Hi, I'm new here

[Guest guest]

Hello Dan, welcome to the group. If you have any questions or worries

about getting a C.I. ask your questions here. There are lots of helpful

people here that will respond to you.

Ted F.

>

> Hi,

>

> This is Dan. I'm new here. I currently do not have a CI but am looking

> into the possibility of getting one. Some of you may know me from

> another -hearing loss related group, smile.

>

[Guest guest]

> >

> > Hi,

> >

> > This is Dan. I'm new here. I currently do not have a CI but am looking

> > into the possibility of getting one. Some of you may know me from

> > another -hearing loss related group, smile.

> >

>

Thanks Ted. I'll keep that in mind.

[Guest guest]

,

I am sorry your son is having to go through this. The teenage years are rough, and throwing a new diagnosis on top of it, makes it worse. I hope things start to look up for him as he learns how to deal with his JRA.

Helen

(mom to nne, poly jra 9, asthma)

Hi, I'm new here

Hi Everyone,

I just joined the group. My 15 year old son has been diagnosed with JRA. He started with mild symptoms in the fall. The doctors didn't even suspect JRA at that point. Then at the end of March his symptoms worsened terribly. He was diagnosed at the end of April. It is effecting his neck, shoulders, spine, wrists, hips, knees and ankles. So far the medications he has taken haven't helped much. He took Naprosyn, then Tolectin. He's on Orudis and Minocin now. He will go back to the rheumatologist on Tuesday and we finally have a consultation with a pediatric rheumatologist on Monday. We have to go to Philadelphia, there is no one local.

Right now my son is struggling with accepting what is happening to him. It's very difficult. School is also tough because in the last two months he's been out more than in. Most of his teachers have been very helpful. It's just tough for him to make up the work because he is exhausted. He comes home from school and goes to sleep. I'm hoping that when his pain is controlled this will get easier for him.

I'm glad I found this group and I hope I can learn a lot from it.

 BMy quilt pictures:http://community. webshots. com/user/ wendyb315

http://www.kendallp arkquiltsforkids .org

[Guest guest]

Hi and welcome to the list. My sonwas 13 when he was diagnosed and his symptoms are similar to your son’s. NSAID’sdidn’t really do a whole lot and he was put on methotrexate (a DMARD) after aperiod of time. Those usually help a lot better than just an anti inflammatoryalone. Just to give you a heads up as to where the rheumy may want to go withthe meds. I know it is very hard on these kids todeal with. My suggestion is to educate your son (and yourself and family) asmuch as possible about the disease. He may resist at first, but once he beginsto understand what is going on in his body it seems to help them cope better.That is not to say they are all fine with it. My son struggled to deal with theidea of having this disease. He even made the decision once he was over 18 tostop treatment. He has finally gone back to a dr recently and I feel that is agood thing. He gets tired of feeling tired all the time, and he is tired of thepain (obviously) but at least he is now working on feeling better again. Evennow, my son will sometimes come home from work and sleep instead of going out.He just has days when he is exhausted. You should check out the arthritiswebsite, www.arthritis.org They have pamphletsyou can order for free that help explain the disease. One helpful one might be “When your student has arthritis†that you can give to his teachers. It is great you are going to a ped rheumy.The disease does affect kids and teens differently than adults and to havesomeone who specializes in kids is really helpful. Please let us know how itall goes, Michele ( 21, spondy) From: [mailto: ] On Behalf Of BSent: Friday, May 16, 2008 11:20AM Subject: Hi, I'm new here Hi Everyone, I just joined the group. My 15 yearold son has been diagnosed with JRA. He started with mild symptoms inthe fall. The doctors didn't even suspect JRA at that point. Thenat the end of March his symptoms worsened terribly. He was diagnosed atthe end of April. It is effecting his neck, shoulders, spine, wrists,hips, knees and ankles. So far the medications he has taken haven'thelped much. He took Naprosyn, then Tolectin. He's on Orudis andMinocin now. He will go back to the rheumatologist on Tuesday and wefinally have a consultation with a pediatric rheumatologist onMonday. We have to go to Philadelphia,there is no one local. Right now my son is struggling withaccepting what is happening to him. It's very difficult. Schoolis also tough because in the last two months he's been out more thanin. Most of his teachers have been very helpful. It's just toughfor him to make up the work because he is exhausted. He comes home fromschool and goes to sleep. I'm hoping that when his pain is controlledthis will get easier for him. I'm glad I found this group and I hope Ican learn a lot from it. BMy quilt pictures:http://community.webshots.com/user/wendyb315http://www.kendallparkquiltsforkids.org

[Guest guest]

Hi , I am not sure where you live - (we are in South Jersey) but we also see the rheumatologists in Philadelphia - they are a wonderful group of doctors. Please let me know if you have any questions or concerns. My 12 year old daughter has JRA - right now she is struggling with a flare in her TMJs and has just been told that we need to add Enbrel to her meds. This is a scary move for us - but I can vouch for the comfort that this group will give. Take care, Lori

[Guest guest]

Hi, and welcome to the group. I have been away for a week or

so. My 14 year old daughter has been having a lot of issues.

She seems to be facing a lot of the same issues as your son. We live

in Texas, but if he wants to talk to her she would love it.

Her name is . Her email address is cassadyn@... or he

can find her on MySpace. He can search her by name or her screen name

is Marie.

Thanks,

, mom to 14, Poly JRA

>

> Hi Everyone,

>

> I just joined the group. My 15 year old son has been diagnosed

with JRA.

> He started with mild symptoms in the fall. The doctors didn't even

suspect

> JRA at that point. Then at the end of March his symptoms worsened

terribly.

> He was diagnosed at the end of April. It is effecting his neck,

shoulders,

> spine, wrists, hips, knees and ankles. So far the medications he

has taken

> haven't helped much. He took Naprosyn, then Tolectin. He's on

Orudis and

> Minocin now. He will go back to the rheumatologist on Tuesday and

we

> finally have a consultation with a pediatric rheumatologist on

Monday. We

> have to go to Philadelphia, there is no one local.

>

> Right now my son is struggling with accepting what is happening to

him. It

> s very difficult. School is also tough because in the last two

months he's

> been out more than in. Most of his teachers have been very

helpful. It's

> just tough for him to make up the work because he is exhausted. He

comes

> home from school and goes to sleep. I'm hoping that when his pain

is

> controlled this will get easier for him.

>

> I'm glad I found this group and I hope I can learn a lot from it.

> 

> B

>

> My quilt pictures:

> http://community.webshots.com/user/wendyb315

> http://www.kendallparkquiltsforkids.org

>

[Guest guest]

,

Welcome to CI Hear. Some thoughts that may help. One, dont give up on

music but put it on the back burner and focus an improving your hearing with

the CI. Have you tried different audis?

You dont state what brand your CI is but one thing for sure, there have

been improvements in many areas since 2004. New mapping software and speech

strategies, new processors.

I have the Nucleus Freedom and while I am not a music pro, I do enjoy

music. Its not perfect but I love what I have. Prior to the CI, I had

given up on music, gave away my records, my stereo. Now I am again back

into music and even found a new genre that I am mad about, Celtic music.

There are many CI'ers on the list who will pipe up about music. But

first, get yours mapped for speech and who knows, music will follow.

*---* *---* *---* *---* *---*

A grenade fell onto a kitchen floor in France, resulted in

Linoleum Blownapart.

& Dreamer Doll ke7nwn

E-mail-

rclark0276@...

Home Page-

http://webpages.charter.net/dog_guide/

[Guest guest]

Hi , I am a musician too and have made some great strives with the CI

and music. It started out for me as noise with speech, music and noise all

sounding the same. I really worked hard at auditory rehab with the CI (I

got my CI back in 1987) and the world of music gradually opened up for me.

I am now playing my violin again, 40 years after receiving my Bachelor of

Music in Violin Performance and having to say good bye to music due to

lifelong progressive hearing loss that had reached a profound level. I can

now tune the instrument without an electronic tuner and have been listened

to by professional musicians who state that my intonation is good. If it

wasn't for Mitochondrial Myopathy, a rare form of Muscular Dystrophy, I

would be able to play in ensembles again, like the local symphony, or

chamber groups. I also enjoy listening to music and even have broadened my

appreciation of music outside of the classical realm, to include Country and

Jazz. Could you email me at rifox@... Ruth

From: [mailto: ] On Behalf Of

renee42861

Sent: Sunday, May 24, 2009 4:17 PM

Subject: Hi, I'm new here

Hi, my name is and I've been implanted since 2004. I got frustrated

and discouraged with the CI and stopped wearing my processor for a while. I

was a musician before I started losing my hearing and as some of you may

know, music is nothing more than noise with that processor and for someone

who has made a living in music it's really hard. Eventually, I gave up music

too because I felt that part of my life was over. I'm trying to wear the

processor again and I'm giving music another try as well. This time, I'm

sure the two dont' mix and it's time to let go of music, wear the processor

and move on. I need to find a new way to make a living. Problem is I'm

nearly 50! Any advice on reinventing myself?

[Guest guest]

Hi , Thanks for the support and encouragement. I have a Med-El Tempo and

I'm waiting to hear from the insurance company concerning coverage for their new

upgrade. According to Med-El it's supposed to be a big improvement over what I

already have and will possibly make music more enjoyable. Right now, Amazing

Grace on the organ sounds like heavy metalLOL! I think I'm going to like .

Looking forward to corresponding!

Like the joke at the end too!

Cassandra

From: <rclark0276@...>

Subject: Re: Hi, I'm new here

Date: Sunday, May 24, 2009, 4:52 PM

,

Welcome to CI Hear. Some thoughts that may help. One, dont give up on

music but put it on the back burner and focus an improving your hearing with

the CI. Have you tried different audis?

You dont state what brand your CI is but one thing for sure, there have

been improvements in many areas since 2004. New mapping software and speech

strategies, new processors.

I have the Nucleus Freedom and while I am not a music pro, I do enjoy

music. Its not perfect but I love what I have. Prior to the CI, I had

given up on music, gave away my records, my stereo. Now I am again back

into music and even found a new genre that I am mad about, Celtic music.

There are many CI'ers on the list who will pipe up about music. But

first, get yours mapped for speech and who knows, music will follow.

*---* *---* *---* *---* *---*

A grenade fell onto a kitchen floor in France, resulted in

Linoleum Blownapart.

& Dreamer Doll ke7nwn

E-mail-

rclark0276charter (DOT) net

Home Page-

http://webpages. charter.net/ dog_guide/

[Guest guest]

,

I would not give up on music totally. I just met someone the other day who's

profession involved music. I can't remember to what capacity, but whatever

it was, he is still able to do his work. He did say it took work to achieve

this. Myself, I have not achieved this. It's okay for me right not because

music is not my life's work, but I would like to be able to enjoy it again

someday.

I think it was who said to not give up, just maybe put it on the

backburner for now. I agree, never give up.

[Guest guest]

Dear and Nina,

 

I  am awaiting for an appointment  from a  New Jersey  hospital  who accepted 

my insurance  for  a hearing test.   I  have  a  social circle, and I would like

to hear the group speak.  I think  that would be a reasonable expectation  while

music appreciation would  not.  In any  case  my hearing aid  Audie mentioned I

still can enjoy music in  my better  right ear.  Hopefully,  the  recruitment,

balance,  vertigo, and  tinnitus would not be  troublesome  if I get a low 

score. It  is  a  risk  that  we all  must take.

 

Gerald

From: Nina <cipalm@...>

Subject: Re: Hi, I'm new here

Date: Sunday, May 24, 2009, 8:21 PM

,

I would not give up on music totally. I just met someone the other day who's

profession involved music. I can't remember to what capacity, but whatever

it was, he is still able to do his work. He did say it took work to achieve

this. Myself, I have not achieved this. It's okay for me right not because

music is not my life's work, but I would like to be able to enjoy it again

someday.

I think it was who said to not give up, just maybe put it on the

backburner for now. I agree, never give up.

[Guest guest]

Hi Gerald and other music hopefuls,

Music listening does take work for most of us but in the end it is very

rewarding. The CI/Hearing aid combo has been found to be the surest way to

music appreciation. I don't have that option and am a unilateral CI and

enjoy music immensely, but it took a lot of practice, patience, and

endurance. Starting with the very simple and working to the complex is the

way to go with both Music and Speech. Cochlear has a rehab program called

Sound and (Way) Beyond that is very helpful towards that end. It has

simple to complex exercises in both speech and music. I also have a

article that I wrote years ago for publication 20 years ago and have updated

since, that outlines how I learned to hear both speech and music starting

from the point of Music, Speech and Noise sounding the same. I will be

willing to share that article with anyone that requests it at

rifox@....

Ruth

From: [mailto: ] On Behalf Of

Gerald Gollinger

Sent: Sunday, May 24, 2009 9:31 PM

Subject: Re: Hi, I'm new here

Dear and Nina,

I am awaiting for an appointment from a New Jersey hospital who

accepted my insurance for a hearing test. I have a social circle,

and I would like to hear the group speak. I think that would be a

reasonable expectation while music appreciation would not. In any case

my hearing aid Audie mentioned I still can enjoy music in my better right

ear. Hopefully, the recruitment, balance, vertigo, and tinnitus would

not be troublesome if I get a low score. It is a risk that we all

must take.

Gerald

From: Nina <cipalm@... <mailto:cipalm%40sbcglobal.net> >

Subject: Re: Hi, I'm new here

<mailto:%40>

Date: Sunday, May 24, 2009, 8:21 PM

,

I would not give up on music totally. I just met someone the other day who's

profession involved music. I can't remember to what capacity, but whatever

it was, he is still able to do his work. He did say it took work to achieve

this. Myself, I have not achieved this. It's okay for me right not because

music is not my life's work, but I would like to be able to enjoy it again

someday.

I think it was who said to not give up, just maybe put it on the

backburner for now. I agree, never give up.

[Guest guest]

Hello , have you had a recent mapping session. What processor are you

using, there might be a more up to date one in use now. 5 years is a long time,

in technology terms. Lots of people can get music pretty well.

Ted F.

>

> Hi, my name is and I've been implanted since 2004. I got frustrated and

discouraged with the CI and stopped wearing my processor for a while. I was a

musician before I started losing my hearing and as some of you may know, music

is nothing more than noise with that processor and for someone who has made a

living in music it's really hard. Eventually, I gave up music too because I felt

that part of my life was over. I'm trying to wear the processor again and I'm

giving music another try as well. This time, I'm sure the two dont' mix and it's

time to let go of music, wear the processor and move on. I need to find a new

way to make a living. Problem is I'm nearly 50! Any advice on reinventing

myself?

>

[Guest guest]

,

Your CI clinic may be able to do wonders and assist in getting insurance

approval for an upgrade if they can show it offers increased benefits over

the current processor.

You have much to look forward to here as I have a huge collection of

quotes that amuse and sometimes forces one to stop and think.

*---* *---* *---* *---* *---*

Dilbert's Words of Wisdom: On the keyboard of life, always keep

one finger on the escape key.

& Dreamer Doll ke7nwn

E-mail-

rclark0276@...

Home Page-

http://webpages.charter.net/dog_guide/

[Guest guest]

hi Ruth

May I know are you a ci user? which brand are you using.?

cheers

superstring

________________________________

From: Ruth Ilean Fox <rifox@...>

Sent: Monday, 25 May 2009 8:09:59

Subject: RE: Hi, I'm new here

Hi Gerald and other music hopefuls,

Music listening does take work for most of us but in the end it is very

rewarding. The CI/Hearing aid combo has been found to be the surest way to

music appreciation. I don't have that option and am a unilateral CI and

enjoy music immensely, but it took a lot of practice, patience, and

endurance. Starting with the very simple and working to the complex is the

way to go with both Music and Speech. Cochlear has a rehab program called

Sound and (Way) Beyond that is very helpful towards that end. It has

simple to complex exercises in both speech and music. I also have a

article that I wrote years ago for publication 20 years ago and have updated

since, that outlines how I learned to hear both speech and music starting

from the point of Music, Speech and Noise sounding the same. I will be

willing to share that article with anyone that requests it at

rifoxcomcast (DOT) net.

Ruth

From: groups (DOT) com [mailto:groups (DOT) com] On Behalf Of

Gerald Gollinger

Sent: Sunday, May 24, 2009 9:31 PM

groups (DOT) com

Subject: Re: Hi, I'm new here

Dear and Nina,

I am awaiting for an appointment from a New Jersey hospital who

accepted my insurance for a hearing test. I have a social circle,

and I would like to hear the group speak. I think that would be a

reasonable expectation while music appreciation would not. In any case

my hearing aid Audie mentioned I still can enjoy music in my better right

ear. Hopefully, the recruitment, balance, vertigo, and tinnitus would

not be troublesome if I get a low score. It is a risk that we all

must take.

Gerald

From: Nina <cipalmsbcglobal (DOT) net <mailto:cipalm% 40sbcglobal. net> >

Subject: Re: Hi, I'm new here

groups (DOT) com <mailto:% 40groups. com>

Date: Sunday, May 24, 2009, 8:21 PM

,

I would not give up on music totally. I just met someone the other day who's

profession involved music. I can't remember to what capacity, but whatever

it was, he is still able to do his work. He did say it took work to achieve

this. Myself, I have not achieved this. It's okay for me right not because

music is not my life's work, but I would like to be able to enjoy it again

someday.

I think it was who said to not give up, just maybe put it on the

backburner for now. I agree, never give up.

[Guest guest]

Hi ,

I played in the band for six years and was a big audiophile back in college.

I've had very good success with music with my CI. At first musice sounded

horrible, but I kept a radio tuned to music around me as much a possible. It

took months, but the results were worth it.

Best regards,

Jim

>

> Hi, my name is and I've been implanted since 2004. I got frustrated and

discouraged with the CI and stopped wearing my processor for a while. I was a

musician before I started losing my hearing and as some of you may know, music

is nothing more than noise with that processor and for someone who has made a

living in music it's really hard. Eventually, I gave up music too because I felt

that part of my life was over. I'm trying to wear the processor again and I'm

giving music another try as well. This time, I'm sure the two dont' mix and it's

time to let go of music, wear the processor and move on. I need to find a new

way to make a living. Problem is I'm nearly 50! Any advice on reinventing

myself?

>

[Guest guest]

I am a Nucleus user. I was implanted in 1987 with the N22 and reimplanted

in 2000 with the N24 as I needed an MRI and the first implants weren't MRI

compatible like they are now. Ruth

From: [mailto: ] On Behalf Of

Batman Catgirl

Sent: Tuesday, May 26, 2009 11:42 AM

Subject: Re: Hi, I'm new here

hi Ruth

May I know are you a ci user? which brand are you using.?

cheers

superstring

________________________________

From: Ruth Ilean Fox <rifox@... <mailto:rifox%40comcast.net> >

<mailto:%40>

Sent: Monday, 25 May 2009 8:09:59

Subject: RE: Hi, I'm new here

Hi Gerald and other music hopefuls,

Music listening does take work for most of us but in the end it is very

rewarding. The CI/Hearing aid combo has been found to be the surest way to

music appreciation. I don't have that option and am a unilateral CI and

enjoy music immensely, but it took a lot of practice, patience, and

endurance. Starting with the very simple and working to the complex is the

way to go with both Music and Speech. Cochlear has a rehab program called

Sound and (Way) Beyond that is very helpful towards that end. It has

simple to complex exercises in both speech and music. I also have a

article that I wrote years ago for publication 20 years ago and have updated

since, that outlines how I learned to hear both speech and music starting

from the point of Music, Speech and Noise sounding the same. I will be

willing to share that article with anyone that requests it at

rifoxcomcast (DOT) net.

Ruth

From: groups (DOT) com [mailto:groups (DOT) com] On Behalf Of

Gerald Gollinger

Sent: Sunday, May 24, 2009 9:31 PM

groups (DOT) com

Subject: Re: Hi, I'm new here

Dear and Nina,

I am awaiting for an appointment from a New Jersey hospital who

accepted my insurance for a hearing test. I have a social circle,

and I would like to hear the group speak. I think that would be a

reasonable expectation while music appreciation would not. In any case

my hearing aid Audie mentioned I still can enjoy music in my better right

ear. Hopefully, the recruitment, balance, vertigo, and tinnitus would

not be troublesome if I get a low score. It is a risk that we all

must take.

Gerald

From: Nina <cipalmsbcglobal (DOT) net <mailto:cipalm% 40sbcglobal. net> >

Subject: Re: Hi, I'm new here

groups (DOT) com <mailto:% 40groups. com>

Date: Sunday, May 24, 2009, 8:21 PM

,

I would not give up on music totally. I just met someone the other day who's

profession involved music. I can't remember to what capacity, but whatever

it was, he is still able to do his work. He did say it took work to achieve

this. Myself, I have not achieved this. It's okay for me right not because

music is not my life's work, but I would like to be able to enjoy it again

someday.

I think it was who said to not give up, just maybe put it on the

backburner for now. I agree, never give up.

[Guest guest]

Hello, My name is Marjorie and I have been off of sugar and candida culprit

foods now for three weeks today. Thank Goodness for this group. I have to admit

I have a lot of catching up to do on educating myself. I am doing my best

though and am really proud of myself so far. I can do this...

Okay, all was great until yesterday. I have been incompasitated for most of the

evening with one of the worst headaches I've ever had. But what really worries

me is I have boils in my armpits!!! Should I be running to the ER for an

emergency dose of antibiotics or is this part of the routine detox?

[Guest guest]

>

> Hello, My name is Marjorie and I have been off of sugar and candida culprit

foods now for three weeks today. Thank Goodness for this group. I have to admit

I have a lot of catching up to do on educating myself. I am doing my best

though and am really proud of myself so far. I can do this...

>

> Okay, all was great until yesterday. I have been incompasitated for most of

the evening with one of the worst headaches I've ever had. But what really

worries me is I have boils in my armpits!!! Should I be running to the ER for

an emergency dose of antibiotics or is this part of the routine detox?

+++Hi Marjorie. Welcome to our group. Headaches are usual die-off symptoms

since candida produces over 79 toxins, most of which are alcohol so that causes

headaches much like a hangover.

Boils are toxins coming out through the skin, so they are also die-off symptoms,

and starting on this program will mobilize toxins more.

You should be taking unrefined coconut oil as your only antifungal at this time,

so ensure you aren't taking too much - start with small amounts and gradually

increase them, otherwise you can get more severe die-off symptoms than are

necessary.

None of your symptoms would be caused by bacteria or a virus, so there is no

need for antibiotics anyway. In any case, there are so many natural antibiotics

that aren't poisonous like antibiotic drugs which also feed candida! Candida

feeds off of poisons, mercury, sugars, etc. so it is a life-saving mechanism by

Nature.

Do what you can to help your body detoxify, i.e. Epsom salt baths, coffee

enemas, dry skin brushing, etc. I suggest you help your boils by applying a

50/50 mixture of oil of oregano with olive on gauze and tape it on your boils

overnight - keep the gauze in a plastic bag in the fridge and replenish the oils

for using over and over.

All the best, Bee

[Guest guest]

Thank you for your quick response Bee. I love your advice and will go out and

get the oil this morning. I'm so relieved that this is normal, my friend had me

a little freaked out, said it could be a staff infection, and the last thing I

want to do of coarse is go on an antibiotic. What felt like defeat yesterday is

looking like a victory today. I know I'm not out of the woods yet, but I feel

much much better just knowing that I have your support. Thank you, Marjorie~

> >

> > Hello, My name is Marjorie and I have been off of sugar and candida culprit

foods now for three weeks today. Thank Goodness for this group. I have to admit

I have a lot of catching up to do on educating myself. I am doing my best

though and am really proud of myself so far. I can do this...

> >

> > Okay, all was great until yesterday. I have been incompasitated for most of

the evening with one of the worst headaches I've ever had. But what really

worries me is I have boils in my armpits!!! Should I be running to the ER for

an emergency dose of antibiotics or is this part of the routine detox?

>

> +++Hi Marjorie. Welcome to our group. Headaches are usual die-off symptoms

since candida produces over 79 toxins, most of which are alcohol so that causes

headaches much like a hangover.

>

> Boils are toxins coming out through the skin, so they are also die-off

symptoms, and starting on this program will mobilize toxins more.

>

> You should be taking unrefined coconut oil as your only antifungal at this

time, so ensure you aren't taking too much - start with small amounts and

gradually increase them, otherwise you can get more severe die-off symptoms than

are necessary.

>

> None of your symptoms would be caused by bacteria or a virus, so there is no

need for antibiotics anyway. In any case, there are so many natural antibiotics

that aren't poisonous like antibiotic drugs which also feed candida! Candida

feeds off of poisons, mercury, sugars, etc. so it is a life-saving mechanism by

Nature.

>

> Do what you can to help your body detoxify, i.e. Epsom salt baths, coffee

enemas, dry skin brushing, etc. I suggest you help your boils by applying a

50/50 mixture of oil of oregano with olive on gauze and tape it on your boils

overnight - keep the gauze in a plastic bag in the fridge and replenish the oils

for using over and over.

>

> All the best, Bee

>

[Guest guest]

>

> Thank you for your quick response Bee. I love your advice and will go out and

get the oil this morning. I'm so relieved that this is normal, my friend had me

a little freaked out, said it could be a staff infection, and the last thing I

want to do of coarse is go on an antibiotic. What felt like defeat yesterday is

looking like a victory today. I know I'm not out of the woods yet, but I feel

much much better just knowing that I have your support.

+++Marjorie, you are so very welcome my friend! Onward to victory!

Healing hugs, Bee