief. And particularly with fibro there are many physical

therapy modalities, ultrasound, massage that can be very helpful. And

acupuncture can help pain, headaches and even energy to some degree. Hot

tubs or jacuzzis can help, but just a bath with Epsom salt can be very good

at relieving pain and stiffness.

There are many things that can help so just keep trying.

Hang in there,

Jill

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Guest guest

Jay,

I know you have received some great posts to this message. Here are a

few more specific ideas to try:

Help for your chronic pain - this could be detox failure of some sort.

You need to bind up the worst of the toxins, solve intestinal dysbiosis

as soon as possible, balance the liver, promote detoxification, and then

start killing the remaining bad bugs. All the while supporting with key

nutrients. Some good natural toxin binders are Modifilan, Chlorella,

Activated Charcoal, Bendonite Clay (Sonne's #7 is good), and Klamath

Blue Green Algae. Also some people like Spirulina. Most of these are

best 30 minutes before a meal, that helps them soak up biotoxins when

they are released in the bile. But in a crisis, you can take any of

these any time, except for chlorella (which has a lot of energizing B12

and should not be taken at night unless you want to stay awake half the

night).

The severe anxiety - this is probably your body's response to the

biotoxin overload from the combination of depleted glutathione and toxic

infections or toxins in your environment. Probably the toxins get in

the nerves and are triggering anxiety responses. Magnesium is certainly

helpful, and also you can re-train your neurological reactions to the

pain and toxins. You can learn to relax even during pain, to sleep

during discomfort and anxiety, etc. But this will take some time and

effort, you must re-condition some semi-autonomic responses.

Visualization exercises and binaural beat meditations can help. Also

you can explore various herbals to help with the anxiety response. Kava

kava is very good for some people for this, as good as some prescription

drugs. Organic or German Chamomile can be sedating, there are many

others. Also be sure to get enough calcium along with the magnesium.

And one of the best treatments is a hot pack, on the chest or around the

back of the neck, very relaxing even when in pain.

The loss of energy in the PM - this is probably when you use up your

cortisol, your adrenals are crashing. May be caused by detox overload,

detox systems require the adrenals. Anyway this is very common with

adrenal exhaustion, I have this also. If you support your adrenals in

the morning, they will last longer in the afternoon. Pre-emptive

resting can also help, rest an hour once in the mid to late morning, for

example, that will extend the adrenal endurance later. Or you can take

adrenal supplements. Salt/c, licorice, many others can be very helpful.

--Kurt

Good Morning

I'm too the end of my rope and hope someone in here may help. I know I

have CFIDS and Fibro. I have walked away from the medical community

alltogether. I'm severly allergic to all prescription drugs now. I

live in chronic pain not only from the Fibro and CF but I survived a

car accident 3 years ago.

It has all been a guessing game to keep me from being so suicidal and

why. All the doctors wanted to was prescribe more. What I did figure

out was not only use my Cpap but use magnesium 2xs a day. Without it I

get nuts, really nuts. I went off all meds 2 months ago after weaning

for weeks. I have been on the prescription wheel for a long time. I

live in Delaware and can't seem to find a doctor here that has a clue.

I seen one and after telling him NO DRUGS, he wrote more scripts. I

threw them out.

I take 400 mgs of Mag in the morning and 400 about 1pm but the

exhaustion hits me so hard by 2 I'm done. I got to lay down. Can

anyone help ??

J

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  • 1 month later...

Well, Im glad you have a good PCP, so did I and half way through my treatment, I fired my gastro cuz he was one who didnt like it that I was as educated about this disease as he was and in the issue of my needing procrit, I was more educated than he.. When I needed it, he just wanted to reduce my Riba dose instead, I DEMANDED procrit, first he said that my insurance probably wouldnt cover it, well it did,, then when it came to it, he didnt know HOW MUCH to write the script for, I had to tell him,, lol,, Please do not continue to drink hon,, it will make your chances of reaching SVR much less and will cause the virus to replicate TWICE as fast and therefore make the treatment unable to keep up with it.. leecuate <leecuate@...> wrote: I thought that I would regret my post last night but I don't.I hate my gastro but my PCP is great. I see him Tuesday. I think that I can go through this with his support. I had my biopsy two weeks ago Thursday and my Gastro just had the courtesy of having her receptionist call my Friday to say that I have some scarring and can start treatment as soon as the medications come in the mail ( blue cross ). I haven't had anything to drink since last May but last night I said F-it. I am ready to start treatment. My goal is to beat this before my 50.. Sorry about all the spanish last night, I had just come from a party where everyone was speaking

spanish.Jackie

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  • 5 months later...

Get copies yourself and take them to the other doctor.

Gail

Good Morning

Hello, I just my blood test taken when over at the VA in Lacanto, here in Florida. I don't have the full results from that day, but I do have my AFP 148.00

Most of my test are high or low?

I do have full work list of test taken on 01-09-07

WBC 3.31 L

RBC 3.65 L

I had a cat scan that I sent to Shands and it says some acities in stomach and lungs. Enlarge spleen, other remarks but when ask them to get me copy they missed some pages when printing from computer and the printer.

I just want to know is all this a sign that my liver is even needing more to work? I was hoping someone new. I ask questions when I get to see the doctor which I will not until Feb 12.07.

What should I ask him, I just feel like since I am being followed at the VA, and I try to get my paper work because they are not sending to Shands for me? Any suggestions on making sure my paper work gets from one to the other?

Love you all,

Glenda

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Hi Everyone this is a friend of the boys. Please pray for him and the family

Blessings

R

-----

How exciting for you; I'd love to be able to fly to see . It's a long time

until August.

In the Kenosha News on Wednesday on the front page was an article about a

soldier from Kenosha injured in Iraq. As it turns out was in DEP (Delayed

Entry Program) with him and he also attended school at Shoreland for his

Freshman and Sophomore year. He then went on to a military school for Junior &

Senior Year. Well, when Jake found out he was hurt, he called his mother to see

how he was. He told her about us MM's, (Military Moms) and how we meet and go

for dinner. She called me and asked if the next time she could come. She is also

going to be meeting with , (Congressman) as he called her too. I told

her that I would too like to talk to him about trying to put something into

effect so that when our boys can fly home, the airlines give them a deal instead

of gouging them. I'd really like to push to do something about this. I think we

need to start writing letters to our Congressman, Senators, Legislatures,

etc..... to get some attention to this issue. What are your thoughts?

God Bless

Armymom01

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Hi Glenda, Somehow your message ended up in my Bulk Mail folder, it's a miracle I didn't just flush it away. To answer your questions - yes your AFP is high, it seems normal for people who are HCV +, mine has never been normal, always high, the WBC is a little low, not bad & the RBC is also a little low. Don't worry about them. Have you been having any "brain fog" lately? Next time ask your doctor to test your blood ammonia level too. An enlarged spleen is also fairly common for us. It's the reason your WBC & RBC are low. The spleen's job is to fight infection & for some reason it starts killing white & red blood cells as if they were diseases, I don't think the doctors know why. Has your doctor told you what stage &

grade your Hep is at? A biopsy is the best way to find that out so see about getting one. I've had 2, 10 years apart & they both said the same thing, cirrhosis but the first one was mild & the more recent one was decompensated or ESLD (end stage liver disease) all I can say is ask your doctor about a biopsy so you know exactly where you stand. Hugs, SuZie & Sir SpYke the Magnificent (in his opinion & I must say mine too)glendajohn25@... wrote: Hello, I just my blood test taken when over at the VA in Lacanto, here in Florida. I don't have the full results from that day, but I do have my AFP 148.00 Most of my test are high or low? I do have full work list of test taken on 01-09-07 WBC 3.31 L RBC 3.65 L I had a cat scan that I sent to Shands and it says some acities in stomach and lungs. Enlarge spleen, other remarks but when ask them to get me copy they

missed some pages when printing from computer and the printer. I just want to know is all this a sign that my liver is even needing more to work? I was hoping someone new. I ask questions when I get to see the doctor which I will not until Feb 12.07. What should I ask him, I just feel like since I am being followed at the VA, and I try to get my paper work because they are not sending to Shands for me? Any suggestions on making sure my paper work gets from one to the other? Love you all, Glenda

Next time I'm coming back as a cat

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I will pray for him , I always keep our brave men and women everywhere

who are doing their duty to keep our country safe in my daily prayers

Love,

C

On 1/26/07, Rettig <drettig@...> wrote:

>

> Hi Everyone this is a friend of the boys. Please pray for him and the

> family

>

> Blessings

> R

> -----

>

> How exciting for you; I'd love to be able to fly to see . It's a long

> time until August.

> In the Kenosha News on Wednesday on the front page was an article about a

> soldier from Kenosha injured in Iraq. As it turns out was in DEP

> (Delayed Entry Program) with him and he also attended school at Shoreland

> for his Freshman and Sophomore year. He then went on to a military school

> for Junior & Senior Year. Well, when Jake found out he was hurt, he called

> his mother to see how he was. He told her about us MM's, (Military Moms) and

> how we meet and go for dinner. She called me and asked if the next time she

> could come. She is also going to be meeting with , (Congressman) as

> he called her too. I told her that I would too like to talk to him about

> trying to put something into effect so that when our boys can fly home, the

> airlines give them a deal instead of gouging them. I'd really like to push

> to do something about this. I think we need to start writing letters to our

> Congressman, Senators, Legislatures, etc..... to get some attention to this

> issue. What are your thoughts?

> God Bless

> Armymom01

>

>

>

>

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Hi ,

I promise that I will pray for all of them!!!

Love always,

Pat

Fw: Good Morning

Hi Everyone this is a friend of the boys. Please pray for him and the family

Blessings

R

-----

How exciting for you; I'd love to be able to fly to see . It's a long time

until August.

In the Kenosha News on Wednesday on the front page was an article about a

soldier from Kenosha injured in Iraq. As it turns out was in DEP (Delayed

Entry Program) with him and he also attended school at Shoreland for his

Freshman and Sophomore year. He then went on to a military school for Junior &

Senior Year. Well, when Jake found out he was hurt, he called his mother to see

how he was. He told her about us MM's, (Military Moms) and how we meet and go

for dinner. She called me and asked if the next time she could come. She is also

going to be meeting with , (Congressman) as he called her too. I told

her that I would too like to talk to him about trying to put something into

effect so that when our boys can fly home, the airlines give them a deal instead

of gouging them. I'd really like to push to do something about this. I think we

need to start writing letters to our Congressman, Senators, Legislatures,

etc..... to get some attention to this issue. What

are your thoughts?

God Bless

Armymom01

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  • 8 months later...

Hello . And attagirls to all the BBW who keep the list going, and dynamic. Lately, I have not been one of those people (grin).

I do have a couple of revelations to share and since I actually had a LOSS this week (which, well, it was a surprise - that's all I'm gonna say), I figured it's time to recommit.

I supply the candy dish at work (my choice - why do you think I started the tradition?) I tend to buy one particularly large bag with a variety of different items. It's easy, there's enough different that everyone can find something they like, including Yours Truly, of course, and schlepping it to work on the bus is strength training, right?. However, until this week, there was a definite pattern. If I bought this particular bag, I would gain that week. Sometimes a little, sometimes a lot. If I buy something else that I didn't care for as much then I would lose (typically, these aren't the popular favorites, either. Things like Smartees and mints), . I'm sure it's an oversimplification, but it has sure seemed that way. This week, I thought for sure I had screwed up BAD. I lost 0.8 !! Realizations:

Even when I think I'm terrible at this, I must be doing a few things right.

I have a serious sugar addiction.

I need to eat breakfast or the candy, whatever kind, WILL call my name. Even if it's a granola bar, string cheese and apple that I take with me on the bus.

This statement really IS true - insanity is doing the same thing over and over and expecting different results.

Phrased another way - if you keep doing what you've always done, then you'll always get what you always got.

I'm just a couple candy bars away from diabetes - mom, aunt, cousins, gfather, 2nd cousin, all have or had it, all Type II. I'm always amazed when my routine blood sugars at the MD come back OK.

My knees are really starting to bother me. Since I've never played pro sports (grin), I figure it's my weight.

I got the Walking Kit at WW 2 weeks ago, put the audios onto my ipod, but haven't played them ONCE. Except by accident when I was looking for Springsteen.

Work responsibilities have recently shifted, increased. I won't be able to do them if I don't take care of myself.

If I have time for internet surfing, A & E, CourtTV, Boston Legal and (watching) Dancing with the Stars, I have time for a walking video or doing handweights in front of the TV.

I do have hypothyroid. I do have a Rx. I need to take it, more than just the 5 days before I know I'm getting a blood test.

I need to get back on the horse, as it were.

I will do the WW 20-minute walk 3 times this week, plus the small amount of walking I do (1/4 mile each way) to and from the bus.

At least twice, I will come home the "long" way, which is about 1/2 mile. I was trying to do this most evenings but I've been slacking off because I was carrying stuff, it was getting dark, etc.

If I don't walk for morning break, I can't knit for afternoon break. I am obsessed with knitting. Obsessed.

In a fitness-conscious city like Portland, with exceptional transit (thank you very much, yes I DO work for the bus company) and bike paths and normally mild weather, there is NO EXCUSE to not walk outside for even 15 minutes a day, every day. Except for the 4 days every 3 years when we get 7 snowflakes and the city shuts down.

So there! I've put it out there. You have my permission to kick me where it counts if I start writing excuses to the list instead of deeds.

I'm so glad you are still here and haven't "given up" on me (grin).

Eileen in OR

-----Original Message-----From: 100-plus [mailto:100-plus ]On Behalf Of ABrite@...Sent: Saturday, October 27, 2007 9:32 AMABrite@...Subject: Good Morning

Good Morning Groupies!! Hope all you had a nice relaxing Friday night!! Ummm unless you are a TGIF partier and went out hooting it up last night, then I hope you had a wild and exciting time!!

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Sue,

I had dental surgery Thursday so wet noodles would be appropriate - that's

about all I can handle right now. I did splurge on a pumpkin milkshake the

day of procedure though. I look forward to it each year, have one and then

I'm done.

Weigh-in in an hour; have no idea what it will say due to reduced activity /

meals the last couple days....

Eileen

PS) I think that oral surgery, with stitches, dressings, etc. is a REASON,

not an excuse (grin). Nothing sounds so good now as a cold apple....

-----Original Message-----

From: 100-plus [mailto:100-plus ]On

Behalf Of Sue in NJ

Sent: Monday, October 29, 2007 12:16 PM

No kicks allowed on this list, only lashes with wet noodles! LOL

>>So there! I've put it out there. You have my permission to kick

me where it counts if I start writing excuses to the list instead of deeds.

Sue in NJ

No virus found in this outgoing message.

Checked by AVG Free Edition.

Version: 0.0.503 / Virus Database: 269.15.18/1104 - Release Date: 11/1/2007

6:47 PM

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In a message dated 10/27/2007 12:31:22 P.M. Pacific Daylight Time, ebax@... writes:

In a fitness-conscious city like Portland, with exceptional transit (thank you very much, yes I DO work for the bus company) and bike paths and normally mild weather, there is NO EXCUSE to not walk outside for even 15 minutes a day, every day. Except for the 4 days every 3 years when we get 7 snowflakes and the city shuts down.

Is that all you get there for snow Elaine?? I outta move to Portland LOL!!

So there! I've put it out there. You have my permission to kick me where it counts if I start writing excuses to the list instead of deeds.

I don't know about kicking you - but how has your week gone??

I'm so glad you are still here and haven't "given up" on me (grin).

Never - LOL!! And glad you all don't give up on me when I am two weeks behind on some emails by now....

(Sigh)

See what's new at AOL.com and Make AOL Your Homepage.

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  • 3 months later...

BEST WISHES TO YOU PAULETTE FOR THE JOB & THE SS ISSUE HUGS DORTette Limegrover <palime22@...> wrote: Good morning EveryoneI'm up far too early as I've got a job interview tomorrow morning. I doubt I'll get the job, but I'm going to show up.I searched through Blingo and learned that social security under certain circumstances will grant SS DI to obese individuals. I'm still waiting on my results as I submitted further information to my attorney and he thinks it

might help.I hope this finds everyone doing well.Hugs Love & Prayersette

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DortI woke up yesterday not feeling well and then something came up which prevented me from attending the interview. I called to advise them of such and hoped they'd return my call to reschedule, but not one called me back.

I'm upset over this being called into the doctors office (nurse/practitioner)for the results so soon instead of waiting for a month. Now I'm up scared to death in reference to my dad's money situation. I'll be cleaning up a lot of my stuff in order to sell at consignment shops, including jewelry given to me by my mom and possibly furs of hers.

I pray my Aunt Helen will be able to help financially as much as possible without upsetting my dad.Hugs Love & Prayersette

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AWWWWWWWWW.. IM SO SORRY ;;PAULETTE;; I PRAY THAT YOU ARE FEELING BETTER & THAT THEY HAVE CALLED YOU BY NOW TO RESCHEDULE & ALSO THAT ALL WORKS OUT FOR YOU;; KEEP YOUR CHIN UP HUGS DORTette Limegrover <palime22@...> wrote: DortI woke up yesterday not feeling well and then something came up which prevented me from attending the interview. I called to advise them of such and hoped they'd return my call to reschedule, but not one called me back.I'm upset over

this being called into the doctors office (nurse/practitioner)for the results so soon instead of waiting for a month. Now I'm up scared to death in reference to my dad's money situation. I'll be cleaning up a lot of my stuff in order to sell at consignment shops, including jewelry given to me by my mom and possibly furs of hers.I pray my Aunt Helen will be able to help financially as much as possible without upsetting my dad.Hugs Love & Prayersette

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Guest guest

HEY MIKE!

YOU ARE SO CORRECT!!! BE HONEST ON THE PAPERWORK...BECAUSE THEY MAY JUST

CHECK YOU OUT...I HAD NO PROBLEM GETTING IT...I FILLED IN ALL THE PAPERWORK AND

HAD MY DOCTOR FILL IN HIS PART...I ALSO SENT IN PHOTOS OF WHAT MY FOOT LOOKS

LIKE...I THINK THAT THIS REALLY DID HELP, AS UNFORTUNATLEY, IT IS HORRIFIC

LOOKING ...AND EVERYTHING THAT I DOCUMENTED WAS BACKED UP BY MY DOCTOR.

MY FRIEND'S DAD APLIED, BUT SINCE HIS FINANCES WERE SO BAD UNTIL HE WAS

APPROVED, HE HAD TO CONTINUE DELIVERING PIZZAS JUST TO MAKE SOME QUICK

CASH....THEY ACTUALLY CAUGHT HIM ON TAPE DOING THIS AND HE WAS PERMANENTLY

DENIED....SO

MAKE SURE WHAT YOU SAY IS ALL TRUE!!!!

I ALSO AGREE WITH WHAT YOU STARTED, MIKE. YOUR GROUP IS REALLY MADE UP OF

GREAT, KIND, AND HELPFUL, FUNNY FOLKS!!!

GOD BLESS YA AND HAVE A GREAT VK!

KATHY

**************Get trade secrets for amazing burgers. Watch " Cooking with

Tyler Florence " on AOL Food.

(http://food.aol.com/tyler-florence?video=4? & NCID=aolfod00030000000002)

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I recieved SSD after filing three months didn't see any of their doctors,I think

it was also my mri of back....I see doctor today for permanant stimulator its a

neurosurgeon and not the pain doctor that put the trial one in...I am afraid

because I am so overweight that he is going to tell me that I have to lose

weight..I am so afraid of that...glad for support here also and education from

others

mike2boys <mike2boys@...> wrote:

good morning all my friends. I sure love this group. it's

freindliness its questions etc.. About ? regarding SSDI it depends I

was accepted after i filled 2 months later. of course they sent me to

a Doctor when I brought my ct scan mri records he said you need SSDI

cant work ever again. then 1 week later SSDI sent approval letter.

the bigest part of getting accepted is the written section you must

fill out. be honest dont say cant say need hrlp with. etc.... mike

owner

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---I was very lucky. I got hurt in May, I went to SS and filed in oct.

was sent to a couple drs. then in April the following April I got my

checks ,back to Nov when I became eligible. you have to off work for 6

months before your eligible. .. good luck !!

In Stimulator , " mike2boys " <mike2boys@...> wrote:

>

> good morning all my friends. I sure love this group. it's

> freindliness its questions etc.. About ? regarding SSDI it depends

I

> was accepted after i filled 2 months later. of course they sent me

to

> a Doctor when I brought my ct scan mri records he said you need

SSDI

> cant work ever again. then 1 week later SSDI sent approval letter.

> the bigest part of getting accepted is the written section you must

> fill out. be honest dont say cant say need hrlp with. etc.... mike

> owner

>

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I haven't worked since the middle of July 2007. I had been on leave of absence

from my work for three surgeries. I finally had to retire in March of this year

due to the pain being so bad from doing everyday housework or trying to do

housework. My husband is trying to sell the farm because he has brachial

plexis in both arms. As soon as he sells it he is going to try to get on

disability.

Re: good morning

---I was very lucky. I got hurt in May, I went to SS and filed in oct.

was sent to a couple drs. then in April the following April I got my

checks ,back to Nov when I became eligible. you have to off work for 6

months before your eligible. .. good luck !!

In Stimulator@gro ups.com, " mike2boys " <mike2boys@. ..> wrote:

>

> good morning all my friends. I sure love this group. it's

> freindliness its questions etc.. About ? regarding SSDI it depends

I

> was accepted after i filled 2 months later. of course they sent me

to

> a Doctor when I brought my ct scan mri records he said you need

SSDI

> cant work ever again. then 1 week later SSDI sent approval letter.

> the bigest part of getting accepted is the written section you must

> fill out. be honest dont say cant say need hrlp with. etc.... mike

> owner

>

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