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Sharon, YOu have a wonderful time.... Just let us know when you are back...my

memory isn't so good. LOL Wish I was going to the coast....one of my

favorite places to be...

Will try my best to have a dull week just for you. LOL

hugs

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  • 2 months later...

I don't know who I'm supposed to contact, but one someone make me no mail until October 6th and then return me to receiving mail? Thanks, I really appreciate it. Sue Park

Re: New to group and to polychondritis

Hi Margaret,

So glad you found our group.

I also had RP for at least ten years before being DX.

I also have Fibromyalgia.

I took 1 mg of Folic Acid when I was on Methotrexate. It prevented me from getting mouth sores.

Who is treating you for the RP.?

I see a Rheumatologist, Pulmonologist, ENT and my PCP.

Feel free to ask questions, I know its hard to deal with at times.

When you need support we are here for you.

Hugs,

Sandy

Hi, I am new to this group, and so glad that I found it. I was diagnosed with relapsing polychondritis about 3 months ago, but after careful review have found that I have had symptoms for over 10 years--since I was 18. In addition, I was diagnosed with fibromyalgia. I am not doing so well coping. I have 4 small children 10, 8, 6 and 15 mo. I don't have any support from family, and because my husband is in the military, am new to an area and have no friends, no support system at all.I am so thankful for this group!!MargaretDISCLAIMER!!WE ARE NOT MEDICAL PROFESSIONALS, THEREFORE ANY INFORMATION THAT IS RECEIVED HERE IS FROM EXPERIENCE ONLY. PLEASE CONSULT WITH YOUR DOCTOR BEFORE TRYING ANYTHING THAT IS SUGGESTED. WE ARE NOT A SUBSTITUTE FOR YOUR PHYSICIAN AND ARE NOT TRYING TO BE. REMEMBER EVERYONE IS DIFFERENT AND TREATMENT MAYBE DIFFERENT FOR MANY OF US. THANK YOU

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I don't know who I'm supposed to contact, but one someone make me no mail until October 6th and then return me to receiving mail? Thanks, I really appreciate it. Sue Park

Re: New to group and to polychondritis

Hi Margaret,

So glad you found our group.

I also had RP for at least ten years before being DX.

I also have Fibromyalgia.

I took 1 mg of Folic Acid when I was on Methotrexate. It prevented me from getting mouth sores.

Who is treating you for the RP.?

I see a Rheumatologist, Pulmonologist, ENT and my PCP.

Feel free to ask questions, I know its hard to deal with at times.

When you need support we are here for you.

Hugs,

Sandy

Hi, I am new to this group, and so glad that I found it. I was diagnosed with relapsing polychondritis about 3 months ago, but after careful review have found that I have had symptoms for over 10 years--since I was 18. In addition, I was diagnosed with fibromyalgia. I am not doing so well coping. I have 4 small children 10, 8, 6 and 15 mo. I don't have any support from family, and because my husband is in the military, am new to an area and have no friends, no support system at all.I am so thankful for this group!!MargaretDISCLAIMER!!WE ARE NOT MEDICAL PROFESSIONALS, THEREFORE ANY INFORMATION THAT IS RECEIVED HERE IS FROM EXPERIENCE ONLY. PLEASE CONSULT WITH YOUR DOCTOR BEFORE TRYING ANYTHING THAT IS SUGGESTED. WE ARE NOT A SUBSTITUTE FOR YOUR PHYSICIAN AND ARE NOT TRYING TO BE. REMEMBER EVERYONE IS DIFFERENT AND TREATMENT MAYBE DIFFERENT FOR MANY OF US. THANK YOU

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In a message dated 9/19/01 8:06:35 PM Pacific Daylight Time, spark@...

writes:

<< I don't know who I'm supposed to contact, but one someone make me no mail

until October 6th and then return me to receiving mail? Thanks, I really

appreciate it. Sue Park

>>

Sue, I will put you on no mail til 10/6. But Please remind me when you get

back. LOL I don't think I can remember that long.... If you find no

posting.... just give a yell and I will put you back on... By the way......

did you at one time have an email address of sspark1? If you did, we still

have you listed under that name too... Do you want us to delete it?

Hope you are doing well... Will miss you while you are gone.

hugs

Clauidia

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In a message dated 9/19/01 8:06:35 PM Pacific Daylight Time, spark@...

writes:

<< I don't know who I'm supposed to contact, but one someone make me no mail

until October 6th and then return me to receiving mail? Thanks, I really

appreciate it. Sue Park

>>

Sue, I will put you on no mail til 10/6. But Please remind me when you get

back. LOL I don't think I can remember that long.... If you find no

posting.... just give a yell and I will put you back on... By the way......

did you at one time have an email address of sspark1? If you did, we still

have you listed under that name too... Do you want us to delete it?

Hope you are doing well... Will miss you while you are gone.

hugs

Clauidia

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  • 2 weeks later...
  • 1 year later...
  • 1 year later...

stay safe laura!!!

jodie c.

> Well, we stayed here and it looks like at the last report the EYE

is coming

> right through Orlando.. So, I know we will loose power and such..

I am

> taking down my computer tonight.. So I will go no mail on all my

groups till

> I can get back on....

>

>

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