Guest guest Posted August 10, 2000 Report Share Posted August 10, 2000 My mom and grandma both have fibro mialgia. Just a little something else to add to our history! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 10, 2000 Report Share Posted August 10, 2000 A few other related conditions that should be noted here are Fibro Mialgia and Rheiters Syndrome. After discovering Skylers condition I found I was surrounded. My rommate has Rheiters, my best friend has Lupus, several ladies I know have Fibro Mialgia two neighbors have AOSD! Suddenly I was wondering how rare this condition(s) is(are). --- Aimee Moles <ssahm@...> wrote: <HR> <html><body> <tt> Thanks to all for the thoughts re: family plagues! & nbsp; I also appreciate <BR> the comment about early treatment. & nbsp; It is really easy to blow off <BR> early symptoms. & nbsp; In fact my doctor said that it can sputter along for <BR> years before becomming really noticable or even showing up in the <BR> blood work. & nbsp; <BR> <BR> What I know about Lupus is that it is different for everyone just <BR> like JRA. & nbsp; Some people have mild symptoms and some have a lot of <BR> trouble. & nbsp; My sis had had it since age 13. & nbsp; There are plenty of <BR> informative websites out there with good information in them.<BR> <BR> Aimee Moles (Karl's mom)<BR> <BR> </tt> <!-- |**|begin egp html banner|**| --> <hr> <!-- |@|begin eGroups banner|@| runid: 8193 crid: 4101 --> <a target= " _blank " href= " 1/8193/3/_/524922/_/965917737/ " ><center> <img width= " 468 " height= " 60 " border= " 0 " alt= " " src= " http://adimg./img/8193/3/_/524922/_/965917737/468x60_maze12k.gif\ " ></center><center><font color= " black " ></font></center></a> <!-- |@|end eGroups banner|@| --> <hr> <!-- |**|end egp html banner|**| --> <tt> For links to websites with JRA info visit: <BR> <a href= " http://www.geocities.com/Heartland/Village/8414/Links.html " >http://www.geo\ cities.com/Heartland/Village/8414/Links.html</a></tt> <br> </body></html> __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 17, 2000 Report Share Posted August 17, 2000 Question: About 4 years ago I was hospitalized over a supposed allergic reaction. It started with a rash on my forearm, thought was chicken pox -- ER said allergic reaction and gave me steriods and corto cream. Within 1 week I was swollen so badly, turning black/blur, ached everywhere, itching was uncontrollable, rash everywhere.....was immediately put in hospital. Docs pumped me full of steriods, took pictures for their educational files and thought I had lupus. Went to a specialist, found no proof of lupus. Technically docs are saying I had a severe allergic reaction to the antibiotic Cephaclor, but no real proof of that either. Then 1 week ago every morning I'd wake up itching with little pimple like bumps on me here and there. Nothing major and thought maybe spider bites. Then three days ago I woke up with a lot more little bumps and major itching. Went to doc yesterday, not regular doc and this one could have cared less. I told him even though I have no rash or swelling, the itching feels the same as 4 years ago. He gave me a corto shot and sent me home with a 6 day taper pack of steriods. He's tentatively thinking a reaction to stopping Macrobid (an antibiotic I was taking for 6 months for bladder infections) 5 days ago. I don't believe this because the original bumps started before I quit the Macrobid. The itching is driving me crazy. I'm taking Atarax to help keeps things at bay. Wondered if anyone can help lead me in the right direction....I know if I'm not better tomorrow, I'm going to try and see my allergist. Wondered if this is lupus still undiagnosed? Thanks, Sandi A. (Ashli's mom) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 17, 2000 Report Share Posted August 17, 2000 Sandi my mother in law has lupus and vasculitis and it took her a long time to be diagnosed. her bloodwork came back borderline her allergist said. Finally she went to a rheumy who did multiple different lupus test. Then she was diagnosed with both. Also she never had the lupus rash on her face. Only the vasculitis rash elsewhere on her body. Charlene(chychys mom) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 18, 2000 Report Share Posted August 18, 2000 Sandi this is very tricky the doctor thought melissa had lupus first before more testing showed JRA is the rash only on the joint area? melissa never has had a rash just swelling and pain but since your on atarax does this seem to help? a few years ago i had noticed my back was itching alot asked my hubby to see what was there he asked me where i had been cause my back was bad with a rash i went to the doctor who said i had a bad case of hives how in the world could it be hives lololol the doctor asked me a bunch of questions and confirmed it was hives gave me a nerve pill and said i would be ok i laughed it off it worked though but he said moms go and go and stress builds up and the body releases it but when it cant it will come out as hives its emotional lolol this one made my day when he said that nerves play a good part of a woman tragedy tramatic happenings arguements different things but if you have not used anything different on your clothes or rubbed up against anything different OR been out where chiggers are and the doctor said no lupus but prescribed a nerve pill ( atarax) it could be just hives but if this continues PLEASE go back to the doctor and MAKE him do something Robbin Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 23, 2000 Report Share Posted August 23, 2000 This sounds identical to what Skyler experienced at onset of JRA - Stills. He had these and other rashes, was treated for Fungal rash, Hives, Excema and Chicken pox. His stills rash was diagnosed as Eruthema Multiforma (a rash normally associated with Ebstein Bar disease) and he was quite the spectical at Phoenix childrens Hospital as these were so rare to see. We were given several topical ointments including steroids. The latter work the best but I am allways concerned about all the steroid uses. The little pimple like things still come around and sometimes do not go away until we physically break them. We are still not sure if he has or has not had chicken pox. [ & Skyler] --- mommytme@... wrote: <HR> <html><body> <tt> Question: & nbsp; About 4 years ago I was hospitalized over a supposed allergic <BR> reaction. & nbsp; It started with a rash on my forearm, thought was chicken pox -- <BR> ER said allergic reaction and gave me steriods and corto cream. & nbsp; Within 1 <BR> week I was swollen so badly, turning black/blur, ached everywhere, itching <BR> was uncontrollable, rash everywhere.....was immediately put in hospital. & nbsp; <BR> Docs pumped me full of steriods, took pictures for their educational files <BR> and thought I had lupus. & nbsp; Went to a specialist, found no proof of lupus. & nbsp; <BR> Technically docs are saying I had a severe allergic reaction to the <BR> antibiotic Cephaclor, but no real proof of that either.<BR> <BR> Then 1 week ago every morning I'd wake up itching with little pimple like <BR> bumps on me here and there. & nbsp; Nothing major and thought maybe spider bites. & nbsp; <BR> Then three days ago I woke up with a lot more little bumps and major itching. <BR> Went to doc yesterday, not regular doc and this one could have cared less. & nbsp; <BR> I told him even though I have no rash or swelling, the itching feels the same <BR> as 4 years ago. & nbsp; He gave me a corto shot and sent me home with a 6 day taper <BR> pack of steriods. & nbsp; He's tentatively thinking a reaction to stopping Macrobid <BR> (an antibiotic I was taking for 6 months for bladder infections) 5 days ago. & nbsp; <BR> I don't believe this because the original bumps started before I quit the <BR> Macrobid. & nbsp; The itching is driving me crazy. & nbsp; I'm taking Atarax to help keeps <BR> things at bay. & nbsp; <BR> <BR> Wondered if anyone can help lead me in the right direction....I know if I'm <BR> not better tomorrow, I'm going to try and see my allergist. & nbsp; Wondered if this <BR> is lupus still undiagnosed?<BR> <BR> Thanks,<BR> Sandi A. (Ashli's mom)<BR> </tt> <!-- |**|begin egp html banner|**| --> <hr> <!-- |@|begin eGroups banner|@| runid: 7752 crid: 3957 --> <a target= " _blank " href= " 1/7752/3/_/524922/_/966539818/ " ><center> <img width= " 468 " height= " 60 " border= " 0 " alt= " " src= " http://adimg./img/7752/3/_/524922/_/966539818/greenaria_new3.gif\ " ></center><center><font color= " black " ></font></center></a> <!-- |@|end eGroups banner|@| --> <hr> <!-- |**|end egp html banner|**| --> <tt> For links to websites with JRA info visit: <BR> <a href= " http://www.geocities.com/Heartland/Village/8414/Links.html " >http://www.geo\ cities.com/Heartland/Village/8414/Links.html</a></tt> <br> </body></html> __________________________________________________ Quote Link to comment Share on other sites More sharing options...
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