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I have chronic regional pain syndrome. Was called rsd. Its from soft

tissue injusries, surgeries, whatever

it can happen to anyone. Im not sure i can post links on here. But there

are a lot of sites about it. I have that on top of the ra and psoriasis...

Jolene

In a message dated 3/20/2008 12:16:32 P.M. Eastern Daylight Time,

pamhunt56@... writes:

What are crps? Someone at work last night told me it sounded like I might

have a bone spur in my foot. I've heard of it but I don't really know what it

is.

Pam

_Jolenefive@..._ (mailto:Jolenefive@...) wrote: I have crps in my

foot.

Jolene

In a message dated 3/19/2008 9:29:36 P.M. Eastern Daylight Time,

_iMarzz@..._ (mailto:iMarzz@...) writes:

You may have some RA associated tendonitis. My feet are full of painful

lumps and

bumps, tendonitis and ganglions - lovely.

I hope you feel better soon.

-- In _ @-- In _RA-S-- In _ @_ @groRA-SUPP_

(mailto: ) ) ,

" Pam Hunt " <pamhunt56@.pa> wrote:

>

> I've been having some pain in my right foot. It is in one spot, on the

> left side right above the heel. It isn't a sore. It looks red but it

> is underneath the skin, but it's not hard like a callus would be. It

> hurts when I walk or push on it with my finger. I have arthritis in my

> feet. Does anyone have any idea what could be causing this. I don't

> know if it's arthritis are caused from something else. Thanks.

> Pam

>

************************<WBR>**Create a Home Theater Like the Pros. Watch

Home.

(_http://home.http://home.http://home.<WBRhttp://home.<Whttp://hohttp://home.<

WBRhttp://ho_

(http://home.aol.com/diy/home-improvement-eric-stromer?video=15?ncid=aolhom00030\

000000001) )

[Non-text portions of this message have been removed]

Pamela Hunt

---------------------------------

Be a better friend, newshound, and know-it-all with Mobile. Try it

now.

[Non-text portions of this message have been removed]

**************Create a Home Theater Like the Pros. Watch the video on AOL

Home.

(http://home.aol.com/diy/home-improvement-eric-stromer?video=15?ncid=aolhom00030\

000000001)

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What are crps? Someone at work last night told me it sounded like I might have a

bone spur in my foot. I've heard of it but I don't really know what it is.

Pam

Jolenefive@... wrote: I have crps in my foot.

Jolene

In a message dated 3/19/2008 9:29:36 P.M. Eastern Daylight Time,

iMarzz@... writes:

You may have some RA associated tendonitis. My feet are full of painful

lumps and

bumps, tendonitis and ganglions - lovely.

I hope you feel better soon.

-- In _ @groRA-SUPP_ (mailto: ) ,

" Pam Hunt " <pamhunt56@.pa> wrote:

>

> I've been having some pain in my right foot. It is in one spot, on the

> left side right above the heel. It isn't a sore. It looks red but it

> is underneath the skin, but it's not hard like a callus would be. It

> hurts when I walk or push on it with my finger. I have arthritis in my

> feet. Does anyone have any idea what could be causing this. I don't

> know if it's arthritis are caused from something else. Thanks.

> Pam

>

**************Create a Home Theater Like the Pros. Watch the video on AOL

Home.

(http://home.aol.com/diy/home-improvement-eric-stromer?video=15?ncid=aolhom00030\

000000001)

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  • 1 month later...
Guest guest

bio identic progesteron cream might help with your pain in your feet.

>

> Hello all. Diagnosed with lupus 2/08. Started ldn 3/29/08 at

1.75 mg

> and now on a week of 4.5 mg. Have had astounding results when

finally

> went to 4.5. (I feel like I am dreaming this). Brain fog is gone

and

> have great energy. One problem seems to persist...pain in the

bottoms

> of my feet. I am not sure it is lupus related as have never heard

> anyone discuss this. I also have some fibro issues but they have

> diminished. It feels as though there is no pad on the bottom at

the

> pressure points and I can only wear croc sandals as they are

soft.

> Any suggestions? It seems to be the most painful when weight

> bearing. Many thanks to all you wonderful folks for all your help

and

> support!! I feel so fortunate that I found LDN so early in my

> disease. At age 60 I sure need a head start!

>

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here you can buy it

http://www.sunrisewd.com/cgi-sunrisewd/sb/productsearch.cgi?

storeid=*1c035af591ca1ea14101578ac71c5048

because it is hormone although bio identical i suggest you buy of dr.

lee .what doctors do not tell you about menopause.if you have the

cream and still do not know how to use it you can mail us.we might be

able to help you.

>

> Thank you Zahavi. Can the bio id. progesterone cream be purchased

at

> a health food store or is it presription?

>

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  • 3 months later...
Guest guest

Hi Sugargpaw - This is a bit delayed in response, but I ran across

this post while looking for Lupus-related info. To answer your

question, Yes, it is possible that the pain on the bottom of your feet

is Lupus related. It's a less common symptom, but could be a

neuropathy. I have it too, but mine seems to present itself a little

differently than yours. Mine is intermittent and when it does happen,

it's first thing in the morning and will subside after walking around

a few minutes. It almost never comes back later in the day and if it

does is so mild it could be overlooked if I weren't so attentive of

keeping track of my body's " status " . Hopefully, whatever's causing it

hasn't done anything permanent and the LDN can correct it.

Wishing the best of health & pain-free feet! - Abby

>

> Hello all. Diagnosed with lupus 2/08. Started ldn 3/29/08 at 1.75 mg

> and now on a week of 4.5 mg. Have had astounding results when finally

> went to 4.5. (I feel like I am dreaming this). Brain fog is gone and

> have great energy. One problem seems to persist...pain in the bottoms

> of my feet. I am not sure it is lupus related as have never heard

> anyone discuss this. I also have some fibro issues but they have

> diminished. It feels as though there is no pad on the bottom at the

> pressure points and I can only wear croc sandals as they are soft.

> Any suggestions? It seems to be the most painful when weight

> bearing. Many thanks to all you wonderful folks for all your help and

> support!! I feel so fortunate that I found LDN so early in my

> disease. At age 60 I sure need a head start!

>

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Hi,

Foot pain is also a classic symptom of bartonella, one of the tick-borne co-infections that may accompany Lyme, or come alone. Just food for thought.

In a message dated 7/29/2008 1:47:11 A.M. Eastern Daylight Time, smylze111@... writes:

Hi Sugargpaw - This is a bit delayed in response, but I ran acrossthis post while looking for Lupus-related info. To answer yourquestion, Yes, it is possible that the pain on the bottom of your feetis Lupus related. It's a less common symptom, but could be aneuropathy. I have it too, but mine seems to present itself a littledifferently than yours. Mine is intermittent and when it does happen,it's first thing in the morning and will subside after walking arounda few minutes. It almost never comes back later in the day and if itdoes is so mild it could be overlooked if I weren't so attentive ofkeeping track of my body's "status". Hopefully, whatever's causing ithasn't done anything permanent and the LDN can correct it. Wishing the best of health & pain-free feet! - Abby>> Hello all. Diagnosed with lupus 2/08. Started ldn 3/29/08 at 1.75 mg > and now on a week of 4.5 mg. Have had astounding results when finally > went to 4.5. (I feel like I am dreaming this). Brain fog is gone and > have great energy. One problem seems to persist...pain in the bottoms > of my feet. I am not sure it is lupus related as have never heard > anyone discuss this. I also have some fibro issues but they have > diminished. It feels as though there is no pad on the bottom at the > pressure points and I can only wear croc sandals as they are soft. > Any suggestions? It seems to be the most painful when weight > bearing. Many thanks to all you wonderful folks for all your help and > support!! I feel so fortunate that I found LDN so early in my > disease. At age 60 I sure need a head start!> Get fantasy football with free live scoring. Sign up for FanHouse Fantasy Football today.

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Yes. Many Lymies are using LDN, with varying results from what I have heard. For me it has been great, but many of my symptoms were/are MS-like, and the LDN seems to be exceptional for that. I've been sick approx 15 years, and on LDN for 10-11 months. It has begun what I hope is to be a turnaround.

The beginning was rough though.

In a message dated 7/29/2008 10:24:38 P.M. Eastern Daylight Time, smylze111@... writes:

Interesting! Has anyone used LDN for Lyme?>> Hi,> > Foot pain is also a classic symptom of bartonella, one of thetick-borne > co-infections that may accompany Lyme, or come alone. Just food forthought.> > Get fantasy football with free live scoring. Sign up for FanHouse Fantasy Football today.

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Guest guest

Interesting! Has anyone used LDN for Lyme?

>

> Hi,

>

> Foot pain is also a classic symptom of bartonella, one of the

tick-borne

> co-infections that may accompany Lyme, or come alone. Just food for

thought.

>

>

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  • 2 weeks later...
Guest guest

>Dear Cookie,

I have the chair mat massager & it really is great. When I have the

pain, I arrange it where I can lay on it for 15-30 minutes, three

times a day if possible. And it truly does wonders. It has even

helped improve the strength in my feet, ankles, and legs.

> Hi Gang,

>

>

>

> I totally forgot about this till now!! When I was having major

pain in my

> feet and hands and neck I had this brush vibrator (I know it sounds

kinky_

> that I bought thru Avon and did not know it was a vibrator. Anyway

I set

> this on the highest setting and it really helped the pain.

>

>

>

> I still get pain in my feet when I used different shoes or really

flat shoes

> and I have a massaging foot machine that I use and wow it is great.

I got it

> for Christmas and have used it for many years. I am sure the new

ones are

> better. Don't get the vibrator foot thing get the one that rolls.

Oh and I

> did use the vibrator foot pillow (at that time from GNC) when I was

first

> diagnosed.

>

>

>

> Hope this helps at lot of you with pain.

>

>

>

> cooky

>

>

>

>

>

>

>

>

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So you know I was on to something here :-)))

_____

From: rheumatic [mailto:rheumatic ] On Behalf

Of mrs_sears_guy1999

Sent: Saturday, August 09, 2008 7:40 PM

rheumatic

Subject: rheumatic Re: foot pain

>Dear Cookie,

I have the chair mat massager & it really is great. When I have the

pain, I arrange it where I can lay on it for 15-30 minutes, three

times a day if possible. And it truly does wonders. It has even

helped improve the strength in my feet, ankles, and legs.

> Hi Gang,

>

>

>

> I totally forgot about this till now!! When I was having major

pain in my

> feet and hands and neck I had this brush vibrator (I know it sounds

kinky_

> that I bought thru Avon and did not know it was a vibrator. Anyway

I set

> this on the highest setting and it really helped the pain.

>

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  • 2 months later...

I've had the same thing, especially after long walks. Soaking my feet in

epsom salts (magnesium sulfate) is very helpful for me

Foot pain

Question:

I am noticing more and more adults starting to have trouble with their

feet.

Pain in the bottom center esp at night when they first get up.

Some are put in a brace, others have inserts put in. Some call it

plantar fasciitis or it may be something else.

Any ideas of natural therapies for this problem.

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I haven't had this myself. However, I was on a thyroid group where a

couple of people said their plantar fascitis was improved after raising

their thyroid hormone levels to a proper level. If one hormone helped

some, then it would seem possible that other hormones may also be

relevant.

I have a friend who developed this, & he used the inserts. It appears

that the inserts strengthened the arch and in time enabled him to walk

longer without pain. That's probably the worth a shot. My friend bought

those Walk Fit inserts that were on an infomercial.

wrote:

>

> Question:

>

> I am noticing more and more adults starting to have trouble with their

> feet.

>

> Pain in the bottom center esp at night when they first get up.

>

> Some are put in a brace, others have inserts put in. Some call it

>

> plantar fasciitis or it may be something else.

>

> Any ideas of natural therapies for this problem.

>

>

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Hi All,

No harm trying Vit-E, 400 units daily.

___________________________________

Apricot85 wrote:

> I haven't had this myself. However, I was on a thyroid group where a

> couple of people said their plantar fascitis was improved after raising

> their thyroid hormone levels to a proper level. If one hormone helped

> some, then it would seem possible that other hormones may also be

> relevant.

>

> I have a friend who developed this, & he used the inserts. It appears

> that the inserts strengthened the arch and in time enabled him to walk

> longer without pain. That's probably the worth a shot. My friend bought

> those Walk Fit inserts that were on an infomercial.

>

>

> wrote:

>

>> Question:

>>

>> I am noticing more and more adults starting to have trouble with their

>> feet.

>>

>> Pain in the bottom center esp at night when they first get up.

>>

>> Some are put in a brace, others have inserts put in. Some call it

>>

>> plantar fasciitis or it may be something else.

>>

>> Any ideas of natural therapies for this problem.

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>

> Question:

>

> I am noticing more and more adults starting to have trouble with

their feet.

>

> Pain in the bottom center esp at night when they first get up.

>

> Some are put in a brace, others have inserts put in. Some call it

>

> plantar fasciitis or it may be something else.

>

> Any ideas of natural therapies for this problem.

Hi ,

I had foot pain, mainly around the heel and arch, and diagnosed

myself with plantar fasciitis. I'm middle aged, and have been

working on cement floors for over 30 yrs.

I started to stretch and massage the foot, and rub the arch and heel

with magnesium oil in the mornings before work. I also wear sneakers

(tennis shoes) everyday, and invested in some Saucony Hurricanes with

arch support and quality cushioning. I have to say that my pain is

gone.

Jean

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I had plantar fasciitis for a while. I am thyroidless, and on my

support groups, we have noticed that many thyroid patients develop

plantar fasciitis and it goes away when thyroid levels are improved enough.

Lynnette

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You are right, it is plantar faciitis.  Symptoms are pain on the bottom of the

foot near the heel, when first arising in the morning. Itr appears massage,

arches and improved thyroid levels will help. Any other therapies for this??  

thanks,

From: Amberlyn <amberlyn@...>

Subject: Re: Foot pain

Longevity

Date: Sunday, November 2, 2008, 7:02 AM

I had plantar fasciitis for a while. I am thyroidless, and on my

support groups, we have noticed that many thyroid patients develop

plantar fasciitis and it goes away when thyroid levels are improved enough.

Lynnette

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Yes, I used the herb safflower.

BJ

Re: Foot pain

Longevity

Date: Sunday, November 2, 2008, 7:02 AM

I had plantar fasciitis for a while. I am thyroidless, and on my

support groups, we have noticed that many thyroid patients develop

plantar fasciitis and it goes away when thyroid levels are improved enough.

Lynnette

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  • 1 year later...

Ok need some advice, went to the fair with my son today, he could only walk

about 15-20 minutes before his feet hurt so much he had to sit down. We were

really having a good time and it was a shame he just couldn't enjoy it so

much. so my question is this, would AFOs help this? He only wears splints

at night currently to help stretch his tendons. His current sneakers are

about a year old, should we replace them possibly? We are going to the

physiatrist next week so will mention this to him but was wondering what has

helped other people with the foot pain.

Lori

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Lori,

Can he describe the pain? Ask him if his feel like they are burning. Burning is

a type of pain. To stop the burning, take shoes off and use some BioFreeze or

any cold lotion. I've had this my whole life, I also walk on cold tiles to cool

my feet, or soak in cold water and my orthotist did make the last topcover in a

special material that helps.

Changing shoes throughout the day can help. Massaging can help. (Your son can

learn to self-massage - even with something as simple as a tennis ball). I doubt

AFOs will help with foot pain, since the pain is on the bottom of the feet (I am

assuming, that's where the burn starts) I also have some Spenco liners which

help too. But no AFOs, because they are for footdrop.

As for his shoes - they should be replaced about every 4 months - and have

plenty of room in the toe and metatarsal area, while snug in the heels.

There are medications that can help - but don't know if you want to go that

route. Your neurologist, orthotist, phys should all work together for your son.

My orthotist also has certain brands and lasts of shoes that he recommends for

his clients.

Gretchen

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Thanks Mark,

Going to dr diamond, our physiatrist next Monday. will ask him

about it. Have to think hard about the trip to Detroit or we are considering

going to CHOP possibly instead. cannot stand all these dr's and therapies

etc so we try and keep it to a minimum. He qualified for a study at CHOP but

refuses to do it. We are heading for Lancaster tomorrow morning (lots of walking

around) and of course he has been in so much pain these last few days. Put new

inserts into his shoes but going to get him new sneakers tonight (fingers

crossed) that will help.

On an aside, I am waiting to hear back from local diner about sept 21st, have to

stop back in I guess and looking into a partylite fundraiser where CMTA would

get 50% of everything sold.

Lori

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Don't feel so dismayed, you have a great son. There are lots of great afo's out

there and they are getting better every day. One thing about CMT I have learned

is it's not fatal and studies have shown that most people with CMT live longer

than the norm. Just find your son some afo's he likes and will wear and get him

started on them.

>

> Hi Lori,

>

> We had our visit with Dr. Shy and the talented staff today. Much to my

> surprise, (and complete dismay, it was very much agreed that it was time

> for Zack to be fit for AFOs. He tried the Blue Rockers like I have.

> After walking the halls for a good amount of time, he very strongly felt

> they helped him walk much easier and everyone in the staff felt it would

> be so much easier for Zack in school and any time he had a lot of

> walking to do. They said he would not need them all the time, but he

> would know when it was right. Maybe the same is true for son too.

>

> Dismay? Yes, it was one of those moments when a parent feels all the

> weight of passing on an inherited disorder to their child. The

> generations up to me did not know about this. I was already an uncle 4

> times over before I was diagnosed, so my bro and sis did not know

> anything other than the " Griffiths Foot " ran in the family, but neither

> of them had any signs of it. So then the heavy guilt and weight of this

> really came crashing down on my today hearing those words. Was I

> narcissistic in having children? What was I thinking?

>

> I know this, my life would be nothing without my family. I guess I have

> to channel this more into the drive to stopping this so no more

> generations have this.

>

> Mark

>

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