tag:blogger.com,1999:blog-7633557036763388530.post3200587205444828114..comments2024-02-10T03:31:45.791-05:00Comments on JRA.... Journal of a Radical Arthritis Chick: The love/hate relationship with MethotrexateMalloryhttp://www.blogger.com/profile/01589044078041288717noreply@blogger.comBlogger10125tag:blogger.com,1999:blog-7633557036763388530.post-18471527422593768232022-08-31T00:49:52.945-04:002022-08-31T00:49:52.945-04:00d6j34u1v42 c3x02q1y20 q8q41n5y94 w0x30s4f28 r0... <a href="https://toughn77800.blogspot.com/" rel="nofollow"><strong>d6j34u1v42</strong></a> c3x02q1y20 <a href="https://thanough32576.blogspot.com/" rel="nofollow"><strong>q8q41n5y94</strong></a> w0x30s4f28 <a href="https://nesasheysh81766.blogspot.com/" rel="nofollow"><strong>r0t31u5r11</strong></a> r9h31h6b18rethehttps://www.blogger.com/profile/11753594297149149223noreply@blogger.comtag:blogger.com,1999:blog-7633557036763388530.post-2836232990193775092021-07-25T12:38:53.057-04:002021-07-25T12:38:53.057-04:00golden goose sale
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Just saw your blog when I typed in I ...Hi Mallory,<br /><br />Just saw your blog when I typed in I hate methotrexate. I stopped taking it about 4 months ago and I know I have to start taking it again. My whole body aches and I feel horrible. I have had RA since I was 10 and I am now 39. I have been on Enbrel for the last 10 years, I am now getting injection site reddness after ten years. I hate methotrexate I only take 6 mg... I am always sick on it and I hate the color but I think I rather feel good all over than worry about an upset stomach. I will not take prednisone. I have only taken that a couple times and I will not take it I would have to be really bad to take it. I pray for all of us who suffer this horrible illness.Anonymousnoreply@blogger.comtag:blogger.com,1999:blog-7633557036763388530.post-1045297449106660192011-08-11T15:10:11.718-04:002011-08-11T15:10:11.718-04:00Mallory...I just came across your blog & am SO...Mallory...I just came across your blog & am SO glad. I've had RA Since 2006, currently taking 25mg methotrexate & getting started on remicade soon. I'm hopeful that this will work! Thank you for your posts, they are greatly appreciated. :)Matchbox Momhttps://www.blogger.com/profile/03277774019952369200noreply@blogger.comtag:blogger.com,1999:blog-7633557036763388530.post-36937037826985150282011-06-22T08:37:43.508-04:002011-06-22T08:37:43.508-04:00The green printer - They did test me for Celiac Di...The green printer - They did test me for Celiac Disease, and I don't have it. I have an Endoscopy next week, so more waiting for me! I personally am not gluten free, but have heard stories from people who do and they feel somewhat of a difference. Thanks everyone who reads my blogs!Mallorynoreply@blogger.comtag:blogger.com,1999:blog-7633557036763388530.post-49172713089817089392011-06-15T00:30:56.781-04:002011-06-15T00:30:56.781-04:00Came across this randomly on Facebook...diagnosed ...Came across this randomly on Facebook...diagnosed ra, sjogrens syndrome and celiac disease.<br /><br />I live gluten free though I cannot tell a difference since I was gluten free prior to ra diagnosis. I would like to think it does.<br /><br />Mallory, I read your post of your digestive problems. Did they rule out celiac disease (another autoimmune sometimes presenting with ra)? Your symptoms sound too familiar... :(. Nothing's farfetched though since my sister also suffers from chrones/colitis.<br /><br />Living in autoimmune city here...the green printerhttps://www.blogger.com/profile/11776033890990101509noreply@blogger.comtag:blogger.com,1999:blog-7633557036763388530.post-21576514165610459942011-06-08T14:41:36.141-04:002011-06-08T14:41:36.141-04:00I was diagnosed with RA 3 years ago. I have been o...I was diagnosed with RA 3 years ago. I have been on Plaquenil since I was diagnosed and up until about 6 months ago, I was doing quite well on it. Now, the bones in my baby toes have eroded substantially and I'm in constant pain pretty much from every joint... especially my feet, hands, wrists and elbows.<br /><br />My doctor wants me to go on Metho and I am too scared to go on it.<br /><br />I have read stories of people following a gluten-free diet either alone or combined with vegan and they seem to have success stories. I know it's not a definite that it'll work but I'm giving it a shot. It's been a week and so far no change.<br /><br />Does anyone have experienc with this (gluten and/or vegan)?<br /><br />Wish you all well.<br /><br />TheresaTheresa's Kitchenhttps://www.blogger.com/profile/13498388546711581929noreply@blogger.comtag:blogger.com,1999:blog-7633557036763388530.post-11990326115340862442011-06-08T09:24:13.707-04:002011-06-08T09:24:13.707-04:00Let's hope the repeat addition of the metho wo...Let's hope the repeat addition of the metho works out for you. I was up to 25 mg tablets per week or thereabouts and had to stop it as I was too sick on the stuff. That was years ago.<br /><br />Amanda - I have been doing low dose pregnisone for years. First, be sure you are taking calcium w/ vit d in it as this med is known to possibly lead to brittle or thinning bones. Next, (I do 7.5 mg dialy: 5mg in the am and 2.5 in the pm/ this split was my magic bullet...did it years ago for the am pain problems), if you are doing the pregnisone for a short term burst, usually there are no long term side effects. If you are doing it for the long term...alot will depend on the dosage and how you handle the medication (meaning your body). As you probably know it can have many side effects (you can search the med online for those). So far for me personally no raised sugar levels, no moon face, no hump at the back of the neck, etc. etc. I do eat pretty healthy though and try to watch my weight although I could loose a few pounds. Hope this helps!Deb aka AbcsOfrahttps://www.blogger.com/profile/12619087592028571941noreply@blogger.comtag:blogger.com,1999:blog-7633557036763388530.post-62189599415123146282011-06-07T16:59:19.826-04:002011-06-07T16:59:19.826-04:00Hi : ) I just came across this on facebook. I was ...Hi : ) I just came across this on facebook. I was diagnosed with RA a little over a year ago. Last summer I was taking the pills, and I felt like I was dying. I couldn't eat, I couldn't get out of bed , and the headache was so bad that the ER couldn't get it to stay away longer than 30 minutes or LESS. Yesterday I did my 3rd injection, we're trying AGAIN! I'm also on Humira and prednisone, along with a nice list ; ( I'd be interested to hear from anyone that has been on Prednisone long term and what if any lasting side effects do they have/had? Thanks for posting this Mallory : )Amandahttps://www.blogger.com/profile/10263324098026022857noreply@blogger.com